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Cat. No. Product Name Field of Application Chemical Structure
DCC1593 Cugamycin
Novel r(CUG) repeat expansion cleaver, specifically recognizing the 3-dimensional structure of r(CUG)exp, cleaving it more selectively among transcripts containing short, nonpathogenic r(CUG) repeats than an oligonucleotide that recognizes RNA sequence vi
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DCC1592 Cu-6pmn
Novel fluorescent RXR agonist
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DCC1591 Ctw0415
Novel Serotonin 5-HT 2C Receptor Positive Allosteric Modulator (PAM) with Enhanced Drug-like Properties
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DCC1590 Ctt-54.2 Potassium
Inhibitor of prostate-specific membrane antigen (PSMA)
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DCC1589 Ctr-32
Novel anticancer agent, effectively killing multi-drug resistant cancer cells and a panel of different cancer cells originated from a variety of different tissues including breast and skin, preventing tubulin polymerization, leading to the cell cycle arre
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DCC1588 Ctr-21
Novel anticancer agent, effectively killing multi-drug resistant cancer cells and a panel of different cancer cells originated from a variety of different tissues including breast and skin, preventing tubulin polymerization, leading to the cell cycle arre
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DCC1587 Ct-mz1
Novel cell permeable degrader of BRD4
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DCC1586 Ct-711
Novel potent dual inhibitor of ALK and c-Met
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DCC1585 Ct-2584
Dual inhibitor of angiogenesis and lysophosphatidic acid acyltransferase
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DCC1584 Csv0c018875 Hydrochloride
Novel G9a (EHMT2) inhibitor, binding tightly inside the active site cavity of G9a, inhibiting the activity of G9a in both enzyme and cell based assays with much lesser toxicity than BIX-0129
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DCC1583 C-src-in-12
Novel substrate-competive c-Src inhibitor
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DCC1582 Csl-32
Novel modulator of PI3K and NF-κB activities, blocking migration and production of inflammatory mediators
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DCC1581 Cryptozepine-2
Novel photoisomerizable potent and selective M1 ligand, mimicing the tricyclic chemical structure and display reversibly controlled activity, showing stronger inhibition upon illumination both in vitro and in cardiac atria ex vivo
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DCC1580 Cryptopleurine
Inhibitor of gene products associated with cell survival, proliferation, invasion, and angiogenesis, targeting NF-κB pathway, showing antiproliferative activity and unique mode of action
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DCC1579 Cryosim-3
Novel water-soluble, potent, and selective TRPM8 receptor agonist
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DCC1578 Cryosim-1
Novel TRPM8 agonist
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DCC1577 Crx-527
Novel potent powerful lipid A analogue as a conjugation-ready TLR4 ligand
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DCC1576 Crx-526
TLR4 antagonist, protecting against advanced diabetic nephropathy
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DCC1575 Crth2 Antagonist K117
Potent and selective CRTH2 antagonist
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DCC1574 Crt0093964
Potent and selective inhibitor of AKR1C3
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DCC1573 Crt0083914
Potent and selective inhibitor of AKR1C3
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DCC1572 Crs400393
Novel potent and mycobacteria-specific antimycobacterial agent, targeting MmpL3, a mycobacterial mycolic acid transporterr, demonstrating MIC = 0.03, 2, and ≤ 0.12 μg/mL against Mabs, Mycobacterium avium complex (MAC), and Mtb respectively
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DCC1571 Crs400359
Novel potent and mycobacteria-specific antimycobacterial agent, targeting MmpL3, improving the antimycobacterial activity and being also potent against Mtb
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DCC1570 Crom-2
Novel potent, selective, and reversible inhibitor of human monoamine oxidase B (hMAO-B)
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DCC1569 Crom-1
Novel potent, selective, and reversible inhibitor of human monoamine oxidase B (hMAO-B)
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DCC1568 Crl-40940
Selective dopaminergic reuptake inhibitor
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DCC1567 Cribrostatin 6
Antineoplastic and Antibacterial; Inducer of death in cancer cells through a reactive oxygen species (ROS)-mediated mechanism; Dark blue cancer cell growth inhibitor
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DCC1566 Cremastranone
Natural antiangiogenic homoisoflavanone, inhibiting the proliferation, migration and tube formation ability of human retinal microvascular endothelial cells
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DCC1565 Crebbp-in-9
Novel CREBBP Bromodomain Inhibitor
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DCC1564 Creb Inhibitor 666-15
Novel potent and cell-permeable inhibitor of cAMP-response element binding protein (CREB)
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