plants Review The Genus Lagochilus (Lamiaceae): A Review of Its Diversity, Ethnobotany, Phytochemistry, and Pharmacology Nilufar Z. Mamadalieva 1,2, * , Davlat Kh. Akramov 1 , Ludger A. Wessjohann 2 , Hidayat Hussain 2 , Chunlin Long 3,4 , Komiljon Sh. Tojibaev 5 , Elham Alshammari 6 , Mohamed L. Ashour 7,8 and Michael Wink 9, * 1 2 3 4 5 6 7 8 9



 Citation: Mamadalieva, N.Z.; Akramov, D.K.; Wessjohann, L.A.; Hussain, H.; Long, C.; Tojibaev, K.S.; Alshammari, E.; Ashour, M.L.; Wink, M. The Genus Lagochilus (Lamiaceae): A Review of Its Diversity, Ethnobotany, Phytochemistry, and Pharmacology. Plants 2021, 10, 132. https://doi.org/10.3390/ plants10010132 Received: 26 November 2020 Accepted: 8 January 2021 Published: 11 January 2021 Publisher’s Note: MDPI stays neutral with regard to jurisdictional clai- * Institute of the Chemistry of Plant Substances of the Academy Sciences of Uzbekistan, Mirzo Ulugbek Str 77, Tashkent 100170, Uzbekistan; a.davlat@inbox.ru Department of Bioorganic Chemistry, Leibniz Institute of Plant Biochemistry, Weinberg 3, 06120 Halle (Saale), Germany; ludger.wessjohann@ipb-halle.de (L.A.W.); hidayat.hussain@ipb-halle.de (H.H.) College of Life and Environmental Sciences, Minzu University of China, Beijing 100081, China; long@mail.kib.ac.cn Key Laboratory of Ethnomedicine, Ministry of Education, Minzu University of China, Beijing 100081, China Institute of Botany of the Academy Sciences of Uzbekistan, Durmon Yuli Str 32, Tashkent 100125, Uzbekistan; ktojibaev@mail.ru Department of Pharmacy Practice, College of Pharmacy, Princess Nourah bint Abdulrahman University, Riyadh 11671, Saudi Arabia; ejalshammari@pnu.edu.sa Department of Pharmaceutical Sciences, Pharmacy Program, Batterjee Medical College, Jeddah 21442, Saudi Arabia; ashour@pharma.asu.edu.eg Department of Pharmacognosy, Faculty of Pharmacy, Ain Shams University, Cairo 11566, Egypt Department of Pharmaceutical Biology, Institute of Pharmacy and Molecular Biotechnology, Heidelberg University, 69120 Heidelberg, Germany Correspondence: nmamadalieva@yahoo.com (N.Z.M.); wink@uni-heidelberg.de (M.W.); Tel.: +49-6221-54-4880 (M.W.); Fax: +49-6221-54-4884 (M.W.) Abstract: The genus Lagochilus (Lamiaceae) is native to Central, South-Central, and Eastern Asia. It comprises 44 species, which have been commonly used as herbal medicines for the treatments of various ailments for thousands of years, especially in Asian countries. This review aims to summarize the chemical constituents and pharmacological activities of species from the genus Lagochilus to unveil opportunities for future research. In addition, we provide some information about their traditional uses, botany, and diversity. More than 150 secondary metabolites have been reported from Lagochilus, including diterpenes, flavonoids, phenolic compounds, triterpenoids, iridoid glycosides, lignans, steroids, alkaloids, polysaccharides, volatile, non-volatile and aromatic compounds, lipids, carbohydrates, minerals, vitamins, and other secondary metabolites. In vitro and in vivo pharmacological studies on the crude extracts, fractions, and isolated compounds from Lagochilus species showed hemostatic, antibacterial, anti-inflammatory, anti-allergic, cytotoxic, enzyme inhibitory, antispasmodic, hypotensive, sedative, psychoactive, and other activities. Keywords: Lagochilus; Lamiaceae; diversity; traditional medicine; phytochemistry; secondary metabolites; pharmacology; biological properties ms in published maps and institutional affiliations. 1. Introduction Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/). Terrestrial plants have been used for centuries as an endless well for supplying many medicinally important secondary metabolites that are used effectively in curing various ailments. They are considered as the milestone of all the traditional medicinal systems used throughout the whole world since antiquity. This fact attracted researchers in drug discovery to explore these plants frequently with the aim of finding new secondary metabolites or to validate the claimed ethnopharmacological uses. Family Lamiaceae (the mint family) is among the largest family that contains about 236 genera and 6900 to 7200 species. The family is famous for many of its widely used Plants 2021, 10, 132. https://doi.org/10.3390/plants10010132 https://www.mdpi.com/journal/plants Plants 2021, 10, 132 2 of 21 genera including Salvia, Scutellaria, Stachys, Plectranthus, Hyptis, Teucrium, Vitex, Thymus, and Nepeta. Members from the Lamiaceae are important ornamental, medicinal, and aromatic plants and have been used as traditional herbal medicines for thousands of years [1]. They are also used as culinary herbs, spices, and vegetables and as ingredients in cosmetics, hygienic products, and perfumes [2]. The genus Lagochilus is a small genus that comprises about 44 species that are native to Central, South-Central, and Eastern Asia [3,4]. It is highly drought-tolerant and is considered a typical mountain plant. Most of these species have been commonly used as herbal medicines for the treatment of various ailments for thousands of years, especially in Asian countries. Species of this genus exhibit various pharmacological effects, such as hemostatic, antispasmodic, and anti-edemic properties, and can be used against bleeding, coronary heart disease, chest pain, skin conditions, stomach pain, and as a tranquilizer. The most reported properties include relaxation, insomnia, dementia, euphoria, and subtle perceptual changes. Lagochilus is also used for the treatment of allergies and skin diseases [5–9]. Pharmacological studies indicated that mainly diterpenoids have hemostatic abilities [10,11]. Previous chemical instigations on the genus are limited due to the fact that many species are classified endangered, and the collection of these plants is not easy. However, this effort on the chemical profiling of the plants belonging to the genus led to the isolation and characterization of many diterpenes, flavonoids, iridoids, triterpenes, and polysaccharides. The diterpene lagochiline and its derivatives are among the promising hemostatic agents [5,7,10,11]. To the best of our knowledge, no reviews in the literature provide comprehensive insights into the medicinal uses and importance of Lagochilus plants. Although there is some work done about limited species that showed the very promising potential of the studied plants nevertheless, many other species of the genus remain untouched. Therefore, this review presented an effort to summarize all the up-to-date published data about the genus and provided comprehensive and condensed references dealing with all the required data about botanic characterization, distribution, traditional uses, primary and secondary metabolites, and pharmacological activities of the undiscovered genus Lagochilus. This review might shed light on the unseen genus that might attract researchers in drug discovery to find new compounds with promising biological potential. 2. Materials and Methods The literature for this review was collected by searching various scientific electronic databases, including GoogleScholar (https://scholar.google.com/), PubMed (https: //pubmed.ncbi.nlm.nih.gov/), SpringerLink (https://link.springer.com), SciFinder (https: //scifinder.cas.org/), ScienceDirect (https://www.sciencedirect.com/), and Web of Science (https://mjl.clarivate.com), via searching of these keywords: “Lagochilus and phytochemistry”, “Lagochilus and chemical compounds”, “Lagochilus and traditional uses”, and “Lagochilus and biological activity” in literature written in English, Russian, and Uzbek. Additional knowledge from other sources of literature was extracted (books, thesis). Altogether, about 94 references covering the isolation of phytoconstituents, as well as the diversity, traditional uses, and biological properties of the Lagochilus genus species from 1954 to 2020, were chosen unbiased to be reviewed in the work. The Plant List (http://www.theplantlist.org/), International Plant Name Index (https://ipni.org/), and Kew Botanical Garden Plant name (https://wcsp.science.kew.org/home.do) databases were used to validate the scientific name. The review is built on giving the general botanical characteristics of the genus, followed by distribution of the species worldwide and a compilation of the traditional uses. Then the chemical isolated secondary metabolites are reported in subclasses based on their chemical structures, and finally, the biological work was subcategorized based on uses. Plants 2021, 10, 132 3 of 21 3. Taxonomy and Botany Within the Lamiaceae family, Lagochilus belongs to the subfamily Lamioideae and tribe Leonureae Dumort [12]. Species of Lagochilus are subshrubs or perennial herbs (Figure 1). Rootstocks are woody. Stems are green-white, rigid, and sparsely hirsute. The leaf blade is rhombic, palmatipartite, or pinnatipartite, with lobes spinescent, sometimes subtending sterile spinescent bracteoles. Normally, 2–10 flowers grow vertically. The calyx is campanulate to tubular-campanulate, 5-veined; throat oblique, straight; teeth five, subequal or three posterior teeth longer, triangular to oblong or broadly ovate, usually longer than the tube, apex spinescent. Corolla is villous outside, pilose annulate inside, 2-lipped; upper lip oblong, straight, slightly concave, 2-lobed or 4-toothed; lower lip obliquely spreading, 3-lobed; middle lobe largest, obcordate, 2-lobulate; lateral lobes straight, acute, or emarginate. Stamens are four, exserted or sub included, anterior two longer; with filaments complanate; anther cells two, parallel or divergent, ciliate. Style is filiform, apex subequally 2-cleft. Nutlets are flattened-obconical, oblong–obovoid or oblong–ovoid, apex truncate or rounded, glandular, dusty hairy, scaly, or glabrous, smooth. Figure 1. Photograph for some Lagochilus species from Uzbekistan Flora (A): L. inebrians Bunge, (B): L. nevskii Knorring, (C): L. occultiflorus Rupr., (D): L. olgae Kamelin, (E): L. platycalyx Schrenk, (F): L. proskorjakovii Ikramov, (G): L. seravschanicus Knorring, (H): L. setulosus Vved., (I): L. vvedenskyi R. Kam. (Photos A, B, D, G are taken by Natalya Beshko, photos C, H are taken by Alim Gaziev, photo E is taken by Tulkin Tillaev, photos F, I are taken by Akbar Akhmedov). 