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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
DCC1614 Cxcr2-in-c5
Novel CXCR2 selective antagonist with a low CXCR1 antagonism preference
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DCC1613 Cxcr2 Antagonist 3e
Novel potent CXCR2 antagonist
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DCC1612 Cx-659s
Nonsteroidal dermatologic and anti-inflammatory agent, blocking the MEK1/2-Erk1/2 pathway, inhibiting chronic contact hypersensitivity responses (CHRs) and the rebound phenomenon following withdrawal of corticosteroid therapy without immunosuppression
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DCC1611 Cx4338
Novel inhibitor of CXCL8-mediated chemotaxis through selective regulation of CXCR2-mediated signaling
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DCC1610 Cx1739
Novel low-impact ampakine that can safely activate AMPA receptors without causing excito-neurotoxicity, rapidly crossing the blood-brain barrier (T max = 2 min), protecting against respiratory depression
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DCC1609 Moxilubant Maleate
Potent LTB4 receptor antagonist
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DCC1608 Cx08005
Novel potent and substrate-competitive PTP1B and TCPTP dual inhibitor
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DCC1607 Cwp231904
Novel Wnt/β-Catenin Inhibitor, Preferentially Inhibiting the Growth of Breast Cancer Stem-like Cells
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DCC1606 Cwhm-505 Hydrochloride
Potent antimalarial agent against Plasmodium falciparum 3D7
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DCC1605 Cwhm-505
Potent antimalarial agent against Plasmodium falciparum 3D7
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DCC1604 Cwhm-1552
Novel orally efficacious antimalarial agent against P. falciparum 3D7 ( IC50: 51 nM)
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DCC1603 Cvs-1578
Potent serine protease inhibitor, targeting the S 2 S 3 thrombin and FXa subsites
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DCC1602 Cvs-1123
Direct thrombin inhibitor, preventing occlusive arterial and venous thrombosis in a canine model of vascular injury
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DCC1601 Cvm-05-002
Novel potent and selective inhibitor of PI5P4Ks
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DCC1600 Cvm-04-70
Inhibitor of PIM, suppressing cyclin-Dependent Kinase 2 (CDK2)
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DCC1599 Cvk-021
Novel potent pregnane X Receptor (PXR) agonist
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DCC1598 Cvk-003
Novel dual PXR and AhR agonist
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DCC1597 Cv21/jr95
Potent anti-cancer agent
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DCC1596 Cuprizone
Inducer of demyelination and motor dysfunction via upregulation of IGF-1
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DCC1595 Cumyl-pica
Agonist for the cannabinoid receptors, with Ki values of 59.21 nM at CB1 and 136.38 nM at CB2 and EC50 values of 11.98 nM at CB1 and 16.2 nM at CB2
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DCC1594 Cumi-101
5-HT1A receptor agonist
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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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