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
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
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
Title | Date | PubMed |
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Evidence for elevation of cytochrome P4502E1 (alcohol-inducible form) mRNA levels in rat kidney following pyridine administration. | 1992 Jul 31 |
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CYP1A1 induction by pyridine and its metabolites in HepG2 cells. | 2002 Aug 15 |
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HIV-chemotherapy and -prophylaxis: new drugs, leads and approaches. | 2004 Sep |
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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 |
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Metal-organic rotaxane frameworks: three-dimensional polyrotaxanes from lanthanide-ion nodes, pyridinium N-oxide axles, and crown-ether wheels. | 2005 Jan 28 |
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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 |
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1H NMR and DFT study of proton exchange in heterogeneous structures of pyridine-N-oxide/HCl/DCl/H2O. | 2005 Mar |
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Evidence of the electronic factor for the highly enantioselective catalytic efficiency of Cinchona-derived phase-transfer catalysts. | 2005 Mar 17 |
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Calculations on the group 15 intraring substituted benzenes (pyridine to bismin series) and their datively bonded oxides and sulfides. | 2005 Oct 13 |
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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 |
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Synthesis development of a naphthyridinone p38 kinase inhibitor. | 2006 Nov |
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Modulation of the luminescence quantum efficiency for blue luminophor {Al(salophen)}(+) by ester-substituents. | 2010 Feb 28 |
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Densely packed Gd(III)-chelates with fast water exchange on a calix[4]arene scaffold: a potential MRI contrast agent. | 2010 Jan 7 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 17:19:40 GMT 2023
by
admin
on
Fri Dec 15 17:19:40 GMT 2023
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Record UNII |
91F12JJJ4H
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Common Name | English |
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Pyridine-N-oxide
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18250
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29136
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211-774-6
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694-59-7
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12753
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91F12JJJ4H
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DTXSID3061007
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C013229
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m9354
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PRIMARY | Merck Index |