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Tubulin polymerization-IN-37

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Catalog No. T61084Cas No. 2011784-92-0

Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 µM) of tubulin polymerization, binding specifically to the colchicine site of tubulin and preventing colchicine binding, with potential applications in cancer research, notably for lymphomas [1].

Tubulin polymerization-IN-37

Tubulin polymerization-IN-37

😃Good
Catalog No. T61084Cas No. 2011784-92-0
Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 µM) of tubulin polymerization, binding specifically to the colchicine site of tubulin and preventing colchicine binding, with potential applications in cancer research, notably for lymphomas [1].
Pack SizePriceAvailabilityQuantity
25 mg$1,5206-8 weeks
50 mg$1,9806-8 weeks
100 mg$2,5006-8 weeks
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Product Introduction

Bioactivity
Description
Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 µM) of tubulin polymerization, binding specifically to the colchicine site of tubulin and preventing colchicine binding, with potential applications in cancer research, notably for lymphomas [1].
In vitro
Tubulin polymerization-IN-37 (also referred to as compound 2f), at a concentration of 1 μM for 72 hours, significantly reduces the proliferation of lymphoma cells by over 50%. At concentrations of 50 and 500 nM over 24 to 72 hours, this compound induces apoptosis and arrests VL51 and MINO cells in the G2/M phase of the cell cycle. Furthermore, at a concentration of 5 μM, it inhibits the binding of colchicine to tubulin by 80%, demonstrating its mechanism of action. Tubulin polymerization-IN-37 also exhibits cytotoxic effects against MCF-7 cells with an IC50 value of 0.21 μM. Additionally, in a cell proliferation assay involving VL51, MINO, HBL1, and SU-DHL-10 cell lines treated with 0-10 μM of the compound for 72 hours, cell proliferation was inhibited to 28.1%, 8.6%, 7.3%, and 13.8% at 1 μM, respectively, with IC50 values of 0.12, 0.07, 0.08, and 0.07 μM respectively. Cell cycle analysis further confirmed the compound's effectiveness in arresting VL51 and MINO cells in the G2/M phase at concentrations of 50 and 500 nM after 24, 48, and 72 hours of treatment.
Chemical Properties
Molecular Weight340.37
FormulaC19H20N2O4
Cas No.2011784-92-0
Storage & Solubility Information
StorageShipping with blue ice.

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