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
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)
| 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
| Title | Date | PubMed |
|---|---|---|
| [Chemical studies the mechanism of action of isoniazid]. | 1966 Nov |
|
| Rat ventral prostate microsomal biotransformation of ethanol to acetaldehyde and 1-hydroxyethyl radicals: its potential contribution to prostate tumor promotion. | 2002 |
|
| Conformational polymorphism in N-(4'-methoxyphenyl)- 3-bromothiobenzamide. | 2007 Apr 2 |
|
| Hydrogen sulfide enhances ulcer healing in rats. | 2007 Dec |
|
| A proteomic analysis of bromobenzene reactive metabolite targets in rat liver cytosol in vivo. | 2007 Mar |
|
| The investigation of structure-activity relationships of tacrine analogues: electronic-topological method. | 2008 Aug 6 |
|
| Protein targets of reactive metabolites of thiobenzamide in rat liver in vivo. | 2008 Jul |
|
| Enantiomeric resolution of N,N'-dimethyldithiodianthranilide through diastereomeric silver(I) complex. Circular dichroism spectra, racemization barrier, and molecular self-assembly. | 2008 Jul 4 |
|
| 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 Jun |
|
| ETM-ANN approach application for thiobenzamide and quinolizidine derivatives. | 2010 |
|
| 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 Feb |
|
| Formation of covalently bound protein adducts from the cytotoxicant naphthalene in nasal epithelium: species comparisons. | 2010 May |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:22:54 GMT 2023
by
admin
on
Fri Dec 15 18:22:54 GMT 2023
|
| Record UNII |
8799VM9SXC
|
| Record Status |
Validated (UNII)
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| Record Version |
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