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2007-02-05 08:02:02 · 2 answers · asked by SS 1 in Science & Mathematics Biology

2 answers

Through the Hantzsch Dihydropyridine (Pyridine) Synthesis.
This reaction allows the preparation of dihydropyridine derivatives by condensation of an aldehyde with two equivalents of a β-ketoester in the presence of ammonia. Subsequent oxidation (or dehydrogenation) gives pyridine-3,5-dicarboxylates, which may also be decarboxylated to yield the corresponding pyridines.
In medicine, dihydropyridines bind to and inhibit the voltage\-gated calcium channel of skeletal muscle T junctional membranes, the principle molecular transducer of excitation\-contraction coupling.

2007-02-05 08:08:11 · answer #1 · answered by Jesus is my Savior 7 · 0 0

Dihydropyridines are molecules based upon pyridine that have been semi-saturated with two substituents replacing one double bond.

Examples include:

* amlodipine
* felodipine
* nicardipine
* nifedipine
* nimodipine

2007-02-05 16:06:51 · answer #2 · answered by MSK 4 · 0 1

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