PP 3

Pricing Availability   Qty
说明: Negative control for PP 2 (Cat. No. 1407)
化学名: 1-Phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-amine
纯度: ≥98% (HPLC)
说明书
引用文献 (7)
评论

生物活性 for PP 3

PP 3 is a negative control for the Src kinase inhibitor, PP 2. Inhibits EGFR kinase (IC50 = 2.7 μM).

Active Analog also available.

化合物库 for PP 3

PP 3 is also offered as part of the Tocriscreen 2.0 Max and Tocriscreen Antiviral Library. 了解 Tocris 化合物库的更多信息。

技术数据 for PP 3

分子量 211.22
公式 C11H9N5
储存 Store at -20°C
纯度 ≥98% (HPLC)
CAS Number 5334-30-5
PubChem ID 4879
InChI Key KKDPIZPUTYIBFX-UHFFFAOYSA-N
Smiles NC1=NC=NC2=C1C=NN2C3=CC=CC=C3

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 PP 3

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
DMSO 21.12 100
ethanol 5.28 25

制备储备液 for PP 3

以下数据基于产品分子量 211.22。 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 4.73 mL 23.67 mL 47.34 mL
5 mM 0.95 mL 4.73 mL 9.47 mL
10 mM 0.47 mL 2.37 mL 4.73 mL
50 mM 0.09 mL 0.47 mL 0.95 mL

Molarity Calculator

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Reconstitution Calculator

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Dilution Calculator

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产品说明书 for PP 3

分析证书/产品说明书
选择另一批次:

参考文献 for PP 3

参考文献是支持产品生物活性的出版物。

Traxler et al (1997) Use of a pharmacophore model for the design of EGF-R tyrosine kinase inhibitors: 4-(phenylamino)pyrazolo[3,4-d]pyrimidines. J.Med.Chem. 40 3601 PMID: 9357527

Hou et al (2007) PP2, a potent inhibitor of Src family kinases, protects against hippocampal CA1 pyramidal cell death after transient global brain ischemia. Neurosci.Letts. 420 235 PMID: 17556100


If you know of a relevant reference for PP 3, please let us know.

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关键词: PP 3, PP 3 supplier, Negative, control, PP, 2, EGFR-kinases, inhibitors, inhibits, Src, negative, Epidermal, Growth, Factors, Receptors, ErbB, Her, EGFR, Receptor, Tyrosine, RTKs, PP3, Kinases, 2794, Tocris Bioscience

7 篇 PP 3 的引用文献

引用文献是使用了 Tocris 产品的出版物。 PP 3 的部分引用包括:

Li et al (2016) Progesterone receptor membrane component-1 regulates hepcidin biosynthesis. J Clin Invest 126 389 PMID: 26657863

Chen et al (2014) BDNF released during neuropathic pain potentiates NMDA receptors in primary afferent terminals. Eur J Neurosci 39 1439 PMID: 24611998

Vijayakumar et al (2015) Tyrosine phosphorylation of WIP releases bound WASP and impairs podosome assembly in macrophages. Neural Regen Res 128 251 PMID: 25413351

Kubota et al (2014) mGluR1-mediated excitation of cerebellar GABAergic interneurons requires both G protein-dependent and Src-ERK1/2-dependent signaling pathways. PLoS One 9 e106316 PMID: 25181481


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