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Classification | API >> Hormone and endocrine-regulating drugs >> Gonadotropin |
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Name | Bicalutamide |
Synonyms | N-[4-Cyano-3-(trifluoromethyl)phenyl]-3-(4-fluorophenyl)sulfonyl-2-hydroxy-2-methyl-propanamide |
Molecular Structure | ![]() |
Molecular Formula | C18H14F4N2O4S |
Molecular Weight | 430.37 |
CAS Registry Number | 90357-06-5 |
EC Number | 618-534-3 |
SMILES | CC(CS(=O)(=O)C1=CC=C(C=C1)F)(C(=O)NC2=CC(=C(C=C2)C#N)C(F)(F)F)O |
Solubility | 86 mg/mL (DMSO), <1 mg/mL (water), 7 mg/mL (ethanol) (Expl.) |
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Density | 1.5±0.1 g/cm3, Calc.* |
Melting point | 191-193 ºC |
Index of Refraction | 1.578, Calc.* |
Boiling Point | 650.3±55.0 ºC (760 mmHg), Calc.* |
Flash Point | 347.1±31.5 ºC, Calc.* |
Hazard Symbols |
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Hazard Statements | H315-H319-H335-H351 Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Precautionary Statements | P203-P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P318-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501 Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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SDS | Available | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Bicalutamide is a synthetic nonsteroidal antiandrogen used primarily in the treatment of prostate cancer. It works by inhibiting the action of androgens, such as testosterone, which promote the growth of prostate cancer cells. Bicalutamide was first developed in the late 1980s by the pharmaceutical company AstraZeneca. Its primary function is to block androgen receptors, preventing testosterone from binding to them and thus inhibiting the growth and proliferation of prostate cancer cells. Bicalutamide is often used in combination with other treatments for prostate cancer, including surgery, radiation therapy, or other hormonal therapies. One of its common applications is in the treatment of advanced or metastatic prostate cancer, where it can be used in combination with other drugs such as luteinizing hormone-releasing hormone (LHRH) agonists to reduce androgen levels. It is usually administered orally, and its therapeutic effects are achieved by blocking the androgen receptor, thus preventing the stimulation of cancerous growth in prostate cells. The drug's effectiveness in treating prostate cancer has been well-documented, with several clinical trials supporting its use in combination therapy to delay disease progression and alleviate symptoms. Bicalutamide is also used in cases of prostate cancer recurrence after initial treatment, providing additional therapeutic options for patients with advanced stages of the disease. Its role in cancer therapy highlights the critical need for targeted treatments in oncology, particularly in hormone-dependent cancers such as prostate cancer. In addition to its application in prostate cancer, bicalutamide has also been investigated for use in the treatment of other hormone-dependent conditions, such as hirsutism in women and as part of gender-affirming treatment in transgender individuals. While its primary use remains in prostate cancer therapy, research continues into its potential broader uses. The development of bicalutamide is part of a broader trend in cancer therapy, where targeting specific molecular pathways, such as androgen signaling, offers a more precise and less invasive approach than traditional chemotherapy. This focus on targeted therapies has significantly improved the prognosis for patients with prostate cancer, making bicalutamide an important drug in modern oncology. |
Market Analysis Reports |
List of Reports Available for Bicalutamide |