Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C13H18N6O5.ClH |
| Molecular Weight | 374.78 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CN1C(\C=N\N2CC(CN3CCOCC3)OC2=O)=NC=C1[N+]([O-])=O
InChI
InChIKey=JMRKBMOVLDCXFV-AWXXIEIHSA-N
InChI=1S/C13H18N6O5.ClH/c1-16-11(14-7-12(16)19(21)22)6-15-18-9-10(24-13(18)20)8-17-2-4-23-5-3-17;/h6-7,10H,2-5,8-9H2,1H3;1H/b15-6+;
Moxnidazole is an antiparasitic drug suitable for oral use against parasites in farm animals. administration of Moxnidazole in the drinking water gave good prophylaxis of dysentery in swine, histomoniasis in hens and turkeys, and trichomoniasis in pigeons. Isolated relapses were due to renfections and were successfully treated by another dose of the drug.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/786594
3-20 mg/kg
Route of Administration:
Oral
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
9577035
Created by
admin on Mon Mar 31 22:16:36 GMT 2025 , Edited by admin on Mon Mar 31 22:16:36 GMT 2025
|
PRIMARY | |||
|
300583
Created by
admin on Mon Mar 31 22:16:36 GMT 2025 , Edited by admin on Mon Mar 31 22:16:36 GMT 2025
|
PRIMARY | |||
|
30185-92-3
Created by
admin on Mon Mar 31 22:16:36 GMT 2025 , Edited by admin on Mon Mar 31 22:16:36 GMT 2025
|
NON-SPECIFIC STOICHIOMETRY | |||
|
30826-72-3
Created by
admin on Mon Mar 31 22:16:36 GMT 2025 , Edited by admin on Mon Mar 31 22:16:36 GMT 2025
|
PRIMARY | |||
|
0I2J76PMVM
Created by
admin on Mon Mar 31 22:16:36 GMT 2025 , Edited by admin on Mon Mar 31 22:16:36 GMT 2025
|
PRIMARY |
ACTIVE MOIETY
SUBSTANCE RECORD