Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H10N4O2S |
| Molecular Weight | 250.277 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1C(CSC2=NC=CC=C2)=NC=C1[N+]([O-])=O
InChI
InChIKey=IRVDBEMWNQAVEV-UHFFFAOYSA-N
InChI=1S/C10H10N4O2S/c1-13-8(12-6-10(13)14(15)16)7-17-9-4-2-3-5-11-9/h2-6H,7H2,1H3
| Molecular Formula | C10H10N4O2S |
| Molecular Weight | 250.277 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Pirinidazole was found to be the compound from a series of 5-nitroimidazoles with the broadest action against protozoans. Its effect against trichomonads is the most pronounced. The comparison of the effective doses of different 5-nitroimidazoles against Trichomonas fetus demonstrates that the compound Pirinidazole is slightly superior to Tinidazole, distinctly superior to Metronidazole, and very much superior to Nitrimidazine. Some toxicological data of Pirinidazole show that the compound is well tolerated.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:27:34 GMT 2025
by
admin
on
Mon Mar 31 18:27:34 GMT 2025
|
| Record UNII |
YL02E256HT
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C277
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
55432-15-0
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
DTXSID20866483
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
SUB09914MIG
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
C66423
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
3637
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
100000081668
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
259-636-4
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
68724
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
YL02E256HT
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY | |||
|
CHEMBL2106974
Created by
admin on Mon Mar 31 18:27:34 GMT 2025 , Edited by admin on Mon Mar 31 18:27:34 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |