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Cat. No. Product Name Field of Application Chemical Structure
DCC1929 El-0052
Novel etomidate analogue, enhancing GABA A receptors currents with a concentration for 50% of maximal effect (EC 50 ) of 0.98 {plus minus} 0.02 μM, which was about three times more potent than etomidate (3.07 {plus minus} 1.67 μM), retaining the favorable
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DCC1928 Ejr-866-81
Novel Cell-active Inhibitor of the Undrugged Oncogenic PTP4A3 Phosphatase
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DCC1927 Ejr-866-75
Novel Cell-active Inhibitor of the Undrugged Oncogenic PTP4A3 Phosphatase
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DCC1926 Ejmch-6
Novel anti-bacterial agent, targeting the MmpL3 transporter in Mycobacterium abscessus
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DCC1925 Eif4a Inhibitor 28
Novel RNA-competitive, ATP-uncompetitive eIF4A Inhibitor, decreasing BJAB Burkitt lymphoma cell viability, engaging a novel pocket in the RNA groove of eIF4A and inhibiting unwinding activity by interfering with proper RNA binding and suppressing ATP hydr
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DCC1924 Eidd-1723
Novel water-soluble analog of progesterone, reducing cerebral edema and lesion size and improving functional recovery, decreasing glial fibrillary acidic protein expression immunoreactivity
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DCC1923 Eidd-1619
Novel water-soluble analog of progesterone
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DCC1922 Eht5372
Novel Mirk kinase inhibitor, inhibiting DYRK1A-induced Tau phosphorylation at multiple AD-relevant sites, blocking the in vivo growth of pancreatic cancer cells
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DCC1921 Ehi2225
Potent and bio-stable inhibitor of the chicken sEH (chxEH)
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DCC1920 Ehi2119
Potent and bio-stable inhibitor of the chicken sEH (chxEH)
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DCC1919 Ehi1471
Potent and bio-stable inhibitor of the chicken sEH (chxEH)
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DCC1918 Eh-201
Arginase Inhibitor, activating EPO-mediated mitochondrial function and haemoglobin expression, stimulating melanogenesis by MAP kinase activation and tyrosinase upregulation
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DCC1917 Egonol
Antibacterial agent
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DCC1916 Egis-8332
Selective, non-competitive AMPA receptor antagonist, improving motor co-ordination
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DCC1915 Egis-11150
Potent inhibitor of adrenergic alpha1, alpha2c, 5-HT2a, 5HT7 receptors; Relatively selective blocker of adrenergic alpha2c over adrenergic alpha2a receptors.
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DCC1914 Egfr-in-557
Novel EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis
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DCC1913 Egfr-in-542
Novel EGFR inhibitor, significantly reducing myocardial inflammation, fibrosis, apoptosis, and dysfunction, showing promises to the treatment on obesity-induced cardiac complications
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DCC1912 Egfr-in-451
Novel EGFR inhibitor, attenuating Ang II-induced Kidney Fibrosis
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DCC1911 Egfr T790m Inhibitor 6a
Novel third-generation EGFR tyrosine kinase inhibitor, targeting EGFR T790M mutation in advanced non-small cell lung cancer
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DCC1910 Efrotomycin
Antibiotic, inhibiting bacterial protein synthesis
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DCC1909 Efrapeptin F
Natural alpha-aminobutyric acid-rich secondary metabolite of fungi, strongly inhibiting the BBMV V-ATPase, acting as a mitochondrial complex V inhibitor, showing antitumor activity in vivo
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DCC1908 Efonidipine
Calcium channel blocker, blocking both T-type and L-type calcium channels
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DCC1907 Efatutazone
Potent agonist of peroxisome proliferator-activated receptor gamma (PPAR-gamma) with potential antineoplastic activity
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DCC1906 Eef2k-in-21i
Novel eEF2K inhibitor, inducing significant apoptosis through classical apoptotic pathways
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DCC1905 Edoxaban Isomer
An impurity of Edoxaban, a novel inhibitor of factor Xa
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DCC1904 Ecraprost
Lipo-pro-prostaglandin E1, preventing hearing disturbance and equilibrium dysfunction due to inner ear microcirculatory disorders
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DCC1903 Echinoside A
Novel marine-derived anticancer saponin, targeting topoisomerase2alpha by unique interference with its DNA binding and catalytic cycle
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DCC1902 Ecdsbb-in-9
Novel specific inhibitor of EcDsbB, targeting disulfide bond forming enzyme DsbB of Gram-negative bacteria
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DCC1901 Ecdsbb-in-12
Novel potent specific inhibitor of EcDsbB, targeting disulfide bond forming enzyme
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DCC1900 Ebv Activator C60
Novel EBV activator, well-performing EBV lytic cycle inducer
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