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Details

Stereochemistry RACEMIC
Molecular Formula C9H10O5
Molecular Weight 198.1727
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-HYDROXY-3-(3,4-DIHYDROXYPHENYL)PROPANOIC ACID

SMILES

OC(CC1=CC(O)=C(O)C=C1)C(O)=O

InChI

InChIKey=PAFLSMZLRSPALU-UHFFFAOYSA-N
InChI=1S/C9H10O5/c10-6-2-1-5(3-7(6)11)4-8(12)9(13)14/h1-3,8,10-12H,4H2,(H,13,14)

HIDE SMILES / InChI

Molecular Formula C9H10O5
Molecular Weight 198.1727
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Evaluation of the effects of cytochrome P450 nonsynonymous single-nucleotide polymorphisms on tanshinol borneol ester metabolism and inhibition potential.
2010-12
Metabolism of tanshinol borneol ester in rat and human liver microsomes.
2010-09
[Effect of isopropyl 3-(3,4-dihydroxyphenyl) -2-hydroxypropanoate on rat pulmonary artery smooth muscle].
2008-12
[Studies on the chemical constituents of Salvia miltiorrhiz of Lijiang].
2008-02
Determination of the main bioactive metabolites of Radix salvia miltiorrhizae in compound Danshen dripping pills and the tissue distribution of Danshensu in rabbit by SPE-HPLC-MSn.
2007-04
Simultaneous determination of six phenolic constituents of danshen in human serum using liquid chromatography/tandem mass spectrometry.
2005-06-05
Protective effects of Danshensu from the aqueous extract of Salvia miltiorrhiza (Danshen) against homocysteine-induced endothelial dysfunction.
2004-11-12
A new acylated quercetin glycoside from Ranunculus lanuginosus.
2004-09
[Determination of danshensu in urine and its pharmacokinetics in human].
2003-10
Simultaneous determination and pharmacokinetic studies on (3,4-Dihydroxyphenyl)-lactic acid and protocatechuic aldehyde in rat serum after oral administration of Radix Salviae miltiorrhizae extract.
2003-07
[A study on the mechanism of the biological roles of danshensu on fibroblast].
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:08:18 GMT 2025
Edited
by admin
on Mon Mar 31 18:08:18 GMT 2025
Record UNII
NA8H56YM3K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(±)-DAN SHEN SU
Preferred Name English
2-HYDROXY-3-(3,4-DIHYDROXYPHENYL)PROPANOIC ACID
Systematic Name English
DANSHENSU, (±)-
Common Name English
3-(3,4-DIHYDROXYPHENYL)-2-HYDROXYPROPANOIC ACID
Systematic Name English
3-(3,4-DIHYDROXYPHENYL)LACTIC ACID DL-.BETA.-(3,4-DIHYDROXYPHENYL)LACTIC ACID
Systematic Name English
.ALPHA.-HYDROXYDIHYDROCAFFEIC ACID
Systematic Name English
Code System Code Type Description
FDA UNII
NA8H56YM3K
Created by admin on Mon Mar 31 18:08:18 GMT 2025 , Edited by admin on Mon Mar 31 18:08:18 GMT 2025
PRIMARY
PUBCHEM
439435
Created by admin on Mon Mar 31 18:08:18 GMT 2025 , Edited by admin on Mon Mar 31 18:08:18 GMT 2025
PRIMARY
EPA CompTox
DTXSID10865081
Created by admin on Mon Mar 31 18:08:18 GMT 2025 , Edited by admin on Mon Mar 31 18:08:18 GMT 2025
PRIMARY
CAS
23028-17-3
Created by admin on Mon Mar 31 18:08:18 GMT 2025 , Edited by admin on Mon Mar 31 18:08:18 GMT 2025
PRIMARY
CHEBI
17807
Created by admin on Mon Mar 31 18:08:18 GMT 2025 , Edited by admin on Mon Mar 31 18:08:18 GMT 2025
PRIMARY