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PP2,Src和RIP2激酶抑制剂

Src和RIP2激酶抑制剂
规格或纯度: ≥98%
有货

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货号 (SKU) 包装规格 是否现货 价格 数量
P125361-1mg
1mg 期货 Stock Image
P125361-5mg
5mg 现货 Stock Image
P125361-25mg
25mg 现货 Stock Image
P125361-100mg
100mg 现货 Stock Image

基本描述

英文别名 172889-27-9|pp2|PP 2|1-(tert-butyl)-3-(4-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine|AG 1879|1-tert-butyl-3-(4-chlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine|1-tert-butyl-3-(4-chlorophenyl)pyrazolo[3,4-d]pyrimidin-4-amine|4-Amino-5-(4-chloropheny
规格或纯度 ≥98%
英文名称 PP2
生化机理 PP 2 is an effective and selective inhibitor of c-Src family kinases. The inhibitor has been shown to inhibit Lck, FynT, phosphorylation of focal adhesion kinase (FAK) and potently inhibits Hck, Lck (p56) and Fyn (p59). Additionally, PP 2 was reported to inhibit tyrosone kinase-dependent TcR-induced T cell proliferation. PP 2 studies indicate that this agent has demonstrated the ability to activate ERK 1, ERK 2 and p38. Research sμggests that PP 2 may be useful to help identify c-Src family member substrates. MCF-7 cell research shows that PP 2 down regulates the expression of both enoyl-CoA hydratase short chain 1 and peroxiredoxin 3 (PRDX3), and induces apoptosis. PP 2 is an inhibitor of casein kinase I δ and RICK.
储存温度 -20°C储存
运输条件 超低温冰袋运输
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产品介绍

PP2(AGL 1879) 是可逆的ATP竞争性的Src家族抑制剂,对p56lck,p59fynT,Hck和Src的IC50分别为4,5,5和100 nM。An effective and selective inhibitor of Src family kinases

PP2, a Src family kinase inhibitor, potently inhibits Lck/Fyn with IC50 of 4 nM/5 nM in cell-free assays, ~100-fold less potent to EGFR, inactive for ZAP-70, JAK2 and PKA.
An effective and selective inhibitor of Src family kinases

名称和标识符

EC号 878-892-3
IUPAC Name 1-tert-butyl-3-(4-chlorophenyl)pyrazolo[3,4-d]pyrimidin-4-amine
INCHI InChI=1S/C15H16ClN5/c1-15(2,3)21-14-11(13(17)18-8-19-14)12(20-21)9-4-6-10(16)7-5-9/h4-8H,1-3H3,(H2,17,18,19)
InChi Key PBBRWFOVCUAONR-UHFFFAOYSA-N
Canonical SMILES CC(C)(C)N1C2=NC=NC(=C2C(=N1)C3=CC=C(C=C3)Cl)N
Isomeric SMILES CC(C)(C)N1C2=NC=NC(=C2C(=N1)C3=CC=C(C=C3)Cl)N
关联CAS 172889-27-9
PubChem CID 4878
MeSH Entry Terms 4-amino-5-(4-chlorophenyl)-7-(t-butyl)pyrazolo(3,4-d)pyrimidine;AG 1879;AG1879;PP2 cpd;Src family kinase inhibitor PP2
分子量 301.77

化学和物理性质

溶解性 DMSO 60 mg/mL Water <1 mg/mL Ethanol 2 mg/mL
密度 1.36
敏感性 对空气敏感,对热敏感
折光率 1.68
沸点 493.54° C at 760 mmHg
熔点 193.32°C

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参考文献

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