Abiraterone Acetate , ≥99% , 154229-18-2
Synonym(s):
17-(Pyridin-3-yl)androsta-5,16-dien-3β-yl acetate;Abiraterone acetate;CB 7598
CAS NO.:154229-18-2
Empirical Formula: C26H33NO2
Molecular Weight: 391.55
MDL number: MFCD00934213
EINECS: 620-314-7
Pack Size | Price | Stock | Quantity |
5MG | RMB23.20 | In Stock |
|
25MG | RMB31.20 | In Stock |
|
100MG | RMB39.20 | In Stock |
|
250mg | RMB63.20 | In Stock |
|
1g | RMB127.20 | In Stock |
|
5g | RMB383.20 | In Stock |
|
25g | RMB1359.20 | In Stock |
|
others | Enquire |
PRODUCT Properties
Melting point: | 127-130°C |
Boiling point: | 506.7±50.0 °C(Predicted) |
Density | 1.14±0.1 g/cm3(Predicted) |
storage temp. | -20°C |
solubility | Chloroform (Slightly), DMSO (Sparingly), Methanol (Sparingly) |
pka | 5.31±0.12(Predicted) |
form | powder |
color | white to beige |
Description and Uses
In April 2011, the United States FDA approved abiraterone acetate (CB7630) in combination with the steroid prednisone for the treatment of metastatic castration-resistant prostate cancer (mCRPC) for patients who were previously treated with a docetaxel containing regimen for late-stage disease. Abiraterone acetate affects prostate, testicular, and adrenal androgens by irreversibly inhibiting both the lyase and hydroxylase activity of cytochrome P450 17A (CYP17) signaling pathways (IC50's of 2.9 and 4 nM, respectively) thereby decreasing testosterone levels.Most common serious adverse events for abiraterone acetate versus placebo included fluid retention (30.5% vs. 22.3%), hypokalemia (17.1% vs. 8.4%), hypertension (9.7% vs. 7.9%), hepatic transaminase abnormalities (10.4% vs. 8.1%), and cardiac abnormalities (13.3% vs. 10.4%).
A novel steroidal inhibitor of human Cytochrome P450(17a-Hydroxylase-C17,20-lyase): potential agent for the treatment of prostatic cancer.
Safety
Symbol(GHS) | GHS08 |
Signal word | Danger |
Hazard statements | H360-H372 |
Precautionary statements | P201-P202-P260-P264-P270-P308+P313 |
WGK Germany | 3 |
RTECS | BV7992100 |
HS Code | 2937290000 |