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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H22O10
Molecular Weight 494.4469
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of SALVIANOLIC ACID A

SMILES

OC(=O)[C@@H](CC1=CC(O)=C(O)C=C1)OC(=O)\C=C\C2=C(/C=C/C3=CC(O)=C(O)C=C3)C(O)=C(O)C=C2

InChI

InChIKey=YMGFTDKNIWPMGF-UCPJVGPRSA-N
InChI=1S/C26H22O10/c27-18-7-2-14(11-21(18)30)1-6-17-16(4-9-20(29)25(17)33)5-10-24(32)36-23(26(34)35)13-15-3-8-19(28)22(31)12-15/h1-12,23,27-31,33H,13H2,(H,34,35)/b6-1+,10-5+/t23-/m1/s1

HIDE SMILES / InChI

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
71.4 nM [Ki]
39.8 nM [Ki]
66.6 nM [Ki]
36.2 µM [IC50]
23.5 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Effects of salvianolic acid a on oxidative stress and liver injury induced by carbon tetrachloride in rats.
2007 Feb
Effects of salvianolic acids on oxidative stress and hepatic fibrosis in rats.
2010 Jan 15
Salvianolic acid A exerts antiamnesic effect on diazepam-induced anterograde amnesia in mice.
2011 Jan
Salvianolic acid A preconditioning confers protection against concanavalin A-induced liver injury through SIRT1-mediated repression of p66shc in mice.
2013 Nov 15
Name Type Language
SALVIANOLIC ACID A
Common Name English
BENZENEPROPANOIC ACID, .ALPHA.-((3-(2-(2-(3,4-DIHYDROXYPHENYL)ETHENYL)-3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-3,4-DIHYDROXY-, (R-(E,E))-
Systematic Name English
(+)-SALVIANOLIC ACID A
Common Name English
DAN PHENOLIC ACID A
Common Name English
BENZENEPROPANOIC ACID, .ALPHA.-(((2E)-3-(2-((1E)-2-(3,4-DIHYDROXYPHENYL)ETHENYL)-3,4-DIHYDROXYPHENYL)-1-OXO-2-PROPENYL)OXY)-3,4-DIHYDROXY-, (.ALPHA.R)-
Systematic Name English
Code System Code Type Description
CAS
96574-01-5
Created by admin on Sat Dec 16 08:26:43 GMT 2023 , Edited by admin on Sat Dec 16 08:26:43 GMT 2023
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FDA UNII
51622542XO
Created by admin on Sat Dec 16 08:26:43 GMT 2023 , Edited by admin on Sat Dec 16 08:26:43 GMT 2023
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DRUG BANK
DB15246
Created by admin on Sat Dec 16 08:26:43 GMT 2023 , Edited by admin on Sat Dec 16 08:26:43 GMT 2023
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PUBCHEM
5281793
Created by admin on Sat Dec 16 08:26:43 GMT 2023 , Edited by admin on Sat Dec 16 08:26:43 GMT 2023
PRIMARY
EPA CompTox
DTXSID701316580
Created by admin on Sat Dec 16 08:26:43 GMT 2023 , Edited by admin on Sat Dec 16 08:26:43 GMT 2023
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