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
NC(=O)CC1=CC=CC=C1
InChI
InChIKey=LSBDFXRDZJMBSC-UHFFFAOYSA-N
InChI=1S/C8H9NO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
An enzyme-labile safety catch linker for synthesis on a soluble polymeric support. | 2001 Mar 2 |
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Novel, potent phenethylamide inhibitors of the hepatitis C virus (HCV) NS3 protease: probing the role of P2 aryloxyprolines with hybrid structures. | 2003 Aug 18 |
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The scent of age. | 2003 May 7 |
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Thyroid receptor ligands. Part 2: Thyromimetics with improved selectivity for the thyroid hormone receptor beta. | 2004 Jul 5 |
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Mandelamide hydrolase from Pseudomonas putida: characterization of a new member of the amidase signature family. | 2004 Jun 22 |
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Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists. | 2004 Mar 11 |
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Studies on anti-Helicobacter pylori agents. Part 3: A novel, efficacious cephem derivative, FR193879. | 2004 May 17 |
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SAR and pharmacokinetic studies on phenethylamide inhibitors of the hepatitis C virus NS3/NS4A serine protease. | 2004 Sep 6 |
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Diastereospecific photocyclization of a isopropylbenzophenone derivative in crystals and the morphological changes. | 2007 Aug 31 |
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Production of enantiomerically pure (S)-beta-phenylalanine and (R)-beta-phenylalanine by penicillin G acylase from Escherichia coli in aqueous medium. | 2007 Dec |
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QSAR and pharmacophore analysis on amides against drug-resistant S. aureus. | 2008 Jan-Mar |
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The influence of leukotriene receptors' antagonists on experimentally induced ulcer in rats. | 2008 Jul-Sep |
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Phenylethylamide and phenylmethylamide derivatives as new tyrosinase inhibitors. | 2009 Feb |
|
N-(3,4-Diethoxy-phen-yl)acetamide. | 2009 May 20 |
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Code System | Code | Type | Description | ||
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103-81-1
Created by
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DTXSID1059282
Created by
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1877
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7680
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C005293
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m8648
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admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
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203-147-0
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5R219M9TJF
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admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
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16562
Created by
admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
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SUBSTANCE RECORD