Dihydropyridines are a class of compounds that contain a pyridine ring with two hydrogen atoms attached to one of the carbon atoms in the ring. These compounds can be synthesized through the Hantzsch reaction and are known for their diverse pharmacological properties. Some dihydropyridines may exhibit antifungal activity by affecting calcium channels in fungal cells or other mechanisms.
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Isoquinoline, 1,2,3,4,5,6,7,8-octahydro-2-methyl-5-(phenylmethyl)-
5-Pyrimidinecarboxylic acid, 1,4-dihydro-2-[[(4-methoxyphenyl)methyl]thio]-6-methyl-4-(3-nitrophenyl) -, 1-methylethyl ester, (R)-
methyl 4,7-dihydro-6-methyl-4-(3-nitrophenyl)-3-phenylthieno[2,3-b]pyridine-5-carboxylate
S-TERT-BUTYL THIOACETATE
3-(4-Bromophenyl)-5-methylisoxazole-4-carboxaldehyde
