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Details

Stereochemistry ACHIRAL
Molecular Formula C7H10N2
Molecular Weight 122.1677
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-PYRIDINEETHANAMINE

SMILES

NCCC1=CC=CC=N1

InChI

InChIKey=XPQIPUZPSLAZDV-UHFFFAOYSA-N
InChI=1S/C7H10N2/c8-5-4-7-3-1-2-6-9-7/h1-3,6H,4-5,8H2

HIDE SMILES / InChI

Molecular Formula C7H10N2
Molecular Weight 122.1677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
5.9 null [pIC50]
PubMed

PubMed

TitleDatePubMed
Regulation of interleukin-6, and macrophage colony-stimulating factor mRNA levels by histamine in stromal cell line (MC3T3-G2/PA6).
1998 May
Synthesis of 17beta-estradiol platinum(II) complexes: biological evaluation on breast cancer cell lines.
2003 Nov 17
Histamine elicits neuronal excitatory response of red nucleus in the rat via H2 receptors in vitro.
2003 Nov 6
Biological evaluation of novel estrogen-platinum(II) hybrid molecules on uterine and ovarian cancers-molecular modeling studies.
2004 Dec 6
Large-scale overproduction, functional purification and ligand affinities of the His-tagged human histamine H1 receptor.
2004 Jul
Involvement of hypothalamic histamine H1 receptor in the regulation of feeding rhythm and obesity.
2004 Sep
Isatin-Schiff base copper(II) complexes and their influence on cellular viability.
2005 Jul
Excitatory effect of histamine on neuronal activity of rat globus pallidus by activation of H2 receptors in vitro.
2005 Nov
Pro-apoptotic activity of novel Isatin-Schiff base copper(II) complexes depends on oxidative stress induction and organelle-selective damage.
2007 Apr 20
Synthesis of 17beta-estradiol-platinum(II) hybrid molecules showing cytotoxic activity on breast cancer cell lines.
2008 Apr 1
Metal-assisted in situ formation of a tridentate acetylacetone ligand for complexation of fac-Re(CO)3+ for radiopharmaceutical applications.
2008 Apr 7
Histamine excites rat lateral vestibular nuclear neurons through activation of post-synaptic H2 receptors.
2008 Dec 19
Antagonist affinity measurements at the Gi-coupled human histamine H3 receptor expressed in CHO cells.
2008 Jun 6
μ-Squarato-κO:O-bis-{[2-(2-amino-ethyl)pyridine-κN,N']aqua-nickel(II)} squarate 0.25-hydrate.
2008 Sep 27
Automated potentiometric titrations in KCl/water-saturated octanol: method for quantifying factors influencing ion-pair partitioning.
2009 Apr 1
2-[2-(2-Pyrid-yl)eth-yl]isoindolinium perchlorate.
2009 Aug 19
2-(2-Ammonio-ethyl)pyridinium hexa-chloridorhenate(IV).
2009 Feb 4
Polymer-bound oxidovanadium(IV) and dioxidovanadium(V) complexes: synthesis, characterization and catalytic application for the hydroamination of styrene and vinyl pyridine.
2009 Nov 21
New photomagnetic cyanido-bridged Cu(II)-Mo(IV) oligonuclear complexes: slight modification of the blocking ligands induces different structures.
2009 Oct 7
Mast cells down-regulate CD4+CD25+ T regulatory cell suppressor function via histamine H1 receptor interaction.
2009 Sep 1
Neuropharmacology of vestibular system disorders.
2010 Mar
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:32:52 GMT 2023
Edited
by admin
on Fri Dec 15 18:32:52 GMT 2023
Record UNII
ATW1AH7OJ5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-PYRIDINEETHANAMINE
Systematic Name English
2-(2-PYRIDINYL)ETHANAMINE
Systematic Name English
2-(2-AMINOETHYL)PYRIDINE
Systematic Name English
DEMETHYLBETAHISTINE
Common Name English
.ALPHA.-(2-AMINOETHYL)PYRIDINE
Common Name English
2-(2'-AMINOETHYL)PYRIDINE
Common Name English
2-(2-PYRIDYL)ETHYLAMINE
Systematic Name English
.ALPHA.-PYRIDYLETHYLAMINE
Systematic Name English
2'-AMINOETHYL-2-PYRIDINE
Common Name English
NSC-71989
Code English
N-(2-(2-PYRIDINYL)ETHYL)AMINE
Systematic Name English
PYRIDINE, 2-(2-AMINOETHYL)-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
2-Pyridylethylamine
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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EPA CompTox
DTXSID5022196
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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MESH
C006183
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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ECHA (EC/EINECS)
220-295-1
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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PUBCHEM
75919
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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CHEBI
74024
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
PRIMARY
CAS
2706-56-1
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
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NSC
71989
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
PRIMARY
FDA UNII
ATW1AH7OJ5
Created by admin on Fri Dec 15 18:32:52 GMT 2023 , Edited by admin on Fri Dec 15 18:32:52 GMT 2023
PRIMARY