4. Diversity The genus Lagochilus is mostly distributed on dry slopes, in valleys, and deserts from Iran to Mongolia, Russia (south Siberia), northwest China, north Pakistan [1] and has a distributional center in Tianshan Mountains and Central Asia. The results of the studies of Zhang et al. [3] showed that the Tianshan Mountains, especially the western Ili-Kirghizia Tianshan, as well as Sunggar and Kaschgar, were the ancestral area. The ancestral biome was mainly in the montane steppe zone of valley and slope at altitudes Plants 2021, 10, 132 4 of 21 of 1700 ± 2700 m above sea level, and the montane desert zone of foothill and fronthill at 800 ± 1700 m. The main center of diversity lies in Central Asia. According to Tskervanik [12], in world flora, there are 44 species that can be distinguished in Lagochilus. According to the taxonomy of this author, 34 species grow in the territory of the CIS (Commonwealth of Independent States). In the flora of Uzbekistan, this genus is represented by 18 species (Table 1) [13]. Taxa of the genus Lagochilus basically occur throughout the territory of Uzbekistan, starting from the deserts to Tian-Shan and Pamir-Alay mountain systems. The majority of species can be found in the Pamir-Alai Mountain, south-west of Tian-Shan and Turanian lowland [13]. Species from the genus Lagochilus belong to the most vulnerable plant species from the Lamiaceae family. Out of the existing 18 Lagochilus species in the flora of Uzbekistan, four are included in the Red Book of the Republic of Uzbekistan [14]: L. vvedenskyi, L. olgae, L. proskorjakovii, and L. inebrians. The main population of these species grows in Nuratau and Kyzylkum deserts. On the basis of occurrence, these Red List plant species belong to category I (disappearing) and II (rare species). In addition, the natural distribution of other species from this genus, such as L. gypsaceus and L. acutilobus, are also limited across the country [15]. In the territory of South Kazakhstan, 10 species of Lagochilus were found, and the areas of these species are located in Karatau, Karzhantau, and Aksu-Zhabagly [16]. In the Flora of China, there are 14 Lagochilus species distributed wildly in the northwest region. One of the species, L. ilicifolius, grows in the desert (sandy land) and steppe in northwestern China (Neimeng, Gansu, Shanxi, and Ningxia provinces), whereas the other 13 species are distributed mainly in the Xinjiang region [3,10,17]. The Flora of Iran comprises six species, and four of them (L. macranthus Fisch and C.A. Mey., L. quadridentatus Jamzad, L. lasiocalyx (Stapf) Jamzad, and L. aucheri Boiss.) are endemic to Iran [4,18,19]. Three species of Lagochilus are found in Mongolian flora, and they are widely distributed in the Khangai, Mongolian Altai, Middle Khalkha, Depression of Great Lakes, Valley of Lakes, East Gobi, Gobi-Altai, Transaltai Gobi, Alashan Gobi regions (Table 1) [20,21]. Table 1. Diversity and distribution of different Lagochilus species in Asia. Distribution Region Afghanistan western Himalaya China northwestern China, Xinjiang region (Ili Valley, the Karakoram and Altai Mountains) Iran Kazakhstan Karatau, Karzhantau, Aksu-Zhabagly Species Reference L. cabulicus Benth., L. cuneatus Benth., L. hindukushi Kamelin and Gubanov, L. schugnanicus Knorring L. ilicifolius Bunge ex Benth., L. grandiflorus C. Y. Wu and Hsuan, L. platyacanthus Rupr., L. kaschgaricus Ruprecht, L. diacanthophyllus (Pall.) Benth, L. hirtus Fisch. and C.A. Mey., L. bungei Benth., L. macrodontus Knorring, L. kaschgaricus Rupr., L. lanatonodus C.Y. Wu and S.J. Hsuan, L. leiacanthus Fisch. and C.A. Mey., L. pungens Schrenk, L. xianjiangensis G.J. Liu L. alutaceus Bunge., L. cabulicus Benth., L. macranthus Fisch and C.A. Mey., L. quadridentatus Jamzad, L. lasiocalyx (Stapf) Jamzad, L. aucheri Boiss. L. acutilobus (Ledeb.) Fisch. and C.A. Mey., L. bungei Benth., L. longidentatus Knorr., L. pulcher Knorr., L. taucumensis Zucker., L. inebrians Bunge, L. androsswii Knorr., L. leiacanthus Fisch. et Mey, L. pungens Schrenk, L. hirtus Fisch. et Mey, L. diacanthophillus Benth., L. kaschgaricus Rupr., L. knorringianus Pavlov, L. occultiflorus Rupr., L. platyacanthus Rupr., L. platycalyx Schrenk ex Fisch. and C.A. Mey, L. seravschanicus Knorring, L. setulosus Vved., L. subhispidus Knorring https: //wcsp.science.kew.org/ [3,10,17] https: //wcsp.science.kew.org/ [4,18,19] [16] https: //wcsp.science.kew.org/ Plants 2021, 10, 132 5 of 21 Table 1. Cont. Distribution Region Species Reference Kyrgyzstan Tian-Shan and Pamir Alai Mountains L. diacanthophyllus (Pall.) Benth, L. drobovii Kamelin and Tzukerv., L. hirsutissimus Vved, L. kaschgaricus Rupr., L. knorringianus Pavlov, L. occultiflorus Rupr., L. paulsenii Briq., L. platyacanthus Rupr., L. platycalyx Schrenk ex Fisch. and C.A. Mey, L. pubescens Vved., L. pulcher Knorring, L. schugnanicus Knorring, L. turkestanicus Knorring https: //wcsp.science.kew.org/ Mongolia Mongolian Altai and Khangai Mountains, Gobi regions L. bungei Benth., L. diacanthophyllus, L. ilicifolius Bge [20,21] Pakistan Western Pakistan https: //wcsp.science.kew.org/ Tajikistan Pamir-Alay Mountains L. cabulicus Benth., L. cuneatus Benth., L. schugnanicus Knorring L. botschantzevii Kamelin and Tzukerv., L. gypsaceus Vved., L. hirsutissimus Vved, L. inebrians Bunge, L. knorringianus Pavlov, L. kschtutensis Knorring, L. nevskii Knorring, L. paulsenii Briq., L. platyacanthus Rupr, L. platycalyx Schrenk ex Fisch. and C.A. Mey, L. pubescens Vved, L. schugnanicus Knorring, L. seravschanicus Knorring, L. turkestanicus Knorring L. balchanicus Czerniak., L. gypsaceus Vved., L. inebrians Bunge, L. cabulicus Benth. L. acutilobus (Ledeb.) Fisch. et C. A. Mey., L. botschantzevii Kamelin et Zukerv., L. diacanthophyllus (Pall.) Benth., L. gypsaceus Vved., L. hirsutissimus Vved., L. inebrians Bunge, L. knorringianus Pavlov, L. kschtutensis Knorr., L. nevskii Knorr., L. occultiflorus Rupr., L. olgae R. Kamelin, L. paulsenii Briq., L. pubescens Vved., L. platyacanthus Rupr., L. setulosus Vved., L. platycalyx Schrenk, L. seravschanicus Knorr., L. vvedenskyi R. Kam. et Zucker. Turkmenistan Uzbekistan Nuratau and Kyzylkum deserts, Tian-Shan and Pamir-Alay Mountains https: //wcsp.science.kew.org/ https: //wcsp.science.kew.org/ [13,15] 5. Traditional Uses The traditional use of Lagochilus plants dates back centuries. L. inebrians is commonly known as Inebriating Mint, Intoxicating Mint, Turkistan Mint, or Intoxicating Hare’s Lip. The name L. inebrians is derived from the Greek words “lagos” and “cheilos”, literally meaning “hare” and “lip/cheek” and “inebrians”, meaning intoxicating, thus translating to “intoxicating hare’s lip” (Wikipedia). A decoction of herb and roots of Lagochilus species are used in folk medicine as a styptic and also against skin conditions, stomach pain, and as tranquilizers. Many species of the Lagochilus genus have been used in traditional medicine to treat hemorrhages and inflammation [8,9]. The most commonly reported effects include relaxation, euphoria, and subtle perceptual changes. It is also used for the treatment of allergies and skin diseases. In Central Asia, L. inebrians has been used during celebrations for its intoxicating and sedative effects [22]. People make infusions with the dried leaves of L. inebrians; honey and sugar are often added to this drink to reduce its bitter taste. A summary of their traditional use is presented in Table 2. Plants 2021, 10, 132 6 of 21 Table 2. Ethnomedicinal uses of different Lagochilus species and the used parts. Species Country Parts Used Traditional Uses Reference L. cabulicus Iran aerial parts [23,24] L. gypsaceus Uzbekistan aerial parts L. hirtus Xinjiang, China whole plant L. ilicifolius Ningxia, China whole plant L. inebrians Uzbekistan L. lanatonodus L. leiacanthus L. platycalyx L. platyacanthus Xinjiang, China Xinjiang, China Uzbekistan leaves, stems, fruits, inflorescences aerial parts whole plant leaves Xinjiang, China whole plant for animals with lung trouble hemostatic, sedative effect, decrease in blood pressure, hemorrhage (traumatic, uterine, hemorrhoidal, pulmonary, lung, and nasal), hemophilia styptic, antihemorrhagic, coronary heart diseases, angina pectoris, ulcer, insomnia, amnesia hemostatic, inflammation, ulcer, hemostasis, spasm, anti-edema, coronary heart disease, angina pectoris, insomnia, dementia antihemorrhagic, allergic dermatosis, skin illnesses, stomach pain, tranquillizer, intoxicating effect, sedative antihemorrhagic, against allergic dermatosis hemostatic, inflammation, ulcer sedative and hypotensive action antihemorrhagic, coronary heart diseases, angina pectoris, ulcer, insomnia, and amnesia [9,25] [10,26] [5–7] [5,8,9] [6,7,27] [28] [29] [10,26] 6. Phytochemical Studies Phytochemical studies performed on different Lagochilus species have demonstrated the occurrence of several classes of primary and secondary metabolites. A literature survey revealed that the genus Lagochilus is a rich source of diterpenoids [30–33], flavonoids [29,34], phenolic compounds, triterpenoids [34], iridoid glycosides, lignans, steroids, alkaloids, polysaccharides [35], volatile, non-volatile and aromatic compounds, lipids, carbohydrates, minerals, vitamins, and others. About 150 secondary metabolites have been reported from all previous classes in the genus. Among these compounds, diterpenoids have been considered as useful taxonomic markers and the major active components of Lagochilus species. In the following section (Table 