CAS NO: | 164656-23-9 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Dutasteride (GG745) is a potent inhibitor of both5α-reductase isozymes. Dutasteride may possess off-target effects on theandrogen receptor(AR) due to its structural similarity to DHT[1]. | ||||||||||||||||
IC50& Target | IC50: 5 alpha-reductase[1] | ||||||||||||||||
体外研究 (In Vitro) | Dutasteride inhibits3H-T conversion to3H-DHT and, as anticipated, inhibits T-induced secretion of PSA and proliferation. However the drug also inhibited DHT-induced PSA secretion and cell proliferation (IC50approximately 1 μM)[1].Dutasteride competes for binding the LNCaP cell AR with an IC50approximately 1.5 μM. High concentrations of dutasteride (10-50 μM), but not finasteride, in steroid-free medium, resulted in enhanced cell death, possibly by apoptosis[1].Dutasteride reduces cell viability and cell proliferation in both cell lines tested (androgen-responsive (LNCaP) and androgen-unresponsive (DU145) human prostate cancer (PCa))[2]. | ||||||||||||||||
体内研究 (In Vivo) | GG745 has a terminal half-life of approximately 240 hr, and single doses of >10 mg decreased DHT levels significantly more than did single 5-mg doses of finasteride[3].In placebo treated men without prostate cancer there was an 8.3% median increase in PSA at month 24 compared with -59.5% in those who received dutasteride, using doubled values to correct for dutasteride treatment[4].Toxicity: Dutasteride may affect male fertility and steroid hormone dynamics. Therefore, a 21-day reproduction study was conducted to determine the effects of dutasteride (10, 32 and 100 μg/L) on fish reproduction. Exposure to dutasteride significantly reduced fecundity of fish and affected several aspects of reproductive endocrine functions in both males and females[5]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 528.53 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C27H30F6N2O2 | ||||||||||||||||
CAS 号 | 164656-23-9 | ||||||||||||||||
中文名称 | 度他雄胺 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 33.33 mg/mL(63.06 mM;Need ultrasonic) 配制储备液
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