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CDK7-IN-27

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Catalog No. T209449

CDK7-IN-27 (Compound 37) is a selective inhibitor of cyclin-dependent kinase 7 (CDK7), with a Ki value of 3 nM. It effectively causes cell cycle arrest at the G0/G1 phase.

CDK7-IN-27

CDK7-IN-27

🥰Excellent
Catalog No. T209449
CDK7-IN-27 (Compound 37) is a selective inhibitor of cyclin-dependent kinase 7 (CDK7), with a Ki value of 3 nM. It effectively causes cell cycle arrest at the G0/G1 phase.
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Product Introduction

Bioactivity
Description
CDK7-IN-27 (Compound 37) is a selective inhibitor of cyclin-dependent kinase 7 (CDK7), with a Ki value of 3 nM. It effectively causes cell cycle arrest at the G0/G1 phase.
Targets&IC50
CDK7:3 nM, CDK2:19.4 nM
In vitro
CDK7-IN-27 effectively inhibits the proliferation of MDA-MB-453 cells with an EC50 of 1.49 μM when used in concentrations ranging from 0.04 to 10 μM over the course of 5 days. At a concentration of 1 μM over 24 hours, CDK7-IN-27 demonstrates good metabolic stability in both mouse and human liver microsomes, with half-life periods of 38.5 minutes and 34.1 minutes, respectively. Additionally, CDK7-IN-27 (0-1 μM, 24 h) arrests the cell cycle in the G0/G1 phase by inhibiting the phosphorylation of retinoblastoma protein through CDK7 inhibition.
Chemical Properties
FormulaC26H37N7O2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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 μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
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