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GSK-F1 Chemical Structure

GSK-F1

Data Sheet For research use only. Not for human use.
Cat. No. :BCP29575CAS No. :1402345-92-9Purity:98%
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  • Chemical Properties&Biological Activity
CAS No. 1402345-92-9 Cat. No. BCP29575
Name GSK-F1
Synonyms 1384097-27-1;rac-GSK-F1;
SMILES COC1=C(C=C(C=N1)C2=CC3=C(C=C2)N=C(N(C3=O)C4=CC=CC=C4C(F)(F)F)N)S(=O)(=O)NC5=C(C=C(C=C5)F)F
Chemical Name
Formula C27H18F5N5O4S M. Wt 603.52
Purity 98% Storage Store at 4-8°C
Description GSK-F1 is a potent inhibitor of PI4KA. It has markedly better pharmacokinetic properties in vivo with respects to GSK-A1 . GSK-F1 does not cross the blood-brain barrier. Phosphatidylinositol 4-kinase type IIIα (PI4KA) is a host factor essential for hepatitis C virus replication and hence is a target for drug development. RNAi studies have shown that PI4KA is a mandatory host factor in HCV replication. Down-regulation of PI4KA appears to be reasonably tolerated by cultured cell models and results.
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