PAK3
- [1]. Kreis P, et al. PAK signalling in neuronal physiology. Cell Signal. 2009 Mar;21(3):384-93. [Content Brief]
- [2]. Meng J, et al. Abnormal long-lasting synaptic plasticity and cognition in mice lacking the mental retardation gene Pak3. J Neurosci. 2005 Jul 13;25(28):6641-50. [Content Brief]
- [3]. Licciulli S, et al. FRAX597, a small molecule inhibitor of the p21-activated kinases, inhibits tumorigenesis of neurofibromatosis type 2 (NF2)-associated Schwannomas. J Biol Chem. 2013 Oct 4;288(40):29105-14. [Content Brief]
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PAK3 関連製品 (10)
関連製品 (10)
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組換えタンパク質 (3)
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PF-3758309
0 Images別名: PF-03758309PF-3758309 (PF-03758309) is a potent, orally available, and reversible ATP-competitive inhibitor of PAK4 (Kd= 2.7 nM; Ki=18.7 nM). PF-3758309 has the expected cellular functions of a PAK4 inhibitor: inhibition of anchorage-independent growth, induction of apoptosis, cytoskeletal remodeling, and inhibition of proliferation. -
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- FRAX597
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- FRAX486
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LDN-0028574
0 Images製品番号: HY-123739CAS 番号: 337500-87-5LDN-0028574 is a PAK3 inhibitor. LDN-0028574 can be used in the research of p53-deficient cancers. -
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PF-3758309 hydrochloride
0 Images製品番号: HY-13007ACAS 番号: 1279034-84-2別名: PF-03758309 hydrochloridePF-3758309 (PF-03758309) hydrochloride is a potent, orally available, and reversible ATP-competitive inhibitor of PAK4 (Kd= 2.7 nM; Ki=18.7 nM). PF-3758309 hydrochloride has the expected cellular functions of a PAK4 inhibitor: inhibition of anchorage-independent growth, induction of apoptosis, cytoskeletal remodeling, and inhibition of proliferation. -
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RN193
0 Images製品番号: HY-184447CAS 番号: 3091508-49-2RN193 is a type II kinase inhibitor with a human PAK1 IC50 of 4.28 μM. RN193 functionally inhibits kinase activity of PAK1, PAK2, and PAK3, and engages with their kinase domains in live cells. RN193 induces thermal shifts in CLK1, GSK3B, ULK1, MELK, MAPK13, BRAF, and STK10, indicating binding and stabilization of these proteins. RN193 induces formation of PAK3:PAK2 heterodimers and displaces PAK2 homodimers in live cells. RN193 acts as a tool compound for studying group I PAK conformational states. -
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PF-3758309 dihydrochloride
0 Images製品番号: HY-13007B別名: PF-03758309 dihydrochloridePF-3758309 (PF-03758309) dihydrochloride is a potent, orally available, and reversible ATP-competitive inhibitor of PAK4 (Kd= 2.7 nM; Ki=18.7 nM). PF-3758309 dihydrochloride has the expected cellular functions of a PAK4 inhibitor: inhibition of anchorage-independent growth, induction of apoptosis, cytoskeletal remodeling, and inhibition of proliferation. -
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PI3Kα-IN-27
0 Images製品番号: HY-178812CAS 番号: 2098649-83-1 -
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ZMF-10
0 Images製品番号: HY-146786CAS 番号: 2415295-37-1 -
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LDN-0044878
0 Images製品番号: HY-118606CAS 番号: 296246-47-4LDN-0044878 is a PAK3 inhibitor. LDN-0044878 inhibits the proliferation or induces the death of p53-deficient cells. LDN-0044878 exhibits moderate trypanocidal activity against Trypanosoma brucei, but does not directly inhibit the core target Rhodesain. LDN-0044878 can be used in studies related to cervical adenocarcinoma and Trypanosoma brucei infection. -
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