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            | Cat. No. | Product Name | Field of Application | Chemical Structure | 
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| DCC1899 | Ebselen Oxide | 
                               Novel dose-dependent inhibitor of HDAC1, HDAC3, HDAC4, HDAC5, HDAC6, HDAC7, HDAC8, and HDAC9, inhibiting Pseudomonas aeruginosa alginate synthesis 
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| DCC1898 | Ebov-in-c31 | 
                               Novel PP1-targeting Ebola Virus (EBOV) inhibitor with improved pharmacological properties 
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| DCC1897 | Ebopiprant | 
                               Novel Oral and Selective Prostaglandin F 2α (PGF 2α ) Receptor Antagonist 
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| DCC1896 | Ebmi-13b | 
                               Highly potent and selective activator of isozymes CA-VA and CA-VII 
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| DCC1895 | Ebi-13a | 
                               Highly potent and selective activator of isozymes CA-VA and CA-VII 
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| DCC1894 | Ea-b3a | 
                               Novel degrader of GST-α and GST-α-EGFP fusion proteins as well as endogenous GST-π in cells and lysates 
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| DCC1893 | E-5842 Citrate | 
                               Sigma1 receptor ligand and potential atypical antipsychotic 
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| DCC1892 | E3-ligase Degrader 10 | 
                               Novel XIAP BIR2 domain-binding degrader of E3 ubiquitin ligases 
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| DCC1891 | E235-1756 | 
                               Potent Activator of P53-Independent Cellular Senescence 
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| DCC1890 | e2012-bpyne | 
                               γ-Secretase modulator (GSM) photoaffinity probe, revealing distinct allosteric binding sites on presenilin 
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| DCC1889 | E09241 | 
                               Novel OPG/RANKL upregulator, increasing OPG expression without affecting RANKL expression, promoting osteoblast differentiation while inhibiting osteoclast differentiation, regulating OPG expression through canonical Wnt/β-catenin signaling 
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| DCC1888 | Dy428174 | 
                               Novel potent Inhibitor of PI3Kalpha 
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| DCC1887 | Dy3002 | 
                               Novel Selective and Potent EGFR Inhibitor, Overcoming T790M-Mediated Resistance in Non-Small Cell Lung Cancer 
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| DCC1886 | Dx-52-1 | 
                               Antitumor antibiotic 
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| DCC1885 | Dx2-hsp70 Inhibitor-1 | 
                               Novel allosteric inhibitor of the tumor-promoting interaction between the oncogenic factor AIMP2-DX2 and HSP70 
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| DCC1884 | Dwn-723-23 | 
                               Novel Hsp70 agonist, showing no cellular toxicity and induced cellular stress response pathways 
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| DCC1883 | Dw-1350 | 
                               Novel and potent leukotriene B(4) receptor antagonist 
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| DCC1882 | Dw10075 | 
                               Novel potent and highly selective inhibitor of VEGFR, exhibiting antitumor activities both in vitro and in vivo. 
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| DCC1881 | Dv-7028 Hydrochloride | 
                               Potent and selective 5-HT 2A receptor antagonist 
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| DCC1880 | Dv-7028 | 
                               Selective 5-HT2A receptor antagonist 
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| DCC1879 | Dutomycin | 
                               Anthracycline antibiotic from Streptomyces 
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| DCC1878 | Duocarmycin A | 
                               Irreversible DNA minor groove binding alkylating agent, disrupting the nucleic acid architecture and leading to tumor cell death 
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| DCC1877 | Du-34569 Maleate | 
                               Antiviral agent against influenza A, parainfluenza Sendai, coxsackie A21, and rhinovirus 
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| DCC1876 | Dtagv-1 | 
                               Potent and selective degrader of mutant FKBP12F36V fusion proteins 
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| DCC1875 | Dt2216nc | 
                               Negative control for DT2216 
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| DCC1874 | Dt-061 | 
                               Novel potent and orally active activator of PP2A 
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| DCC1873 | Ds-sg-44 | 
                               Agonist of S1P receptors 
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| DCC1872 | Dsr-98776 | 
                               Novel selective mGlu5 receptor negative allosteric modulator (NAM) with potent antidepressant and antimanic activity 
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| DCC1871 | Dsm705 | 
                               Novel potent Dihydroorotate Dehydrogenase (DHODH) inhibitor 
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| DCC1869 | Dsm-338 | 
                               Novel Plasmodium falciparum Dihydroorotate Dehydrogenase (PfDHODH) Inhibitor (Pfalcip cells: 0.0018 μM) 
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