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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC2906 | Kcal01 | 
                               Potent PDZ domain peptide inhibitor that rescues CFTR activity 
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| DCC2905 | Kca2 Positive Modulator 2q | 
                               Novel potent and Subtype-Selective Positive Modulator of KCa2 Channels 
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| DCC2904 | Kca-1490 | 
                               Dual PDE3/4 inhibitor 
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| DCC2903 | Kca075 | 
                               Highly specific transglutaminase 2 (TG2) inhibitor 
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| DCC2902 | Kc-11404 | 
                               LTB4 inhibitor for the treatment of b-cell leukemias and lymphomas, potently inhibiting histamine, platelet activating factor,and 5-lipoxygenase 
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| DCC2901 | Kb-r7785 | 
                               Novel ADAM12 and MMP inhibitor, ameliorating cardiac function in a transverse aortic constriction (TAC) model by inhibiting the proteolytic activation of HB-EGF signaling, exerting its antidiabetic effect by ameliorating insulin sensitivity through the in 
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| DCC2900 | Kbp-088 | 
                               Novel highly potent dual amylin and calcitonin receptor agonist (DACRA), showing long-lasting improvement of food preference and body weight loss 
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| DCC2899 | Kb-nb165-09 | 
                               Selective inhibitor of Protein_kinase_D1>protein kinase D (PKD); Inhibitor of cell adhesion and HIV; Inhibitor of herpes simplex virus type 1 replication 
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| DCC2898 | Kbjk557 | 
                               Novel Plk1 PBD inhibitor, showing a remarkable in vitro anticancer effect by inducing Plk1 delocalization, mitotic arrest, and apoptosis in HeLa cells 
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| DCC2897 | Kbh-a42 | 
                               Novel histone deacetylase inhibitor 
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| DCC2896 | Kb130015 | 
                               Novel activator of hERG1 potassium channels, blocking native and recombinant hERG1 channels at high voltages, but activating them at low voltages 
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| DCC2895 | Kasugamycin | 
                               Antibiotic, binding within the mRNA channel of the 30S subunit and inhibiting protein synthesis 
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| DCC2894 | Kar425 | 
                               Novel antimalarial agent, providing protection to malaria-infected mice 
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| DCC2893 | Kalb001 | 
                               Novel mGlu4 ligand 
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| DCC2892 | Kaempulchraol Q | 
                               Natural anti-inflammatory agent, inhibiting the NF-κB-mediated transactivation of a luciferase reporter gene, IL-6 production, and COX-2 expression 
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| DCC2891 | Kaempulchraol P | 
                               Natural anti-inflammatory agent, inhibiting the NF-κB-mediated transactivation of a luciferase reporter gene, IL-6 production, and COX-2 expression 
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| DCC2890 | K-8012 | 
                               Novel inhibitor of the interaction of the N-terminally truncated RXR 
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| DCC2889 | K-8008 | 
                               Novel inhibitor of the interaction of the N-terminally truncated RXR 
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| DCC2888 | K4610422 | 
                               Novel norditerpenoid inhibitor of testosterone-5α-reductase 
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| DCC2887 | K-14585 | 
                               Novel antagonist for proteinase-activated receptor 2 (PAR2) 
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| DCC2886 | K103 Hydrochloride | 
                               Novel inhibitor of peptidoglycan synthesis targeting the lipid II precursor 
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| DCC2885 | K00518 | 
                               Novel dual CLK1 and CLK3 inhibitor 
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| DCC2884 | K00135 | 
                               Novel potent and selective inhibitor of PIM kinases 
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| DCC2883 | Jzp-430 | 
                               Potent, highly selective, and irreversible ABHD6 Inhibitor 
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| DCC2882 | jzad-iv-22 | 
                               Inhibitor of all three monoamine transporters 
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| DCC2881 | Jz-5029 | 
                               Novel irreversible β-Glucocerebrosidase modulator 
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| DCC2880 | Jz-4109 | 
                               Novel β-Glucocerebrosidase modulator, promoting dimerization of β-glucocerebrosidase and revealing an allosteric binding site, stabilizing wild-type and N370S mutant GCase and increases GCase abundance in patient-derived fibroblast cells 
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| DCC2879 | Jy-xhe-053 | 
                               Selective modulator of GABAA receptors containing the α5 subunit 
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| DCC2878 | Jyl-79 | 
                               Potent vanilloid receptor (VR1) agonist 
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| DCC2877 | Jyl-273 | 
                               Potent TRPV1 agonist 
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