U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2
Molecular Weight 94.1147
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-AMINOPYRIDINE

SMILES

c1ccnc(c1)N

InChI

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

HIDE SMILES / InChI

Molecular Formula C5H6N2
Molecular Weight 94.1147
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Evaluation of pyridoindoles, pyridylindoles and pyridylpyridoindoles as matrices for ultraviolet matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2001
Structures of the N-linked sugar chains in PAS-7 glycoprotein sharing the same protein core with PAS-6 glycoprotein from the bovine milk fat globule membrane.
2001 Apr
Triclinic polymorph of sulfasalazine.
2001 Apr
A synthetic analogue of the active site of Fe-containing nitrile hydratase with carboxamido N and thiolato S as donors: synthesis, structure, and reactivities.
2001 Apr 11
Synthesis and biological activity of analogues of the antidiabetic/antiobesity agent 3-guanidinopropionic acid: discovery of a novel aminoguanidinoacetic acid antidiabetic agent.
2001 Apr 12
Structural characterization of fucose-containing oligosaccharides by high-performance liquid chromatography and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2001 Feb
Theoretical analysis of the molecular determinants responsible for the K(+) channel blocking by aminopyridines.
2001 Jun 15
N-glycan structures from the major glycoproteins of pigeon egg white: predominance of terminal Galalpha(1)Gal.
2001 Jun 29
Inhibition of class C beta-lactamases: structure of a reaction intermediate with a cephem sulfone.
2001 May 29
Glycoproteins secreted from suspension-cultured tobacco BY2 cells have distinct glycan structures from intracellular glycoproteins.
2001 Nov
Infrared studies of tautomerism in 2-hydroxypyridine 2-thiopyridine and 2-aminopyridine.
2001 Nov
Spectral characteristics of 2-(4'-N,N-dimethylaminophenyl)pyrido[3,4-d]imidazole in AOT/n-heptane/water reverse micelles.
2001 Nov
Inhibition of copper amine oxidases by pyridine-derived aldoximes and ketoximes.
2001 Nov-Dec
Complexation-induced unfolding of heterocyclic ureas. Simple foldamers equilibrate with multiply hydrogen-bonded sheetlike structures.
2001 Oct 31
Synthesis and anti-HIV activity of some isatin derivatives.
2001 Sep-Oct
Synthesis of some new quinoline derivatives: new routes to synthesize polysubstituted 2(1H)-quinolone derivatives.
2001 Sep-Oct
Structural model of nicotinic acetylcholine receptor isotypes bound to acetylcholine and nicotine.
2002
The nature of the receptor site for the reversible K+ channel blocking by aminopyridines.
2002 Apr 10
Alkylation reactions of [WS(4)](2)(-) and [(eta(5)-C(5)Me(5))WS(3)](-) with 2,6-bis(bromomethyl)pyridine: the first isolation of bisalkylated tetrathiometalate WS(2)[2,6-(SCH(2))(2)(C(5)H(3)N)].
2002 Aug 12
Analysis of fluorogenic Smith degradation products of 7-(1,3-disulfonaphtyl)amino-disaccharides for linkage position analysis of carbohydrates.
2002 Dec
[N.1.1]-(2,6)-Pyridinophanes: a new ligand type imposing unusual metal coordination geometries.
2002 Dec 16
Syntheses and magnetic properties of hexanuclear [Cp2Mn3(L1)4]2 and octanuclear [Mn8(L2)12(mu 4-O)2] (L1 = 2-HNC5H5N, L2 = 2-NH-3-Br-5-MeC5H3N, Cp = C5H5).
2002 Dec 21
Hydrogen bond vibrations of 2-aminopyridine.2-pyridone, a Watson-Crick analogue of adenine.uracil.
2002 Dec 4
Characterization of glycosphingolipids from Schistosoma mansoni eggs carrying Fuc(alpha1-3)GalNAc-, GalNAc(beta1-4)[Fuc(alpha1-3)]GlcNAc- and Gal(beta1-4)[Fuc(alpha1-3)]GlcNAc- (Lewis X) terminal structures.
2002 Jan
Analysis of alpha-amylase-derived pyridylamino-dextran sulfate oligomers by the combination of size-exclusion and reversed-phase high-performance liquid chromatography.
2002 Jan 25
Examination of molar-based distribution of A, B and C chains of amylopectin by fluorescent labeling with 2-aminopyridine.
2002 Jul 16
Oxidative damage due to copper ion and hydrogen peroxide induces GlcNAc-specific cleavage of an Asn-linked oligosaccharide.
2002 Mar
Modulation of the internal aldimine pK(a)'s of 1-aminocyclopropane-1-carboxylate synthase and aspartate aminotransferase by specific active site residues.
2002 Mar 19
New stereoselective reaction of methylglyoxal with 2-aminopyridine and adenine derivatives: formation of imino acid-nucleic base derivatives in water under mild conditions.
2002 May 21
Synthesis and characterization of new linear pi-conjugated molecules containing bis(ethynylpyridine) units with a benzothiadiazole spacer.
2002 Nov 1
Amination of pyridylketenes: experimental and computational studies of strong amide enol stabilization by the 2-pyridyl group.
