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・ Dihydromethysticin
・ Dihydromorin
・ Dihydromorphine
・ Dihydroneopterin aldolase
・ Dihydronicotinamide adenine dinucleotide-coenzyme Q reductase
・ Dihydroorotase
・ Dihydroorotate dehydrogenase
・ Dihydroorotate dehydrogenase (fumarate)
・ Dihydroorotate dehydrogenase (quinone)
・ Dihydrophloroglucinol
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Dihydropyridine
・ Dihydropyrimidinase
・ Dihydropyrimidine dehydrogenase
・ Dihydropyrimidine dehydrogenase (NADP+)
・ Dihydropyrimidine dehydrogenase deficiency
・ Dihydroquinidine
・ Dihydroquinine
・ Dihydrosanguinarine
・ Dihydrosanguinarine 10-monooxygenase
・ Dihydrostilbenoid
・ Dihydrostreptomycin
・ Dihydrostreptomycin-6-phosphate 3'alpha-kinase
・ Dihydrotachysterol
・ Dihydrotanshinone
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Dihydropyridine : ウィキペディア英語版
Dihydropyridine

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Dihydropyridine is a molecule based upon pyridine, and the parent of a class of molecules that have been semi-saturated with two substituents replacing one double bond. They are particularly well known in pharmacology as L-type calcium channel blockers, used in the treatment of hypertension. Compared with certain other L-type calcium channel blockers (for example those of the phenylalkylamine class such as verapamil) which have significant action at the heart, they are relatively vascular selective in their mechanism of action in lowering blood pressure.
==Class members==
Dihydropyridine class L-type calcium channel blockers include, in alphabetical order (brand names vary in different countries):
The pharmaceutical drug finerenone is also a dihydrophyridine derivative, but does not act as a calcium channel blocker but as an antimineralocorticoid.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Dihydropyridine」の詳細全文を読む



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