Details
Stereochemistry | ACHIRAL |
Molecular Formula | C8H9NO |
Molecular Weight | 135.1632 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O=CNCC1=CC=CC=C1
InChI
InChIKey=IIBOGKHTXBPGEI-UHFFFAOYSA-N
InChI=1S/C8H9NO/c10-7-9-6-8-4-2-1-3-5-8/h1-5,7H,6H2,(H,9,10)
Molecular Formula | C8H9NO |
Molecular Weight | 135.1632 |
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 |
---|---|---|
Peptoid inhibition of trypanothione reductase as a potential antitrypanosomal and antileishmanial drug lead. | 2002 Jun |
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Structure of three class I human alcohol dehydrogenases complexed with isoenzyme specific formamide inhibitors. | 2004 Oct 5 |
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Optimum culture conditions for the production of N-substituted formamide deformylase by Arthrobacter pascens F164. | 2005 Jan |
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Probing stereoselective inhibition of the acyl binding site of cholesterol esterase with four diastereomers of 2'-N-alpha-methylbenzylcarbamyl-1, 1'-bi-2-naphthol. | 2005 Sep 22 |
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Generation and cyclization of unsaturated carbamoyl radicals derived from S-4-pentynyl carbamothioates under tin-free conditions. | 2006 Apr 14 |
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New 2-arylpyrazolo[3,4-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonists. Synthesis, pharmacological evaluation, and ligand-receptor modeling studies. | 2007 Aug 23 |
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N-Benzylformamide at 150 K. | 2008 Dec |
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Design, synthesis, and biological evaluation of benzylamino-methanone based cholesteryl ester transfer protein inhibitors. | 2010 Aug 19 |
|
(E)-N-Benzyl-2-cyano-3-phenyl-acryl-amide. | 2010 Dec 4 |
|
Novel isonitrile hydratase involved in isonitrile metabolism. | 2010 Nov 5 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:37:20 GMT 2023
by
admin
on
Fri Dec 15 19:37:20 GMT 2023
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Record UNII |
L363D92ELK
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Record Status |
Validated (UNII)
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Record Version |
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