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)
| Molecular Formula | C8H7NO4 |
| Molecular Weight | 181.1455 |
| 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 |
|---|---|---|
| Studies on the catalytic behaviour of a cholinesterase-like abzyme in an AOT microemulsion system. | 2002 Aug 7 |
|
| Synthesis and characterization of photolabile o-nitrobenzyl derivatives of urea. | 2002 Dec 13 |
|
| Comparative analysis of inhibitory effects of caged ligands for the NMDA receptor. | 2005 Mar 15 |
|
| Mechanisms of cholinesterase inhibition by inorganic mercury. | 2007 Apr |
|
| Studies of decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl (CNB) caged compounds. | 2008 Jan |
|
| Leveraging a small-molecule modification to enable the photoactivation of rho GTPases. | 2009 Dec 14 |
|
| Competition between cleavage and decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl protected cysteine derivatives. | 2009 Jun 14 |
|
| 5-(3-Nitro-benz-yl)-1,3,4-thia-diazol-2-amine. | 2009 Nov 25 |
|
| Total synthesis of (+/-)- and (-)-actinophyllic acid. | 2010 Apr 7 |
|
| Delta9-tetrahydrocannabinol is a full agonist at CB1 receptors on GABA neuron axon terminals in the hippocampus. | 2010 Jul-Aug |
|
| (2-Nitrophenyl)acetyl: a new, selectively removable hydroxyl protecting group. | 2010 May 7 |
|
| The α,5-dicarboxy-2-nitrobenzyl caging group, a tool for biophysical applications with improved hydrophilicity: synthesis, photochemical properties and biological characterization. | 2010 Nov-Dec |
|
| Inhibition of human carboxylesterases hCE1 and hiCE by cholinesterase inhibitors. | 2013 Mar 25 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:46:55 GMT 2023
by
admin
on
Fri Dec 15 17:46:55 GMT 2023
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| Record UNII |
05TN0SUY38
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| Record Status |
Validated (UNII)
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| Record Version |
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3740-52-1
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05TN0SUY38
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77337
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223-128-0
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DTXSID0063157
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16624
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