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Details

Stereochemistry ACHIRAL
Molecular Formula C5H5NO
Molecular Weight 95.0993
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PYRIDINE N-OXIDE

SMILES

[O-][N+]1=CC=CC=C1

InChI

InChIKey=ILVXOBCQQYKLDS-UHFFFAOYSA-N
InChI=1S/C5H5NO/c7-6-4-2-1-3-5-6/h1-5H

HIDE SMILES / InChI

Molecular Formula C5H5NO
Molecular Weight 95.0993
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Evidence for elevation of cytochrome P4502E1 (alcohol-inducible form) mRNA levels in rat kidney following pyridine administration.
1992 Jul 31
CYP1A1 induction by pyridine and its metabolites in HepG2 cells.
2002 Aug 15
HIV-chemotherapy and -prophylaxis: new drugs, leads and approaches.
2004 Sep
In vitro microsomal metabolic studies on a selective mGluR5 antagonist MTEP: characterization of in vitro metabolites and identification of a novel thiazole ring opening aldehyde metabolite.
2005 Aug
Metal-organic rotaxane frameworks: three-dimensional polyrotaxanes from lanthanide-ion nodes, pyridinium N-oxide axles, and crown-ether wheels.
2005 Jan 28
Enantioselective approach to the hetisine alkaloids. Synthesis of the 3-methyl-1-aza-tricyclo[5.2.1.0(3,8)]decane core via intramolecular dipolar cycloaddition.
2005 Jul 21
1H NMR and DFT study of proton exchange in heterogeneous structures of pyridine-N-oxide/HCl/DCl/H2O.
2005 Mar
Evidence of the electronic factor for the highly enantioselective catalytic efficiency of Cinchona-derived phase-transfer catalysts.
2005 Mar 17
Calculations on the group 15 intraring substituted benzenes (pyridine to bismin series) and their datively bonded oxides and sulfides.
2005 Oct 13
Discovery of 3-methyl-N-(1-oxy-3',4',5',6'-tetrahydro-2'H-[2,4'-bipyridine]-1'-ylmethyl)benzamide (ABT-670), an orally bioavailable dopamine D4 agonist for the treatment of erectile dysfunction.
2006 Dec 14
Synthesis development of a naphthyridinone p38 kinase inhibitor.
2006 Nov
Modulation of the luminescence quantum efficiency for blue luminophor {Al(salophen)}(+) by ester-substituents.
2010 Feb 28
Densely packed Gd(III)-chelates with fast water exchange on a calix[4]arene scaffold: a potential MRI contrast agent.
2010 Jan 7
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:19:40 GMT 2023
Edited
by admin
on Fri Dec 15 17:19:40 GMT 2023
Record UNII
91F12JJJ4H
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PYRIDINE N-OXIDE
Systematic Name English
PYRIDINE 1-OXIDE
MI  
Systematic Name English
NSC-18250
Code English
PYRIDINE 1-OXIDE [MI]
Common Name English
Code System Code Type Description
WIKIPEDIA
Pyridine-N-oxide
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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NSC
18250
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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CHEBI
29136
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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ECHA (EC/EINECS)
211-774-6
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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CAS
694-59-7
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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PUBCHEM
12753
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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FDA UNII
91F12JJJ4H
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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EPA CompTox
DTXSID3061007
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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MESH
C013229
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
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MERCK INDEX
m9354
Created by admin on Fri Dec 15 17:19:40 GMT 2023 , Edited by admin on Fri Dec 15 17:19:40 GMT 2023
PRIMARY Merck Index