3), we will summarize the reported natural products isolated from each species. Out of 44 species presented in the genus, only 19 species have been phytochemically explored. Therefore, the genus still holds more than half of its species unseen by researchers. Table 3. Chemical profiling of the isolated compounds from each Lagochilus species. Species Compounds References L. aucheri germacrene D (107), α-pinene (108), β-bourbonene (109) tricetin 3’-methylether (39), quercetin (40), quercetin 3-O-α-L-rhamnopyranosyl (1→6) β-D-glucopyranoside (41), quercetin 3-O-β-D-glucopyranoside (42), α-pinene (108), β-springene (110), geranyllinalool (111), sitosteryl acetate (122), stigmasteryl acetate (124), lupeol (126) lagochilin (1), lagochirsine (16), 7- cinnamoyllamalbide (106), 5-hydroxy-7,4′ -dimethoxyflavone (48), daucosterol (125), β-sitosterol (121), 8-acetylharpagide (99) lagochilin (1), lagohirzidin (19), di-O-acetyllagohirsin (18) [33], lagochirzin, mono- and diacetyllagochirsins (16–18) [37,39], stachydrine (127), tannins (2.0–3.3%), coumarins (0.3–2.5%), lipids (4.25–8.30%) [41], diterpenoid lactone quercetin (40), rutin (43), myricetin (44), isoquercitrin (45), kaempferol-3-O-rutinoside (46), kaempferol-3-O-β-D-(6”-O-p-coumaryl) glycoside (47), (+)-syringaresinol (138), scopoletin (150), 8-O-acetylharpagide (99), harpagide (100), ajugoside (101), ajujol (102), geniposidic acid (103), mussaenosidic acid (104) and 8-deoxyshanzhiside (105), phytol (142), 12-hentriacontanol (143), octacosanol (144), citrusin C (94), 4-(1E)-hydroxy-1-prophenyl)-2-methoxyphenol (95), 4-acetoxycinnamic acid (96), 3-methyl-1,2,3,4-tetrahydroquinoline (128), 4-hydroxyisoquinoline (129), songoramine (130), songorine (131), erythro-1-[(4-O-β-D-glucopyranosyl-3-methoxyl)phenyl]-2-[(5’-methoxyl)-pinoresinol]-propane-1,3-diol (132), tortoside C (133), sisymbrifolin (134) [18] L. cabulicus L. gypsaceus L. hirsutissimus L. ilicifolius [24,36] [37–40] [41–43] [5–7,21] Plants 2021, 10, 132 7 of 21 Table 3. Cont. Species L. inebrians L. kotschyanus L. lanatonodus L. leiacanthus L. macranthus L. occultiflorus L. olgae L. platyacanthus L. platycalyx L. proskorjacovii L. pubescens L. setulosus L. usunachmaticus L. zeravschanicus Compounds lagochilin (1), lagochilin and its mono-, di-, tetraacetates (1–15), vulgarol and its acetate (37–38), 5-hydroxy-4’,7-dimethoxyflavone (48), β-sitosterol (121), nonacosane (139), hentriacontane (140), tritriacontane (141), 8-O-acetylharpagide (99), harpagide (100), stachydrine (127) α-pinene (108), myrcene (115), β-caryophyllene (116) acetovanillone (72), androsin (97), neolloydosin (98), erythrodiol (118), β-sitosterol (121), dacosyl ester (145), scopoletin (150) 15-demethoxyscupolin I (35), scupolin I (36), 5,2’,6’-trihydroxy-7,8-dimethoxyflavanone (49), 5,2’,6’-trihydroxy-6,7,8-trimethoxyflavanone (50), 5,2’,6’-trihydroxy-7,8-dimethoxyflavanone-2’-O-β-D-glucoside (51), 5,2’-dihydroxy-7,8,6’-trimethoxyflavanone (53), 5,2’-dihydroxy-6,7,8,6’-tetramethoxyflavanone (54), pinocembrin (55), oroxylin A (56), chrysin (57), 5,6-dihydroxy-7,8-dimethoxyflavone (58), isoscutellarein-8-methyl ester (59), apigenin (60), hispidulin (61), 5,2’-dihydroxy- 6,7,8-trimethoxyflavone (62), skullcapflavone I (63), 5,8- dihydroxy-7,2’-dimethoxyflavone (64), 5,2’,6’-trihydroxy6,7,8-trimethoxyflavone (65), 5,7,2’-trihydroxy-8,6’-dimethoxyflavone (66), 5,6,2’-trihydroxy-7,8,6’-trimethoxyflavone (67), neobaicalein (68), rivularin (69), oleanolic acid (118), ursolic acid (119), vanillin (70), p-hydroxyacetophenone (71), acetovanillone (72), dihydroxyskullcapflavanone I (73), wogonin (74), liquiritin (75), viscidulin II 2’-O-glucoside (76), 5,2’,6’-trihydroxy-6,7,8- trimethoxyflavone 2’-O-glucoside (77) caryophyllene oxide (112), humulene epoxide II (113), viridiflorol (114) laballenic (146), octadeca -5,8-dienoic (147), eicos -11-enoic (148) and eicosa-9,11-dienoic acids (149) lagochirsine (16) lagoditerpenes A-E (20–24), (13E)-labd-l3-ene-8α,15-diol (25), leojaponins B (26), leoheteronin D (27), enantioagathic acid (28), isocupressic acid (29), 7β,13 S-dihydroxylabda-8 (17),14-dien-19-oic acid (30), 8α,13(R),14(S/R),15-tetrahydroxylabdane (31), 15-nor-14-oxolabda-8(17),12E-diene-18-oic acid (32), 12β,19-dihydroxymanoyl oxide (33), ent-12α,19-dihydroxy-13-epi-manoyl oxide (34) (Zhang et al. 2015), rutin (43), apigenin (60), apigenin-7,4’-dimethylether (78), acacetin (79), luteolin-7,3’,4’-trimethyl ether (80), luteolin-7,4’-dimethyl ether (81), diosmetin (82), chrysoeriol (83), quercetin-3-O-rutinoside-7-O-glucoside (84), horridin (85), apigenin-6,8-di-C-β-D-glucopyranoside (86), isorhamnetin-3-O-rutinoside (87), isorhamnetin-3-O-robinobioside (88), isorhamnetin-3-O-β-D-glucoside (89), isorhamnetin-3-O-rutinoside-4’-O-glucoside (90), lavandulifolioside (91), 8-O-acetylharpagide (99), geniposidic acid (103), 1-(4-hydroxy-3-methoxy)-phenyl-2-[4-(1,2,3-trihydroxypropyl)-2-methoxy]-phenoxy1,3-propandiol (135), (+)-isolarisiresinol 3-α-O-β-D-glucopyranoside (136), (-)-isolarisiresinol 3-α-O-β-D-glucopyranoside (137) quercetin (40), rutin (43), myricetin (44), kaemferol (92), 8-O-acetylharpagide (99), harpagide (100), stachydrine (127) lagochilin (1), tetraacetyllagochilin (10), 5-hydroxy-4’,7-dimethoxyflavone (48), 5,7-dihydroxy-3,4’-dimethoxyflavone (93), β-sitosterol (121), nonacosane (139) 15-mono-O-acetyllagochilin (3), 16-mono-O-acetyllagochilin (4), 3,18-di-O-acetyllagochilin (5), 15,16-di-O-acetyllagochilin (6), 3,15,18-tri-O-acetyllagochilin (7), 3,16,18-tri-O-acetyllagochilin (8), 15,16,18-tri-O-acetyllagochilin (9), tetraacetyllagochilin (10), 3,18-O-isopropylidenelagochilin-15-acetate (12), 3,18-O-isopropylidenelagochilin-15,16-diacetate (14), lagochilin (1), di-O-isopropylidenelagochilins (5–6), 3,18-O-isopropylidenelagochilin (11), 16-O-acetyl-3,18-O-isopropylidenelagochilin (13), di-O-acetyl-3,18-O-isopropylidenelagochilin (15), lagochilin (1), 3,18-O-isopropylidenelagochilin (11), 5-hydroxy-4’,7-dimethoxyflavone (48), β-sitosterol (121), nonacosane (139), stachydrine (127) lagochilin (1), 8-O-acetylharpagide (99), harpagide (100), lagochirsine (16), stachydrine (127), ascorbic acid (151), β-carotene (152) carbohydrates, polysaccharides, pectin, hemicellulose polysaccharides, pectins, hemicelluloses References [32,37,40,44–55] [19] [27] [28] [56] [57] [37] [58] [29,42,52,53,59] [12,60,61] [30,31,53,60,62] [37,39,52–54,63] [64,65] [35,64] Plants 2021, 10, 132 8 of 21 In the following part, we will classify the isolated compounds from the species based on their chemical structures. The most relevant citation about the isolation and characterization of these secondary metabolites will be given and highlighted. 6.1. Diterpenes Diterpenes are the most characteristic and important phytochemicals in Lagochilus, the highest numbers of which were reported in L. inebrians [48], L. pubescens [60], and L. platyacanthus [26] (Table 4, Figure S1). Lagochilin (1) is the main component of the total extractive substances of many species of the genus. Lagochilin (1) identified in L. inebrians, L. setulosus, L. gypsaceus [37], L. hirsutissimus [33], L. proskorjacovii [61], and L. pubescens [62]. L. inebrians gathered in Samarkand province contained 2.3% lagochilin, L. setulosus gathered in Chimkent province 1.1%, and L. gypsaceus gathered in Kashkadar’ya province 2.1% [66]. Lagochirsine (16) is found free in the three plant species L. hirsutissimus, L. setulosus, and L. gypsaceus. However, its content in these plants was 0.2–0.3% [39]. Table 4. The isolated diterpenes of Lagochilus species as described in the literature. Identified Compounds Lagochilin (1) 3-Mono-O-acetyllagochilin (2) 15-Mono-O-acetyllagochilin (3) 16-Mono-O-acetyllagochilin (4) 3,18-di-O-Acetyllagochilin (5) 15,16-di-O-Acetyllagochilin (6) 3,15,18-tri-O-Acetyllagochilin (7) 3,16,18-tri-O-Acetyllagochilin (8) 15,16,18-tri-O-Acetyllagochilin (9) tetra-Acetyllagochilin (10) 3,18-O-Isopropylidene-lagochilin (11) 3,18-O-Isopropylidene-lagochilin-15-acetate (12) 16-O-Acetyl-3,18-O-isopropylidene-lagochilin (13) 3,18-O-Isopropylidene-lagochilin-15,16-diacetate (14) di-O-Acetyl-3,18-O-isopropylidene-lagochilin (15) Lagochirsine (16) O-Acetyl-lagohirsin (17) di-O-Acetyl-lagohirsin (18) Lagohirzidin (19) Lagoditerpenes A (20) Lagoditerpenes B (21) Lagoditerpenes C (22) Lagoditerpenes D (23) Lagoditerpenes E (24) (13E)-Labd-l3-ene-8α,15-diol (25) Leojaponins B (26) Leoheteronin D (27) Enantioagathic acid (28) Isocupressic acid (29) 7β,13 S-Dihydroxylabda-8 (17),14-dien-19-oic acid (30) 8α,13(R),14(S/R),15-Tetrahydroxylabdane (31) 15-Nor-14-oxolabda-8(17),12E-diene-18-oic acid (32) 12β,19-Dihydroxymanoyl oxide (33) ent-12α,19-Dihydroxy-13-epi-manoyl oxide (34) 15-Demethoxyscupolin I (35) Scupolin I (36) Vulgarol (37) Vulgarol acetate (38) Sources L. gypsaceus, L. inebrians, L. setulosus, L. pubescens, L. proskorjacovii, L. hirsutissimus L. inebrians L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens, L. proskorjacovii L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. inebrians, L. pubescens L. hirsutissimus, L. setulosus, L. gypsaceus, L. olgae L. hirsutissimus L. hirsutissimus L. hirsutissimus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. leiacanthus L. leiacanthus L. inebrians L. inebrians Reference [12,30,32,37,38,41,44– 49,60,61,63] [12,30,32,37,38,41,44–49,60–63] [32,44–49,60] [32,44–49,60] [31,32,44–49,60,62] [31,32,44–49,60,62] [32,44–49,60] [32,44–49,60] [32,44–49,60] [12,32,44–49,60,61] [30–32,44–49,60,62] [30–32,44–49,60,62] [30–32,44–49,60,62] [30–32,44–49,60,62] [30–32,44–49,60,62] [37,39] [37,39] [33,37,39] [33] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [26] [28] [26] [44,45,47] [44,45,47] Plants 2021, 10, 132 9 of 21 6.2. Flavonoids and Phenolic Glycosides Lagochilus species are characterized by rich biological activities, such as antioxidant, anti-allergic, and enzyme inhibitory activities