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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2738 | Ips-02001 |
Novel inhibitor of protein-protein interaction (PPI), targeting integrin αvβ3-osteopontin interface, blocking OC maturation from murine bone marrow-derived macrophages, as well as the resorptive function of OCs, impairing downstream signaling of integrin
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| DCC2737 | Iproclozide |
Irreversible and nonselective Monoamine_oxidase_inhibitor>monoamine oxidase inhibitor (MAOI)
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| DCC2736 | ipr-456 |
Inhibitor of the uPAR·uPA protein-protein interaction, blocking cancer cell invasion
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| DCC2735 | Ipr-2025 |
Novel inhibitor of glioblastoma multiforme (GBM), inhibiting cell viability of low-passage patient-derived GBM spheroids, blocking tube-formation of endothelial cells in Matrigel, showing no effect on primary hematopoietic CD34+ progenitor spheroids or as
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| DCC2734 | Ipomoeassin F |
Natural inhibitor of the in vitro biogenesis of the SARS-CoV-2 spike protein and its host cell membrane receptor, binding Sec61α to Inhibit Protein Translocation
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| DCC2733 | Ipomeamarone |
Natural toxic furanoterpenoid found in mold-damaged sweet potatoes
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| DCC2732 | Ipi-269609 |
Orally bioavailable inhibitor of Hedgehog signaling, inhibiting tumor initiation and metastasis in pancreatic cancer
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| DCC2731 | Iperoxo-bqca C6 |
Muscarinic Acetylcholine Receptor Hybrid Ligand, possessing noticeable M2/M4 mAChR selectivity
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| DCC2730 | Ipcs-1 |
Novel inhibitor of the plant inositol phosphorylceramide synthase ((IPCS), demonstrating herbicidal activity
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| DCC2729 | Iodoclorgyline |
Selective monoamine oxidase A inhibitor
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| DCC2728 | Iodiconazole |
Novel antifungal agent, exhibiting broad spectrum and potent activity against 12 kinds of clinically pathogenic fungi
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| DCC2727 | Inz-4 [1585213-98-4] |
Novel Potent Fungal-Selective Inhibitor of Mitochondrial Cytochrome bc1
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| DCC2726 | Inuloxin A |
Natural Activator of Programmed Cell Death, leading to membrane damage, mitochondria alteration, chromatin condensation, and ROS accumulation
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| DCC2725 | Intoplicine |
Inhibitor of both topoisomerase I and II via intercalating DNA helix
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| DCC2724 | Intervenolin |
Natural potent inhibitor of H. pylori DHODH, having greater efficacy for treatment of H. pylori infection
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| DCC2723 | Int2-31 |
Blocker of the interaction of FAK and IGF-1R; Antagonist of the phosphorylation of tumor AKT
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| DCC2722 | Ins48823 |
Activator of the P2Y6 receptor in bone, increasing survival of osteoclasts
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| DCC2721 | Ins3-54-a26 |
Novel inhibitor of the DNA-binding domain (DBD) of STAT3, suppressing tumor growth, metastasis and STAT3 target gene expression in vivo
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| DCC2720 | Ins015_037 |
Novel potent inhibitor of DDR1 tyrosine kinase
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| DCC2719 | Inp1750 |
Novel putative inhibitor of type III secretion (T3S) in the Gram-negative pathogen Yersinia pseudotuberculosis and Chlamydia trachomatis
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| DCC2718 | Inos-in-d27 |
Novel Potent and Orally Active Inducible Nitric Oxide Synthase (iNOS) Dimerization Inhibitor with Efficacy in Rheumatoid Arthritis Mouse Model
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| DCC2717 | Inos-in-18 |
Novel Potent and Selective Inducible Nitric Oxide Synthase (iNOS) Inhibitor (IC50 = 74 nM) with high BBB permeability (Pe = 19.1 × 10-6 cm/s) for Parkinson's Disease
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| DCC2716 | Inos-in-10 |
Novel selective inhibitor of the iNOS, without affecting the eNOS isoform
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| DCC2715 | Inhibitor R3 |
Novel Potent Inhibitor of Microbiome ß-Glucuronidases
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| DCC2714 | Inhibitor R1 |
Novel Potent Inhibitor of Microbiome ß-Glucuronidases
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| DCC2713 | Inhib1x |
Novel dual inhibitor of MAPKAPK5 and MAPKAPK2
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| DCC2712 | inh-32 |
Novel inhibitor of Ark1, the fission yeast member of the conserved Aurora kinase family
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| DCC2711 | Ingavirin |
Novel inhibitor of the influenza virus reproduction, inhubiting the formation of the virus specific hemagglutinin
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| DCC2710 | Infraluciferin |
NIR emitting firefly luciferin analogue
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| DCC2709 | Indoxyl Sulfate |
Metabolite of tryptophan, showing adverse effects on bones and the central nervous system, having been most frequently implicated as a contributor to renal disease progression and vascular disease
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