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・ 4-alpha-D-((1-4)-alpha-D-glucano)trehalose trehalohydrolase
・ 4-alpha-glucanotransferase
・ 4-Aminoacridine
・ 4-aminobenzoate 1-monooxygenase
・ 4-Aminobenzoic acid
・ 4-Aminobiphenyl
・ 4-aminobutyrate aminotransferase
・ 4-aminobutyrate transaminase
・ 4-aminobutyrate—pyruvate transaminase
・ 4-aminobutyric acid aminotransferase
・ 4-Aminophenol
・ 4-Aminopyridine
・ 4-Aminoquinoline
・ 4-Aminosalicylic acid
・ 4-Androstene-3,6,17-trione
4-Androstenediol
・ 4-Androstenedione
・ 4-Anisaldehyde
・ 4-beat
・ 4-Benzylpiperidine
・ 4-bit
・ 4-bolt main
・ 4-Bromo-3,5-dimethoxyamphetamine
・ 4-Bromoaniline
・ 4-Bromofluorobenzene
・ 4-Bromomethcathinone
・ 4-by the Beatles
・ 4-Caffeoyl-1,5-quinide
・ 4-carboxy-2-hydroxymuconate-6-semialdehyde dehydrogenase
・ 4-carboxymethyl-4-methylbutenolide mutase


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

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Δ4-Androstenediol is an androstenediol that is converted to testosterone. The conversion rate is about 15.76%, almost triple that of Δ4-androstenedione, due to utilization of a different enzymatic pathway. There is also some conversion into estrogen, since testosterone is the metabolic precursor of the estrogens.
Δ4-Androstenediol is closer to testosterone structurally than Δ5-androstenediol, and has androgenic effects, acting as a weak partial agonist of the androgen receptor. However, due to its lower intrinsic activity in comparison, in the presence of full agonists like testosterone or dihydrotestosterone (DHT), Δ4-androstenediol has antagonistic actions, behaving more like an antiandrogen.〔
==Medical and commercial use==
Patrick Arnold holds a 1999 patent on "Use of 4-androstenediol to increase testosterone levels in humans".〔http://www.patentstorm.us/patents/5880117/description.html〕

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-Androstenediol」の詳細全文を読む



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