2002 Nov 20
Antitumor agents. 2. Synthesis, structure-activity relationships, and biological evaluation of substituted 5H-pyridophenoxazin-5-ones with potent antiproliferative activity.
2002 Nov 21
Example of highly stereoregulated ruthenium amidine complex formation: synthesis, crystal structures, and spectral and redox properties of the complexes [Ru(II)(trpy)[NC(5)H(4)-CH=N-N(C(6)H(5))C(CH(3))=NH]](ClO(4))(2) (1) and [Ru(II)(trpy)(NC(5)H(4)-CH=N-NH-C(6)H(5))Cl]ClO(4) (2) (trpy = 2,2':6',2"-terpyridine).
2002 Nov 4
Ru3(CO)12-catalyzed C-H/CO/olefin coupling of N-pyridylindolines. Direct carbonylation at a C-H bond delta to the pyridine nitrogen.
2002 Oct 18
Solid-phase synthesis of imidazo[1,2-a]pyridine using sodium benzenesulfinate as a traceless linker.
2002 Oct 31
X-ray diffraction and (1)H NMR in solution: structural determination of lanthanide complexes of a Py(2)N(6)Ac(4) ligand.
2002 Oct 7
N-glucuronidation of nicotine and cotinine in human: formation of cotinine glucuronide in liver microsomes and lack of catalysis by 10 examined UDP-glucuronosyltransferases.
2002 Sep
Enzymatic synthesis and characterization of oligosaccharides structurally related to the repeating unit of Pullulan.
2002 Sep 20
Site of protonation of nicotine and nornicotine in the gas phase: pyridine or pyrrolidine nitrogen?
2002 Sep 4
A mild method for the formation and in situ reaction of imidoyl chlorides: conversion of pyridine-1-oxides to 2-aminopyridine amides.
2002 Sep 5
Reduced inotropic heart response in selenium-deficient mice relates with inducible nitric oxide synthase.
2003 Feb
Magnetic interaction of pyridyl-substituted thioaminyl stable free radicals.
2003 Feb 21
Structural modulation of Cu(I) and Cu(II) complexes of sterically hindered tripyridine ligands by the bridgehead alkyl groups.
2003 Feb 24
2-aminopyridinium benzoate.
2003 Jan
Syntheses and structures of isoindoline complexes of Zn(II) and Cu(II): an unexpected trinuclear Zn(II) complex.
2003 Jan 13
Structural chemistry and In vitro antitubercular activity of acetylpyridine benzoyl hydrazone and its copper complex against Mycobacterium smegmatis.
2003 Jan 6
N-glycan structures of human transferrin produced by Lymantria dispar (gypsy moth) cells using the LdMNPV expression system.
2003 Jul
Investigations into the interactions between DNA and conformationally constrained pyridylamineplatinum(II) analogues of AMD473.
2003 Jun 2
Plant cultured cells expressing human beta1,4-galactosyltransferase secrete glycoproteins with galactose-extended N-linked glycans.
2003 Mar
Thermodynamic, kinetic and structural studies on the mixed ligand complexes of palladium(II) with tridentate and monodentate ligands.
2003 Mar 1
Patents
Substance Class Chemical
Created
by admin
on Sat Jun 26 11:19:57 UTC 2021
Edited
by admin
on Sat Jun 26 11:19:57 UTC 2021
Record UNII
WSX981HEWU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-AMINOPYRIDINE
HSDB  
Systematic Name English
NSC-431
Code English
.ALPHA.-AMINOPYRIDINE
MI  
Common Name English
MEPYRAMINE MALEATE IMPURITY C [EP]
Common Name English
.ALPHA.-AMINOPYRIDINE [MI]
Common Name English
2-PYRIDINAMINE
Systematic Name English
TENOXICAM IMPURITY A [EP]
Common Name English
PYRIDIN-2-AMINE
Systematic Name English
PIROXICAM RELATED COMPOUND A [USP-RS]
Common Name English
2-AMINOPYRIDINE [HSDB]
Common Name English
PIROXICAM SPECIFIED IMPURITY A [EP]
Common Name English
AMINOPYRIDINE, 2-
Systematic Name English
Code System Code Type Description
HSDB
2068
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
MERCK INDEX
M1739
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY Merck Index
EPA CompTox
504-29-0
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
CAS
504-29-0
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
PUBCHEM
10439
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
MESH
C032439
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
WIKIPEDIA
2-AMINOPYRIDINE
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
ECHA (EC/EINECS)
207-988-4
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
USP_CATALOG
1544519
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY USP-RS
FDA UNII
WSX981HEWU
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
EVMPD
SUB117598
Created by admin on Sat Jun 26 11:19:58 UTC 2021 , Edited by admin on Sat Jun 26 11:19:58 UTC 2021
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
correction factors: for the calculation of content, multiply the peak areas of the following impurities by the corresponding correction factor: impurity A = 0.2
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
ACTIVE MOIETY