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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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This compound is a selective and BBB-permeable inhibitor of CDK4/6, with half-maximal inhibitory concentrations (IC50s) of 2 nM and 10 nM for CDK4 and CDK6, respectively.
Selective inhibition of key enzymes involved in cell cycle regulation.
Permeates the blood-brain barrier.
Reduces cell viability in various human cell lines, including HCT-116, MCF7, and PANC-1.
Inhibits Rb phosphorylation, leading to a G1 arrest and suppressed proliferation.
Activity is specific for cells that are proficient in Rb.
Effective in reducing cell viability across multiple cancer cell lines.
Demonstrates antiproliferative activity against human HCT116 and MCF7 cells.
Shows inhibition in resistant cell lines.
Causes a cooperative antitumor effect when combined with other agents in xenograft models.
Leads to significant tumor growth inhibition in xenograft models.
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This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.for further information and support please go to the website of the issuing Pharmacopoeia.
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