Alpelisib (BYL719)

99%

  • Product Code: 99501
  CAS:    1217486-61-7
Molecular Weight: 441.47 g./mol Molecular Formula: C₁₉H₂₂F₃N₅O₂S
EC Number: MDL Number: MFCD22417085
Melting Point: Boiling Point:
Density: Storage Condition: -20℃
Product Description: Alpelisib is primarily used in the treatment of advanced or metastatic breast cancer, specifically in cases where the cancer is hormone receptor-positive (HR+), HER2-negative, and has a PIK3CA mutation. It is often prescribed in combination with fulvestrant, an estrogen receptor antagonist, to enhance its efficacy. The drug works by inhibiting the PI3K pathway, which is often overactive in these types of cancers, thereby slowing tumor growth and progression. Alpelisib is particularly beneficial for patients who have previously undergone endocrine therapy but have seen their cancer progress. Its targeted approach helps in managing the disease more effectively, offering a therapeutic option for those with specific genetic mutations.
Product Specification:
Test Specification
APPEARANCE White to off-white powder or crystals
PURITY 98.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.001 10-20 days $53.16
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-
0.005 10-20 days $132.89
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-
0.025 10-20 days $316.45
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-
0.100 10-20 days $777.42
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Alpelisib (BYL719)
Alpelisib is primarily used in the treatment of advanced or metastatic breast cancer, specifically in cases where the cancer is hormone receptor-positive (HR+), HER2-negative, and has a PIK3CA mutation. It is often prescribed in combination with fulvestrant, an estrogen receptor antagonist, to enhance its efficacy. The drug works by inhibiting the PI3K pathway, which is often overactive in these types of cancers, thereby slowing tumor growth and progression. Alpelisib is particularly beneficial for patients who have previously undergone endocrine therapy but have seen their cancer progress. Its targeted approach helps in managing the disease more effectively, offering a therapeutic option for those with specific genetic mutations.
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