due in part to the presence of a diversity of flavonoids and phenolic compounds [21,27–29,40,50,58]. Flavonoids accumulate in different plant parts of the Lagochilus species. It is believed that most flavonoids in the Lagochilus are derivatives of quercetin, luteolin, and kaempferol. To date, about 60 flavonoids have been identified in Lagochilus. The structural formulas of major flavonoids and their glycosides isolated or identified from raw materials of Lagochilus species are shown in Table 5 and Figure S2. Table 5. The isolated phenylpropanoids of Lagochilus species described in the literature. Identified compounds Sources Reference Tricetin 3’-methylether (39) L. cabulicus Quercetin (40) L. cabulicus, L. ilicifolius, L. platycalyx Quercetin 3-O-α-L-rhamnopyranosyl (1→6)-β-D-glucopyranoside (41) Quercetin 3-O-β-D-glucopyranoside (42) L. cabulicus L. cabulicus L. ilicifolius, L. platyacanthus, L. platycalyx L. ilicifolius, L. platycalyx L. ilicifolius L. ilicifolius L. ilicifolius L. gypsaceus L. inebrians L. proskorjacovii, L. pubescens L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus, L. platyacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus, L. lanatonodus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. leiacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus [23,36] [7,23,29,36, 59] [23,36] [23,36] Rutin (43) Myricetin (44) Isoquercitrin (45) Kaempferol-3-O-rutinoside (46) Kaempferol-3-O-β-D-(6”-O-p-coumaryl) glycoside (47) 5-Hydroxy-4’,7-dimethoxyflavone (48) 5,2’,6’-Trihydroxy-7,8-dimethoxyflavanone (49) 5,2’,6’-Trihydroxy-6,7,8-trimethoxyflavanone (50) 5,2’,6’-Trihydroxy-7,8-dimethoxyflavanone-2’-O-β-D-glucoside (51) 5,2’,6’-Trihydroxy-6,7,8-trimethoxyflavanone-2’-O-β-D-glucoside (52) 5,2’-Dihydroxy-7,8,6’-trimethoxyflavanone (53) 5,2’-Dihydroxy-6,7,8,6’-tetramethoxyflavanone (54) Pinocembrin (55) Oroxylin A (56) Chrysin (57) 5,6-Dihydroxy-7,8-dimethoxyflavone (58) Isoscutellarein-8-methyl ester (59) Apigenin (60) Hispidulin (61) 5,2’-Dihydroxy-6,7,8-trimethoxyflavone (62) Skullcapflavone I (63) 5,8- Dihydroxy-7,2’-dimethoxyflavone (64) 5,2’,6’-Trihydroxy- 6,7,8-trimethoxyflavone (65) 5,7,2’-Trihydroxy-8,6’-dimethoxyflavone (66) 5,6,2’-Trihydroxy-7,8,6’-trimethoxyflavone (67) Neobaicalein (68) Rivularin (69) Vanillin (70) p-Hydroxyacetophenone (71) Acetovanillone (72) Dihydroxyskullcapflavanone I (73) Wogonin (74) Liquiritin (75) Viscidulin II 2’-O-glucoside (76) 5,2’,6’-Trihydroxy-6,7,8- trimethoxyflavone 2’-O-glucoside (77) Apigenin-7,4’-dimethylether (78) Acacetin (79) Luteolin-7,3’,4’-trimethyl ether (80) Luteolin-7,4’-dimethyl ether (81) Diosmetin (82) [7,29,58,59] [7,29,59] [7] [7] [7] [12,30,50,51, 60,61] [28] [28] [28] [28] [28] [28] [28] [28] [28] [28] [28] [28,58] [28] [28] [28] [28] [28] [28] [28] [28] [28] [28] [28] [27,28] [28] [28] [28] [28] [28] [58] [58] [58] [58] [58] Plants 2021, 10, 132 10 of 21 Table 5. Cont. Identified compounds Sources Reference Chrysoeriol (83) Quercetin-3-O-rutinoside-7-O-glucoside (84) Horridin (85) Apigenin-6,8-di-C-β-D-glucopyranoside (86) Isorhamnetin-3-O-rutinoside (87) Isorhamnetin-3-O-robinobioside (88) Isorhamnetin-3-O-β-D-glucoside (89) Isorhamnetin-3-O-rutinoside-4’-O-glucoside (90) Lavandulifolioside (91) Kaemferol (92) 5,7-Dihydroxy-3,4’-dimethoxyflavone (93) Citrusin C (94) 4-(1E)-Hydroxy-1-prophenyl)-2-methoxyphenol (95) 4-Acetoxycinnamic acid (96) Androsin (97) Neolloydosin (98) L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platyacanthus L. platycalyx L. pubescens L. ilicifolius L. ilicifolius L. ilicifolius L. lanatonodus L. lanatonodus [58] [58] [58] [58] [58] [58] [58] [58] [58] [29,59] [12,30,60,61] [5,21] [5,21] [5,21] [27] [27] 6.3. Iridoids and Their Glycosides Iridoids are a type of monoterpenoids in the general form of cyclopentanopyran and are found in a wide variety of plants as glucosides. 8-O-Acetylharpagide (99) and harpagide (100) are common iridoids in Lagochilus [6,50,52]. The latest results of our investigations showed that L. inebrians and L. gypcaseus are rich for 8-O-acetylharpagide [40,50]. However, only a few (seven) iridoids could be reported in the genus. From the aerial parts of L. ilicifolius ajugoside (101), ajugol (102), geniposidic acid (103), mussaenosidic acid (104), and 8-deoxyshanzhiside (105) were identified and isolated [5,58] (Table 3, Figure S3). 6.4. Essential Oils The species of Lagochilus are aromatic with a pleasant scent. Germacrene D (107), αpinene (108), and β-bourbonene (109) are the main components of the oil of L. aucheri [18]. In the oil of L. cabulicus α-pinene (108), β-springene (110), and geranyllinalool (111) are major compounds [23]. The oil of L. macranthus mainly contains the oxygenated sesquiterpenes caryophyllene oxide (112), humulene epoxide II (113), and viridiflorol (114) [56]. The major constituents of L. kotschyanus appear to be α-pinene (108), myrcene (115), and βcaryophyllene (116), respectively [19]. In the oil of L. diacanthophyllus, the main components are α-pinene (108) and dillapiol (117) [67,68]. The chemical composition of three Lagochilus species essential oils: L. gypsaceus, L. inebrians, and L. setulosus, were determined using the GC-MS method [69]. The results showed that the studied essential oils are made up mainly of linalool, β-ionone, trans-chrysanthenyl acetate, α-terpineol for L. gypsaceus; transchrysanthenyl acetate, eugenol, trans-verbenol, bicyclo [3.1.1]hept-3-en-2-one, pinocarvone for L. inebrians; and finally 2,4-bis(1,1-dimethylethyl)phenol, bicyclo[3.1.1]hept-2-en-4-ol, hexadecanoic acid, limonene, 2-hexenal for L. setulosus. Our results indicated that limonene, furfural, benzaldehyde, 4-terpineol, myrtenal, α-terpineol, myrtenol, and p-cymen-7-ol are the common compounds to these species. Monoterpens linalool, trans-chrysanthenyl acetate, α-terpineol, eugenol have been reported as the most abundant compounds in the oil of L. gypsaceus and L. inebrians, while L. setulosus oil consists of aliphatic alcohol, aldehyde, and ketons. Especially, oxygenated monoterpenes trans-chrysanthenyl acetate and eugenol were found for the first time in substantial amounts in the oil from L. gypsaceus and L. inebrians. A comparison of our studies confirms that the dissimilarities in the composition of the essential oils of three Lagochilus species may be considered as an indication of several chemotypes existing within the genus (Table 3, Figure S4). Plants 2021, 10, 132 11 of 21 6.5. Triterpenes Plant triterpenoids represent a large and structurally diverse class of natural products. However, they represent a minor class of compounds reported from Lagochilus species. Only erythrodiol (118) from L. lanatonodus [27], oleanolic (119), and ursolic acid (120) from L. leiacanthus [28] were isolated (Table 3, Figure S5). 6.6. Steroids Plant steroids are a diverse group of secondary metabolites. Up to now, phytochemical studies have afforded six steroids from the Lagochilus genus, which sitosteryl acetate (122), stigmasteryl acetate (124), lupeol (126) from L. cabulicus [23,36] (Table 3, Figure S6). L. gypsaceus afforded daucosterol (125) and β-sitosterol (121) [40]. β-Sitosterol (121), stigmasterol (123), and daucosterol (125) were isolated from L. inebrians [50]. β-Sitosterol (121) was identified in L. lanatonodus and L. pubescens [12,27,30,51,60,61]. 6.7. Alkaloids Alkaloids are a group of important secondary metabolites. Alkaloids and extracts of alkaloid-containing plants have been used throughout human history as remedies, poisons, and psychoactive drugs. Stachydrine has been identified in many Lamiaceae species [53,54]. Multiple studies have confirmed that stachydrine has strong neuroprotective, anti-fibrotic, and anti-inflammatory effects [70]. Stachydrine (127) was reported in L. inebrians and L. hirsutissimus [42,54,63]. 3-Methyl-1,2,3,4-tetrahydroquinoline (128), 4-hydroxyisoquinoline (129), songoramine (130), and songorine (131) were determined from L. ilicifolius [21] (Table 3, Figure S7). 6.8. Lignans The lignans are fiber-associated compounds found in plants, particularly seeds, nuts, grains, and vegetables. Lignans are rare in the Lagochilus genus, with only three lignans named erythro-1-[(4-O-β-D-glucopyranosyl-3-methoxyl)- phenyl]-2-[(5’-methoxyl)pinoresinol]-propane-1,3-diol (132), tortoside C (133), and sisymbrifolin (134) isolated from L. ilicifolius [7] (Table 3, Figure S8). Another three lignans: 1-(4-hydroxy-3-methoxy)phenyl-2-[4-(1, 2, 3-trihydroxypropyl)-2-methoxy]-phenoxy- 1, 3-propandiol (135), (+)isolarisiresinol 3-α-O-β-D-glucopyranoside (136), and (-)-isolarisiresinol 3-α-O-β-Dglucopyranoside (137) were isolated from whole herb of L. platyacanthus [58]. From L. ilicifolius (+)-syringaresinol (138) was identified by Qian et al. [7]. 6.9. Aliphatic Alkanes and Alcohols Plants have an outer surface layer of wax, which is usually a complex mixture of aliphatic lipid compounds, such as straight and branched chain alkanes, alkenes, long-chain fatty acids and esters, long-chain fatty alcohols, long-chain fatty aldehydes, and ketones. Nonacosane (139) (in L. inebrians, L. proskorjacovii, L. pubescens) [12,51,60,61], hentriacontane (140), tritriacontane (141) (in L. inebrians) [51], phytol (142), 12-hentriacontanol (143), and octacosanol (144) (in L. ilicifolius) [5], dacosyl ester (145) (in L. lanatonodus) [27] are present in Lagochilus species (Table 3, Figure S9). 