(redirected from 1,4-Dihydropyridine)
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References in periodicals archive ?
Im et al., "Design and synthesis of 1,4-dihydropyridine derivatives as BACE-1 inhibitors," European Journal of Medicinal Chemistry, vol.
List of studied eleven 1,4-dihydropyridine derivatives, their structural formulas, molecular weight data, [LD.sub.50] values in mg/kg (on NIH 3T3 cells), and antiradical activity data (DPPH assay, in %) (ARA) and data for previously reported compound Z41-74 for more detailed analysis of relationships are given in Table 1.
Davoodnia, "Microwave assisted sol-gel synthesis of MgO nanoparticles and their catalytic activity in the synthesis of Hantzsch 1,4-dihydropyridines," Chinese Journal of Catalysis, vol.
The synthesis of several 2,3,4,5,6-pentasubstituted 1,4-dihydropyridines was successfully performed using the Hantzch reaction and various modifications of it.
[68] reported about the synthesis and antioxidant activity of a series of novel 3-chalcone-substituted 1,4-dihydropyridine derivatives, based on dimethyl or diethyl 2,6-dimethyl-4-phenyl-1,4-DHP-3,5-dicarboxylate.
Hernandez-Gallegos, "Novel halogenated 1,4-dihydropyridines: synthesis, bioassay, microsomal oxidation and structure-activity relationships," European Journal of Medicinal Chemistry, vol.
1,4-dihydropyridine derivatives are a class of important heterocyclic compounds, and was used as high-performance calcium antagonists since 1960's.
A broad group of 1,4-dihydropyridine derivatives as long time known compounds with antioxidant potential have been extensively evaluated during last three decades.
Sadeghi, "Rapid and efficient one-pot synthesis of 1,4-dihydropyridine and polyhydroquinoline derivatives through the hantzsch four component condensation by zinc oxide," Journal of the Iranian Chemical Society, vol.
Squella, "Differential pulse polarographic and UV-vis spectrophotometric study of inclusion complexes formed by 1,4-dihydropyridine calcium antagonists, nifedipine and nicardipine with [beta]-cyclodextrin," Electroanalysis, vol.
Triggle, 1,4-Dihydropyridines as Calcium Channel Ligands and Privileged Structures.
Novel structurally varied N-alkyl 1,4-dihydropyridines as ABCB1 inhibitors: structure-activity relationships, biological activity and first bioanalytical evaluation.