目錄:MedChemExpress LLC>>信號通路>> Anastrozole | 阿那曲唑 | MedChemExpress (MCE)
CAS | 120511-73-1 | 純度 | 99.99% |
---|---|---|---|
分子量 | 293.37 | 分子式 | C??H??N? |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 10 mM * 1 mL |
貨號 | HY-14274 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 120511-73-1
MCE 國際站:Anastrozole
產(chǎn)品活性:Anastrozole 是一種選擇性的芳香酶 (aromatase) 抑制劑,抑制胎盤芳香化酶,IC50 為 15 nM。
研究領(lǐng)域:Metabolic Enzyme/Protease
作用靶點:Cytochrome P450
In Vitro: Anastrozole is a comparatively simple, achiral benzyltriazole derivative, that inhibits human placental aromatase with an IC50 of 15 nM. In the same assay it is 200 times as potent as aminoglutethimide (AG), twice as potent as 4-OHA and one third as potent as Fadrozole.
In Vivo: Groups of eight immature (22-day-old) female rats are given androstenedione (AD) (30 mg/kg) in arachis oil s.c. daily for3 days with or without various doses of Anastrozole p.o. on day 4 the uteri are dissected, blotted and weighed. An oral dose of 0.1 mg/kg of Anastrozole given on day 2 or day 3 of the cycle completely blocked ovulation. At the same daily dosage (0.1 mg/kg), Anastrozole completely extinguished the uterotrophic activity of exogenous AD in immature rats. In male pigtailed monkeys, twice-daily oral treatment with 0.1 mg/kg and above of Anastrozole reduced circulating oestradiol concentrations by 50-60%.
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