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=CC=C1[N+]([O-])=O
InChI
InChIKey=BUNFNRVLMKHKIT-UHFFFAOYSA-N
InChI=1S/C8H8N2O3/c1-6(11)9-7-4-2-3-5-8(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 |
|---|---|---|
| Hydrolysis of acetylthiocoline, o-nitroacetanilide and o-nitrotrifluoroacetanilide by fetal bovine serum acetylcholinesterase. | 2009-04 |
|
| High aryl acylamidase activity associated with cobra venom acetylcholinesterase: biological significance. | 2009-01-27 |
|
| The level of aryl acylamidase activity displayed by human butyrylcholinesterase depends on its molecular distribution. | 2008-09-25 |
|
| Human butyrylcholinesterase components differ in aryl acylamidase activity. | 2008-04 |
|
| Kinetic analysis of butyrylcholinesterase-catalyzed hydrolysis of acetanilides. | 2007-09 |
|
| Aryl acylamidase activity of human serum albumin with o-nitrotrifluoroacetanilide as the substrate. | 2007-08 |
|
| Human serum cholinesterase from liver pathological samples exhibit highly elevated aryl acylamidase activity. | 2007-05-01 |
|
| EstA from Arthrobacter nitroguajacolicus Rü61a, a thermo- and solvent-tolerant carboxylesterase related to class C beta-lactamases. | 2007-03 |
|
| Diisopropylfluorophosphate-sensitive aryl acylamidase activity of fatty acid free human serum albumin. | 2006-08-15 |
|
| On the active site for hydrolysis of aryl amides and choline esters by human cholinesterases. | 2006-07-01 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 21:21:41 GMT 2025
by
admin
on
Mon Mar 31 21:21:41 GMT 2025
|
| Record UNII |
Q4KJC83992
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
209-009-6
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
11090
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
1313
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
Q4KJC83992
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
DTXSID4060282
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
m7937
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | Merck Index | ||
|
C539848
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY | |||
|
552-32-9
Created by
admin on Mon Mar 31 21:21:41 GMT 2025 , Edited by admin on Mon Mar 31 21:21:41 GMT 2025
|
PRIMARY |