Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C11H9N |
| Molecular Weight | 155.1959 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1=CC=C(C=C1)C2=CC=CN=C2
InChI
InChIKey=HJKGBRPNSJADMB-UHFFFAOYSA-N
InChI=1S/C11H9N/c1-2-5-10(6-3-1)11-7-4-8-12-9-11/h1-9H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Chemistry of a Ni(II) acetohydroxamic acid complex: formation, reactivity with water, and attempted preparation of zinc and cobalt analogues. | 2005 Oct 3 |
|
| Metal-directed self-assembly of cavitand frameworks. | 2006 Mar 31 |
|
| Biarylaniline phenethanolamines as potent and selective beta3 adrenergic receptor agonists. | 2006 May 4 |
|
| Novel substituted (pyridin-3-yl)phenyloxazolidinones: antibacterial agents with reduced activity against monoamine oxidase A and increased solubility. | 2007 Oct 4 |
|
| Design, synthesis, and evaluation of isoindolinone-hydroxamic acid derivatives as histone deacetylase (HDAC) inhibitors. | 2007 Sep 1 |
|
| 1H, 13C and 15N nuclear magnetic resonance coordination shifts in Au(III), Pd(II) and Pt(II) chloride complexes with phenylpyridines. | 2009 Aug |
|
| Potent biphenyl- and 3-phenyl pyridine-based inhibitors of acetyl-CoA carboxylase. | 2009 Oct 15 |
|
| SCH 530348: a novel oral thrombin receptor antagonist. | 2009 Sep |
|
| Emerging antiplatelet agents, differential pharmacology, and clinical utility. | 2010 |
|
| Fluorescent chemosensors for toxic organophosphorus pesticides: a review. | 2010 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
13886
Created by
admin on Fri Dec 15 19:36:00 GMT 2023 , Edited by admin on Fri Dec 15 19:36:00 GMT 2023
|
PRIMARY | |||
|
DTXSID0061404
Created by
admin on Fri Dec 15 19:36:00 GMT 2023 , Edited by admin on Fri Dec 15 19:36:00 GMT 2023
|
PRIMARY | |||
|
EDZ6KB7JVC
Created by
admin on Fri Dec 15 19:36:00 GMT 2023 , Edited by admin on Fri Dec 15 19:36:00 GMT 2023
|
PRIMARY | |||
|
1008-88-4
Created by
admin on Fri Dec 15 19:36:00 GMT 2023 , Edited by admin on Fri Dec 15 19:36:00 GMT 2023
|
PRIMARY | |||
|
213-762-6
Created by
admin on Fri Dec 15 19:36:00 GMT 2023 , Edited by admin on Fri Dec 15 19:36:00 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
