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Country: China (Mainland)
Business Type:Trading Company
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Tel: +86 18233902561
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CAS NO.154229-19-3
medical grade(1-50)Metric Tonmedical grade(50-500)Metric Ton
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Molecular Formula | C24H31NO |
Molar Mass | 349.52 |
Density | 1.14±0.1 g/cm3(Predicted) |
Melting Point | 227-228 °C(Solv: toluene (108-88-3)) |
Boling Point | 500.2±50.0 °C(Predicted) |
Flash Point | 256.3°C |
Solubility | DMSO 0.1 mg/mL Water 0.02 mg/mL Ethanol 0.2 mg/mL |
Vapor Presure | 7.99E-11mmHg at 25°C |
Appearance | Solid |
Color | White to Pale Yellow |
pKa | 14.71±0.70(Predicted) |
Storage Condition | 2-8°C |
Refractive Index | 1.605 |
Use | Androgen antagonists |
In vitro study | Abiraterone binds to wild-type and mutant androgen receptors (AR). In Vitro, Abiraterone inhibits proliferation and androgen receptor-regulated gene expression in androgen receptor-positive prostate cancer cells, explaining the mechanism by inhibition of steroid and antiandrogen receptors. In fact, the mutant androgen receptor activated by Eplerenone can be inhibited by higher concentrations of Abiraterone. The Abiraterone replaces the ligand in WT-AR and T877A with an EC50 of 13.4 μm and 7.9 μm, respectively. Abiraterone acts on rat testis microparticles and inhibits lyase activity with an IC50 of 5.8 nM. Abiraterone acetate significantly inhibited T secretion (− 48%) and in turn increased LH concentrations. (192 percent). |
In vivo study | In human testis microsomes, Abiraterone inhibits CYP17 with an IC50 of 72 nM. Abiraterone did not significantly reduce any organ size. Abiraterone strongly reduces the level of testosterone, almost to the level of removal of the testicles. Compared with the control group, Abiraterone reduced testosterone levels by more than 95%. |