Structure | Cat No. | Product Name | CAS No. | Product Description |
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V41975 | PF-1018 | 131256-42-3 | PF-1018, biochemical |
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V41980 | PF-257 | 52237-22-6 | PF-257, biochemical |
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V39572 | PF-3758309 HCl | 1279034-84-2 | PF-3758309 (PF3758309) HCl is a novel,ATP-competitive and potent inhibitor of PAK4 with anticancer activity. |
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V41966 | PF-4363467 | 2040055-84-1 | PF-4363467, dopamine D3/D2 receptor antagonist |
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V32936 | PF-543 Citrate | 1415562-83-2 | PF-543 Citrate (PF-543; PF 543), the citrate salt ofPF-543, is a novel cell-permeable and sphingosine-competitive SphK1inhibitor with potential anticancer activity. |
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V41969 | PF-945863 | 893556-85-9 | PF-945863 is an orally bioactive macrolide antibiotic that may be utilized to study multidrug-resistant strains of the respiratory tract. |
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V41978 | PF-DcpSi | 2092917-19-4 | PF-DcpSi, inhibitor of the mRNA decapping scavenger enzyme (DcpS) |
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V41932 | PF-06939999 | 2159123-14-3 | PF-06939999 (PRMT5-IN-3) is a PRMT5 inhibitor that is synthetically lethal to tumor cells in combination with DNA damaging agents. |
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V39959 | PfDHODH-IN-1 | 183945-55-3 | PfDHODH-IN-1 is an analog of the bioactive metabolite of Leflunomide. |
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V41770 | PFI-5 | 2423057-75-2 | PFI-5 is an inhibitor of SMYD2 with IC50 of 8 nM. |
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V34123 | PGLa | 102068-15-5 | PGLa is a 21-residue antimicrobial peptide. |
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V40397 | PGLa TFA | PGLa TFA is a 21-residue antimicrobial peptide. | |
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V40216 | PGlu-3-methyl-His-Pro-NH2 TFA | PGlu-3-methyl-His-Pro-NH2 TFA is a novel and potent thyrotropin-releasing hormone (TRH) peptide | |
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V33281 | pGlu-Pro-Arg-MNA | 130835-45-9 | pGlu-Pro-Arg-MNA is a chromogenic substrate. |
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V31824 | pGlu-Pro-Arg-MNA monoacetate | 2070009-26-4 | pGlu-Pro-Arg-MNA monoacetate is a chromogenic substrate. |
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V34116 | PGS-IN-1 | 102271-49-8 | PGS-IN-1 is a potent prostaglandin synthetase inhibitor (antagonist) with IC50 of 0.28 μM; it can also inhibit the activity of 5-lipoxygenase with IC50 of 1.05 μM. |
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V39215 | Ph-Bis(C1-N-(C2-NH-Boc)2) | 1807521-06-7 | Ph-Bis(C1-N-(C2-NH-Boc)2) is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain class, may be utilized to prepare PROTAC protein degraders. |
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V38755 | PHD-1-IN-1 | 2009343-14-8 | PHD-1-IN-1 is an orally bioactive and potent inhibitor of hypoxia-inducible factor prolyl hydroxylase domain 1 (PHD-1) with IC50 of 0.034 μM. |
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V32550 | Phe-Met-Arg-Phe amide trifluoroacetate | 159237-99-7 | Phe-Met-Arg-Phe amide trifluoroacetate is a neuropeptide that activates/agonizes K+ currents in peptidergic neurons with ED50 of 23 nM in a dose-dependent fashion. |
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V32083 | Phosphocreatine dipotassium | 18838-38-5 | Phosphocreatine dipotassium mainly exists in the skeletal muscles of vertebrates. |