Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C5H7N3O2.CH4O3S |
| Molecular Weight | 237.234 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CS(O)(=O)=O.CN1C(C)=NC=C1[N+]([O-])=O
InChI
InChIKey=FKWSWLFYXRLGRR-UHFFFAOYSA-N
InChI=1S/C5H7N3O2.CH4O3S/c1-4-6-3-5(7(4)2)8(9)10;1-5(2,3)4/h3H,1-2H3;1H3,(H,2,3,4)
| Molecular Formula | CH4O3S |
| Molecular Weight | 96.106 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C5H7N3O2 |
| Molecular Weight | 141.128 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Dimetridazole is an anti-fungal and anti-protozoal drug traditionally used in veterinary for the prevention and treatment of histomoniasis in turkeys, genital trichomoniasis in cattle and hemorrhagic enteritis in pigs. Results from the in vitro and in vivo tests suggested, that dimetridazole was not genotoxic compound, but its use is legally limited, although this compound is still can be found in eggs.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and evaluation of nitroheterocyclic carbamate prodrugs for use with nitroreductase-mediated gene-directed enzyme prodrug therapy. | 2003-12-04 |
|
| Determination of dimetridazole in poultry tissues and eggs using liquid chromatography-thermospray mass spectrometry. | 1997-09 |
|
| The therapeutic effect of 16 antimicrobial agents on Cryptosporidium infection in mice. | 1982-04 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8950108
in veterinary: After laying hens had been dosed orally with dimetridazole (DMZ) for 3 days (50 and 250 mg/kg body weight (b.w.)) or intramuscularly, also for 3 days (50 mg/kg b.w.), the residues were determined in serum, liver, breast and thigh muscle by liquid chromatography.
Route of Administration:
Other
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/9786623
The in vitro susceptibility of four Trichomonas gallinae isolates to five nitroimidazolic drugs, that is, carnidazole, dimetridazole, metronidazole, ornidazole and ronidazole, was also determined. Minimal lethal concentrations (MLCs) of these drugs were obtained. For carnidazole, dimetridazole, metronidazole and ornidazole the MLC ranged between 93.75-500 microg ml.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:33:41 GMT 2025
by
admin
on
Mon Mar 31 21:33:41 GMT 2025
|
| Record UNII |
8WI17L7FIJ
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
93856-85-0
Created by
admin on Mon Mar 31 21:33:41 GMT 2025 , Edited by admin on Mon Mar 31 21:33:41 GMT 2025
|
PRIMARY | |||
|
DTXSID40917486
Created by
admin on Mon Mar 31 21:33:41 GMT 2025 , Edited by admin on Mon Mar 31 21:33:41 GMT 2025
|
PRIMARY | |||
|
8WI17L7FIJ
Created by
admin on Mon Mar 31 21:33:41 GMT 2025 , Edited by admin on Mon Mar 31 21:33:41 GMT 2025
|
PRIMARY | |||
|
16205819
Created by
admin on Mon Mar 31 21:33:41 GMT 2025 , Edited by admin on Mon Mar 31 21:33:41 GMT 2025
|
PRIMARY | |||
|
299-119-0
Created by
admin on Mon Mar 31 21:33:41 GMT 2025 , Edited by admin on Mon Mar 31 21:33:41 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |