Details
Stereochemistry | ACHIRAL |
Molecular Formula | C6H8N2 |
Molecular Weight | 108.1411 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC=NC(N)=C1
InChI
InChIKey=ORLGLBZRQYOWNA-UHFFFAOYSA-N
InChI=1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8)
Molecular Formula | C6H8N2 |
Molecular Weight | 108.1411 |
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 |
---|---|---|
2-Amino-4-methylpyridine as a potent inhibitor of inducible NO synthase activity in vitro and in vivo. | 1996 Nov |
|
Synthesis and evaluation of 3-aminopropionyl substituted fentanyl analogues for opioid activity. | 2006 Sep 15 |
|
Hexakis(2-amino-4-methyl-pyridine-κN)dioxidohexa-μ(4)-sulfido-hexa-copper(I)divanadium(V). | 2008 Aug 30 |
|
Bis(2-amino-4-methyl-pyridinium) tetra-chloridocuprate(II). | 2008 Dec 17 |
|
2-Amino-4-methyl-pyridinium 4-amino-benzoate. | 2008 May 21 |
|
tert-Butyl N-(4-methyl-2-pyrid-yl)-carbamate. | 2008 Oct 31 |
|
2-Ferrocenyl-N-(2-ferrocenylbenzo-yl)-N-(4-methyl-2-pyrid-yl)benzamide. | 2009 Feb 28 |
|
Dimethyl 4-eth-oxy-1-(4-methyl-2-pyri-dyl)-5-oxo-2,5-dihydro-1H-pyrrole-2,3-dicarboxyl-ate. | 2010 Apr 17 |
|
Bis(2-amino-5-bromo-pyridinium) fumarate dihydrate. | 2010 Aug 11 |
|
2-Amino-4-methyl-pyridinium hexa-2,4-dienoate dihydrate. | 2010 Aug 25 |
|
2-Amino-4-methyl-pyridinium 6-carb-oxy-pyridine-2-carboxyl-ate methanol monosolvate. | 2010 Dec 8 |
|
2-Amino-5-methyl-pyridinium 4-nitro-benzoate. | 2010 Feb 13 |
|
2-Amino-4-methyl-pyridinium 4-nitro-benzoate. | 2010 Jan 13 |
|
Cyclosporine A-induced nitration of tyrosine 34 MnSOD in endothelial cells: role of mitochondrial superoxide. | 2010 Jul 15 |
|
2-Amino-4-methyl-pyridinium 3-carb-oxy-4-hy-droxy-benzene-sulfonate monohydrate. | 2010 Jul 24 |
|
4-Methyl-N-[(E)-4-methyl-1-(4-methyl-phenyl-sulfon-yl)-1,2-dihydropyridin-2-yl-idene]benzene-sulfonamide. | 2010 Jul 3 |
|
2-Amino-4-methyl-pyridinium 2-hy-droxy-benzoate. | 2010 Jul 31 |
|
2-Amino-4-methyl-pyridinium 2-carb-oxy-benzoate. | 2010 Jul 7 |
|
2-Amino-4-methyl-pyridinium 3-chloro-benzoate. | 2010 Jun 26 |
|
Quantitative morphometry of respiratory tract epithelial cells as a tool for testing chemopreventive agent efficacy. | 2010 Mar |
|
2-Amino-4-methyl-pyridinium trifluoro-acetate. | 2010 Mar 10 |
|
2-Amino-4-methyl-pyridinium trifluoro-acetate: a monoclinic polymorph. | 2010 Mar 17 |
|
DNA binding ability and hydrogen peroxide induced nuclease activity of a novel Cu(II) complex with malonate as the primary ligand and protonated 2-amino-4-picoline as the counterion. | 2010 May 6 |
|
2-Amino-4-methyl-pyridinium 6-carb-oxy-pyridine-2-carboxyl-ate sesquihydrate. | 2010 Nov 20 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:14:17 GMT 2023
by
admin
on
Fri Dec 15 18:14:17 GMT 2023
|
Record UNII |
394N1Z644H
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Code | English | ||
|
Brand Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
1490
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
394N1Z644H
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
176165
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
m1732
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | Merck Index | ||
|
172
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
695-34-1
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
1533
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
6972
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
DTXSID1044720
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY | |||
|
211-780-9
Created by
admin on Fri Dec 15 18:14:18 GMT 2023 , Edited by admin on Fri Dec 15 18:14:18 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|