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Abiraterone
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Abiraterone图片
CAS NO:154229-19-3
包装与价格:
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

产品名称
CB-7598
产品介绍
Abiraterone 是一种有效的不可逆的CYP17A1抑制剂,具有抗雄激素活性,抑制细胞色素 p450 酶 CYP17 的 17α-羟化酶和 17,20-裂合酶活性,IC50值 分别为 2.5 nM 和 15 nM.
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
Powder-20°C3 years
4°C2 years
In solvent-80°C6 months
-20°C1 month
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
浓度溶剂体积质量1 mg5 mg10 mg
1 mM2.8611 mL14.3057 mL28.6115 mL
5 mM0.5722 mL2.8611 mL5.7223 mL
10 mM0.2861 mL1.4306 mL2.8611 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80℃, 6 months; -20℃, 1 month。-80℃ 储存时,请在 6 个月内使用,-20℃ 储存时,请在 1 个月内使用。