SL 0101-1

Discontinued Product

2250 has been discontinued.

View all RSK products.
说明: Selective ribosomal S6 kinase (RSK) inhibitor
化学名: 3-[(3,4-Di-O-acetyl-6-deoxy-α-L-mannopyranosyl)oxy]-5,7-dihydro-2-(4-hydroxyphenyl)-4H-1benzopyran-4-one
纯度: ≥95% (HPLC)
说明书
引用文献 (7)
评论

生物活性 for SL 0101-1

SL 0101-1 is a selective inhibitor of ribosomal S6 kinase (RSK) (IC50 = 89 nM for RSK2). Does not inhibit upstream kinases such as MEK, Raf and PKC. Inhibits the growth of MCF-7 human breast cancer cells with no effect on the normal breast cell line.

技术数据 for SL 0101-1

分子量 516.46
公式 C25H24O12
储存 Store at -20°C
纯度 ≥95% (HPLC)
CAS Number 77307-50-7
PubChem ID 14825856
InChI Key SXOZSDJHGMAEGZ-UHFFFAOYSA-N
Smiles O=C1C3=C(C=C(O)C=C3O)OC(C4=CC=C(O)C=C4)=C1OC2C(O)C(OC(C)=O)C(OC(C)=O)C(C)O2

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

产品说明书 for SL 0101-1

分析证书/产品说明书
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参考文献 for SL 0101-1

参考文献是支持产品生物活性的出版物。

Smith et al (2005) Identification of the first specific inhibitor of p90 ribosomal S6 kinase (RSK) reveals an unexpected role for RSK in cancer cell proliferation. Cancer Res. 65 1027 PMID: 15705904

Bain et al (2007) The selectivity of protein kinase inhibitors: a further update. Biochem.J. 408 297 PMID: 17850214

Godeny and Sayeski (2006) ERK1/2 regulates ANG II-dependent cell proliferation via cytoplasmic activation of RSK2 and nuclear activation of elk1. Am.J.Cell.Physiol. 291 1308

Saha et al (2012) RSK phosphorylates SOS1 creating 14-3-3-docking sites and negatively regulating MAPK activation. Biochem.J. 447 159 PMID: 22827337

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关键词: SL 0101-1, SL 0101-1 supplier, Selective, p90, ribosomal, S6, kinases, RSK, inhibitors, inhibits, SL0101-1, 2250, Tocris Bioscience

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