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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2777 | Ivq Hydrochloride |
Prodrug of QVO, being quickly converted to QVO in mice and rats following administration, ameliorating hyperglycemia, and suppressing hepatic gluconeogenesis and activating AMPK signaling pathway in the liver tissues
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| DCC2776 | Ivde77 |
The first Ang IV-analogue being able to abolish IRAP-availability completely at the cell surface in vitro
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| DCC2775 | Ivabradine |
Selective inhibitor of the funny channel pacemaker current (If) in the sinoatrial node in a dose-dependent fashion, resulting in a lower heart rate and thus more blood to flow to the myocardium
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| DCC2774 | Ityr-dbrmd |
First-in-class iodothyronine deiodinase type 3 (DIO3) inhibitor, demonstratig attenuated cell counts, induction in apoptosis, and a reduction in cell proliferation in DIO3-positive HGSOC cells (OVCAR3 and KURAMOCHI)
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| DCC2773 | Itx-4520 |
Novel highly potent, orally bioavailable hepatitis C virus (HCV) entry inhibitor
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| 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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