JNJ 10198409

Pricing Availability   Qty
说明: Potent PDGFRα and PDGFRβ inhibitor; also inhibits c-Abl, Lck, c-Src and Fyn kinases
化学名: N-(3-Fluorophenyl)-1,4-dihydro-6,7-dimethoxyindeno[1,2-c]pyrazol-3-amine
纯度: ≥98% (HPLC)
说明书
引用文献 (8)
评论
实验方案 (1)
文献 (1)

生物活性 for JNJ 10198409

JNJ 10198409 is a potent platelet-derived growth factor receptor (PDGFR) inhibitor (IC50 values are 4.2 and 45 nM for PDGFRβ and PDGFRα, respectively). Also inhibits c-Abl, Lck, c-Src and Fyn kinases (IC50 values are 22, 100, 185 and 378 nM respectively). Displays antiproliferative activity in multiple tumor cell lines. Accelerates down regulation of fibroblast genes in transdifferentiation of human fibroblasts into functional cardiomyocytes, within 9C cocktail.

For more information about how JNJ 10198409 may be used, see our protocol: Converting Fibroblasts into Cardiomyocytes (9C Cocktail)

许可信息

Sold with the permission of Janssen Pharmaceutica N.V.

化合物库 for JNJ 10198409

JNJ 10198409 is also offered as part of the Tocriscreen 2.0 Max, Tocriscreen Kinase Inhibitor Library, Tocriscreen Antiviral Library and Tocriscreen Stem Cell Library. 了解 Tocris 化合物库的更多信息。

技术数据 for JNJ 10198409

分子量 325.34
公式 C18H16FN3O2
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 627518-40-5
PubChem ID 9797370
InChI Key ZDNURMVOKAERHZ-UHFFFAOYSA-N
Smiles COC1=C(OC)C=C2C(CC3=C2NN=C3NC2=CC(F)=CC=C2)=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.

溶解性数据 for JNJ 10198409

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 6.51 20
ethanol 32.53 100

制备储备液 for JNJ 10198409

以下数据基于产品分子量 325.34。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
1 mM 3.07 mL 15.37 mL 30.74 mL
5 mM 0.61 mL 3.07 mL 6.15 mL
10 mM 0.31 mL 1.54 mL 3.07 mL
50 mM 0.06 mL 0.31 mL 0.61 mL

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参考文献 for JNJ 10198409

参考文献是支持产品生物活性的出版物。

Ho et al (2005) (6,7-Dimethoxy-2,4-dihydroindeno[1,2-c]pyrazol-3-yl)phenylamines: platelet-derived growth factor receptor tyrosine kinase inhibitors with broad antiproliferative activity against tumor cells. J.Med.Chem. 29 8163 PMID: 16366598

Cao et al (2016) Conversion of human fibroblasts into functional cardiomyocytes by small molecules. Science. 352 1216 PMID: 27127239


If you know of a relevant reference for JNJ 10198409, please let us know.

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关键词: JNJ 10198409, JNJ 10198409 supplier, JNJ10198409, stem, cell, reprogramming, 9C, cocktail, cardiomyocytes, myocytes, platelet-derived, growth, factor, receptor, alpha, beta, inhibitors, inhibits, PDGFR, PDGFRb, PDGFRa, transdifferentiation, Src, Kinases, Other, Stem, Cell, Reprogramming, Cardiomyocyte, Cells, 6976, Tocris Bioscience

8 篇 JNJ 10198409 的引用文献

引用文献是使用了 Tocris 产品的出版物。 JNJ 10198409 的部分引用包括:

Ulrich et al (2019) Self-organization of modular network architecture by activity-dependent neuronal migration and outgrowth. Elife 8 PMID: 31526478

Stephen H et al (2016) Tyrosine Binding Protein Sites Regulate the Intracellular Trafficking and Processing of Amyloid Precursor Protein through a Novel Lysosome-Directed Pathway. PLoS One 11 e0161445 PMID: 27776132

Anisur et al (2014) Mesenchymal chemotaxis requires selective inactivation of myosin II at the leading edge via a noncanonical PLCγ/PKCα pathway. Dev Cell 31 747-60 PMID: 25482883

Donghong et al (2020) Anaplastic Lymphoma Kinase Regulates Internalization of the Dopamine D2 Receptor. Mol Pharmacol 97 123-131 PMID: 31734646


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JNJ 10198409 实验方案

以下实验方案包含使用 JNJ 10198409(目录编号 6976)的更多信息。

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