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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2
Molecular Weight 94.1145
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of M-AMINOPYRIDINE

SMILES

NC1=CN=CC=C1

InChI

InChIKey=CUYKNJBYIJFRCU-UHFFFAOYSA-N
InChI=1S/C5H6N2/c6-5-2-1-3-7-4-5/h1-4H,6H2

HIDE SMILES / InChI

Molecular Formula C5H6N2
Molecular Weight 94.1145
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Theoretical analysis of the molecular determinants responsible for the K(+) channel blocking by aminopyridines.
2001 Jun 15
Design and synthesis of a new binucleating ligand via cobalt-promoted C-N bond fusion reaction. Ligand isolation and its coordination to nickel, palladium, and platinum.
2003 Aug 25
A quantitative structure-activity relationship and pharmacophore modeling investigation of aryl-X and heterocyclic bisphosphonates as bone resorption agents.
2003 Jul 3
3-pyridylcarbene and 3-pyridylnitrene: ring opening to nitrile ylides.
2003 Jul 30
SSR182289A, a selective and potent orally active thrombin inhibitor.
2004 Apr 1
Uridine release during aminopyridine-induced epilepsy.
2004 Aug
Sensitive determination of propoxur by spectrophotometry using 3-aminopyridine.
2004 Dec
Surface complexation modeling of the sorption of 2-, 3-, and 4-aminopyridine by montmorillonite.
2005 Apr 15
Hydrogen bonding patterns in the cocrystals of 5-nitrouracil with several donor and acceptor molecules.
2005 Dec 9
Examining the out-of-center distortion in the [NbOF5]2- anion.
2005 Feb 21
Synthesis and characterization of the face-sharing bioctahedral [Mo2O6F3]3- anion.
2005 Jun 27
catena-Poly[bis[(eta2-1-allyl-3-aminopyridinium)copper(I)]-di-mu-chloro-copper(I)-di-mu-chloro-copper(I)-di-mu-chloro].
2005 Mar
Theoretical prediction of relative and absolute pKa values of aminopyridines.
2006 Nov 20
N-(2-Chloro-benzo-yl)-N'-(3-pyrid-yl)thio-urea.
2008 Jul 5
Effects of 3-aminopyridine-induced seizures on platelet eicosanoid synthesis.
2008 May-Jun
Precolumn derivatization reagents for high-speed analysis of amines and amino acids in biological fluid using liquid chromatography/electrospray ionization tandem mass spectrometry.
2009 May
Isolation of somatic Na+ currents by selective inactivation of axonal channels with a voltage prepulse.
2010 Jun 2
4-aminopyridine-sensitive K+ channels contributes to NaHS-induced membrane hyperpolarization and relaxation in the rat coronary artery.
2010 Sep-Oct
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 20:23:11 GMT 2023
Edited
by admin
on Sat Dec 16 20:23:11 GMT 2023
Record UNII
69JE8P2L84
Record Status Validated (UNII)
Record Version
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Name Type Language
M-AMINOPYRIDINE
Systematic Name English
3-AMINOPYRIDINE
Systematic Name English
BETA-AMINOPYRIDINE
Common Name English
3-PYRIDYLAMINE
Systematic Name English
3-PYRIDINAMINE
Systematic Name English
.BETA.-AMINOPYRIDINE
MI  
Common Name English
UN-2671
Code English
.BETA.-AMINOPYRIDINE [MI]
Common Name English
UN2671
Code English
3-PYRIDINYLAMINE
Systematic Name English
NSC-15040
Code English
Code System Code Type Description
MESH
C031283
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
FDA UNII
69JE8P2L84
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
WIKIPEDIA
3-AMINOPYRIDINE
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
207-322-2
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
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NSC
15040
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
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PUBCHEM
10009
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
MERCK INDEX
m1739
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID9047461
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
CAS
462-08-8
Created by admin on Sat Dec 16 20:23:11 GMT 2023 , Edited by admin on Sat Dec 16 20:23:11 GMT 2023
PRIMARY
Related Record Type Details
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