6.10. Lipids In plants, lipids play especially important roles as signaling and energy storage compounds [55]. Lipid compounds were identified and analyzed in Lagochilus species by some researchers [41,55,57]. Laballenic (146), octadeca -5,8-dienoic (147), eicos -11enoic (148), and eicosa-9,11-dienoic acids (149) were detected in L. occultifloris [57] (Table 3, Figure S10). Free and polar lipids from ripe seeds of L. inebrians were investigated by Yuldasheva et al. [55], and the findings showed that seeds have a very high percentage of oil content, a large fraction of unsaturated ω-3 and ω-6 fatty acids. Plants 2021, 10, 132 12 of 21 6.11. Miscellaneous Compounds Some other metabolites were also discovered in this genus, such as scopoletin (150) [7,27,41], ascorbic acid (151), β-caroten (152) [63] (Figure S11). The following class of metabolites were identified in Lagochilus species: carbohydrates [35,64], sugars [63], polysaccharides, pectin, hemicellulose [64,65,71], tannins [63], organic acids, resins [63], and microelements [63,72,73]. 7. Biological Activities The biological activities, including hemostatic, antibacterial, anti-inflammatory, antiallergic, cytotoxic, enzyme inhibitory, antispasmodic, sedative, hypotensive, psychoactive, and other activities, have been reported in some publications. Different biological activities have been reported from the extracts, fractions, essential oils, and their isolated compounds. Mostly, Lagochilus species have been used as a folk medicine for treating hemostatic [10,11,25,35,39,58,64,65,71,74–85], inflammation [10,85–87], and ulcers [7] in Chinese and Central Asian traditional medicine. Reported biological activities of the genus Lagochilus are written in subcategories below. 7.1. Hemostatic Effect The plants of the genus Lagochilus have been known for their therapeutic effects and have been included in medicinal practice as valuable hemostatic agents [10,11,25,35,39,58,64,65,71,74–85]. The mechanism of the hemostatic action of Lagochilus preparations was evaluated using different in vivo tests (Table 6). The extracts of Lagochilus species have shown a promising activity when applied to treat hemophilia. In China and Central Asian countries, the species of Lagochilus are widely used as effective hemostatic agents. Table 6. The hemostatic effect of different Lagochilus species extracts and their isolated components. Species Tested Sample Test Type Lagochilus species Lagochilus preparations in vivo Lagochilus species lagochiline acetic acid ester in vivo Lagochilus species Lagochilus infusion and pure lagochilin (1) in vivo L. inebrians Lagoden drug (5% solution of lagohirisine sodium salt) has been developed and approved for public use in vivo Main Finding increased the coagulation ability of the blood both by activating plasma and cellular blood coagulation factors and by depressing the anticoagulant system, and also have a suppressive effect on plasma fibrinolytic activity; accelerating the blood coagulation process, reducing vascular permeability, lowering blood pressure, sedative and analgesic effects showed sedative properties; LD50 for mice was 3.6 g/kg. Injected subcutaneously into rabbits in doses of 0.05 g/kg, it hastened the process of blood coagulation by 30–40%; it affected a reduction in the bleeding time and the volume of blood lost in doses of 0.05 g/kg in dogs shortened the blood-clotting and prothrombin times by 40–60%; the effects were even more pronounced in dicoumarol hemophilia. Lagoden is prescribed for the treatment and prevention of acute and chronic bleeding (gastrointestinal, hemorrhoidal, pulmonary, uterine, etc.), parenchymal hemorrhage (renal, splenic, brain), capillary, and other bleeding, for surgical interventions in otolaryngology practice (for tonsillary tumors, juvenile nasopharyngeal angiofibroma), microsurgery on the ear, etc., in dentistry for removing teeth, cysts, granulomas, during surgery of the gastrointestinal tract, prostate adenomectomy, gynecological operations on the uterus, including bleeding associated with a violation of the blood coagulation system Reference [25,74–77] [78] [79] Pharmacological Committee of the Republic of Uzbekistan (registration Certificate N 01/195/1 of 08.05.2001) Plants 2021, 10, 132 13 of 21 Table 6. Cont. Species Tested Sample Test Type Main Finding Reference L. inebrians Inebrin drug (extractive substances) in vivo recommended in the form of tablets for the treatment of chronic uterine, nasal, gastrointestinal, and other bleeding [80–82] in vivo hemostatic activity [11,39,71,82,83] in vivo possessed a marked direct-action activity and exceeded heparin during affection [35,64,65] L. inebrians L. usunachmaticus compound 1 and 16 and their natural and synthetic derivatives (with cellulose acetate, mono-, di-, tri- and tetrasodium succinates, supramolecular complexes of lagochilin with glycyrrhizic acid and its monoammonium salt, etc.) polysaccharides and carbohydrates isolated from the epigeal part of the plant L. setulosus Setulin (obtained from a dry extract of the plant) in vivo L. diacanthophyllus H2 O and 95% EtOH extracts in vivo L. platyacanthus lagoditerpenes 20, 21 and 24 in vivo L. lanatonodus, L. diacanthophyllus, L. platyacanthus L. hirtus, L. ilicifolius H2 O and EtOH extracts in vivo Setulin hemostatic drug excipient in rabbits in a dose of 50 mg/kg causes the expressed hemostatic effect associated with the activation of thromboplastin formation and transformation of prothrombin into thrombin owing to the acceleration of contact and phospholipid coagulation starting mechanisms (I and II phases of blood coagulation). At 60–90 min after introduction, Setulin completely removes the hypocoagulative effect of heparin EtOH extract significantly shorten the clotting time of mice, bleeding time, show some hemostatic activity lagoditerpenes 20, 21, and 24 showed that moderate hemostatic activities by shortening the values of activated partial thromboplastin time (APTT). These compounds were able to shorten the values of APTT, while the values of prothrombin time and thromboplastin time were not obviously shorted L. lanatonodus and L. diacanthophyllus showed better hemostatic activities among five species. The extracts of L. lanatonodus and L. diacanthophyllus showed dose-dependent hemostatic effects. Both H2 O and EtOH extracts of L. lanatonodus at 400 mg/kg in rats greatly reduced the blood clotting time and tail bleeding time [84] [85] [58] [10] 7.2. Anti-Inflammatory Activity Some species of the Lagochilus genus have been used in Chinese traditional medicine to treat inflammation. The results of anti-inflammatory activities of the components from Lagochilus species are summarized in Table 7 [10,85–87]. This could be due to iridoid glucosides, which have been shown to be potent anti-inflammatory compounds [10,85]. Plants 2021, 10, 132 14 of 21 Table 7. The anti-inflammatory activities of different Lagochilus species extracts. Species Tested Sample Test Performed L. inebrians 5% infusion of leaves in vivo L. inebrians tincture of aerial parts in vivo L. diacanthophyllus H2 O extract or 95% EtOH extract in vivo L. diacanthophyllus H2 O extract or 95% EtOH extract in vitro five Lagochilus species (L. hirtus, L. platyacanthus, L. lanatonodus, L. diacanthophyllus, and L. ilicifolius) H2 O and EtOH extracts in vivo Main Finding from 10 guinea pigs, 8 were less sensitive to L. inebrians most active inhibitor of edema in frog legs among the tested samples extracts can suppress xylene-induced ear edema in mice, showed some anti-inflammatory activity in vivo EtOH extract significantly inhibit macrophage release of NO, TNF-α, IL-6, showed strong in vitro anti-inflammatory activity the extracts of L. lanatonodus and L. diacanthophyllus showed strong inhibitory effects on the acute phase of inflammation in both xylene-induced ear edema mouse model and carrageenan-induced paw edema rat model. Aqueous extract of L. lanatonodus showed the best anti-inflammatory activities among the five Lagochilus species. L. lanatonodus extracts can significantly modulate inflammatory indexes, that is, lower NO, MDA, and PEG2 and elevate SOD. L. platyacanthus, L. hirtus, and L. ilicifolius, exhibited little potency in alleviating edema Reference [86] [87] [85] [85] [10] 7.3. Antibacterial Activity The antibacterial effect of the components (different extracts, essential oils, total alkaloids, and some individual compounds) from Lagochilus species were evaluated [5–7,19,21,24,88]. The results indicated that the components of L. ilicifolius, L. cabulicus, L. acutilobus, L. gypsaceus, L. inebrians, L. olgae, L. proskorjakovii, L. setulosus, L. vvedenskyi had weak antibacterial effects on human pathogens (Table 8). However, Taban et al. [19] reported that the essential oil obtained from the flowers of L. kotschyanus showed strong inhibitory activity against Gram-positive bacteria S. pyogenes, S. agalactia, and B. anthracis (MIC 3.1 mg/mL). Table 8. The antibacterial activities of the components from Lagochilus species. Species Tested sample L. ilicifolius EtOH, petroleum ether, CHCl3 , EtOAc, n-BuOH extracts, water remainder, and total alkaloids S. aureus, B. subtilis, B. cereus, E. coli L. kotschyanus essential oils of flowers and leaves S. aureus, S. pyogenes, S. agalactia, B. anthracis, K. pneumoniae, P. aeruginosa H2 O and EtOH extracts S. aureus ATCC 6538; E. coli ATCC 11229; B. subtilis ATCC 6633; P. aeriginosa ATCC 9027 L. cabulicus Microorganism Main finding EtOAc ext. inhibited B. subtilis (3.0 ± 0.1 mm), EtOH, EtOAc, n-BuOH extracts inhibited B. cereus (5.0 ± 0.1 mm) (at 100 µg/disc concentration) flowers oil showed strong inhibitory activity against S. pyogenes, S. agalactia, B. anthracis, K. pneumoniae, and P. aeruginosa; leaves oil only showed inhibitory activity against S. pyogenes only EtOH extract inhibited S. aureus ATCC 6538 at 0.5 mg/mL Reference [5–7,21] [19] [24] Plants 2021, 10, 132 15 of 21 Table 8. Cont. Species Tested sample L. acutilobus, L. gypsaceus, L. inebrians, L. olgae, L. proskorjakovii, L. setulosus, L. vvedenskyi compounds lagochilin (1), 5-hydroxy-4’,7dimethoxyflavone (48), 8-O-acetylharpagide (99), β-sitosterol (121), stigmasterol (123), daucosterol (125), MeOH extracts obtained from the aerial parts of plants Microorganism Main finding Reference S. aureus ATCC 25923, B. subtilis RKMUz 5, P. aeruginosa ATCC 27879, E. coli RKMUz 