產(chǎn)品名稱 STK16-IN-1
產(chǎn)品貨號(hào) Axon 2743 CAS [1223001-53-3] MF C17H12FN3OMW 293.30 Purity: 99% Soluble in DMSO Description STK16-IN-1 is a highly selective ATP-competitive inhibitor which exhibits potent inhibitory activity against STK16 kinase (IC50 value of 0.295 μM). In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics results in a slight potentiation of the antiproliferative effects of the chemotherapeutics. References Certificates Categories Extra info F Liu et al. Discovery of a Highly Selective STK16 Kinase Inhibitor. ACS Chem Biol. 2016 Jun 17;11(6):1537-43. Certificate of Analysis Material Safety Data Sheet Cell Signaling & Oncology EC 2.7.10.2 STK16 ATP-competitive STK16 inhibitor Chemical name 1-(4-Fluoro-3-methylphenyl)-1H-pyrrolo[2,3-h][1,6]naphthyridin-2(7H)-one Parent CAS No. [1223001-53-3] Order Size Unit Price Stock 10 mg €125.00 In Stock
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STK16-IN-1

Based on 1 reference(s) in Google Scholar 8 10 1

Axon 2743

CAS [1223001-53-3]

MF C17H12FN3O
MW 293.30

  • Purity: 99%
  • Soluble in DMSO

STK16-IN-1

Description

STK16-IN-1 is a highly selective ATP-competitive inhibitor which exhibits potent inhibitory activity against STK16 kinase (IC50 value of 0.295 μM). In MCF-7 cells, treatment with STK16-IN-1 results in a reduction in cell number and accumulation of binucleated cells, which can be recapitulated by RNAi knockdown of STK16. Co-treatment of STK16-IN-1 with chemotherapeutics results in a slight potentiation of the antiproliferative effects of the chemotherapeutics.
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