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Cat. No. Product Name Field of Application Chemical Structure
DCC2772 Ith15004
Novel, potent, selective, and BBB-permeable P2X7 antagonist
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DCC2771 Ith12505
Novel neuroprotective agent
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DCC2770 ith12246
Novel PP2A ligand, protecting against memory impairment and focal cerebral ischemia in mice
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DCC2769 Itf3985
Novel selective HDAC6 inhibitor
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DCC2768 Itf3756
Novel Potent and Selective Histone Deacetylase 6 (HDAC6) Inhibitor, showing a remarkably low toxicity both in vitro and in vivo and increasing the function of regulatory T cells (Tregs) at well-tolerated concentrations
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DCC2767 Ite-conhch3
Novel highly potent (EC 50 = 1.6 nM) aryl hydrocarbon receptor (AhR) agonist with high affinity (K i = 88 nM)
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DCC2766 Ite-atra
Novel degrader of CRABP proteins
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DCC2765 Isvy130
Novel Potent and Selective A3 Antagonist
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DCC2764 Ist-622
Unique topoisomerase inhibitor, showing significant growth-inhibitory effects against large-cell lung cancer (Lu-116) and gastric adenocarcinoma (St-4)
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DCC2763 Isq-1 Hydrochloride
Distinct IKur blocker
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DCC2762 Isp-vt
Novel inhibitor of COX and neutrophil migration
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DCC2761 Isph Inhibitor 23.20-tpp
Novel prodrug of potent IspH inhibitor, killing clinical isolates of several multidrug-resistant bacteria, including those from the genera Acinetobacter, Pseudomonas, Klebsiella, Enterobacter, Vibrio, Shigella, Salmonella, Yersinia, Mycobacterium and Baci
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DCC2760 Isox-inact
Biological Active Reagents
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DCC2759 Isoxaben
Inhibitor of the cellulose biosynthesis, inhibiting anisotropic cell expansion resulting in a severely swollen and stunted growth phenotype
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DCC2758 Isowighteone
Natural genistein derivetive with antibacterial and antifungal activities
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DCC2757 Iso-ppads
P2X-purinoceptor antagonist
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DCC2756 Isopedopeptin B
Natural antibacterial agent with cytotoxicity and hemolytic properties against a larger panel of Gram-negative bacteria
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DCC2755 Isomyristicin
Natural essential oil, showing activity against T. muris
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DCC2754 Isomazole
Potent inotropic agent, inhibiting both PDE3 and PDE4
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DCC2753 Isofagomine
Iminosugar, binding selectively to N370S glucocerebrosidase and restoring its correct conformation and, consequently, enhancing its activity
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DCC2752 Iso-dehydrozingerone
Novel osteoclastogenesis inhibitor, preventing ovariectomy-induced osteoporosis in ddY mice
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DCC2751 Isir-005
Natural Stabilizer of the 14-3-3/Gab2 Protein-Protein Interaction (PPI) Interface
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DCC2750 Isbogrel
Selective thromboxane A2 (TXA2) synthase inhibitor
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DCC2749 Isatin-o
Neutral BBB crossing reactivator for acetylcholinesterase inhibited by paraoxon, also acting as anticonvulsant
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DCC2748 Isam-c032
Novel potent hA2BAR antagonist (Ki = 3.66 nM)
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DCC2747 Irl-1620
ET B receptor agonist, showing anti-apoptotic activity and protecting neural cells in rats with cerebral ischemia
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DCC2746 ire1-in-vii
Inhibitor of IRE1 endoribonuclease activity, strongly inhibiting XBP-1 splicing in an in vivo model of acute endoplasmic reticulum stress.
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DCC2745 Irc-083864
Novel inhibitor of CDC25 phosphatases, actively against human cancer cells
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DCC2744 Irak4-in-13
Novel Orally Efficacious IRAK4 Inhibitor, Targeting MyD88L265P Mutant Diffuse Large B Cell Lymphoma
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DCC2743 Irak3 Degrader 23
Novel potent and selective degrader of IRAK3, inducing proteasome-dependent degradation of IRAK3 and showing both CRBN and IRAK3 binding for activity
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