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

Details

Stereochemistry ABSOLUTE
Molecular Formula C42H64O19
Molecular Weight 872.9462
Optical Activity UNSPECIFIED
Defined Stereocenters 22 / 22
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of K-STROPHANTHOSIDE

SMILES

[H][C@@]1(C[C@H](OC)[C@H](O[C@]2([H])O[C@H](CO[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)[C@@H](O)[C@H](O)[C@H]2O)[C@@H](C)O1)O[C@H]4CC[C@]5(C=O)[C@@]6([H])CC[C@]7(C)[C@H](CC[C@]7(O)[C@]6([H])CC[C@]5(O)C4)C8=CC(=O)OC8

InChI

InChIKey=GILGYKHFZXQALF-FBPIOBPTSA-N
InChI=1S/C42H64O19/c1-19-36(61-38-35(51)33(49)31(47)27(60-38)17-56-37-34(50)32(48)30(46)26(15-43)59-37)25(54-3)13-29(57-19)58-21-4-9-40(18-44)23-5-8-39(2)22(20-12-28(45)55-16-20)7-11-42(39,53)24(23)6-10-41(40,52)14-21/h12,18-19,21-27,29-38,43,46-53H,4-11,13-17H2,1-3H3/t19-,21+,22-,23+,24-,25+,26-,27-,29+,30-,31-,32+,33+,34-,35-,36-,37-,38+,39-,40+,41+,42+/m1/s1

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Antiherpes activity of glucoevatromonoside, a cardenolide isolated from a Brazilian cultivar of Digitalis lanata.
2011 Oct
Patents
Name Type Language
K-STROPHANTHOSIDE
Common Name English
NSC-7530
Code English
CARD-20(22)-ENOLIDE, 3-((O-.BETA.-D-GLUCOPYRANOSYL-(1->6)-O-.BETA.-D-GLUCOPYRANOSYL-(1->4)-2,6-DIDEOXY-3-O-METHYL-.BETA.-D-RIBO-HEXOPYRANOSYL)OXY)-5,14-DIHYDROXY-19-OXO-, (3.BETA.,5.BETA.)-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID60954919
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY
ECHA (EC/EINECS)
251-439-1
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY
PUBCHEM
20055295
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY
NSC
7530
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY
CAS
33279-57-1
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY
FDA UNII
8141H9654J
Created by admin on Fri Dec 15 16:29:23 GMT 2023 , Edited by admin on Fri Dec 15 16:29:23 GMT 2023
PRIMARY