CAS NO: | 154229-19-3 |
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 |
1 g | 电议 |
2 g | 电议 |
5 g | 电议 |
10 g | 电议 |
50 g | 电议 |
生物活性 | Abiraterone is a potent and irreversibleCYP17A1inhibitor with antiandrogen activity, which inhibits both the 17α-hydroxylase and 17,20-lyase activity of thecytochrome p450enzymeCYP17withIC50s of 2.5 nM and 15 nM, respectively. | ||||||||||||||||
IC50& Target | IC50:17α-hydroxylase (2.5 nM), 17,20-lyase (15 nM)[6] | ||||||||||||||||
体外研究 (In Vitro) | Significant inhibition of proliferation of the AR-positive prostate cancer cell lines LNCaP and VCaP with doses of Abiraterone ≥5 μM is confirmed[2]. Abiraterone shows IC50values of 15 nM and 2.5 nM for the 17,20-lyase and 17α-hydroxylase (CYP17 is a bifunctional enzyme with both 17α-hydroxylase and 17,20-lyase activity). Abiraterone inhibits human 17,20-lyase and 17α-hydroxylase with IC50of 27 and 30 nM respectively[3]. Abiraterone inhibits recombinant human 3βHSD1 and 3βHSD2 activity with competitive Kivalues of 2.1 and 8.8 μM. 10 μM Abiraterone is sufficient to completely block synthesis of 5α-dione and DHT in both cell lines.Treatment with abi significantly inhibited CRPC progression in the robustly growing subset, effectively putting a ceiling on tumor growth over 4 weeks of treatment (P<0.00001). [3H]-dehydroepiandrosterone (DHEA) depletion and Δ4-androstenedione (AD) accumulation are inhibited by Abiraterone in LNCaP, with an IC50<1 μm[4]. | ||||||||||||||||
体内研究 (In Vivo) | The 0.5 mmol/kg/d Abiraterone treatment dose is previously shown to yield serum concentrations of about 0.5 to 1 μM. Xenograft tumor growth in the control group is widely variable, with some tumors growing slowly and only a subset of tumors exhibiting robust growth[4]. Following i.v. administration (5 mg/kg) the clearance (Cl) and volume of distribution (Vd) are found to be 31.2 mL/min/kg and 1.97 L/kg, respectively. The AUC0-∞(area under the plasma concentration-time curve from time zero to infinity time point) is found to be 2675 ng*h/mL. The terminal half-life (t1/2) is 0.73 h. Because of high clearance, Abiraterone (ART) is quantifiable only until 2 h following i.v. administration[5]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 349.51 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C24H31NO | ||||||||||||||||
CAS 号 | 154229-19-3 | ||||||||||||||||
中文名称 | 阿比特龙;坦度酮罗;阿比特伦 | ||||||||||||||||
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: DMF : 8.75 mg/mL(25.04 mM;Need ultrasonic and warming) Ethanol : 5.4 mg/mL(15.45 mM;Need ultrasonic) DMSO : 5 mg/mL(14.31 mM;Need ultrasonic) 配制储备液
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