Dihydropyridine

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Dihydropyridine is a class of calcium channel blockers used primarily in the treatment of hypertension. These compounds are derivatives of the parent compound pyridine, and are characterized by the presence of two hydrogen atoms on the pyridine ring.

Chemistry[edit | edit source]

Dihydropyridines are synthesized from pyridine through a process known as hydrogenation. This involves the addition of hydrogen atoms to the pyridine ring, resulting in a dihydropyridine molecule. The structure of dihydropyridines is characterized by a six-membered ring with two nitrogen atoms and four carbon atoms. The two hydrogen atoms are attached to one of the carbon atoms in the ring.

Pharmacology[edit | edit source]

Dihydropyridines exert their therapeutic effects by blocking calcium channels in the vascular smooth muscle. This results in relaxation of the smooth muscle, leading to a decrease in blood pressure. Dihydropyridines are particularly effective in treating hypertension because they selectively target the calcium channels in the vascular smooth muscle, without significantly affecting the calcium channels in the heart.

Clinical Use[edit | edit source]

The most commonly used dihydropyridines in clinical practice are amlodipine, nifedipine, and felodipine. These drugs are used primarily in the treatment of hypertension, but they are also effective in managing angina pectoris and certain types of arrhythmia. Dihydropyridines are generally well tolerated, but they can cause side effects such as edema, flushing, and dizziness.

Research[edit | edit source]

Research into dihydropyridines is ongoing, with scientists exploring their potential use in other medical conditions. For example, some studies suggest that dihydropyridines may have neuroprotective effects, making them potential candidates for the treatment of neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD