Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H8N2O3 |
| Molecular Weight | 180.1607 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(C=C1)[N+]([O-])=O
InChI
InChIKey=NQRLPDFELNCFHW-UHFFFAOYSA-N
InChI=1S/C8H8N2O3/c1-6(11)9-7-2-4-8(5-3-7)10(12)13/h2-5H,1H3,(H,9,11)
| Molecular Formula | C8H8N2O3 |
| Molecular Weight | 180.1607 |
| 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 |
|---|---|---|
| Molecular characterization of a novel bacterial aryl acylamidase belonging to the amidase signature enzyme family. | 2010-05 |
|
| A novel aryl acylamidase from Nocardia farcinica hydrolyses polyamide. | 2009-03-01 |
|
| Gene cloning and characterization of arylamine N-acetyltransferase from Bacillus cereus strain 10-L-2. | 2009-01 |
|
| Human butyrylcholinesterase components differ in aryl acylamidase activity. | 2008-04 |
|
| Kinetic properties of wild-type and altered recombinant amidases by the use of ion-selective electrode assay method. | 2006-08-15 |
|
| N-(4-Trifluoromethylphenyl)amide group of the synthetic histamine receptor agonist inhibits nicotinic acetylcholine receptor-mediated catecholamine secretion. | 2006-02-28 |
|
| Role of protein conformational mobility in enzyme catalysis: acylation of alpha-chymotrypsin by specific peptide substrates. | 2004-01-27 |
|
| Enzymatic hydrolysis of p-nitroacetanilide: mechanistic studies of the aryl acylamidase from Pseudomonas fluorescens. | 2002-01-22 |
|
| Substitutions of Thr-103-Ile and Trp-138-Gly in amidase from Pseudomonas aeruginosa are responsible for altered kinetic properties and enzyme instability. | 2001-03 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:20:00 GMT 2025
by
admin
on
Mon Mar 31 21:20:00 GMT 2025
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| Record UNII |
PH3B066365
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| Record Status |
Validated (UNII)
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| Record Version |
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C033553
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m7937
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7691
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104-04-1
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DTXSID5059290
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Nitroacetanilide
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PH3B066365
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1315
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203-169-0
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