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PAK Related Products (48)
Related Products (48)
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Pak5 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09997 -
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PAK2 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09989 -
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ZMF-23
0 ImagesCat. No.: HY-155179Purity: 99.83%ZMF-23 is a PAK1/HDAC6 dual inhibitor. ZMF-23 inhibits PAK1 and HDAC6 regulated aerobic glycolysis and migration. ZMF-23 induces TNF-α-regulated necroptosis, and further enhances apoptosis. ZMF-23 inhibits the Warburg effect and cell migration. ZMF-23 can be used for research of triple-negative breast cancer (TNBC). -
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Pak5 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09998 -
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Pak6 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS10000 -
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5-Aminosalicylic acid-13C6
0 ImagesCat. No.: HY-15027S2CAS No.: 1189709-96-3Synonyms: Mesalamine-13C6; 5-ASA-13C6; Mesalazine-13C65-Aminosalicylic acid-13C6 is the 13C labeled 5-Aminosalicylic Acid. 5-Aminosalicylic acid (Mesalamine) acts as a specific PPARγ agonist and also inhibits p21-activated kinase 1 (PAK1) and NF-κB. -
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PAK3 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09990 -
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Rac/Cdc42-IN-1
0 ImagesCat. No.: HY-183246CAS No.: 2143950-05-2Rac/Cdc42-IN-1, the major phase I metabolite of the oral Rac/Cdc42 inhibitor MBQ-167 (HY-112842) in vivo, is a selective Rac inhibitor. Rac/Cdc42-IN-1 functions by blocking the GTP-binding activation of Rac1, targeting the autophosphorylation of Thr423/Thr402/Thr436 and Ser141/Ser144/Ser154 in downstream PAK1/2/3, with an inhibitory effect superior to that of MBQ-167. Rac/Cdc42-IN-1 significantly inhibits cell migration, and suppresses tumor growth and distant metastasis to the lung, liver and kidney in HER2+ breast cancer mouse models. Rac/Cdc42-IN-1 can be used for targeted research on metastatic breast cancer. -
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PAK4 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09993 -
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Pak2 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09988 -
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Anti-aging agent 2
0 ImagesCat. No.: HY-187429Anti-aging agent 2 is an anti-aging agent. Anti-aging agent 2 attenuates senescence-associated secretory phenotype (SASP), alleviates cell cycle arrest, reduces the levels of senescence markers in renal tissues, and downregulates the expression of p21, p16 and p53 in the kidney. Anti-aging agent 2 improves renal function and alleviates renal fibrosis. Anti-aging agent 2 extends the lifespan of Caenorhabditis elegans. Anti-aging agent 2 can be used in the research of chronic kidney disease. -
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- TAT-PAK18 inhibitory peptide
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PAK5 Human Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09996 -
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- PAK4-IN-6
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Pak4 Mouse Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09994 -
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- PAK4-IN-3
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st-Ht31
0 ImagesCat. No.: HY-P2624CAS No.: 188425-80-1st-Ht31 is a membrane-permeable peptide inhibitor of protein kinase A (PKA) anchoring. st-Ht31 induces robust cholesterol/phospholipid efflux. st-Ht31 completely reverses foam cell formation and restores the metabolic health of macrophage. -
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Fingolimod hydrochloride (Standard)
0 ImagesSynonyms: FTY720 (Standard)Fingolimod (hydrochloride) (Standard) is the analytical standard of Fingolimod (hydrochloride). This product is intended for research and analytical applications. Fingolimod hydrochloride (FTY720), an analog of sphingosine, is a potent sphingosine 1-phosphate (S1P) receptors modulator. Fingolimod hydrochloride is phosphorylated by sphingosine kinases, particularly by SK2, and then binds S1PR1, 3, 4, and 5. Fingolimod hydrochloride induces the internalization of S1P1, and consequently, inhibits S1P activity. Fingolimod hydrochloride also is a pak1 activator. -
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5-Aminosalicylic Acid-d3 hydrochloride
0 ImagesSynonyms: Mesalamine-D3 hydrochloride; 5-ASA-D3 hydrochloride; Mesalazine-D3 hydrochloride5-Aminosalicylic Acid-d3 (hydrochloride) is the deuterium labeled 5-Aminosalicylic Acid. 5-Aminosalicylic acid (Mesalamine) hydrochloride acts as a specific PPARγ agonist and also inhibits p21-activated kinase 1 (PAK1) and NF-κB. -
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Pak1 Rat Pre-designed siRNA Set A
0 ImagesCat. No.: HY-RS09985 -
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