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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC1960 | Endosidin8.0 | 
                               Novel modulator of the PIN1 accumulation, selectively modifying PIN1 basal plasma membrane targeting in Arabidopsis with minimal effects on apical plasma membrane proteins 
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| DCC1959 | Endosidin7 | 
                               Specific inhibitor for plant callose deposition during cytokinesis without affectting endomembrane trafficking during interphase or cytoskeletal organization 
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| DCC1957 | Endosidin4 | 
                               Novel inhibitor of eukaryotic ARF-GEFs (ADP-ribosylation factor guanine nucleotide exchange factors) 
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| DCC1956 | Endosidin3 | 
                               Specific inhibitor of trafficking pathways, disrupting recycling at the PM via interference with ROP6/RIC1 signalling 
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| DCC1955 | Endosidin1 | 
                               Natural vesicle trafficking inhibitor 
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| DCC1954 | Endochin | 
                               Antimalarial 
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| DCC1953 | Endo-3-aminotropane Dihydrochloride | 
                               Useful pharmceutical building block 
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| DCC1952 | Encenicline | 
                               Novel Potentiator of α7 Receptor Signaling 
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| DCC1951 | Ena739155 | 
                               Novel butyrylcholinesterase inhibitor against Alzheimer's disease 
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| DCC1950 | En3356 | 
                               Novel non-steroidal CYP17 inhibitor. reducing androgen synthesis for treatment of castration-resistant prostate cancer 
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| DCC1949 | Emoxypine Succinate | 
                               Antioxidant, inhibiting free radical oxidation of biomembrane lipids, modulating the activity of membrane-bound enzymes and the receptor complexes of the brain membranes 
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| DCC1948 | Eml981 | 
                               Novel Potent and Selective Inhibitor of Protein Arginine Methyltransferase 4 (PRMT4) 
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| DCC1947 | Eml108 | 
                               Novel PRMT inhibitor, preventing arginine methylation of cellular proteins, being essentially inactive against the lysine methyltransferase SET7/9 
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| DCC1946 | Emitefur | 
                               5-FU derivative, with various anticancer agents against human cancer xenografts 
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| DCC1945 | Emicerfont | 
                               Novel corticotropin-release factor 1 antagonist 
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| DCC1944 | Emdb-3 | 
                               Novel peptide endomorphin (EM) degradation blocker 
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| DCC1943 | Emdb-2 | 
                               Novel peptide endomorphin (EM) degradation blocker 
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| DCC1942 | Emdb-1 | 
                               Novel peptide endomorphin (EM) degradation blocker 
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| DCC1941 | Emd-66684 | 
                               Non-peptide angiotensin II receptor antagonist 
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| DCC1940 | Emd57439 | 
                               PDE 3 inhibitor 
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| DCC1939 | Emd-1204831 | 
                               Novel potent and highly selective c-Met inhibitor 
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| DCC1938 | Emac4001 | 
                               Novel potent antitumor agent, inducing apoptosis in a panel of tumor cell lines 
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| DCC1937 | em-800 | 
                               High affinity ligand for estrogen receptor- 
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| DCC1936 | Em20-25 | 
                               Novel BCL-2 inhibitor, neutralizing the antiapoptotic activity of overexpressed BCL-2 toward staurosporine and sensitizing BCL-2-expressing cells from leukemic patients to the killing effects of staurosporine, chlorambucil, and fludarabine 
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| DCC1935 | Elx-02 | 
                               Eukaryotic Ribosomal Selective Glycoside (ERSG), inducing read-through of premature stop codons (PSCs) and resulting in translation of full-length protein 
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| DCC1934 | Elovl1 Inhibitor 22 | 
                               Novel highly potent, selective, and CNS-penetrant inhibitor of elongation of very long chain fatty acid 1 (ELOVL1) enzyme 
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| DCC1933 | Elnd006 | 
                               Novel γ-secretase inhibitor 
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| DCC1932 | elaidyl-sulfamide | 
                               Oleoylethanolamide-modelled PPAR 
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| DCC1931 | Ela23-32 | 
                               Novel ligand of the apelin receptor (APJ), possessing high affinity for APJ (Ki 4.6 nM) and producing cardiorenal effects in vivo similar to those of ELA 
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| DCC1930 | El-228 | 
                               Novel inhibitor of Aurora B kinase 
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