| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| 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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| 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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| DCC1699 | Dc-prc2in-01 | Novel PRC2 Inhibitor, Targeting EZH2-EED Interaction |
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| DCC1700 | Dc-s100 | Novel, Selective Histone Methyltransferase SET7 Inhibitor |
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| DCC1701 | Dc-s238 | Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor |
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| DCC1702 | Dc-s239 | Novel, Potent and Selective Histone Methyltransferase SET7 Inhibitor |
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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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| DCC1704 | Dcz3112 | Novel Hsp90 inhibitor, exerts potent antitumor activity against HER2-positive breast cancer through disruption of Hsp90-Cdc37 interaction |
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| DCC1705 | Dd-04-015 | Novel selective BTK degrader, demonstrating prolonged pharmacodynamic effects |
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| DCC1706 | Dd04107 Featured | Novel inhibitor of α-calcitonin gene-related peptide (α-CGRP) exocytotic release from primary sensory neurons, selectively interacting with Synaptotagmin 1 |
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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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| DCC1708 | Ddd00015314 | Novel activator of the GUS reporter activity, specific increasing in stumpy reporter gene expression |
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| DCC1709 | Ddd01035881 | Novel transmission blocker of antimalarials, targeting male gametes |
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| DCC1710 | Ddd-028 | Potent potential non-opioid, non-cannabinoid analgesic for neuropathic and inflammatory pain |
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| DCC1711 | Ddd100097 | Potent inhibitor of Trypanosoma brucei N-myristoyltransferase (TbNMT) with markedly improved blood-brain barrier permeability |
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| DCC1712 | Ddhctp Sodium Salt | Novel potent and broad-spectrum antiviral agent, acting as a chain terminator for viral RNA polymerase |
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| DCC1713 | Ddo-2117 | Novel potent blocker of mixed lineage leukemia 1 (MLL1)-WDR5 interaction, inhibiting MLL1 complex H3K4 methyltransferase activity |
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| DCC1714 | Ddo-2213 | Novel Potent and Orally Bioavailable Inhibitor of the WDR5-Mixed Lineage Leukemia 1 (MLL1) Protein-Protein Interaction for the Treatment of MLL Fusion Leukemia |
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| DCC1715 | Ddo-7132 | Novel NQO1 substrate, inhibiting cancer cell (NQO1-rich A549 cell line) growth |
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| DCC1716 | Ddo-7204 | Novel Nrf2 activator |
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| DCC1717 | ddpm-1457 | Potent mGAT4 inhibitor |
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| DCC1718 | Ddr1-in-2 | Potent and selective DDR1 receptor tyrosine kinase inhibitor |
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| DCC1719 | Ddri-18 | Inhibitor of nonhomologous end-joining (NHEJ) DNA repair following double strand DNA breaks induced by ionizing radiation, enhancing the effects of DNA-damaging cancer drugs like etoposide, camptothecin and doxorubicin |
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| DCC1720 | Ddr-trk-1n | Negative control for DDR-TRK-1 |
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| DCC1721 | Dea Nonoate Sodium Salt | NO donor, generating a controlled release of nitric oxide in solution. |
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| DCC1722 | Deacm-caged D-luciferin | Coumarin-caged D-luciferin, being excited in the caged group only by light of wavelength ranging within 400-430 nm |
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| DCC1723 | Deac-pda-atp | Fluorophore to myosin or actomyosin |
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| DCC1724 | Debio-1452-nh3 | Novel potent inhibitor of the enoyl-acyl carrier protein reductase FabI, reducing bacterial burden in mice and rescuing mice from lethal infections with clinical isolates of Acinetobacter baumannii, Klebsiella pneumoniae and E. coli |
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| DCC1725 | Deferasirox Ferrate(iii) Tripotassium Complex | Deferasirox iron complex |
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| DCC1726 | Deferoxamine Hydrochloride | Iron chelating agent, chelating iron from intra-lysosomal ferritin and hemosiderin forming ferrioxamine, a water-soluble chelate excreted by the kidneys and in the feces via the bile |
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