PHA-793887

≥95%

  • Product Code: 77734
  CAS:    718630-59-2
Molecular Weight: 361.48 g./mol Molecular Formula: C₁₉H₃₁N₅O₂
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: -20°C
Product Description: PHA-793887 is primarily utilized in research settings as a potent and selective inhibitor of cyclin-dependent kinases (CDKs), particularly CDK2, CDK5, and CDK7. Its application is significant in studying cell cycle regulation and understanding the mechanisms of CDKs in cellular processes. Researchers employ it to investigate the role of CDKs in cancer development, as dysregulation of these kinases is often associated with tumor growth and progression. Additionally, PHA-793887 is used in preclinical studies to explore potential therapeutic strategies for targeting CDKs in various cancers. Its ability to inhibit CDK activity makes it a valuable tool for elucidating pathways involved in cell proliferation and apoptosis, contributing to the development of novel anticancer therapies.
Product Specification:
Test Specification
APPEARANCE Yellow solid
PURITY 95-100
NMR Consistent with structure
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days ฿9,360.00
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-
0.025 10-20 days ฿30,850.00
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-
PHA-793887
PHA-793887 is primarily utilized in research settings as a potent and selective inhibitor of cyclin-dependent kinases (CDKs), particularly CDK2, CDK5, and CDK7. Its application is significant in studying cell cycle regulation and understanding the mechanisms of CDKs in cellular processes. Researchers employ it to investigate the role of CDKs in cancer development, as dysregulation of these kinases is often associated with tumor growth and progression. Additionally, PHA-793887 is used in preclinical studies to explore potential therapeutic strategies for targeting CDKs in various cancers. Its ability to inhibit CDK activity makes it a valuable tool for elucidating pathways involved in cell proliferation and apoptosis, contributing to the development of novel anticancer therapies.
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