Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H7N |
Molecular Weight | 81.1158 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C1C=CNC=C1
InChI
InChIKey=YNGDWRXWKFWCJY-UHFFFAOYSA-N
InChI=1S/C5H7N/c1-2-4-6-5-3-1/h2-6H,1H2
Approval Year
PubMed
Title | Date | PubMed |
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Inhibition of human cytochrome P450 enzymes by 1,4-dihydropyridine calcium antagonists: prediction of in vivo drug-drug interactions. | 2000 Feb-Mar |
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Stereoselective trans- and cis-dihydroxylations of 2H-pyranyl and dihydropyridinyl heterocycles synthesized from formal [3 + 3]-cycloaddition reactions of alpha,beta-unsaturated iminium ions with 1,3-dicarbonyl equivalents. | 2001 Jul 12 |
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Productive trapping of NAD-type radicals. Non-biomimetic reduction of pyridinium salts. | 2002 Apr 21 |
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Regulation of the homologous two-component systems KvgAS and KvhAS in Klebsiella pneumoniae CG43. | 2006 Nov |
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Oxidation of C4-hydroxyphenyl 1,4-dihydropyridines in dimethylsulfoxide and its reactivity towards alkylperoxyl radicals in aqueous medium. | 2007 Jun 15 |
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Synthesis, coordination chemistry and bonding of strong N-donor ligands incorporating the 1H-pyridin-(2E)-ylidene (PYE) motif. | 2009 Oct 26 |
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50075
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C038806
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Dihydropyridine
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104822
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DTXSID20274185
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100000142184
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3337-17-5
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SUB115812
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SUBSTANCE RECORD