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Cat. No. Product Name Field of Application Chemical Structure
DCC4032 Pcsk9 Modulator
Novel modulator of proprotein convertase subtilisin kexin like type 9 (PCSK9)
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DCC4031 Pcpma-(1s,2s)-22e
Novel potent dopamine D3R antagonist
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DCC4030 Pcpma-(1r,2r)-30q
Novel potent and selective dopamine D3R partial agonist
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DCC4029 Pcpma-(1r,2r)-22e
Novel potent dopamine D3R agonist (Ki=4.1nM)
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DCC4028 p-come 102
Highly selective α1L adrenaline receptor agonist
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DCC4027 pcm126
Potent antagonist of the series disrupting EphA2-ephrinA1 interaction, blocking EphA2 phosphorylation in prostate cancer cells at low
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DCC4026 p-chloro-diphenyl Diselenide
Organoselenium compound with antidepressant-like and memory enhancer actions
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DCC4025 P-cf3-diepp
Novel α7 nAChR weak partial agonist, showing antinociceptive and anti-inflammatory properties
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DCC4024 Pcc0208018
Novel activator of effector T cells, enhancing T cell proliferation and activation to release interferon gamma (IFN-γ) and interleukin-2 (IL-2) without blocking the programmed cell death 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) binding and not dire
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DCC4022 Pcb-te2p
Novel Chelator for Cu-64
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DCC4021 Pcb153
Non-dioxin-like (NDL) congener
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DCC4020 Pc407-ws
Water-soluble novel potential COX-2 inhibitor
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DCC4019 pc-046
Potent tubulin-binding agent with anti-tumor efficacy in hematologic cancers
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DCC4018 Pb-wut-01
Novel calcineurin inhibitor in the C. albicans cells, enhancing susceptibility of the cells
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DCC4017 Pbs-1086
Novel dual inhibitor of the canonical and noncanonical NF-κB pathways, increasing the magnitude and duration of initial EGFR inhibitor response in multiple NSCLC models, decreasing PDHK1 expression, and suppressing phosphorylation of the PDHK1 protein sub
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DCC4016 P-bi-tat
Novel αvβ3 inhibitor, showing excellent efficacy in a glioblastoma multiforme (GBM) mouse model
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DCC4015 Pbiilh2
Pyridobenzimidazole infraluciferin, an analog of D-luciferin, increasing bioluminescence activity while maintaining nIR bioluminescence
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DCC4014 Pbi-1393
Novel enhancer of Th1 type cytokine production and primary T cell activation
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DCC4013 Pbi.120
Novel Inhibitor of Parasite Proliferation of Asexual Blood Stage P. falciparum Parasites
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DCC4012 Pbi.105
Novel Inhibitor of Parasite Proliferation of Asexual Blood Stage P. falciparum Parasites
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DCC4011 pbdnj0804
Novel potent glucosidase inhibitor, suppressing HCV virion assembly and secretion, potently inhibiting DENV infection in vitro
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DCC4010 pbdnj0802
Novel potent inhibitor of
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DCC4009 Pazinaclone
Partial agonist at GABAA benzodiazepine receptors with sedative and anxiolytic effects
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DCC4008 Pav-866
Novel antiviral agent, potently against Rabies virus (RABV) targeting host-rabies virus protein-protein interactions
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DCC4007 Parvifoline Aa
Natural ent-kaurane diterpenoid, markedly stimulates the expression of NKG2D ligands on hepatocellular carcinoma (HCC) cells, considerably enhancing their recognition and lysis by NK cells, covalently inhibiting peroxiredoxins I/II (Prxs-I/II) catalytic a
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DCC4006 Parpi-fl
Fluorescent PARP1 Inhibitor for Glioblastoma Imaging
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DCC4005 Parp10-in-22
Novel Selective Cell-Active Inhibitor of PARP10
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DCC4004 Parp1/brd4 Inhibitor Iii-7
Novel highly selective dual PARP1/BRD4 inhibitor (PARP1 IC 50 =49nM; BRD4 IC 50 =202nM), repressing the expression and activity of PARP1 and BRD4 to synergistically inhibit the malignant growth of pancreatic cancer cells in vitro and in vivo
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DCC4003 Parp/brd4 Inhibitor Iii-16
Potent and Novel Dual PARP/BRD4 Inhibitor for Efficient Treatment of Pancreatic Cancer
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DCC4002 Parogrelil Hydrochloride
Novel potent phosphodiesterase 3 inhibitor, suppressing the asthmatic response and showing both bronchodilating and anti-inflammatory effects
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