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

Details

Stereochemistry ACHIRAL
Molecular Formula C8H5N3O3S2
Molecular Weight 255.274
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TENONITROZOLE

SMILES

[O-][N+](=O)C1=CN=C(NC(=O)C2=CC=CS2)S1

InChI

InChIKey=ZLOXYEZYWCTXHU-UHFFFAOYSA-N
InChI=1S/C8H5N3O3S2/c12-7(5-2-1-3-15-5)10-8-9-4-6(16-8)11(13)14/h1-4H,(H,9,10,12)

HIDE SMILES / InChI

Molecular Formula C8H5N3O3S2
Molecular Weight 255.274
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
ATRICAN

Approved Use

This medicine contains the active ingredient tenonitrozole which belongs to a group of antiprotozoal agents. This medicine is prescribed for the treatment of urogenital trichomoniasis, which is an infection caused by the parasite Trichomonas vaginalis.
Overview

OverviewOther

Other InhibitorOther SubstrateOther Inducer



Drug as perpetrator​Drug as victim

Drug as victim

TargetModalityActivityMetaboliteClinical evidence
no
Tox targets

Tox targets

TargetModalityActivityMetaboliteClinical evidence
PubMed

PubMed

TitleDatePubMed
Development of 5-nitrothiazole derivatives: identification of leads against both replicative and latent Mycobacterium tuberculosis.
2012-12-15
[THE INFLUENCE OF ATRICAN (ALPHA-THENOYL-AMINO-2-NITRO-5-THIAZOLE) ON THE PREGNANCY AND FETAL DEVELOPMENT OF THE RAT, MOUSE AND RABBIT].
1964-05-20
[UROGENITAL SYNDROMES CAUSED BY "TRICHOMONAS VAGINALIS" AND "CANDIDA ALBICANS". RESULTS OF TREATMENT BY 2-(ALPHA-THENOYLAMINO)-5-NITROTHIAZOLE].
1963-12-28
Patents

Sample Use Guides

Urogenital trichomoniasis treatment: The usual dose is 1 capsule in the morning and 1 capsule (250 mg) in the evening during meals, for 4 days. Both partners should be treated simultaneously.
Route of Administration: Oral
Tenonitrozole inhibited Giardia with IC50 value of 0.19 uM
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:55:34 GMT 2025
Edited
by admin
on Mon Mar 31 17:55:34 GMT 2025
Record UNII
PBQ7WLE1WP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TENONITROZOLE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
ATRICAN
Preferred Name English
N-(5-NITRO-2-THIAZOLYL)-2-THIOPHENECARBOXAMIDE
Systematic Name English
Tenonitrozole [WHO-DD]
Common Name English
tenonitrozole [INN]
Common Name English
TENONITROZOLE [MI]
Common Name English
TENONITROZOLE [MART.]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C277
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
WHO-ATC P01AX08
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
Code System Code Type Description
CAS
3810-35-3
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
NCI_THESAURUS
C152561
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
DRUG BANK
DB13659
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
INN
5150
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
ECHA (EC/EINECS)
223-282-9
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
MERCK INDEX
m10560
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY Merck Index
FDA UNII
PBQ7WLE1WP
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
WIKIPEDIA
TENONITROZOLE
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
DRUG CENTRAL
2594
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
SMS_ID
100000082950
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
RXCUI
236186
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY RxNorm
EVMPD
SUB10897MIG
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
ChEMBL
CHEMBL1082354
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
PUBCHEM
19646
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
EPA CompTox
DTXSID5046277
Created by admin on Mon Mar 31 17:55:34 GMT 2025 , Edited by admin on Mon Mar 31 17:55:34 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY