Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H10O3 |
| Molecular Weight | 226.2274 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC1=C(O)C2=CC3=CC=CC=C3C(O)=C2C=C1
InChI
InChIKey=TZIQWQARHPGHIG-UHFFFAOYSA-N
InChI=1S/C14H10O3/c15-12-6-5-10-11(14(12)17)7-8-3-1-2-4-9(8)13(10)16/h1-7,15-17H
| Molecular Formula | C14H10O3 |
| Molecular Weight | 226.2274 |
| 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 |
|---|---|---|
| Prediction of genotoxicity of chemical compounds by statistical learning methods. | 2005-06 |
|
| Evidence for the existence of PAH-quinone reductase and catechol-O-methyltransferase in Mycobacterium vanbaalenii PYR-1. | 2004-12 |
|
| Differential and special properties of the major human UGT1-encoded gastrointestinal UDP-glucuronosyltransferases enhance potential to control chemical uptake. | 2004-01-09 |
|
| Structure-activity relationships for inhibition of human 5alpha-reductases by polyphenols. | 2002-03-15 |
|
| Hydroxyquinones are competitive non-peptide inhibitors of HIV-1 proteinase. | 1995-11-15 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:34:22 GMT 2025
by
admin
on
Mon Mar 31 21:34:22 GMT 2025
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| Record UNII |
E0T985Y674
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| Record Status |
Validated (UNII)
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