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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC1707 | Ddc4002 |
First-generation allosteric EGFR inhibitor, binding to the allosteric site of EGFR along with ATP that leads to inhibition of cell proliferation and arrest of EGFR L858R/T790M/C797S signalling
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| DCC1705 | Dd-04-015 |
Novel selective BTK degrader, demonstrating prolonged pharmacodynamic effects
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| DCC1704 | Dcz3112 |
Novel Hsp90 inhibitor, exerts potent antitumor activity against HER2-positive breast cancer through disruption of Hsp90-Cdc37 interaction
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| DCC1703 | Dc-teadin02 |
Novel potent and selective TEAD autopalmitoylation inhibitor, inhibiting TEADs transcription activity and downstream gene expression
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| DCC1702 | Dc-s239 |
Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor
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| DCC1701 | Dc-s238 |
Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor
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| DCC1700 | Dc-s100 |
Novel, Selective Histone Methyltransferase SET7 Inhibitor
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| DCC1699 | Dc-prc2in-01 |
Novel PRC2 Inhibitor, Targeting EZH2-EED Interaction
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| DCC1698 | Dcn1-ubc12 Inhibitor Dn-2 |
Novel potent and selective DCN1-UBC12 inhibitor for anticardiac fibrotic effects, specifically targetinbg DCN1 at molecular and cellular levels, effectively reversing angiotensin (Ang) II-induced cardiac fibroblast activation
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| DCC1697 | Dc-k2in212 |
Novel potent CDK2 inhibitor with selectivities above 10-fold over CDK1/4/6/7/9/12 above 10-fold, displaying anti-proliferative activity against A2058 melanoma and MV4-11 leukemia cell lines and low toxicity on human normal cell lines, inhibiting CDK2-medi
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| DCC1696 | dcg-iv |
Highly potent agonist for group II mGlu receptors
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| DCC1695 | Dcg066 |
Novel inhibitor of lysine methyltransferase G9a
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| DCC1694 | Dc-ebio |
Activator of IK and SK channels
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| DCC1693 | Dce_42 |
Novel potent EZH2 inhibitor
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| DCC1692 | Dce_254 |
Novel potent EZH2 inhibitor
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| DCC1691 | Dc-cpin734 |
Novel potent CBP bromodomain inhibitor with a TR-FRET IC50 value of 19.5 ± 1.1 nM and over 400-fold of selectivity against BRD4 bromodomains
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| DCC1690 | Dc-bpi-7 |
Novel potent BPTF-BRD inhibitor, showing selectivities 100-fold higher than those of other BRD targets
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| DCC1689 | Dc-bpi-11 |
Novel potent BPTF-BRD inhibitor, showing selectivities 100-fold higher than those of other BRD targets, significantly inhibiting leukemia cell proliferation
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| DCC1688 | Dcat Maleate [57915-90-9] |
Inhibitor of N-methyl transferases (NMT), preventing the formation of Parkinson's syndrome neurotoxins via methylation of non-methylated pre-neurotoxins.
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| DCC1687 | Dc_ym26 |
Novel inhibitor of menin-MLL interaction
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| DCC1686 | Dc_ym25 |
Novel inhibitor of menin-MLL interaction
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| DCC1685 | Dc_ym21 Maleate |
Novel inhibitor of menin-MLL interaction
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| DCC1684 | Dc_m5_2 |
Novel inhibitor of WDR5-MLL1 interaction
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| DCC1683 | Dc_501 |
Novel selective non-nucleoside inhibitor of DNA methyltransferase 1 (DNMT1)
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| DCC1682 | Dbpr110 |
Potent HCV NS5A inhibitor
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| DCC1681 | Dbm-1285 Dihydrochloride |
p38 MAPK inhibitor, supressing p38 phosphorylation and LPS-induced TNF-α production in macrophages
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| DCC1680 | Dbco-stco |
Novel protein cross-linking agent
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| DCC1679 | Db1960 |
Novel antileishmanial agent, against both intracellular Leishmania donovani and intracellular Leishmania amazonensis and displaying dose-dependent reduction of liver parasitemia
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| DCC1678 | Db1255 |
Novel ERG/DNA binding inhibitor, targeting the DNA-binding activity of the human ERG transcription factor
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| DCC1677 | Db07107 |
Novel tyrosine kinase inhibitor for drug resistant T315I mutant BCR-ABL
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