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Cat. No. Product Name Field of Application Chemical Structure
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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