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Details

Stereochemistry ACHIRAL
Molecular Formula C9H9NO4
Molecular Weight 195.1721
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-HYDROXYHIPPURIC ACID

SMILES

OC(=O)CNC(=O)C1=CC=CC(O)=C1

InChI

InChIKey=XDOFWFNMYJRHEW-UHFFFAOYSA-N
InChI=1S/C9H9NO4/c11-7-3-1-2-6(4-7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)

HIDE SMILES / InChI

Molecular Formula C9H9NO4
Molecular Weight 195.1721
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bioavailability of coffee chlorogenic acids and green tea flavan-3-ols.
2010-08
Flavanols and anthocyanins in cardiovascular health: a review of current evidence.
2010-04-13
Yoghurt impacts on the excretion of phenolic acids derived from colonic breakdown of orange juice flavanones in humans.
2009-05
Crystal structure of the Homo sapiens kynureninase-3-hydroxyhippuric acid inhibitor complex: insights into the molecular basis of kynureninase substrate specificity.
2009-01-22
The metabolism of dietary polyphenols and the relevance to circulating levels of conjugated metabolites.
2002-11
The metabolic fate of dietary polyphenols in humans.
2002-07-15
Novel biomarkers of the metabolism of caffeic acid derivatives in vivo.
2001-06-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:55:16 GMT 2025
Edited
by admin
on Mon Mar 31 19:55:16 GMT 2025
Record UNII
17HCX0HNRT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
HIPPURIC ACID, M-HYDROXY-
Preferred Name English
M-HYDROXYHIPPURIC ACID
Systematic Name English
GLYCINE, N-(3-HYDROXYBENZOYL)-
Systematic Name English
N-M-HYDROXYLBENZOYLGLYCINE
Systematic Name English
3-HYDROXYHIPPURIC ACID
Systematic Name English
3-HYDROXYBENZOYLGLYCINE
Systematic Name English
HYDROXYHIPPURIC ACID, M-
Common Name English
Code System Code Type Description
MESH
C535238
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
CAS
1637-75-8
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
CHEBI
70824
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
PUBCHEM
450268
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
DRUG BANK
DB07069
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
FDA UNII
17HCX0HNRT
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY
EPA CompTox
DTXSID30167650
Created by admin on Mon Mar 31 19:55:16 GMT 2025 , Edited by admin on Mon Mar 31 19:55:16 GMT 2025
PRIMARY