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Details

Stereochemistry ACHIRAL
Molecular Formula C8H13N3O4S
Molecular Weight 247.272
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TINIDAZOLE

SMILES

CCS(=O)(=O)CCN1C(C)=NC=C1[N+]([O-])=O

InChI

InChIKey=HJLSLZFTEKNLFI-UHFFFAOYSA-N
InChI=1S/C8H13N3O4S/c1-3-16(14,15)5-4-10-7(2)9-6-8(10)11(12)13/h6H,3-5H2,1-2H3

HIDE SMILES / InChI
Molecular Formula C8H13N3O4S
Molecular Weight 247.272
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:20:29 UTC 2023
Edited
by admin
on Sat Dec 16 16:20:29 UTC 2023
Record UNII
033KF7V46H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TINIDAZOLE
EP   HSDB   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
1H-IMIDAZOLE, 1-(2-(ETHYLSULFONYL)ETHYL)-2-METHYL-5-NITRO-
Systematic Name English
FASIGIN
Brand Name English
TRICOLAM
Brand Name English
TINIDAZOLE [MI]
Common Name English
TINIDAZOLE [MART.]
Common Name English
TINIDAZOLE [JAN]
Common Name English
CP-12,574
Code English
FASIGYN
Brand Name English
TINIDAZOLE [USP-RS]
Common Name English
TRIMONASE
Brand Name English
TINIDAZOLE [USAN]
Common Name English
TINIDAZOLE [HSDB]
Common Name English
IMIDAZOLE, 1-(2-(ETHYLSULFONYL)ETHYL)-2-METHYL-4-NITRO-
Systematic Name English
1-[2-(Ethylsulfonyl)ethyl]-2-methyl-5-nitroimidazole
Systematic Name English
TINIDAZOLE [VANDF]
Common Name English
TINDAMAX
Brand Name English
NSC-758189
Code English
TINIDAZOLE [ORANGE BOOK]
Common Name English
Tinidazole [WHO-DD]
Common Name English
CP-12574
Code English
tinidazole [INN]
Common Name English
SIMPLOTAN
Brand Name English
HAISIGYN
Brand Name English
TINIDAZOLE [USP MONOGRAPH]
Common Name English
TINIDAZOLE [EP MONOGRAPH]
Common Name English
Classification Tree Code System Code
CFR 21 CFR 530.41
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-ATC J01RA11
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-ATC A02BD09
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-VATC QJ01XD02
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-ATC J01RA13
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
NDF-RT N0000175435
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
FDA ORPHAN DRUG 155402
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-VATC QP51AA02
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
LIVERTOX NBK548538
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-ATC J01XD02
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
WHO-ATC P01AB02
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
NDF-RT N0000007663
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
NDF-RT N0000007663
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
FDA ORPHAN DRUG 173603
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
Code System Code Type Description
ChEMBL
CHEMBL1220
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
MERCK INDEX
m10874
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY Merck Index
SMS_ID
100000092535
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
NCI_THESAURUS
C890
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
INN
2653
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
PUBCHEM
5479
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
DRUG BANK
DB00911
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
EVMPD
SUB11074MIG
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
DAILYMED
033KF7V46H
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
FDA UNII
033KF7V46H
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
WIKIPEDIA
TINIDAZOLE
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
MESH
D014011
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
DRUG CENTRAL
2671
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
ECHA (EC/EINECS)
243-014-4
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
CAS
19387-91-8
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
NSC
758189
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
RS_ITEM_NUM
1667520
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
EPA CompTox
DTXSID4023676
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
RXCUI
10612
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY RxNorm
HSDB
7362
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
LACTMED
Tinidazole
Created by admin on Sat Dec 16 16:20:30 UTC 2023 , Edited by admin on Sat Dec 16 16:20:30 UTC 2023
PRIMARY
Related Record Type Details
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
CYTOCHROME P450 3A4
METABOLIC ENZYME -> SUBSTRATE
MAJOR
Structure of TINIDAZOLE
EXCRETED UNCHANGED
URINE
Related Record Type Details
Structure of ETHYL 2-(5-HYDROXY-2-METHYL-4-NITRO-1-IMIDAZOLYL)ETHYL SULPHONE
METABOLITE -> PARENT
MAJOR
URINE
Structure of 2-HYDROXYMETHYLTINIDAZOLE
METABOLITE ACTIVE -> PARENT
The hydroxy metabolite of tinidazole was similarly more active than its parent compound.
Related Record Type Details
Structure of 2-METHYL-5-NITROIMIDAZOLE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
Ph.Eur.; USP
Structure of ISOTINIDAZOLE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
Ph.Eur.; USP
Related Record Type Details
Structure of TINIDAZOLE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC
Tmax PHARMACOKINETIC SINGLE DOSE

following an overnight fast

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