U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C23H22O7
Molecular Weight 410.4166
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TEPHROSIN

SMILES

[H][C@@]12COC3=C(C=C(OC)C(OC)=C3)[C@]1(O)C(=O)C4=C(O2)C5=C(OC(C)(C)C=C5)C=C4

InChI

InChIKey=AQBZCCQCDWNNJQ-AUSIDOKSSA-N
InChI=1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1

HIDE SMILES / InChI

Molecular Formula C23H22O7
Molecular Weight 410.4166
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Rotenone and rotenoids in cubè resins, formulations, and residues on olives.
2004 Jan 28
Preparative isolation and purification of three rotenoids and one isoflavone from the seeds of Millettia pachycarpa Benth by high-speed counter-current chromatography.
2008 Jan 18
Phenolic constituents of Amorpha fruticosa that inhibit NF-kappaB activation and related gene expression.
2008 Oct
Phthalides from Pittosporum illicioides var. illicioides with inhibitory activity on superoxide generation and elastase release by neutrophils.
2008 Oct
Optimising resolution for a preparative separation of Chinese herbal medicine using a surrogate model sample system.
2009 Jun 26
Natural toxins for use in pest management.
2010 Aug
Concise modular asymmetric synthesis of deguelin, tephrosin and investigation into their mode of action.
2010 Aug 23
Tephrosin induces internalization and degradation of EGFR and ErbB2 in HT-29 human colon cancer cells.
2010 Jul 1
Chloroquine potentiates the anti-cancer effect of 5-fluorouracil on colon cancer cells.
2010 Jul 15
Tephrosin-induced autophagic cell death in A549 non-small cell lung cancer cells.
2010 Nov
Rotenoids from Lablab purpureus L. and their bioefficacy against human disease vectors.
2010 Nov
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:34:25 GMT 2023
Edited
by admin
on Sat Dec 16 09:34:25 GMT 2023
Record UNII
9C081V83CC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TEPHROSIN
MI  
Common Name English
TEPHROSIN [MI]
Common Name English
HYDROXYDEGUELIN
Common Name English
3H-BIS(1)BENZOPYRANO(3,4-B:6',5'-E)PYRAN-7(7AH)-ONE, 13,13A-DIHYDRO-7A-HYDROXY-9,10-DIMETHOXY-3,3-DIMETHYL-, (7AR,13AR)-
Systematic Name English
TOXICAROL
Common Name English
DEGUELINOL I
Common Name English
Code System Code Type Description
CHEBI
9442
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY
CAS
76-80-2
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY
FDA UNII
9C081V83CC
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY
PUBCHEM
114909
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY
MERCK INDEX
m10563
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID20878627
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY
WIKIPEDIA
Tephrosin
Created by admin on Sat Dec 16 09:34:25 GMT 2023 , Edited by admin on Sat Dec 16 09:34:25 GMT 2023
PRIMARY