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Details

Stereochemistry ACHIRAL
Molecular Formula C11H12N4O2
Molecular Weight 232.2386
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PANIDAZOLE

SMILES

CC1=NC=C(N1CCC2=CC=NC=C2)[N+]([O-])=O

InChI

InChIKey=ARYPMCPJIWUCIP-UHFFFAOYSA-N
InChI=1S/C11H12N4O2/c1-9-13-8-11(15(16)17)14(9)7-4-10-2-5-12-6-3-10/h2-3,5-6,8H,4,7H2,1H3

HIDE SMILES / InChI

Molecular Formula C11H12N4O2
Molecular Weight 232.2386
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Panidazole, an antiprotozoal agent that was studied in patients for the treatment of intestinal amoebiasis and vaginal trichomoniasis. However, information about the further development of this drug is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
The mutagenic action of nitroimidazoles. II. Tinidazole, ipronidazole, panidazole and ornidazole.
1977-04
Laboratory evaluation of panidazole (1-(2'-( -pyridyl) ethyl-2-methyl)-5-nitroimidazole), a new amoebicide.
1972-06
1-(2-(gamma-pyridyl)ethyl)-2-methyl-5-nitro-imidazole (panidazole), a new amoebicide.
1970-09-26

Sample Use Guides

In Vivo Use Guide
panidazole between 1.0 and 2.0 g per day for six days
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:20:29 GMT 2025
Edited
by admin
on Mon Mar 31 18:20:29 GMT 2025
Record UNII
08AHL2YV5K
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PANIDAZOLE
INN  
INN  
Official Name English
panidazole [INN]
Preferred Name English
4-(2-(2-METHYL-5-NITROIMIDAZOL-1-YL)ETHYL)PYRIDINE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C277
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
Code System Code Type Description
FDA UNII
08AHL2YV5K
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
EVMPD
SUB09604MIG
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
ChEMBL
CHEMBL2105336
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
CAS
13752-33-5
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
NCI_THESAURUS
C66302
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
PUBCHEM
72080
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
INN
2963
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
MESH
C016029
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
237-334-3
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
EPA CompTox
DTXSID50160209
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
SMS_ID
100000082767
Created by admin on Mon Mar 31 18:20:29 GMT 2025 , Edited by admin on Mon Mar 31 18:20:29 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY