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・ 1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate dehydrogenase
・ 1,6-Hexanediol
・ 1,6-Methano(10)annulene
・ 1,68
・ 1,7-Bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one
・ 1,778 Stories of Me and My Wife
・ 1,8-Bis(dimethylamino)naphthalene
・ 1,8-Cineole 2-endo-monooxygenase
・ 1,8-Cineole 2-exo-monooxygenase
・ 1,8-cineole synthase
・ 1,8-Diaminonaphthalene
・ 1,8-Diazabicycloundec-7-ene
・ 1,8-Diazafluoren-9-one
・ 1,8-Octanediol
・ 1,837 Seconds of Humor
1,9-Pyrazoloanthrone
・ 1-(2-Dimethylaminoethyl)dihydropyrano(3,2-e)indole
・ 1-(2-Diphenyl)piperazine
・ 1-(2-Nitrophenoxy)octane
・ 1-(3-Chlorophenyl)-4-(2-phenylethyl)piperazine
・ 1-(4-(Trifluoromethyl)phenyl)piperazine
・ 1-(4-Nitrophenylethyl)piperidylidene-2-(4-chlorophenyl)sulfonamide
・ 1-(5-phosphoribosyl)-5-((5-phosphoribosylamino)methylideneamino)imidazole-4-carboxamide isomerase
・ 1-(Furan-2-yl)undecan-1-ol
・ 1-1
・ 1-2-1-1 zone press
・ 1-2-3
・ 1-2-3 (APO Hiking Society album)
・ 1-2-3 (fuel station)
・ 1-2-3 (Gloria Estefan and Miami Sound Machine song)


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1,9-Pyrazoloanthrone : ウィキペディア英語版
1,9-Pyrazoloanthrone

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1,9-Pyrazoloanthrone is a chemical compound that is a derivative of anthrone. It is used in biochemical studies as an inhbitor of c-Jun N-terminal kinases (JNKs).
Derivatives of 1,9-pyrazoloanthrone have a variety of biological activities. For example, 5-(aminoalkyl)amino derivatives have been investigated as anticancer agents.
== Synthesis ==
1,9-Pyrazoloanthrone can be synthesized by the condensation of 2-chloroanthraquinone with anhydrous hydrazine in pyridine at 100 °C. Purification is achieved via conversion to the ''N''-acetyl derivative which is crystallized from acetic acid, followed by hydrolysis of the acetyl group with ammonium hydroxide in methanol.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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