Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8O4 |
| Molecular Weight | 168.1467 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(O)C(=CC=C1)C(O)=O
InChI
InChIKey=AUZQQIPZESHNMG-UHFFFAOYSA-N
InChI=1S/C8H8O4/c1-12-6-4-2-3-5(7(6)9)8(10)11/h2-4,9H,1H3,(H,10,11)
| Molecular Formula | C8H8O4 |
| Molecular Weight | 168.1467 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| 2-Hydr-oxy-3-methoxy-benzoic acid monohydrate. | 2008-03-12 |
|
| Doxorubicin inhibits oxidation of 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonate) (ABTS) by a lactoperoxidase/H(2)O(2) system by reacting with ABTS-derived radical. | 2007-10-15 |
|
| Inactivation of anthracyclines by serum heme proteins. | 2007-06 |
|
| Inactivation of anthracyclines by cellular peroxidase. | 2005-07-15 |
|
| The enhancement of riboflavin-mediated photo-oxidation of doxorubicin by histidine and urocanic acid. | 2001-04 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 20:39:38 GMT 2025
by
admin
on
Mon Mar 31 20:39:38 GMT 2025
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| Record UNII |
3J31Y0E2IM
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| Record Status |
Validated (UNII)
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| Record Version |
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