Purvalanol A

Pricing Availability   Qty
说明: Cdk inhibitor; potently inhibits cdk1, cdk2 and cdk5
别名: NG 60
化学名: (2R)-2-[[6-[(3-Chlorophenyl)amino]-9-(1-methylethyl)-9H-purin-2-yl]amino]-3-methyl-1-butanol
纯度: ≥98% (HPLC)
说明书
引用文献 (8)
评论

生物活性 for Purvalanol A

Purvalanol A is a cyclin-dependent kinase (cdk) inhibitor (reported IC50 values are 4, 4 - 70, 75 - 240 and 100 nM for cdk1, cdk2, cdk5 and cdk 7, respectively). Reversibly arrests synchronised cells in G1 and G2, and inhibits cell proliferation and cell death.

许可信息

Sold under license from the Regents of the University of California

化合物库 for Purvalanol A

Purvalanol A is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for Purvalanol A

分子量 388.9
公式 C19H25ClN6O
储存 Store at +4°C
纯度 ≥98% (HPLC)
CAS Number 212844-53-6
PubChem ID 456214
InChI Key PMXCMJLOPOFPBT-HNNXBMFYSA-N
Smiles ClC1=CC=CC(NC2=C3C(N(C(C)C)C=N3)=NC(N[C@H]([C@@H](C)C)CO)=N2)=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 Purvalanol A

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
ethanol 19.45 50
DMSO 38.89 100

制备储备液 for Purvalanol A

以下数据基于产品分子量 388.9。 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 2.57 mL 12.86 mL 25.71 mL
5 mM 0.51 mL 2.57 mL 5.14 mL
10 mM 0.26 mL 1.29 mL 2.57 mL
50 mM 0.05 mL 0.26 mL 0.51 mL

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产品说明书 for Purvalanol A

分析证书/产品说明书
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参考文献 for Purvalanol A

参考文献是支持产品生物活性的出版物。

Bain et al (2003) The specificities of protein kinase inhibitors: an update. Biochem.J. 371 199 PMID: 12534346

Gray et al (1998) Exploiting chemical libraries, structure, and genomics in the search for kinase inhibitors. Science 281 533 PMID: 9677190

Gray et al (1999) ATP-site directed inhibitors of cyclin-dependent kinases. Curr.Med.Chem. 6 859 PMID: 10495356

Villerbu et al (2002) Cellular effects of purvalanol A: a specific inhibitor of cyclin-dependent kinase activities. Int.J.Cancer 97 761 PMID: 11857351

Jorda et al (2018) How selective are pharmacological inhibitors of cell-cycle-regulating cyclin-dependent kinases? J.Med.Chem. 61 9105 PMID: 30234987


If you know of a relevant reference for Purvalanol A, please let us know.

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查看全部 Non-selective CDK Inhibitors

关键词: Purvalanol A, Purvalanol A supplier, Cyclin-dependent, protein, kinases, inhibitors, inhibits, Cdk, PurvalanolA, NG60, NG, 60, Kinase, Non-selective, CDKs, 1580, Tocris Bioscience

8 篇 Purvalanol A 的引用文献

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

Gayek and Ohi (2016) CDK-1 Inhibition in G2 Stabilizes Kinetochore-Microtubules in the following Mitosis. PLoS One 11 e0157491 PMID: 27281342

Seldin et al (2013) NuMA localization, stability, and function in spindle orientation involve 4.1 and Cdk1 interactions. Mol Biol Cell 24 3651 PMID: 24109598

Origanti et al (2013) Synthetic lethality of Chk1 inhibition combined with p53 and/or p21 loss during a DNA damage response in normal and tumor cells. Oncogene 32 577 PMID: 22430210

Ozlü et al (2010) Binding partner switching on microtubules and aurora-B in the mitosis to cytokinesis transition. Mol Cell Proteomics 9 336 PMID: 19786723


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