Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)C1=CN=C2C=CC=CC2=N1
InChI
InChIKey=UPUZGXILYFKSGE-UHFFFAOYSA-N
InChI=1S/C9H6N2O2/c12-9(13)8-5-10-6-3-1-2-4-7(6)11-8/h1-5H,(H,12,13)
| Molecular Formula | C9H6N2O2 |
| Molecular Weight | 174.1561 |
| 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 |
|---|---|---|
| Synthesis and antimycobacterial activity of pyrazine and quinoxaline derivatives. | 2002 Dec 5 |
|
| Synthesis and AMPA receptor antagonistic activity of a novel class of quinoxalinecarboxylic acid with a substituted phenyl group at the C-7 position. | 2003 Oct 20 |
|
| Development of HPLC methods for the determination of cyadox and its main metabolites in goat tissues. | 2005 Dec |
|
| Effects of cooking and storage on residues of cyadox in chicken muscle. | 2005 Dec 14 |
|
| Confirmation of carbadox and olaquindox metabolites in porcine liver using liquid chromatography-electrospray, tandem mass spectrometry. | 2005 Feb 25 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:13:13 GMT 2023
by
admin
on
Fri Dec 15 19:13:13 GMT 2023
|
| Record UNII |
M5OE8SN42M
|
| Record Status |
Validated (UNII)
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| Record Version |
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96695
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879-65-2
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M5OE8SN42M
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C042218
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DTXSID80236688
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86873
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