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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC1992 | Er-38925 | 
                               Retinoic acid receptor (RAR) subtype α-selective agonist 
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| DCC1991 | Er-119884 | 
                               Selective squalene synthase (SQS) inhibitor 
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| DCC1990 | Er Degrader 40 | 
                               Novel Oral Selective Estrogen Receptor Degrader with Highly Improved Antitumor Effect and Favorable Druggability 
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| DCC1989 | Epz033294 | 
                               Novel SMYD2 inhibitor 
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| DCC1988 | Epz032597 | 
                               Novel selective SMYD2 inhibitor 
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| DCC1986 | Epz005687n | 
                               Inactive isomer of EPZ005687 and can be used as the negative control for EPZ005687 
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| DCC1985 | Eptapirone Fumarate | 
                               Potent, selective, high efficacy 5-HT1A receptor agonist 
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| DCC1984 | Eps-in-1 | 
                               Novel inhibitor of extracellular polymeric substances (EPS) 
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| DCC1983 | Eprazinone | 
                               Mucolytic and bronchospasm relieving agent 
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| DCC1982 | Epi-nocardicin G | 
                               The precursor of the nocardicins 
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| DCC1981 | Epinastine Hydrobromide | 
                               Second-generation antihistamine and mast cell stabilizer, being highly selective for the H1 receptor 
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| DCC1980 | Epibestatin Hydrochloride | 
                               Novel stabilizer of 14-3-3 PPIs, Diastereoepimer of aminopeptidase inhibitor bestatin 
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| DCC1979 | Epi-0023 | 
                               Novel selrctive SETD8 inhibitor without inhibiting G9a, SETD7, RmtA, and PRMT1 
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| DCC1978 | Ephb3-in-9 | 
                               The first potent and specific inhibitor of a single Eph isoform EphB3 
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| DCC1977 | Ephb3-in-10 | 
                               Novel clickable potent and specific inhibitor of EphB3 
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| DCC1976 | Ephb1-in-10 | 
                               Potent and selective covalent inhibitor of receptor tyrosine kinase EphB1 
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| DCC1975 | Epha2-agonist-27 | 
                               Novel agonist of EphA2 receptor tyrosine kinase 
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| DCC1974 | Epetraborole R-mandelate | 
                               Novel potent and selective leucyl-tRNA synthetase inhibitor 
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| DCC1973 | Epc-k1 | 
                               Vitamin E derivative, suppressing inflammation during hepatic ischemia-reperfusion injury and exerting hepatoprotective effects 
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| DCC1972 | Ep-7041 | 
                               Novel, potent, and selective Factor XIa inhibitor 
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| DCC1971 | Ent-verticilide | 
                               Unnatural verticilide enantiomer, inhibiting type 2 ryanodine receptor-mediated calcium leak and being antiarrhythmic. 
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| DCC1970 | Entpd5-in-2f | 
                               Novel inhibitor of Ectonucleoside Triphosphate Diphosphohydrolase 5 (ENTPD5) 
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| DCC1969 | Entpd5-in-1a | 
                               Novel inhibitor of Ectonucleoside Triphosphate Diphosphohydrolase 5 (ENTPD5) 
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| DCC1967 | Ent Naxagolide Hydrochloride | 
                               Dopamine D2-receptor agonist for the treatment of extrapyramidal disorders, also being an antiparkinson agent 
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| DCC1966 | Enprostil | 
                               PGE2 analog, inhibiting gastric acid secretion 
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| DCC1965 | Enpp1 Inhibitor 43 | 
                               Novel potent inhibitor of ecto-nucleotide pyrophosphatase/phosphodiesterases 1 (ENPP1 or NPP1), showing good in vitro potency, stability in SGF/SIF/PBS, selectivity, ADME properties and pharmacokinetic profile and finally potent anti-tumor response in viv 
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| DCC1964 | Enmd-2076 Tartrate | 
                               Novel oral inhibitor of angiogenic and proliferation kinases, having activity in recurrent, platinum resistant ovarian cancer 
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| DCC1963 | Enl-in-7 | 
                               Novel potent inhibitor of eleven-nineteen leukemia (ENL) protein, selectively targeting the ENL YEATS domain 
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| DCC1962 | Eniporide Hydrochloride | 
                               Sodium/hydrogen exchange inhibitor 
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| DCC1961 | Endosidin8.1 | 
                               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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