221, C. albicans RKMUz 247 compounds 1, 48, 99, 121, 123, 125 were inactive against the tested microorganisms; B. subtilis (9.12 ± 0.13 mm for MeOH ext. of L. proskorjakovii and 9.04 ± 0.10 mm for MeOH ext. of L. olgae) MeOH extracts of L. inebrians, L. olgae, and L. proskorjakovii were more active against B. subtilis with MIC = 125 µg/mL [88] 7.4. Antioxidant Activity The antioxidant activity of methanol extracts of seven Lagochihis species was evaluated using a metal chelating (MC), phosphomolybdenum (PPBD), ferric reducing power (FRAP), cupric reducing antioxidant capacity (CUPRAC), 2,2’-azino-bis (3-ethylbenzothiazoline-6sulphonic acid) (ABTS), and 2,2-diphenyl-1-picrylhydrazyl (DPPH) assays. In these assays, we reported the antioxidant activities as Trolox equivalents, whereas ethylenediaminetetraacetic acid (EDTA) was used for metal chelating assay [40]. Regarding quenching of DPPH radical activity, the observed abilities decreased in the order: L. inebrans (collected from Djizzakh)>L. vvedenskyi>L. olgae>L. setulosus>L. proskorjakovii>L. gypsaceus>L. acutilobus>L. inebrans (collected from the Surkhandarya region). Similar to DPPH, the best cupric (CUPRAC) and ferric reducing power (FRAP) ability were determined by L. inebrans (from Djjzzakh), followed by L. vvedenskyi. The antioxidant activity is probably due to the polyphenols present. The highest amount of total phenolic compounds was found in L. inebrans, followed by L. vvedenskyi and L. proskorjakovii, and we observed a strong correlation between total phenolic content and antioxidant (DPPH, CUPRAC, and FRAP) properties of the tested extracts. In the PPBD assay, L. proskorjakovii exhibited the strongest ability with 2.00 mmolTE/g, while L. inebrians (from Surkhandarya) was the weakest. In the ferrozine assay, the MC ability of L. acutilobus was the best, followed by L. olgae and L. setulosus. We also evaluated the antioxidant potential of 3 Lagochilus essential oils mentioned above in vitro assays [69]. L. inebrians oil exhibited the best antioxidant effect in these assays. For example, L. inebrians had about a 16-fold higher activity than that of L. setulosus in DPPH assay. Similarly, L. inebrians exhibited a significant reducing power effect with 2093.33 mgTE/g in FRAP assay. The second highest antioxidant value was noted in L. setulosus, except for the MC assay. The observed activity for L. inebrians may be explained with its chemical profiles. The main components (trans-chrysanthenyl acetate, eugenol, and verbenol) have already been reported as strong antioxidant compounds, and they could be considered as the main contributors to the observed activity [69]. On the other hand, only very rare work could be traced regarding the in vivo antioxidant activity of the plants belonging to the genus Lagochilus. Only three species were examined by Jiao et al. [10] for their effect on inducible nitric oxide synthase, malondialdehyde, and superoxide dismutase. In this study, both aqueous and alcohol extracts of L. lanatonodus were able to inhibit the enzymes at 200 and 400 mg/kg doses similar to aspirin (positive control). 7.5. Anti-Allergic Activity Lagochilus leiacanthus is a folk medicine used for the treatment of inflammation and ulcers in Xinjiang, China. Mast cells and basophils play a central role in allergic and inflammatory reactions. The β-hexosaminidase release from RBL-2H3 (rat basophilic leukemia) mast cells was measured as an indicator of the inhibitory activity against allergic reactions. In biological studies on the alcoholic extracts of the whole herb of this plant, Furukawa et al. [28] found that the extract inhibits the release of β-hexosaminidase from RBL-2H3 cells. They also examined the inhibitory activity of the isolated compounds. Plants 2021, 10, 132 16 of 21 Among the isolated compounds, flavanones 51–52 and flavones 54, 56, 61, 65–67 showed inhibition of β-hexosaminidase release more potently than ketotifen used as a positive control. It is worth mentioning that no work could be found regarding the in vivo antiallergic effect of Lagochilus species, although most of these plants showed promising anti-inflammatory activity. This point might present a future point for many researchers. 7.6. Cytotoxic Activity The whole herb of L. ilicifolius has been used as a folk medicine for treating hemostatic, inflammation, and ulcers in China. The cytotoxic activities of three lignans 132–134 isolated from L. ilicifolius were evaluated using the MTT assay against the PC12 cell line derived from rat adrenal pheochromocytoma [7]. Erythro-1-[(4-O-β-D-glucopyranosyl-3-methoxyl)phenyl]-2-[(5’-methoxyl)-pinoresinol]-propane -1,3-diol (132) exhibited strong cytotoxic activity against PC12 cell line with an IC50 value of 1.22 ± 0.03 µmol/L, while sisymbrifolin and tortoside C was not cytotoxic. 7.7. Enzyme Inhibition Urease plays an important role in the pathogenesis of many illnesses, such as pyelonephritis, hepatic coma, and peptic ulceration. Tyrosinase plays an important role in melanogenesis (i.e., biosynthesis of melanin pigments, also known as pigmentation). Amylase is an enzyme produced primarily by the pancreas and the salivary glands to help digest carbohydrates. Acetylcholinesterase (AChE) is one of the most efficient enzymes of the nervous system. AChE inhibitors are employed in the treatment of Alzheimer’s disease, myasthenia gravis, glaucoma, smooth muscle atony, and assorted disorders of autonomic nervous system functions. The results of inhibitory enzyme activities of the components from Lagochilus species are summarized in Table 9 [34,40,69]. Table 9. Enzyme inhibitory activities of the components from Lagochilus species. Species Tested Sample Enzyme L. cabulicus EtOAc and MeOH ext urease L. inebrians, L. setulosus, L. gypsaceus essential oils AChE, BChE, tyrosinase, glucosidase, amylase L. acutilobus, L. gypsaceus, L. inebrians, L. olgae, L. proskorjakovii, L. setulosus, L. vvedenskyi MeOH extracts and compounds lagochilin (1), 5-hydroxy-4’,7dimethoxyflavone (48), 8-O-acetylharpagide (99), β-sitosterol (121), daucosterol (125) AChE, BChE, tyrosinase, glucosidase, amylase Main Finding the extracts showed no Jack bean urease inhibitory activity no inhibition was observed by L. gypsaceus EO; L. setulosus EO had no effect against glucosidase; tyrosinase inhibitory activity of EO followed L. inebrans>L. setulosus>L. gypsaceus; L. setulosus EO and L. inebrans EO showed amylase and glucosidase inhibitory effects compound 48 exhibited the strongest inhibitory effects on both AChE and BChE; the highest tyrosinase inhibitory effect was found for MeOH ext of L. inebrians (from Djizzakh) and 48; MeOH ext of L. acutilobus and 48 showed the best amylase inhibitory effects; MeOH ext of L. inebrians and 48 exhibited stronger glucosidase inhibitory effects; compound 99 had the weakest effect on tested enzymes Reference [34] [69] [40,88] Plants 2021, 10, 132 17 of 21 7.8. Acute Toxicity Oral administration of Lagochilus extracts, including aqueous and ethanol extracts from L. lanatonodus, L. diacanthophyllus, L. platyacanthus, L. hirtus, and L. ilicifolius, did not show visible signs of toxicity in mice at the highest dose of 5000 mg/kg of body weight [10]. An acute toxicity study was performed in mice according to the Organization for Economic Cooperation and Development (OECD/OCED) guidelines 423 (Acute Oral Toxicity-Acute Toxicity Class Method) [89] with each group comprising of ten mice. The animals were orally administered a dose of 5000 mg/kg aqueous and ethanol extracts from five Lagochilus species and were observed continuously for 30 min and 4 h, intermittently for 24 h, and then once a day for the next 14 days for general behavioral change, signs of toxicity and mortality. There was no evidence of differences in physiological or behavioral responses between the normal control group and extract-treated groups and also no differences in the consumption of food and water, which implied that the five Lagochilus species are not toxic. 7.9. Other Activities Preliminary biological investigations on Lagochilus components (extracts, fractions, and individual compounds) have indicated their antispasmodic [90], sedative and hypotensive [29], psychoactive [91], and other activities. Lagochilus components may be valuable in the treatment of glaucoma [92], dermoplasty [93], hypertension, heart failure, and angina [29,94]. Lagochilus species have been traditionally and ethnopharmacologically used to treat many diseases, such as hemorrhages, inflammation, allergies, skin diseases, and stomach pain. The phytochemical and biological results validate and support the ethnopharmacological use of Lagochilus species in traditional medicine. Various chemical constituents have been isolated and identified in different groups of compounds, e.g., flavonoids, diterpenes, terpenoids, steroids, iridoids, polysaccharides, and other compounds. Diterpenes and flavonoids are the main bioactive compounds in Lagochilus species, and a wide spectrum of biological studies have focused on these compounds. However, the biological effects of other compounds, such as terpenoids, steroids, iridoids, polysaccharides isolated from this genus, have mostly not been investigated. In certain cases, only plant extracts have been tested for biological activities. Lagochilus species are a valuable medicinal resource with specific pharmacological activities in vitro and in vivo studies; however, more comprehensive studies on their pharmacokinetics, metabolism, side effects, and toxicity are required to demonstrate the efficacy and safety of plant extracts or bioactive compounds from this genus. 