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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| 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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