AZANIDAZOLE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C10H10N6O2
Molecular Weight	246.2254
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	1
Charge	0

SHOW SMILES / InChI

Structure of AZANIDAZOLE

Structure Search

SMILES

CN1C(\C=C\C2=NC(N)=NC=C2)=NC=C1[N+]([O-])=O

InChI

InChIKey=LHIALLMPKJMSIQ-NSCUHMNNSA-N

InChI=1S/C10H10N6O2/c1-15-8(13-6-9(15)16(17)18)3-2-7-4-5-12-10(11)14-7/h2-6H,1H3,(H2,11,12,14)/b3-2+

HIDE SMILES / InChI

Molecular Formula	C10H10N6O2
Molecular Weight	246.2254
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	1
Optical Activity	NONE

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3322753 | https://www.ncbi.nlm.nih.gov/pubmed/6682212 | https://www.ncbi.nlm.nih.gov/pubmed/6132457

Azanidazole (or Triclose), an antitrichomonal agent that is used to treat the vaginal trichomoniasis in Italy. This drug causes genotoxicity in liver and kidney that is not separated from its biological activity.

Approval Year

PubMed

PubMed

Title	Date	PubMed
Combined systemic and topical treatment of trichomoniasis vaginalis with azanidazol.	1981	7307267

Substance Class	Chemical Created by `admin` on `Sat Dec 16 18:00:55 GMT 2023` Edited by `admin` on `Sat Dec 16 18:00:55 GMT 2023`
Record UNII	YP2Y0DRX4S
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

AZANIDAZOLE

Official Name

English

2-PYRIMIDINAMINE, 4-(2-(1-METHYL-5-NITRO-1H-IMIDAZOL-2-YL)ETHENYL)-, (E)-

Common Name

English

azanidazole [INN]

Common Name

English

Azanidazole [WHO-DD]

Common Name

English

AZANIDAZOLE [MART.]

Common Name

English

AZANIDAZOLE [MI]

Common Name

English

(E)-2-Amino-4-[2-(1-methyl-5-nitroimidazol-2-yl)vinyl]pyrimidine

Systematic Name

English

AZANIDAZOLE [USAN]

Common Name

English

Classification Tree Code System Code

WHO-ATC

G01AF13

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

NCI_THESAURUS

C277

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

WHO-ATC

P01AB04

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

WHO-VATC

QG01AF13

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

WHO-VATC

QP51AA04

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

Code System Code Type Description

MESH

C023624

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

PRIMARY

SMS_ID

100000086891

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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WIKIPEDIA

AZANIDAZOLE

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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FDA UNII

YP2Y0DRX4S

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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MERCK INDEX

m2160

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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Merck Index

INN

4274

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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ChEMBL

CHEMBL134920

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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CAS

62973-76-6

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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PUBCHEM

6436171

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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NCI_THESAURUS

C73274

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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DRUG CENTRAL

264

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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EVMPD

SUB05635MIG

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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DRUG BANK

DB13350

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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EPA CompTox

DTXSID40212180

Created by admin on Sat Dec 16 18:00:55 GMT 2023 , Edited by admin on Sat Dec 16 18:00:55 GMT 2023

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Related Record Type Details


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