Flavopiridol
is a constructed flavone admixture that inhibits the phosphorylation of
cyclin-dependent kinases (Cdks) and suppresses announcement of cyclin D1 and
D3, arresting the axial role of Cdks in the adjustment of the corpuscle aeon
and appropriately announcement apoptosis. This activity has been exploited in
studies investigating the abolishment of oncogenic proliferation, synovial
hyperplasia, and collective abolition accompanying to rheumatoid arthritis.
Flavopiridol is an inhibitor of Cdk1, Cdk10, Cdk11, Cdk2, Cdk3, Cdk4, Cdk5,
Cdk6, Cdk7, Cdk8 and Cdk9.
Flavopiridol
is an important beginning drug, acquired from a alleviative bulb from India
which has been acclimated for centuries in abounding aboriginal medicines.
Flavopiridol is getting developed by Aventis Oncology in accord with the
National Cancer Institute (NCI). Its use is anon beneath analysis for a array
of solid tumors as able-bodied as hematological cancers. Several actual ablaze
advisers whose horse faculty I assurance assume to anticipate this biologic has
"legs", that it will survive the aboriginal appearance enhancement
trials to become a above biologic for the analysis of CLL.
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