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)
Approval Year
PubMed
Title | Date | PubMed |
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[Chemical studies the mechanism of action of isoniazid]. | 1966 Nov |
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Rat ventral prostate microsomal biotransformation of ethanol to acetaldehyde and 1-hydroxyethyl radicals: its potential contribution to prostate tumor promotion. | 2002 |
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Synthesis of 1,3-thiazine derivatives and their evaluation as potential antimycobacterial agents. | 2002 Apr |
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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 |
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Planar chiral dianthranilide and dithiodianthranilide molecules: optical resolution, chiroptical spectra, and molecular self-assembly. | 2004 Feb 20 |
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Flavin-containing monooxygenase activity can be inhibited by nitric oxide-mediated S-nitrosylation. | 2004 Oct 8 |
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Covalent modification of microsomal lipids by thiobenzamide metabolites in vivo. | 2007 Apr |
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Conformational polymorphism in N-(4'-methoxyphenyl)- 3-bromothiobenzamide. | 2007 Apr 2 |
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A proteomic analysis of bromobenzene reactive metabolite targets in rat liver cytosol in vivo. | 2007 Mar |
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DTXSID8062280
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C015539
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218-765-6
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683563
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2227-79-4
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8799VM9SXC
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SUBSTANCE RECORD