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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NS
Molecular Weight 137.202
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of THIOBENZAMIDE

SMILES

NC(=S)C1=CC=CC=C1

InChI

InChIKey=QIOZLISABUUKJY-UHFFFAOYSA-N
InChI=1S/C7H7NS/c8-7(9)6-4-2-1-3-5-6/h1-5H,(H2,8,9)

HIDE SMILES / InChI

Molecular Formula C7H7NS
Molecular Weight 137.202
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Formation of covalently bound protein adducts from the cytotoxicant naphthalene in nasal epithelium: species comparisons.
2010-05
Cytotoxic activity of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides.
2010-02
ETM-ANN approach application for thiobenzamide and quinolizidine derivatives.
2010
Mechanism of unusual formation of 3-(5-phenyl-3H-[1,2,4]dithiazol-3-yl)chromen-4-ones and 4-oxo-4H-chromene-3-carbothioic acid N-phenylamides and their antimicrobial evaluation.
2009-08
Bioinformatic analysis of xenobiotic reactive metabolite target proteins and their interacting partners.
2009-06-12
Hexa-thiocarbamoyl phenyl PEG5K Hb: vasoactivity and structure: influence of rigidity of the conjugation linkage on the PEGylation induced plasma expander-like solution properties of PEG-Hb adducts.
2009-06
The investigation of structure-activity relationships of tacrine analogues: electronic-topological method.
2008-08-06
Enantiomeric resolution of N,N'-dimethyldithiodianthranilide through diastereomeric silver(I) complex. Circular dichroism spectra, racemization barrier, and molecular self-assembly.
2008-07-04
Chemical Research in Toxicology. In this issue.
2008-07
Protein targets of reactive metabolites of thiobenzamide in rat liver in vivo.
2008-07
Hydrogen sulfide enhances ulcer healing in rats.
2007-12
Conformational polymorphism in N-(4'-methoxyphenyl)- 3-bromothiobenzamide.
2007-04-02
Covalent modification of microsomal lipids by thiobenzamide metabolites in vivo.
2007-04
The reactive metabolite target protein database (TPDB)--a web-accessible resource.
2007-03-16
A proteomic analysis of bromobenzene reactive metabolite targets in rat liver cytosol in vivo.
2007-03
Flavin-containing monooxygenase activity can be inhibited by nitric oxide-mediated S-nitrosylation.
2004-10-08
Planar chiral dianthranilide and dithiodianthranilide molecules: optical resolution, chiroptical spectra, and molecular self-assembly.
2004-02-20
Rat breast microsomal biotransformation of ethanol to acetaldehyde but not to free radicals: its potential role in the association between alcohol drinking and breast tumor promotion.
2003
Structure-activity relationships for a series of thiobenzamide influenza fusion inhibitors derived from 1,3,3-trimethyl-5-hydroxy-cyclohexylmethylamine.
2002-12-02
The antituberculosis drug ethionamide is activated by a flavoprotein monooxygenase.
2002-04-12
Synthesis of 1,3-thiazine derivatives and their evaluation as potential antimycobacterial agents.
2002-04
Rat ventral prostate microsomal biotransformation of ethanol to acetaldehyde and 1-hydroxyethyl radicals: its potential contribution to prostate tumor promotion.
2002
[Chemical studies the mechanism of action of isoniazid].
1966-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:11:51 GMT 2025
Edited
by admin
on Mon Mar 31 19:11:51 GMT 2025
Record UNII
8799VM9SXC
Record Status Validated (UNII)
Record Version
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Name Type Language
BENZOTHIOAMIDE
Preferred Name English
THIOBENZAMIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID8062280
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
MESH
C015539
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
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ECHA (EC/EINECS)
218-765-6
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
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PUBCHEM
683563
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
CAS
2227-79-4
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY
FDA UNII
8799VM9SXC
Created by admin on Mon Mar 31 19:11:51 GMT 2025 , Edited by admin on Mon Mar 31 19:11:51 GMT 2025
PRIMARY