Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7NO3 |
| Molecular Weight | 165.1461 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CC=CC=C1NC=O
InChI
InChIKey=LLLPDUXGHXIXIW-UHFFFAOYSA-N
InChI=1S/C8H7NO3/c10-5-9-7-4-2-1-3-6(7)8(11)12/h1-5H,(H,9,10)(H,11,12)
| Molecular Formula | C8H7NO3 |
| Molecular Weight | 165.1461 |
| 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 |
|---|---|---|
| Crystallization and diffraction data of 1H-3-hydroxy-4-oxoquinoline 2,4-dioxygenase: a cofactor-free oxygenase of the alpha/beta-hydrolase family. | 2007-05-01 |
|
| Dioxygenases without requirement for cofactors and their chemical model reaction: compulsory order ternary complex mechanism of 1H-3-hydroxy-4-oxoquinaldine 2,4-dioxygenase involving general base catalysis by histidine 251 and single-electron oxidation of the substrate dianion. | 2004-11-16 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:55:12 GMT 2025
by
admin
on
Mon Mar 31 19:55:12 GMT 2025
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| Record UNII |
6670418F9K
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| Record Status |
Validated (UNII)
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| Record Version |
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