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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC4001 Parogrelil
Novel potent phosphodiesterase 3 inhibitor, suppressing the asthmatic response and showing both bronchodilating and anti-inflammatory effects
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DCC4000 Paraquat Diiodide
Non-selective contact herbicide, killing green plant tissue on contact, being highly toxic and linked to Parkinson's disease, generating reactive oxygen species (ROS), which causes cell death and potentially leading to acute respiratory distress syndrome
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DCC3999 Paraoxon
Acetylcholinesterase inhibitor, the active metabolite of the insecticide parathion
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DCC3998 Para-nitroblebbistatin
Selective cell-permeable inhibitor of non-muscle myosin II ATPases, being more stable and less phototoxic than Blebbistatin
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DCC3997 Para-cid-5951923
Isomer of CID-5951923
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DCC3996 Para-aminoblebbistatin
Blebbistatin derivative, increasing water solubility, decreases the inherent fluorescence, stabilizing the molecule to circumvent its degradation by prolonged blue light exposure, and decreasing its phototoxicity while retaining the in vitro and in vivo a
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DCC3994 Pape-1
Pathway Preferential Estrogen, activating the extranuclear signaling pathway without activity on the nuclear signaling pathway
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DCC3993 Pao-pdt
Potent and highly selective small molecule inhibitor of thioredoxin reductase (TrxR)
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DCC3992 Pan-raf/rtk Inhibitor I-16
Novel potent pan-Raf and receptor tyrosine kinase inhibitor, potently inhibits all subtypes of Rafs with IC50 values of 3.49 (BRafV600E), 8.86 (ARaf), 5.78 (BRafWT), and 1.65 nM (CRaf), respectively
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DCC3991 panomifene
Tamoxifen analogue; antiestrogenic
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