产品名称 TG 003
产品货号 Axon 1765 CAS [719277-26-6] MF C13H15NO2SMW 249.33 Purity: 98% Soluble in DMSO Description Potent and specific inhibitor of Cdc2-like kinase (Clk) family (Ki = 10 nM for mClk1/Sty; IC50 = 15 nM, 20 nM, 200 nM, and > 10 mM for mClk4, mClk1, mClk2, and mClk3, respectively); a valuable tool to dissect the regulatory mechanisms involving serine/arginine-rich protein phosphorylation signaling pathways in vivo, and potential for the therapeutic manipulation of abnormal splicing References Certificates Categories Extra info M Muraki et al. Manipulation of alternative splicing by a newly developed inhibitor of Clks. J Biol Chem. 2004, 279(23), 24246-24254.   A Nishida et al. Chemical treatment enhances skipping of a mutated exon in the dystrophin gene. Nature Commun. 2011, 2, 308. Certificate of Analysis Material Safety Data Sheet Cell Cycle Regulation Cell Signaling & Oncology EC 2.7.12.1 CLK Inhibitor of Cdc2-like kinase (Clk) family Chemical name (Z)-1-(3-ethyl-5-methoxybenzo[d]thiazol-2(3H)-ylidene)propan-2-one Parent CAS No. [719277-26-6; 300801-52-9(mix E/Z); 1164521-02-1 (E)] Order Size Unit Price Stock 10 mg €115.00 In Stock
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TG 003

Based on 18 reference(s) in Google Scholar 9 10 18

Axon 1765

CAS [719277-26-6]

MF C13H15NO2S
MW 249.33

  • Purity: 98%
  • Soluble in DMSO

TG 003

Description

Potent and specific inhibitor of Cdc2-like kinase (Clk) family (Ki = 10 nM for mClk1/Sty; IC50 = 15 nM, 20 nM, 200 nM, and > 10 mM for mClk4, mClk1, mClk2, and mClk3, respectively); a valuable tool to dissect the regulatory mechanisms involving serine/arginine-rich protein phosphorylation signaling pathways in vivo, and potential for the therapeutic manipulation of abnormal splicing
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