VE-821

≥98%

Reagent Code: #77805
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CAS Number 1232410-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 368.41 g/mol
Formula C₁₈H₁₆N₄O₃S
badge Registry Numbers
MDL Number MFCD19443686
inventory_2 Storage & Handling
Storage -20°C

description Product Description

VE-821 is primarily utilized in research settings as a potent and selective inhibitor of ATR kinase, a key enzyme involved in the DNA damage response pathway. Its application is significant in studying the mechanisms of DNA repair and cellular responses to genotoxic stress. Researchers use VE-821 to investigate the role of ATR in cancer biology, as inhibiting ATR can sensitize cancer cells to DNA-damaging therapies like chemotherapy and radiation. This makes it a valuable tool for exploring potential combination therapies to enhance the efficacy of existing cancer treatments. Additionally, VE-821 aids in understanding the broader implications of ATR inhibition in normal cells, helping to assess the therapeutic window and potential side effects of targeting this pathway.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Green to Beige Solid
NMR Consistent with structure
Purity 98-100%

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿750.00
inventory 25mg
10-20 days ฿2,080.00
inventory 100mg
10-20 days ฿6,980.00
VE-821
VE-821 is primarily utilized in research settings as a potent and selective inhibitor of ATR kinase, a key enzyme involved in the DNA damage response pathway. Its application is significant in studying the mechanisms of DNA repair and cellular responses to genotoxic stress. Researchers use VE-821 to investigate the role of ATR in cancer biology, as inhibiting ATR can sensitize cancer cells to DNA-damaging therapies like chemotherapy and radiation. This makes it a valuable tool for exploring potential combination therapies to enhance the efficacy of existing cancer treatments. Additionally, VE-821 aids in understanding the broader implications of ATR inhibition in normal cells, helping to assess the therapeutic window and potential side effects of targeting this pathway.
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