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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| 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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