8. Conclusions We conclude that the genus Lagochilus is a good source of phytochemical diversity. This genus is native to Central, South-Central, and Eastern Asia and is mainly distributed in arid and semiarid regions of China, Kazakhstan, Uzbekistan, Mongolia, Iran, Pakistan, Afghanistan, and endemic to the Asian mountains. The obtained results demonstrated that not even the well-studied species of Lagochilus had been exhaustively investigated for secondary metabolites, and it should certainly be worthwhile to explore them for new bioactive molecules further. Some species of Lagochilus are rare in nature and endangered. Due to the rapid economic development of regions, climate change, over-collection by people, and continuing resource exploitation, some species in this genus face severe threats, and serious efforts are needed to save and protect rare and endangered species from overharvesting and extinction. Efforts should, therefore, be made to cultivate and naturalize the economically relevant species. Supplementary Materials: The following are available online at https://www.mdpi.com/2223-7 747/10/1/132/s1, The chemical structures isolated from Lagochilus species are available online, alongside Figures S1–S11. Figure S1. Chemical structures of isolated diterpenes from the genus Lagochilus, Figure S2. Chemical structures of isolated phenylpraponoids from the genus Lagochilus, Plants 2021, 10, 132 18 of 21 Figure S3. Chemical structures of isolated iridoids from the genus Lagochilus, Figure S4. Chemical structures of some isolated terpenoids from the genus Lagochilus, Figure S5. Chemical structures of isolated triterpenoids from the genus Lagochilus, Figure S6. Chemical structures of isolated steroids from the genus Lagochilus, Figure S7. Chemical structures of isolated alkaloids from the genus Lagochilus, Figure S8. Chemical structures of isolated lignans from the genus Lagochilus, Figure S9. Chemical structures of isolated aliphatic alkanes and alcohols from the genus Lagochilus, Figure S10. Chemical structures of some of isolated lipids from the genus Lagochilus, Figure S11. Chemical structures of other isolated compounds from the genus Lagochilus. Author Contributions: N.Z.M. and D.K.A. conceptualization and writing the original draft preparation; C.L., H.H. and K.S.T. collecting of data; E.A. and M.L.A. revising and funding; L.A.W. and M.W. review and editing. All authors have read and agreed to the published version of the manuscript. Funding: This research was funded by the Deanship of Scientific Research at Princess Nourah bint Abdulrahman University through the Fast-track Research Funding Program. Acknowledgments: The authors (N.Z.M. and H.H.) thank the Alexander von Humboldt Foundation for its generous support in providing the opportunity to do work in Germany. The authors extend their appreciation to the Deanship of Scientific Research at Princess Nourah Bint Abdulrahman University for funding this work through the Fast-track Research Funding Program. Conflicts of Interest: The authors declare no conflict of interest. References 1. 2. 3. 4. 5. 6. 7. 8. 9. 10. 11. 12. 13. 14. 15. 16. 17. 18. Harley, R.M.; Atkins, S.; Budantsev, A.L.; Cantino, P.D.; Conn, B.J.; Grayer, R.; Harley, M.M.; De Kok, R.; Krestovskaja, T.; Morales, R.; et al. The Families and Genera of Vascular Plants VII; Kadereit, J.W., Kubitzki, K., Eds.; Flowering Plants. Dicotyledons: Lamiales (Except Acanthaceae Including Avicenniaceae); Springer: Berlin, Germany, 2004; pp. 167–275. Agostini, F.; Santos, C.A.; Rossato, M.; Márcia, R.P.; Paula, L.S.; Serafini, L.A.; Molon, R.; Patrick, M. Essential oil yield and composition of Lamiaceae species growing in southern Brazil. Braz. Arch. Biol. Technol. 2009, 52, 473–478. [CrossRef] Zhang, M.L.; Zeng, X.Q.; Sanderson, S.C.; Byalt, V.V.; Sukhorukov, A.P. Insight into Central Asian flora from the Cenozoic Tianshan montane origin and radiation of Lagochilus (Lamiaceae). PLoS ONE 2017, 12, e0178389. [CrossRef] [PubMed] Jamzad, Z. The genus Lagochilus (Labiatae) in Iran. Iran J. Bot. 1988, 4, 91–103. Li, G.; Mishig, D.; Pu, X.; Yi, J.; Zhang, G.; Luo, Y. Chemical components of aerial parts of Lagochilus ilicifolius. Chin. J. Appl. Environ. Biol. 2012, 18, 924–927. [CrossRef] Qian, J.S.; Zhang, B.F.; Wang, W.; Liu, Q.; Wang, C.H.; Jiao, Y.; Chou, G.X.; Xu, H.; Wang, Z.T. Chemical constituents of Lagochilus ilicifolius. Chin. Tradit. Herb. Drugs 2012, 43, 869–872. Qian, J.S.; Zhang, C.G.; Wang, W.; Zhang, T.; Xu, H.X.; Chou, G.X. A new lignan glucoside from Lagochilus ilicifolius. Pharmacogn. Mag. 2015, 11, 191–195. [CrossRef] Sezik, E.; Yesilada, E.; Shahidoyatov, K.; Kuliev, Z.; Nigmatullaev, A.M.; Aripov, H.; Takaishi, Y.; Takeda, Y.; Honda, G. Traditional medicine in Uzbekistan I. Folk medicine in Uzbekistan I. Toshkent, Djizzax and Samarqand provinces. J. Ethnopharmacol. 2004, 92, 197–207. [CrossRef] Eisenman, S.W.; Zaurov, D.E.; Struwe, L. Medicinal Plants of Central Asia: Uzbekistan and Kyrgyzstan; Springer: New York, NY, USA, 2013; p. 155. Jiao, Y.; Chen, P.-H.; Xiong, A.-Z.; Wang, Z.-T.; Tsim, K.W.-K.; Chou, G.-X.; Xu, H. Evaluation of hemostatic and anti-inflammatory activities of extracts from different Lagochilus species in experimental animals: Comparison of different extractives and sources. Phytother. Res. 2015, 29, 22–29. [CrossRef] Zainutdinov, U.N.; Islamov, R.; Dalimov, D.N.; Abdurakhmanov, T.R.; Matchanov, O.D.; Vypova, N.L. Structure-activity relationship for hemostatic lagochilin diterpenoids. Chem. Nat. Compd. 2002, 38, 161–163. [CrossRef] Tskervanik, T.I. System of the genus Lagochilus (Lamiaceae). Bot. Zhurnal. 1985, 70, 1183–1190. Shomurodov, H.F.; Akhmedov, A.; Saribayeva, S.U. Distribution and the current state of Lagochilus acutilobus (Lamiaceae) in connection with the oil and gas sector development in Uzbekistan. Ecol. Quest. 2014, 19, 45–49. [CrossRef] Red Data Book of Republic of Uzbekistan. Plants (Tashkent: Chinor ENK) 2009, 1, 256. Akhmedov, A.K.; Shomurodov, H.F.; Nomozova, Z.B. The ontogenesis and ontogenetic structure of Lagochilus proskorjakovii Ikram (Lamiaceae) coenopopulations in Nuratau mountain range (Uzbekistan). Am. J. Plant Sci. 2016, 7, 928–936. [CrossRef] Aimenova, Z.E.; Eshibaev, A.A.; Zaynutdinov, U.N. Research of areas of distribution of valuable medicinal species of plants of Lagochilus Bunge (Lamiaceae) genus of South Kazakhstan territory. In Proceedings of the 4th European Conference on Biology and Medical Sciences, Vienna, Austria, 13 January 2015; pp. 4–9. Li, H.; Hedge, I. Lamiaceae. In Flora of China; Wu, Z.Y., Raven, P.H., Eds.; Science Press: Beijing, China; Missouri Botanical Garden Press: St. Louis, MO, USA, 1994; Volume 17, pp. 50–299. Jamzad, M.; Ghorbanalipoor, B.; Hafez Taghva, P.; Jamzad, Z.; Yari, M. Chemical composition of Hymnocrater elegans Bunge. and Lagochilus aucheri Boiss, two Labiatae species from Iran. J. Essent. Oil-Bear Plants. 2015, 18, 833–839. [CrossRef] Plants 2021, 10, 132 19. 20. 21. 22. 23. 24. 25. 26. 27. 28. 29. 30. 31. 32. 33. 34. 35. 36. 37. 38. 39. 40. 41. 42. 43. 44. 45. 46. 47. 48. 49. 19 of 21 Taban, S.; Masoudi, S.; Chalabian, F.; Delnavaz, B.; Rustaiyan, A. Chemical composition and antimicrobial activities of the essential oils from flower and leaves of Lagochilus kotschyanus Boiss. A new species from Iran. J. Med. Plants. 2009, 8, 58–63. Grubov, V.I. Key to the Vascular Plants of Mongolia; Science Publishers: Ulaanbaatar, Mongolia, 2001; p. 261. Dumaa, M.; Gerelt-Od, Y.; Javzan, S.; Otgonhkishig, D.; Doncheva, T.; Yordanova, G.; Philipov, S.; Selenge, D. GC-MS analysis and antibacterial activity of some fractions from Lagochilus ilicifolius Bge. grown in Mongolia. Mong. J. Chem. 2015, 16, 39–43. [CrossRef] Pratov, U.P.; Kholmatov, H.K.; Makhsumov, M.M. Natural Medicaments; Tashkent: Tashkent, Uzbekistan, 2006; p. 208. Jeppesen, A.S.; Soelberg, J.; Jager, A.K. Chemical composition of the essential oil from nine medicinal plants of the Wakhan corridor, Afghanistan. J. Essent Oil-Bear Plants. 2012, 15, 204–212. [CrossRef] Jeppesen, A.S.; Soelberg, J.; Jager, A.K. Antibacterial and COX-1 inhibitory effect of medicinal plants from the Pamir mountains, Afghanistan. Plants 2012, 1, 74–81. [CrossRef] Akopov, I.E. Hemostatic Plants, 2nd ed.; Meditsina: Moscow, Russia, 1981; p. 268. (In Russian) Zhang, C.G.; Wang, L.; Lu, Y.; Ye, Z.; Han, Z.Z.; Xu, H.; Chou, G.X. Diterpenoids from the whole plant of Lagochilus platyacanthus. Planta Med. 2015, 81, 1345–1352. [CrossRef] Ba, H.; Tolhen, M.S.; Wang, B.D.; Zhu, D.Y. Studies on the chemical constituents of Lagochilus lanatonodus. Nat. Prod. Res. Dev. 1997, 9, 44–48. Furukawa, M.; Suzuki, H.; Makino, M.; Ogawa, S.; Iida, T.; Fujimoto, Y. Studies on the constituents of Lagochilus leiacanthus (Labiatae). Chem. Pharm. Bull. 2011, 59, 1535–1540. [CrossRef] Nasrullaev, F.D.; Makhsudova, B.T. Flavonoids of Lagochilus platycalyx. Chem. Nat. Compd. 1991, 27, 511–512. [CrossRef] Zainutdinov, U.N.; Mavlyankulova, Z.I.; Aslanov, K.A. A chemical study of Lagochilus pubescens. Chem. Nat. Compd. 1975, 11, 287–288. [CrossRef] Mavlankulova, Z.I.; Zainutdinov, U.N.; Aslanov, K.A. Diterpenes of Lagochilus pubescens. Chem. Nat. Compd. 1977, 13, 39–41. [CrossRef] Islamov, R.; Zainutdinov, U.N.; Aslanov, K.A. Lagochilin 3-monoacetate from Lagochilus inebrians. Chem. Nat. Compd. 1978, 14, 342–343. [CrossRef] Nurmatova, M.P.; Zainutdinov, U.N.; Kamaev, F.G.; Aslanov, K.A. Structure and configuration of a new diterpenoid lactone from Lagochilus hirsutissimus. Chem. Nat. Compd. 1979, 15, 695–699. [CrossRef] Gohari, A.R.; Nabati, F.; Saeidnia, S.; Malmir, M.; Amanlou, M. Urease inhibitory activity of some Iranian medicinal plants. Asian J. Chem. 2012, 24, 1527–1529. Malikova, M.K.; Rakhimov, D.A. Plant polysaccharides VIII. Polysaccharides of Lagochilus zeravschanicus. Chem. Nat. Comp. 1997, 33, 438–440. [CrossRef] Saeidnia, S.; Barari, E.; Shakeri, A.; Gohari, A.R. Isolation and identification of main compounds of Lagochilus cabulicus. Asian J. Chem. 2013, 25, 1509–1511. Zainutdinov, U.N.; Pulatova, M.P.; Badalbaeva, T.A.; Umarova, R.U.; Mavlyankulova, Z.I.; Pulatova, T.P.; Aslanov, K.A. Diterpene lactones and iridoid glycosides of the genus Lagochilus. Chem. Nat. Compd. 