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 |
---|---|---|
The enhancement of riboflavin-mediated photo-oxidation of doxorubicin by histidine and urocanic acid. | 2001 Apr |
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Inactivation of anthracyclines by cellular peroxidase. | 2005 Jul 15 |
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Inactivation of anthracyclines by serum heme proteins. | 2007 Jun |
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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 Oct 15 |
|
2-Hydr-oxy-3-methoxy-benzoic acid monohydrate. | 2008 Mar 12 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 00:43:08 GMT 2023
by
admin
on
Sat Dec 16 00:43:08 GMT 2023
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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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