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MilliporeSigma™ Calbiochem™ LFM-A13
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Quantity:
5 mg
Description
A potent, cell-permeable, reversible, substrate competitive, and specific inhibitor of Bruton’s Tyrosine Kinase (BTK; IC50 = 17.2μM for human BTK in vitro and IC50 = 2.5μM for recombinant BTK). Also inhibits Polo-like kinase in an ATP-competitive manner (IC50 = 10μM and 61μM for Plx1 and Plk3, respectively), and displays antitumor properties. Does not affect the enzymatic activity of other protein tyrosine kinases, including EGFR, HCK, IRK JAK1, and JAK3 even at concentrations of 278μM. Enhances the chemosensitivity of BTK-positive B-lineage leukemia cells to ceramide- and vincristine-induced apoptosis.

Specifications
Specifications
Color | Light Brown |
Description | 97% by HPLC |
Target Proteins | Human Bruton's Tyrosine Kinase (BTK) |
CAS | 62004-35-7 |
Molecular Formula | C11H8Br2N2O2 |
Formula Weight | 360g/mol |
Solubility | DMSO |
Content And Storage | Protect from light |
Form | Solid |
Quantity | 5 mg |
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