1994, 30, 27–30. [CrossRef] Radchenko, L.I. Phytochemical investigation of Lagochilus gypsaceus and Lagochilus seravschanicus. Aptechnoe Delo. 1963, 12, 24–26. [PubMed] Matchanov, A.D.; Dalimov, D.N.; Zainutdinov, U.N.; Vypova, N.L.; Islamov, A.K.; Bekpolatova, B.M. Preparation and physicochemical and biological properties of molecular associates of lagochilin and lagochirsine with glycyrrhizic acid and its monoammonium salt. Chem. Nat. Compd. 2017, 53, 665–669. [CrossRef] Akramov, D.K.; Bacher, M.; Böhmdorfer, S.; Rosenau, T.; Zengin, G.; Potthast, A.; Nahar, L.; Sarker, S.D.; Mamadalieva, N.Z. Phytochemical analysis and biological evaluation of Lagochilus species from Uzbekistan. Ind. Crops Prod. 2020, 154, 112715. [CrossRef] Sharipova, S.T.; Otroshchenko, O.S.; Sadykov, A.S. Chemical studies of some species of plants of the genus Lagochilus. Nauchnye Trudy—Tash. Gos. Univ. 1972, 419, 215–218. Proskurnina, N.F.; Utkin, L.M. DL-stachydrine in Lagochilus. Meditsinskaya Promyshlennost SSSR 1960, 14, 30–31. Nurmatova, M.P.; Zainutdinov, U.N.; Kamaev, F.G.; Aslanov, K.A.; Sadykov, A.S. Novel diterpenoid lactone from Lagochilus hirsutissimus. Tezisy Doklady Sovetsko-Indiyskii Simposium. Khim. Prir. Soedin. 1978, 5, 66. Zainutdinov, U.N.; Islamov, R. The active substances of Lagochilus inebrians. Khim-Farmi Zhurnal. 1986, 20, 583–584. Abramov, M.M.; Yaparova, S.A. Preparation of main active principle from Lagochilus inebrians. Zhurnal Priklad. Khim. 1963, 11, 2554–2556. Islamov, R.; Zainutdinov, U.N.; Aslanov, K.A. Lagochilin diacetates from Lagochilus inebrians. Chem. Nat. Compd. 1981, 17, 50–53. [CrossRef] Islamov, R.; Zainutdinov, U.N.; Aslanov, K.A. Vulgarol from Lagochilus inebrians. Khim. Prir. Soedin. 1981, 100–101. Zainutdinov, U.N.; Mavlankulova, Z.I.; Aslanov, K.A.; Khagi, M.S.; Kambarova, D.M.; Alimova, M.K. Determination of lagochilin diacetates in Lagochilus inebrians tincture. Khim-Farm Zhurnal. 1988, 22, 450–451. Pulatova, T.P. Proceedings of a Jubilee Scientific Conference of Tashkent Pharmaceutical Institute; Tashkent Pharmaceutical Institute: Tashkent, Uzbekistan, 1970; p. 14. (In Russian) Plants 2021, 10, 132 50. 51. 52. 53. 54. 55. 56. 57. 58. 59. 60. 61. 62. 63. 64. 65. 66. 67. 68. 69. 70. 71. 72. 73. 74. 75. 76. 77. 78. 79. 80. 81. 82. 20 of 21 Akramov, D.K.; Bacher, M.; Zengin, G.; Bohmdorfer, S.; Rosenau, T.; Azimova, S.S.; Mamadalieva, N.Z. Chemical composition and anticholinesterase activity of Lagochilus inebrians. Chem. Nat. Compd. 2019, 55, 575–577. [CrossRef] Islamov, R.; Zainutdinov, U.N.; Aslanov, K.A. Substances from the waxy fraction of the plant Lagochilus inebrians. Sint. Reakts. Sposobn. Org. Soedin. 1983, 61–63. Kotenko, L.D.; Yakubova, M.Y.; Tselishcheva, N.A.; Turakhozhaev, M.T.; Badalbaeva, T.A. Quantitative determination of the total iridoids in plants of the genus Lagochilus. Chem. Nat. Compd. 1994, 30, 669–672. [CrossRef] Pulatova, T.P. Alkaloid content of some plants of the family Labiatae. Chem. Nat. Compd. 1969, 5, 55. [CrossRef] Pulatova, T.P.; Khazanovich, R.L. Alkaloid content of some species of Lagochilus and the nature of lagochiline. Aptechnoe Delo. 1962, 11, 29–32. Yuldasheva, N.K.; Ul’chenko, N.T.; Abdukhomidova, F.; Glushenkova, A.I.; Zainutdinov, U.N. Lipids from seeds of Lagochilus inebrians. Chem. Nat. Compd. 2015, 51, 1154–1156. [CrossRef] Aboee-Mehrizi, F.; Farjam, M.H.; Rustaiyan, A.; Zare, A.; Salari, M. Volatile constituents of Salvia compressa and Logochilus macranthus, two Labiatae herbs growing wild in Iran. Res. J. Recent Sci. 2013, 2, 66–68. Gusakova, S.D.; Umarov, A.U. The oils from plants of the family Labiatae. Chem. Nat. Comp. 1972, 8, 23–28. [CrossRef] Zhang, C.; Lu, Y.; Wang, Z.; Yu, G.; Xu, H. Chemical constituents from whole herb of Lagochilus platyacanthus. Chin. Tradit. Herb. Drugs 2014, 45, 3224–3229. Geissman, T.A. The Chemistry of Flavonoid Compounds; Pergamon: Oxford, MS, USA, 1962; pp. 338–339. Mavlyankulova, Z.I.; Zainutdinov, U.N.; Aslanov, K.A. Acetyllagochilins from Lagochilus pubescens and their investigation by PMR spectroscopy. Chem. Nat. Compd. 1978, 14, 66–69. [CrossRef] Mavlyankulova, Z.I.; Dimchuk, Y.S.; Pulatova, T.P. Phytochemical study of Lagochilus proskorjacovii. Chem. Nat. Compd. 1989, 25, 721–722. [CrossRef] Mavlankulova, Z.I.; Zainutdinov, U.N.; Aslanov, K.A. 3,18-O-isopropylidinelagochilin from Lagochilus pubescens. Chem. Nat. Compd. 1976, 12, 106–107. [CrossRef] Pulatova, T.P. Pharmacognostic study of Lagochilus setulosus. Aptechnoe Delo. 1960, 9, 26–29. Rakhimov, D.A.; Malikova, M.K.; Vakhabov, A.A.; Ruziev, I.O.; Abdurakhmanov, T.R. Plant polysaccharides. Lagochilus polysaccharides and their biological activity. Chem. Nat. Compd. 1995, 31, 260–261. [CrossRef] Rakhimov, D.A.; Malikova, M.K.; Vakhabov, A.A.; Abdurakhmanov, T.R.; Ruziev, O.I. Plant polysaccharides. IX. Isolation and anticoagulant activity of the polysaccharides of Lagochilus usunachmaticus. Chem. Nat. Compd. 1997, 33, 534–535. [CrossRef] Zainutdinov, U.N.; Khaitboev, K.; Khafizov, A.R.; Aslanov, K.A. Method of isolating lagochilin from plans of the genus Lagochilus. Chem. Nat. Compd. 1994, 30, 129. [CrossRef] Atazhanova, G.A. Composition and biological activity of essential oil from plants endemic to Kazakhstan. Chem. Nat. Compd. 2008, 44, 266–269. [CrossRef] Casiglia, S.; Jemia, M.B.; Riccobono, L.; Bruno, M.; Scandolera, E.; Senatore, F. Chemical composition of the essential oil of Moluccella spinosa L. (Lamiaceae) collected wild in Sicily and its activity on microorganisms affecting historical textiles. Nat. Prod. Res. 2015, 2, 1201–1206. [CrossRef] Akramov, D.K.; Zengin, G.; Kang, S.C.; Tojibaev, K.S.; Mahomoodally, M.F.; Azimova, S.S.; Mamadalieva, N.Z. Comparative study on the chemical composition and biological activities of the essential oils of three Lagochilus species collected from Uzbekistan. Nat. Prod. Res. 2019. [CrossRef] Cheng, F.; Zhou, Y.; Wang, M.; Guo, C.; Cao, Z.; Zhang, R.; Peng, C. A review of pharmacological and pharmacokinetic properties of stachydrine. Pharm. Res. 2020, 155, 104755. [CrossRef] [PubMed] Rakhmonberdiev, G.R.; Sidikov, A.S.; Yusupov, R.D.; Zainutdinov, U.N.; Kazantseva, D.S. Synthesis of a hemostatic drug from cellulose acetate. Chem. Nat. Compd. 1998, 34, 192–194. [CrossRef] Mursaliev, A.M. Distribution of some chemical elements in soils and plants of the Kirgiz SSR. Rast. Resur. Kirg. 1969, 74–76. Lobanov, E.M.; Khatamov, S.; Talipov, R.M. Efficiency of neutron activation logging during biogeochemical prospecting for gold ore deposits (in Central Kazakhstan). Uzb. Geol. Zhurnali. 1966, 10, 49–54. Akopov, I.E. The effect of Lagochilus preparations upon clot retraction. Byull. Eksperim. Biol. Med. 1954, 37, 49–54. Akopov, I.E. Mechanism of the hemostatic action of Lagochilus preparations. Farm. Toksik. 1954, 17, 51–55. Akopov, I.E. Pharmacotherapy of hemophilia with the preparation of Lagochilus inebrians BGE. Folia Haematol. 1971, 95, 72–83. Budyka, L.P. Effect of Lagochilus preparations on blood coagulation in patients with hemophilia. Ter. Arkhiv 1970, 1, 86–89. Asliddinov, F.A. The pharmacology of lagochiline ester. Sbornik Nauch. Trudov Samarkand. Med. Inst. 1956, 11, 177–181. Akopov, I.E. The effect of lagochilus preparations on the rate of blood clotting and prothrombin time in normal and pathologic states. Za Sotsial. Zdr. Uzb. 1956, 2, 49–52. Abdurakhmanov, O.B. The use of Lagoden in operative interventions for nasopharyngeal angiofibroma. Res. Otolaryngol. 2015, 4, 35–37. [CrossRef] Zainutdinov, U.N. Diterpenoids of the plants from genus Lagochilus. Ph.D. Thesis, National University of Uzbekistan, Tashkent, Uzbekistan, 1993; p. 253. Zainutdinov, O.U. Evaluation of the Effectiveness of Hemostatic Drug Lagoden in Treatment of Prostate Adenomectomy. Ph.D. Thesis, National University of Uzbekistan, Tashkent, Uzbekistan, 1997; p. 20. Plants 2021, 10, 132 83. 84. 85. 86. 87. 88. 89. 90. 91. 92. 93. 94. 21 of 21 Matchanov, A.D.; Zaynutdinov, U.N.; Islamov, A.K.; Vypova, N.L.; Tashpulatov, F.N.; Matchanov, U.D. Supramolecular complexes of glycyrrhizic acid, its monoammonium salt with diterpenoid lagochilin and their hemostatic activity. Biochem. Ind. J. 2017, 11, 118/1–118/5. Aimenova, Z.E.; Eshibaev, A.A.; Elemanova, Z.R.; Abil’daeva, R.A.; Daulbaj, A.D. Effect of setulin hemostatic drug excipient on the hemostasis in rabbits with experimental hypocoagulation. Res. J. Pharm. Biol. Chem. Sci. 2016, 1, 1946–1951. Xu, H.; Jiao, Y.; Zhang, C.; Chou, G. Application of Lagochilus diacanthophyllus extract in preparation of hemostatic and antiinflammatory agents. CN Patent 103405499A, 27 September 2013. Asliddinov, F.A. Influence of lagochyle infusions on sensitivity of guinea pigs to disease. Farm. Toksikol. 1955, 18, 40. Derevyanko, L.D. Effects of some drugs on edema development in isolated frog legs. Farm. Toksikol. 1963, 26, 465–467. Akramov, D.K.; Sasmakov, S.A.; Zengin, G.; Ashirov, O.N.; Azimova, S.S.; Mamadalieva, N.Z. Antimicrobial and antioxidant activities of the components of Lagochilus species from Uzbekistan. Uzb. Biol. J. 2019, 3, 3–7. OECD. OECD Guidelines for Acute Toxicity of Chemicals; Organization for Economic Co-operation and Development: Paris, France, 2001; p. 420. Akopov, E. Antispasmodic action of Lagochilus extract. Farm. Toksikol. 1954, 17, 34–37. Riedlinger, T.J. Wasson’s alternative candidates for soma. J. Psychoact. Drugs 1993, 25, 149–156. [CrossRef] Kadyrova, K.K. Lagochilus in the treatment of glaucoma. Vestn. Oftalmol. 1955, 34, 32–35. Rasulov, K.K.; Levin, S.I.; Aripov, B.A. Use of Lagochilus tincture in dermoplasty. Ortoped. Travm. Protezir. 1984, 9, 43–44. Derevyanko, L.D. Effects of some vasodilators and desensitizers on vessels in isolated rabbit ear before and after sensitization. Farm. Toksikol. 1963, 26, 611–616.