GSK319347A

≥98%

Reagent Code: #62678
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CAS Number 862812-98-4

science Other reagents with same CAS 862812-98-4

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scatter_plot Molecular Information
Weight 469.53 g/mol
Formula C₂₂H₁₉N₃O₅S₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

GSK319347A is a potent and selective inhibitor of the bromodomains in BET (bromodomain and extra-terminal) proteins, primarily used in research settings to study its potential therapeutic effects, particularly in the field of oncology. It targets epigenetic reader domains involved in cancer progression by disrupting the interaction between BET proteins and acetylated histones, thereby affecting gene expression. Researchers utilize this compound to investigate its efficacy in blocking tumor growth and metastasis, making it a valuable tool for understanding cancer biology and developing novel treatments. Additionally, it is employed in preclinical studies to assess its pharmacokinetics, safety profile, and potential as a lead compound for drug development. Its role in modulating key molecular targets also aids in exploring its application in other diseases beyond cancer, such as inflammatory and autoimmune disorders.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿19,494.00
inventory 5mg
10-20 days ฿59,508.00

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GSK319347A
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GSK319347A is a potent and selective inhibitor of the bromodomains in BET (bromodomain and extra-terminal) proteins, primarily used in research settings to study its potential therapeutic effects, particularly in the field of oncology. It targets epigenetic reader domains involved in cancer progression by disrupting the interaction between BET proteins and acetylated histones, thereby affecting gene expression. Researchers utilize this compound to investigate its efficacy in blocking tumor growth and met

GSK319347A is a potent and selective inhibitor of the bromodomains in BET (bromodomain and extra-terminal) proteins, primarily used in research settings to study its potential therapeutic effects, particularly in the field of oncology. It targets epigenetic reader domains involved in cancer progression by disrupting the interaction between BET proteins and acetylated histones, thereby affecting gene expression. Researchers utilize this compound to investigate its efficacy in blocking tumor growth and metastasis, making it a valuable tool for understanding cancer biology and developing novel treatments. Additionally, it is employed in preclinical studies to assess its pharmacokinetics, safety profile, and potential as a lead compound for drug development. Its role in modulating key molecular targets also aids in exploring its application in other diseases beyond cancer, such as inflammatory and autoimmune disorders.

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