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Submit ReviewW-13 hydrochloride is a calmodulin antagonist (inhibits calmodulin activated PDE activity with an IC50 of 68 μM). Inhibits growth of tamoxifen-resistant breast cancer cells.
分子量 | 349.27 |
公式 | C14H17ClN2O2S.HCl |
储存 | Store at RT |
纯度 | ≥98% (HPLC) |
CAS Number | 88519-57-7 |
PubChem ID | 16760706 |
InChI Key | QKAALLVQBOLELJ-UHFFFAOYSA-N |
Smiles | Cl.NCCCCNS(=O)(=O)C1=CC=C2C(Cl)=CC=CC2=C1 |
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.
参考文献是支持产品生物活性的出版物。
Bosch et al (1998) Calmodulin inhibitor W13 induces sustained activation of ERK2 and expression of p21cip1. J.Biol.Chem. 273 22145 PMID: 9705360
Hidaka and Tanaka (1983) Naphthalenesulfonamides as calmodulin antagonists. Methods Enzymol. 102 185 PMID: 6139736
Stroble and Peterson (1992) Tamoxifen-resistant human breast cancer cell growth: inhibition by thionidazine, pim. and the calmodulin antagonist, W-13. J.Pharmacol.Exp.Ther. 263 186 PMID: 1403784
关键词: W-13 hydrochloride, W-13 hydrochloride supplier, Calmodulin, antagonists, Ca2+, Binding, Protein, modulators, Calcium, Signaling, Signalling, W13, 0361, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 W-13 hydrochloride 的部分引用包括:
Sethna et al (2016) Calmodulin activity regulates group I metabotropic glutamate receptor-mediated signal transduction and synaptic depression. J Neurosci Res 94 401 PMID: 26864654
Yanda et al (2017) Histone deacetylase 6 inhibition reduces cysts by decreasing cAMP and Ca(2+) in knock-out mouse models of polycystic kidney disease. J Biol Chem 292 17897 PMID: 28887310
平均评分: 5 (Based on 1 Review.)
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PN and PH cells were treated with W-7 (catalog no. 0369) and W-13(catalog no. 0361) purchased from Tocris.