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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC42640 | J014 |
Novel cGAS-specific inhibitor for repression of dsDNA-triggered interferon expression ( IC50 of 100 nM and 60.0 nM for h-cGAS and m-cGAS, respectively)
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| DC42639 | RIm13 |
Novel potent inhibitor of Proprotein convertase subtilisin/kexin 9 (PCSK9), targeting the PCSK9/LDLR protein-protein interaction
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| DC42638 | OATD-01 |
First-in-Class Chitotriosidase (CHIT1) Inhibitor as Potential New Therapeutics for Idiopathic Pulmonary Fibrosis
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| DC42637 | KHK-IN-2 |
Novel potent and selective inhibitor of ketohexokinase (KHK)
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| DC42636 | ZINC4326719 |
Novel potent dCTP Pyrophosphatase 1 (DCTPP1) inhibitor
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| DC42635 | ZINC4511851 |
Novel potent dCTP Pyrophosphatase 1 (DCTPP1) inhibitor
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| DC42633 | NCGC1481 |
Novel potent inhibitor of IRAK1/4 and FLT3 with improved solubility, stability, and permeability properties suitable for in vivo utility
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| DC42632 | DAPK1-IN-6d |
The first selective inhibitor of DAPK1
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| DC42630 | NMO-IgG blocker A-01 |
Idiotype-specific blocker of neuromyelitis opticaimmunoglobulin G (NMO-IgG) binding to aquaporin-4 (AQP4)
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| DC42629 | SHMT-IN-2 |
Novel serine hydroxymethyltransferase (SHMT) inhibitor, potently inhibiting both human SHMT1/2
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| DC42626 | Amfonelic Acid |
A research chemical with highly selective dopaminergic stimulant and antibiotic properties.
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| DC42625 | JMS-053 |
Novel allosteric PTP4A3 inhibitor, increasing Emilin 1 gene expression
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| DC42624 | BH-IAA |
Novel potent auxin antagonist
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| DC42622 | ML328 |
Novel specific inhibitor of bacterial RecBCD helicase-nuclease DNA repair enzyme; Inhibitor of autotaxin (ATX, NPP2)
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| DC42621 | CPD3.1 HCl |
Novel YAP-TEAD Interaction Inhibitor, inhibiting TEAD activity, cell proliferation, and cell migration
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| DC42620 | ARI-3099 hydrochloride |
Selective and Potent Inhibitor of Fibroblast Activation Protein and Prolyl Oligopeptidase
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| DC42619 | Z-FL-COCHO hydrate |
Novel cathepsin S inhibitor, enhancing oxaliplatin-induced apoptosis through upregulation of Bim expression
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| DC42618 | NC9 |
Novel irreversible transglutaminase 2 (TG2) inhibitor
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| DC42617 | AA9 |
Novel tissue transglutaminase (TG2) inhibitor
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| DC42615 | Coproporphyrin dihydrochloride |
Appropriate clinical biomarker to recapitulate drug-drug interactions mediated by OATP inhibition
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| DC42614 | UNC7938 |
Novel destabilizer of the endosome membrane, enhancing the endosome-leakage activity of cell-penetrating peptides and facilitating the endosomal escape of macromolecules initially internalized by mammalian cells via endocytosis
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| DC42612 | Glybenclamide Potassium Salt |
Water soluble glyburide, inhibitor of the sulfonylurea receptor 1 (SUR1), regulating subunit of the ATP-sensitive potassium channels (KATP) in pancreatic beta cells
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| DC42610 | Z-VAD-FMK |
Cell-permeable, Irreversible, Non-cytotoxic Pan Caspase Inhibitor
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| DC42608 | IN04 |
Novel inhibitor of LRRK1, suppressing osteoclast function, but not osteoclast differentiation
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| DC42605 | cjoc42 |
Novel inhibitor of the oncoprotein gankyrin, preventing the decrease in p53 protein levels associated with high amounts of gankyrin, restoring p53-dependent transcription and sensitivity to DNA damage
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| DC42603 | GSK205 |
Selective Transient receptor potential vanilloid 4 (TRPV4) antagonist
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| DC42602 | DB-310 |
Novel LMP2 inhibitor as a potential treatment for Alzheimer's disease
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| DC42601 | NC03 |
Novel PI4K2A inhibitor, decreasing the PI4P pools in Golgi and endosomes
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| DC42599 | Quinabactin |
Aba-mimicking agonist, preferentially activating dimeric ABA receptors and possesses ABA-like potency in vivo
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| DC42598 | DC_Y134 |
Novel Selective, Cell Active Inhibitor of Protein Arginine Methyltransferase 5 (PRMT5)
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