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・ 4-Phenyl-1,2,4-triazole-3,5-dione
・ 4-Phenyl-4-(1-piperidinyl)cyclohexanol
・ 4-Phenylazepane
・ 4-Phenylfentanyl
・ 4-Phenylpiperidine
・ 4-Phenylthiosemicarbazide
・ 4-phosphoerythronate dehydrogenase
・ 4-phosphopantoate—beta-alanine ligase
・ 4-phytase
・ 4-Piperidinone
・ 4-Player Bowling Alley
・ 4-polytope
・ 4-poster
・ 4-PPBP
・ 4-pyridoxolactonase
4-Pyridylnicotinamide
・ 4-Pyrone
・ 4-Sight Fax
・ 4-Starr Collection
・ 4-string banjo
・ 4-sulfobenzoate 3,4-dioxygenase
・ 4-Sulfomuconolactone hydrolase
・ 4-tert-Butylcatechol
・ 4-Toluenesulfonyl chloride
・ 4-track
・ 4-Track Demos
・ 4-Track Mind
・ 4-trimethylammoniobutyraldehyde dehydrogenase
・ 4-Vinylcyclohexene
・ 4-Vinylphenol


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4-Pyridylnicotinamide : ウィキペディア英語版
4-Pyridylnicotinamide

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4-Pyridylnicotinamide (4-PNA), also known as ''N''-(pyridin-4-yl)nicotinamide, is a kinked dipodal dipyridine which was originally developed for use in chemotherapy. As in its isomer 3-pyridylnicotinamide, the nitrogen atoms on its pyridine rings can donate their electron lone pairs to metal cations, allowing it to bridge metal centers and act as a bidentate ligand in coordination polymers. It is synthesized through the reaction of nicotinoyl chloride and 4-aminopyridine.〔
==References==



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