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Tubulin polymerization-IN-37

Tubulin polymerization-IN-37
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Tubulin polymerization-IN-37

Catalog No. T61084Cas No. 2011784-92-0
Tubulin polymerization-IN-37 is a potent inhibitor (IC50: 2.3 μΜ) of tubulin polymerization by binding specifically to the colchicine site of tubulin and preventing colchicine binding. It has potential applications in cancer research, notably for lymphomas [1].
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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 μΜ) of tubulin polymerization by binding specifically to the colchicine site of tubulin and preventing colchicine binding. It has 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
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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