
Other Inhibitors
This category encompasses a wide variety of inhibitors that do not fit into the standard classifications but are still critical for various biochemical and pharmacological research. These inhibitors may target unique or less-studied pathways, enzymes, and molecular interactions, providing valuable tools for specialized research areas. At CymitQuimica, we offer a diverse selection of high-quality inhibitors across multiple biological targets and research disciplines, enabling you to explore novel therapeutic avenues and deepen your understanding of complex biological processes.
Found 35858 products of "Other Inhibitors"
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S07-2009
CAS:S07-2009 is a potent and selective inhibitor of aldo-keto reductase 1C3 (AKR1C3) (IC 50 = 0.20 μM) [1].Formula:C16H19N3O5Color and Shape:SolidMolecular weight:333.34Dp2mT
CAS:Dp2mT is an iron chelator which inhibits HIV-1 transcription.Formula:C13H13N5SColor and Shape:SolidMolecular weight:271.34TRK-IN-21
CAS:TRK-IN-21 (5n) is an oral TRK inhibitor targeting multiple TRK mutants; useful for cancer research.Formula:C22H22F2N6OColor and Shape:SolidMolecular weight:424.45Hepta-histidine
CAS:Hepta-histidine is a novel inhibitor of Tau aggregation against Tau-related neurodegenerative diseases including Alzheimer's disease (AD).Formula:C42H51N21O8Color and Shape:SolidMolecular weight:977.99HSP-117 free base
CAS:HSP-117 free base is a novel tachykinin NK1-receptor antagonist.Formula:C23H30N2OColor and Shape:SolidMolecular weight:350.5FKBP12-IN-Q2
CAS:FKBP12-IN-Q2 is an inhibitor of FKBP12.Formula:C13H17NO2SColor and Shape:SolidMolecular weight:251.34Pidnarulex HCl
CAS:Pidnarulex HCl is CX-5461, a selective Pol I inhibitor and p53 activator without DNA damage, showing potent anti-cancer efficacy.Formula:C27H28ClN7O2SColor and Shape:SolidMolecular weight:550.08NPC-18915
CAS:NPC-18915 is a benzofuran compound, inhibitor of neutophil activation.Formula:C23H16O3Color and Shape:SolidMolecular weight:340.37Lonetil M3
CAS:Lonetil M3 is a tranquilizer.Formula:C17H16N2O2Color and Shape:SolidMolecular weight:280.32N2-Methyl-L-arginine
CAS:Selective L-arginine uptake inhibitorFormula:C7H16N4O2Purity:98%Color and Shape:SolidMolecular weight:188.23RO2443
CAS:RO2443 is a dual inhibitor of the MDM2-p53 or MDMX-p53 protein-protein interaction, inducung MDM2 and MDMX dimerization and activating the p53 pathway.Formula:C20H14ClF2N3O2Color and Shape:SolidMolecular weight:401.79PNU-142372
CAS:PNU-142372 is an MMP-3 inhibitor.Formula:C13H10F5N5O2S2Color and Shape:SolidMolecular weight:427.37SLC26A3-IN-3
CAS:SLC26A3-IN-3 (compound 4az), a potent SLC26A3 inhibitor with an IC50 of 40 nM, is utilized for constipation and cystic fibrosis research [1].Formula:C20H17IO5Color and Shape:SolidMolecular weight:464.25DOCK2-IN-1
CAS:DOCK2-IN-1, a CPYPP analogue, inhibits DOCK2 (IC50=19.1μM), reversibly binds DHR-2, and suppresses lymphocyte chemotaxis and T cell activation.Formula:C16H11ClN2O2Color and Shape:SolidMolecular weight:298.72GBS-149
CAS:GBS-149 is a novel non-toxic and mammalian-specific LINE-1 inhibitor.Formula:C8H12N4O3Color and Shape:SolidMolecular weight:212.21ABT-925 fumarate dihydrate
CAS:ABT-925 is a dopamine D3 receptor antagonist with ~100x selectivity over D2 receptors in vitro.Formula:C24H35F3N6O7SColor and Shape:SolidMolecular weight:608.63UBTR008295a
CAS:UBTR008295a is USP5 Inhibitor.Formula:C13H16O3Color and Shape:SolidMolecular weight:220.26Nordimaprit dihydrochloride
CAS:Nordimaprit dihydrochloride is a metabolite of Dimaprit -- a histamine analog and selective H2 histamine receptor agonist.Formula:C5H15Cl2N3SColor and Shape:SolidMolecular weight:220.16JTP-4819
CAS:JTP-4819: potent PEP inhibitor, may treat Alzheimer's, boosts brain peptides and acetylcholine, aiding memory.Formula:C19H25N3O4Color and Shape:SolidMolecular weight:359.42LB42908
CAS:LB42908 is a highly potent Ras farnesyltransferase inhibitor(IC(50)=0.9 nM against H-Ras and 2.4 nM against K-Ras) with potential anticancer activity.Formula:C32H31N5O3Color and Shape:SolidMolecular weight:533.62
