- Source: 1,4-Dihydropyridine
1,4-Dihydropyridine (DHP) is an organic compound with the formula CH2(CH=CH)2NH. The parent compound is uncommon, but derivatives of 1,4-dihydropyridine are important commercially and biologically. The pervasive cofactors NADH and NADPH are derivatives of 1,4-dihydropyridine. 1,4-Dihydropyridine-based drugs are L-type calcium channel blockers, used in the treatment of hypertension. 1,2-Dihydropyridines are also known.
Properties and reactions
A recurring feature of 1,4-dihydropyridines is the presence of substituents at the 2- and 6-positions. Dihydropyridines are enamines, which otherwise tend to tautomerize or hydrolyze.
The dominant reaction of dihydropyridines is their ease of oxidation. In the case of dihydropyridines with hydrogen as the substituent on nitrogen, oxidation yields pyridines:
CH2(CH=CR)2NH → C5H3R2N + H2
The naturally-occurring dihydropyridines NADH and NADPH contain N-alkyl groups. Therefore, their oxidation does not yield pyridine, but N-alkylpyridinium cations:
CH2(CH=CR)2NR' → C5H3R2NR' + H−
Hantzsch ester
Hantzsch ester
See also
Dihydropyridine calcium channel blockers
Dihydropyridine receptor
Ryanodine receptor
References
External links
Dihydropyridines at the U.S. National Library of Medicine Medical Subject Headings (MeSH)