Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H9N5O3 |
| Molecular Weight | 271.2316 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+]1=C2C=CC=CC2=[N+]([O-])C(C=NNC(=O)CC#N)=C1
InChI
InChIKey=MBCZYLSVSCJJJQ-AUWJEWJLSA-N
InChI=1S/C12H9N5O3/c13-6-5-12(18)15-14-7-9-8-16(19)10-3-1-2-4-11(10)17(9)20/h1-4,7-8H,5H2,(H,15,18)/b14-7-
| Molecular Formula | C12H9N5O3 |
| Molecular Weight | 271.2316 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Ciadox is Quinoxaline 1,4-dioxide derivative with antimicrobial and promoting activities. Cyadox supplied as premix in the final feed in Eastern Europe and may be used in pigs up to four months of age. Some evidence demonstrated that the mechanism of Ciadox for improving pig growth performance was correlated with several metabolic hormones and growth factors. Cyadox also did not show any adverse effects in carcinogenicity tests with rats and long-term toxicity tests with mice and rats. Cyadox subchronic oral toxicity evaluation shows mild toxicity in non-rodents animals. Metabolic transformation of Ciadox leads to three major metabolites, including 1,4-bisdesoxycyadox, 4-desoxycyadox, and quinoxaline-2-carboxylic acid. Ciadox and metabolites shows virtually no toxic effects in the acute and subchronic oral toxicity study and no mutagenic, carcinogenic activivt.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26408151
pigs: 20 mg/kg of body weight for five consecutive days.
dogs: 100, 450 and 2500 mg/kg of cyadox, for 13 weeks.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 08:45:30 GMT 2025
by
admin
on
Wed Apr 02 08:45:30 GMT 2025
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| Record UNII |
HX312O5UGN
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| Record Status |
Validated (UNII)
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C52588
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ACTIVE MOIETY |