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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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