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Details

Stereochemistry ACHIRAL
Molecular Formula C11H9N
Molecular Weight 155.1959
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-PHENYLPYRIDINE

SMILES

C1=CC=C(C=C1)C2=CC=NC=C2

InChI

InChIKey=JVZRCNQLWOELDU-UHFFFAOYSA-N
InChI=1S/C11H9N/c1-2-4-10(5-3-1)11-6-8-12-9-7-11/h1-9H

HIDE SMILES / InChI

Molecular Formula C11H9N
Molecular Weight 155.1959
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and structural and magnetic characterisation of cobalt(ii) complexes of mixed phosphonate-antimonate ligands.
2010-10-28
Synthesis, characterization and cytotoxic activities of the [RuCl2(NO)(dppp)(L)]PF6 complexes.
2010-05
Bis(μ-phenyl-tellurido-κTe:Te)bis-[tetra-carbonyl-rhenium(I)].
2010-04-24
Heptacarbonyl-1κC,2κC-(4-phenyl-pyridine-1κN)di-μ-phenyltellurido-1:2κTe:Te-dirhenium(I).
2010-04-14
Excited-state properties of octahedral hexarhenium(III) complexes with redox-active N-heteroaromatic ligands.
2010-01-18
Tripodal 4-pyridyl-derived host ligands and their metallo-supramolecular chemistry: stella octangula and bowl-shaped assemblies.
2010-01-18
1H, 13C and 15N nuclear magnetic resonance coordination shifts in Au(III), Pd(II) and Pt(II) chloride complexes with phenylpyridines.
2009-08
Thermal- and light-induced spin crossover in novel 2D Fe(II) metalorganic frameworks {Fe(4-PhPy)(2)[M(II)(CN)(x)](y)}.sH(2)O: spectroscopic, structural, and magnetic studies.
2009-07-06
Decreased susceptibility of the cytochrome P450 2B6 variant K262R to inhibition by several clinically important drugs.
2009-03
Syntheses, structures and magnetic properties of a family of metal carboxylate polymers via in situ metal-ligand reactions of benzene-1,2,3-tricarboxylic acid.
2009-02-28
Regioselectivity and stereoselectivity of dioxygenase catalysed cis-dihydroxylation of mono- and tri-cyclic azaarene substrates.
2008-11-07
Squamosamide derivative FLZ protects dopaminergic neurons against inflammation-mediated neurodegeneration through the inhibition of NADPH oxidase activity.
2008-05-28
Synthesis, growth and characterization of a new nonlinear optical material: 4-phenylpyridinium hydrogen squarate (4PHS).
2008-04
N-Phenyl-N-{4-[5-(4-pyrid-yl)-1,3,4-oxadiazol-2-yl]phen-yl}aniline.
2007-12-12
Dissecting the thermodynamics and cooperativity of ligand binding in cytochrome P450eryF.
2007-02-21
The novel squamosamide derivative (compound FLZ) attenuated 1-methyl, 4-phenyl-pyridinium ion (MPP+)-induced apoptosis and alternations of related signal transduction in SH-SY5Y cells.
2007-02
Angiotensin type 1 receptor antagonist losartan, reduces MPTP-induced degeneration of dopaminergic neurons in substantia nigra.
2007-01-15
Mass spectrometric studies on 4-aryl-1-cyclopropyl-1,2-dihydropyridinyl derivatives: an examination of a novel fragmentation pathway.
2006-12
Simple chip-based interfaces for on-line monitoring of supramolecular interactions by nano-ESI MS.
2005-10
Rhenium(V) complexes with thiolato and dithiolato ligands: synthesis, structures, and monomerization reactions.
2005-05-16
Parkinson's disease: the first common neurological disease due to auto-intoxication?
2005-03
Autotoxicity, methylation and a road to the prevention of Parkinson's disease.
2005-01
Richness of isomerism in labile octahedral Werner-type cobalt(II) complexes demonstrated by 19F NMR spectroscopy: structure and stability.
2004-09
Tuning the electronic structures of platinum(II) complexes with a cyclometalating aryldiamine ligand.
2004-01-26
Pyrido[2,1-f]purine-2,4-dione derivatives as a novel class of highly potent human A(3) adenosine receptor antagonists.
2002-08-01
The human organic cation transporter (hOCT2) recognizes the degree of substrate ionization.
2002-06-21
Tetra-mu-acetato-kappa2O:O'-bis[(4-phenylpyridine-kappaN)copper(II)].
2002-04
Pentacarbonyl(4-phenylpyridine)tungsten(0) and pentacarbonyl(2-phenylpyridine)chromium(0).
2001-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:49:44 GMT 2025
Edited
by admin
on Mon Mar 31 19:49:44 GMT 2025
Record UNII
452KD9YCG7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-PHENYLPYRIDINE
Systematic Name English
NSC-70375
Preferred Name English
NSC-77935
Code English
Code System Code Type Description
FDA UNII
452KD9YCG7
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
PRIMARY
PUBCHEM
13651
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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CAS
939-23-1
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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NSC
70375
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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NSC
77935
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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MESH
C051448
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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ECHA (EC/EINECS)
213-357-4
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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EPA CompTox
DTXSID5022140
Created by admin on Mon Mar 31 19:49:44 GMT 2025 , Edited by admin on Mon Mar 31 19:49:44 GMT 2025
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