翻訳と辞書
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・ 4-Nitroquinoline 1-oxide
・ 4-Nitrotoluene
・ 4-Nonanoylmorpholine
・ 4-Nonylphenylboronic acid
・ 4-O-beta-D-mannosyl-D-glucose phosphorylase
・ 4-O-Methylhonokiol
・ 4-oxalmesaconate hydratase
・ 4-oxalocrotonate decarboxylase
・ 4-Oxalocrotonate tautomerase
・ 4-oxalomesaconate tautomerase
・ 4-Oxo-2-nonenal
・ 4-oxoproline reductase
・ 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


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

4-Phenylfentanyl is an opioid analgesic that is a derivative of fentanyl. It was developed during the course of research that ultimately resulted in super-potent opioid derivatives such as carfentanil, though it is a substantially less potent analogue. 4-Phenylfentanyl is around 8x the potency of fentanyl in analgesic tests on animals, but more complex 4-heteroaryl derivatives such as substituted thiophenes and thiazoles are more potent still, as they are closer bioisosteres to the 4-carbomethoxy group of carfentanil.
Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.
== References ==




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「4-Phenylfentanyl」の詳細全文を読む



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