Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H5NO |
| Molecular Weight | 107.11 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
O=CC1=CN=CC=C1
InChI
InChIKey=QJZUKDFHGGYHMC-UHFFFAOYSA-N
InChI=1S/C6H5NO/c8-5-6-2-1-3-7-4-6/h1-5H
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Apoptosis induced by picolinic acid-related compounds in HL-60 cells. | 2001 Oct |
|
| Efficient enantiomeric synthesis of pyrrolidine and piperidine alkaloids from tobacco. | 2001 Sep 21 |
|
| Molecular cloning and characterization of a novel lactate dehydrogenase gene from Clonorchis sinensis. | 2006 Jun |
|
| 1,3-Di-3-pyridyl-2,3-dihydro-1H-naphth[1,2-e][1,3]oxazine. | 2008 Feb 13 |
|
| Synthesis and pharmacological evaluation of novel N-alkyl/aryl substituted thiazolidinone arecoline analogues as muscarinic receptor 1 agonist in Alzheimer's dementia models. | 2009 Dec |
|
| Aroylguanidine-based factor Xa inhibitors: the discovery of BMS-344577. | 2009 Dec 15 |
|
| Bis(ethanol-κO)bis-(pyridine-3-carb-aldehyde-κN thio-semicarbazone)bis-(thio-cyanato-κN)iron(II)-pyridine-3-carbaldehyde thio-semicarbazone (1/2). | 2009 Jul 1 |
|
| N'-[(E)-3-Pyridylmethyl-idene]benzo-hydrazide. | 2009 Oct 3 |
|
| Methyl 3-(3-pyridylmethyl-ene)carbazate. | 2009 Oct 31 |
|
| Characterization of nicotinamidases: steady state kinetic parameters, classwide inhibition by nicotinaldehydes, and catalytic mechanism. | 2010 Dec 14 |
|
| Betulin and ursolic acid synthetic derivatives as inhibitors of Papilloma virus. | 2010 Jul 15 |
|
| Novel and convenient synthesis of 1-(pyridinylmethyl)-2-naphthols and 1-(pyridinylmethylene)-2-tetralones from 2-tetralones. | 2010 May |
|
| Kinetics and inhibition of nicotinamidase from Mycobacterium tuberculosis. | 2010 Nov 9 |
|
| Pharmacological evaluation and characterizations of newly synthesized 1,2,4-triazoles. | 2010 Sep |
|
| 4-Dimethyl-amino-N'-(3-pyridyl-methyl-idene)benzohydrazide. | 2010 Sep 25 |
Patents
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C014785
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
DTXSID2022044
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
8952
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
28345
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
SUB14644MIG
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
500-22-1
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
Pyridine-3-carboxaldehyde
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
207-900-4
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
100000079971
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
840R4IDQ1T
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY | |||
|
10371
Created by
admin on Fri Dec 15 17:12:57 GMT 2023 , Edited by admin on Fri Dec 15 17:12:57 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD
