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cisplatin/flavopiridol/paclitaxel

Known as: CDDP/FLAVO/TAX 
 
National Institutes of Health

Papers overview

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2016
2016
Structural analogs of flavopiridol {2-(2-chlorophenyl)-5,7-dihydroxy-8-[(3S,4R)-3-hydroxy-1-methyl-4-piperidinyl]4-chromenone… Expand
2013
2013
BackgroundDormant cells are characterised by low RNA synthesis. In contrast, cancer cells can be addicted to high RNA synthesis… Expand
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2012
2012
PurposeImatinib is an inhibitor of the Bcr-Abl tyrosine kinase; however, resistance is common. Flavopiridol, a cyclin-dependent… Expand
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2010
2010
Background:Flavopiridol (HMR 1275) is a synthetic flavone with antineoplastic properties through inhibition of cyclin-dependent… Expand
2007
2007
Non-compact three-dimensional QED is studied by computer simulations to understand its chiral symmetry breaking features for… Expand
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2007
2007
Non-compact three-dimensional QED is studied by computer s imulations to understand its chiral symmetry breaking features for… Expand
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2003
2003
BACKGROUND Flavopiridol is a flavonoid with antiproliferative effects mediated, in part, by inhibition of cyclin-dependent… Expand
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2002
2002
Flavopiridol [2-(2-chlorophenyl 5 ,7-dihydroxy-8-[cis-(3-hydroxy-1-methyl-4-piperidinyl)-4H-1-benzopyran-4-one, hydrochloride] is… Expand
Highly Cited
2000
Highly Cited
2000
Flavopiridol, the first potent cyclin-dependent kinase inhibitor to enter clinical trials, was recently found to be cytotoxic to… Expand
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Highly Cited
1999
Highly Cited
1999
This study investigates the roles of both ionized and un-ionized species of flavopiridol in solubilization by complexation… Expand