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1-NM-PP1 (PP1 Analog II)

    
98.40%

4-Amino-1-tert-butyl-3-(1’-naphthylmethyl)pyrazolo[3,4-d]pyrimidine

源叶(MedMol)
S84489 一键复制产品信息
221244-14-0
C20H21N5
331.41
4-Amino-1-tert-butyl-3-(1’-naphthylmethyl)pyrazolo[3,4-d]pyrimidine;1-tert-butyl-3-(naphthalen-1-ylmethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine; 1-(1,1-dimethylethyl)-3-(1-naphthalenylmethyl)-1H-pyrazo
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S84489-5mg买3赠1
98.40%

¥400.00

9 - - - -
S84489-10mg买3赠1
98.40%

¥720.00

9 - - - -
S84489-50mg买3赠1
98.40%

¥3040.00

5 - - - -
S84489-100mg买3赠1
≥98%

¥4800.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: 1-NM-PP1, a cell-permeable PP1 analog, is a potent Src family kinases inhibitor with IC50s of 4.3 nM and 3.2 nM for v-Src-as1 and c-Fyn-as1, respectively
靶点: IC50: 4.3 nM (v-Src-as1), 3.2 nM (c-Fyn-as1), 28 μM (v-Src), 1 μM (c-Fyn), 3.4 μM (c-Abl), 29 μM (CDK2), 24 μM (CAMKII), 120 nM (cAbl-as2), 5 nM (CDK2-as1), 8 nM (CAMKII-as1);Serine/threoninkinase; CDK; Src
参考文献: 1. Bishop A C, et al. Generation of Monospecific Nanomolar Tyrosine Kinase Inhibitors via a Chemical Genetic Approach. Journal of the American Chemical Society, 1999, 121(4):627-631. 2. Bishop AC, et al. A chemical switch for inhibitor-sensitive alleles of any protein kinase. Nature. 2000 Sep 21;407(6802):395-401. 3. Larochelle S, et al. Requirements for Cdk7 in the assembly of Cdk1/cyclin B and activation of Cdk2 revealed by chemical genetics in human cells. Mol Cell. 2007 Mar 23;25(6):839-50.
溶解性: DMSO  :  27.5  mg/mL  (82.98  mM;  Need  ultrasonic  and  warming)
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 3.017 ml 15.087 ml 30.174 ml
5 mM 0.603 ml 3.017 ml 6.035 ml
10 mM 0.302 ml 1.509 ml 3.017 ml
50 mM 0.06 ml 0.302 ml 0.603 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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