Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H7NO4 |
| Molecular Weight | 181.1455 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC1=CC=CC=C1[N+]([O-])=O
InChI
InChIKey=WMUZDBZPDLHUMW-UHFFFAOYSA-N
InChI=1S/C8H7NO4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Inhibition of human carboxylesterases hCE1 and hiCE by cholinesterase inhibitors. | 2013-03-25 |
|
| The α,5-dicarboxy-2-nitrobenzyl caging group, a tool for biophysical applications with improved hydrophilicity: synthesis, photochemical properties and biological characterization. | 2010-10-01 |
|
| (2-Nitrophenyl)acetyl: a new, selectively removable hydroxyl protecting group. | 2010-05-07 |
|
| Total synthesis of (+/-)- and (-)-actinophyllic acid. | 2010-04-07 |
|
| Leveraging a small-molecule modification to enable the photoactivation of rho GTPases. | 2009-12-14 |
|
| Delta9-tetrahydrocannabinol is a full agonist at CB1 receptors on GABA neuron axon terminals in the hippocampus. | 2009-12-09 |
|
| 5-(3-Nitro-benz-yl)-1,3,4-thia-diazol-2-amine. | 2009-11-25 |
|
| Competition between cleavage and decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl protected cysteine derivatives. | 2009-06-14 |
|
| Studies of decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl (CNB) caged compounds. | 2008-01 |
|
| Mechanisms of cholinesterase inhibition by inorganic mercury. | 2007-04 |
|
| Comparative analysis of inhibitory effects of caged ligands for the NMDA receptor. | 2005-03-15 |
|
| Synthesis and characterization of photolabile o-nitrobenzyl derivatives of urea. | 2002-12-13 |
|
| Studies on the catalytic behaviour of a cholinesterase-like abzyme in an AOT microemulsion system. | 2002-08-07 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
3740-52-1
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY | |||
|
05TN0SUY38
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY | |||
|
77337
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY | |||
|
223-128-0
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY | |||
|
DTXSID0063157
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY | |||
|
16624
Created by
admin on Mon Mar 31 18:52:34 GMT 2025 , Edited by admin on Mon Mar 31 18:52:34 GMT 2025
|
PRIMARY |
SUBSTANCE RECORD