U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C13H18N6O5
Molecular Weight 338.3192
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of MOXNIDAZOLE

SMILES

CN1C(\C=N\N2CC(CN3CCOCC3)OC2=O)=NC=C1[N+]([O-])=O

InChI

InChIKey=RILWUTQZRXWBOB-GIDUJCDVSA-N
InChI=1S/C13H18N6O5/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/b15-6+

HIDE SMILES / InChI

Molecular Formula C13H18N6O5
Molecular Weight 338.3192
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

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

PubMed

PubMed

TitleDatePubMed
[Field trials with Moxnidazole in poultry and pigs].
1976 Jun 5
Patents

Patents

Sample Use Guides

In Vivo Use Guide
3-​20 mg​/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:53:16 GMT 2023
Edited
by admin
on Sat Dec 16 17:53:16 GMT 2023
Record UNII
9J21260BCQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOXNIDAZOLE
INN   USAN  
INN   USAN  
Official Name English
moxnidazole [INN]
Common Name English
2-OXAZOLIDINONE, 3-(((1-METHYL-5-NITRO-1H-IMIDAZOL-2-YL)METHYLENE)AMINO)-5-(4-MORPHOLINYLMETHYL)-
Systematic Name English
SH 240
Code English
3-[[(1-Methyl-5-nitroimidazol-2-yl)methylene]amino]-5-(morpholinomethyl)-2-oxazolidinone
Systematic Name English
MOXNIDAZOLE [USAN]
Common Name English
SH-240
Code English
Classification Tree Code System Code
NCI_THESAURUS C277
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
Code System Code Type Description
SMS_ID
100000080601
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
FDA UNII
9J21260BCQ
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106791
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
INN
3740
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
PUBCHEM
9571039
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
MESH
C013139
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
EVMPD
SUB09091MIG
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
CAS
52279-59-1
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID40866248
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
NCI_THESAURUS
C90756
Created by admin on Sat Dec 16 17:53:17 GMT 2023 , Edited by admin on Sat Dec 16 17:53:17 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY