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
SMILES
OC(=O)CNC(=O)C1=CC=C(O)C=C1
InChI
InChIKey=ZMHLUFWWWPBTIU-UHFFFAOYSA-N
InChI=1S/C9H9NO4/c11-7-3-1-6(2-4-7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Ca(2+)-Mg (2+)-dependent ATP-ase activity in hemodialyzed children. Effect of a hemodialysis session. | 2010-12 |
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| The metabolic fate of red wine and grape juice polyphenols in humans assessed by metabolomics. | 2010-07 |
|
| Dihydroxylated phenolic acids derived from microbial metabolism reduce lipopolysaccharide-stimulated cytokine secretion by human peripheral blood mononuclear cells. | 2009-07 |
|
| The uraemic retention solute para-hydroxy-hippuric acid attenuates apoptosis of polymorphonuclear leukocytes from healthy subjects but not from haemodialysis patients. | 2008-08 |
|
| Uraemic toxins induce proximal tubular injury via organic anion transporter 1-mediated uptake. | 2002-01 |
|
| Characterization of p-hydroxy-hippuric acid as an inhibitor of Ca2+-ATPase in end-stage renal failure. | 2001-02 |
Patents
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| Code System | Code | Type | Description | ||
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4E2MH5995F
Created by
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71018
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151012
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DTXSID50179518
Created by
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2482-25-9
Created by
admin on Mon Mar 31 19:58:49 GMT 2025 , Edited by admin on Mon Mar 31 19:58:49 GMT 2025
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C056283
Created by
admin on Mon Mar 31 19:58:49 GMT 2025 , Edited by admin on Mon Mar 31 19:58:49 GMT 2025
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SUBSTANCE RECORD