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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2574 | Hmr1426 |
Novel food intake-reducing agent
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| DCC2573 | Hmr1031 |
Potent and specific integrin α4ß1 or very late antigen 4 (VLA-4) receptor antagonist, binding to vascular cell adhesion molecule-1 (VCAM-1) and fibronectin
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| DCC2572 | Hm-mc4-ppea |
Potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt)
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| DCC2571 | Hmk-32 |
Irriversible inhibitor of GSK3
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| DCC2570 | Hmi-1a3 |
Protein kinase C partial agonist, targeting the C1 domain, inhibiting cell proliferation, decreasing cell viability and inducing an apoptotic response
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| DCC2569 | Hmbpp Triammonium Salt |
Potent stimulator of gamma delta T cells
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| DCC2568 | Hmao-b Inhibitor 5 |
Novel highly potent, selective, and competitive hMAO-B inhibitor with high BBB permeability profile and neuroprotective action (IC 50 = 42 nM; SI > 2375)
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| DCC2567 | Hm90822 |
Novel antagonist to the inhibitors of apoptosis (IAPs), potentiating cell death in EGFR-overexpressing non-small-cell lung cancer cells
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| DCC2566 | Hm-50316 |
Potent and highly selective FABP4 inhibitor
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| DCC2565 | Hlö-7 Dimesylate |
Novel Nerve Agent Reactivator
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| DCC2564 | Hlcl-61 |
First-in-class inhibitor of protein arginine methyltransferase 5 (PRMT5)
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| DCC2563 | Hlb-0532247 |
Novel phosphoramidate prodrug of ddhCTP, effectively reducing titers of Zika and West Nile viruses in cell culture with minimal nonspecific toxicity to host cells
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| DCC2562 | hla20a |
Selective Acetylcholinesterase Inhibitor
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| DCC2561 | Hl-3-68 |
Novel SARS-CoV-2 Main Protease (Mpro) inhibitor, binding to Subsites S1 and S2 (K d =0.69 µM)
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| DCC2560 | hl010183 |
Novel Metformin Derivative; Inhibitor of Proliferation and Invasion of Triple-Negative Breast Cancer Cells
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| DCC2559 | Hk2 Modulator-1 |
Novel allosteric hexokinase 2 (HK2) modulator, selectively detaching HK2 from the mitochondria
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| DCC2558 | Hk Inhibitor 2 |
Novel inhibitor of YycG histidine kinase (HK), showing potent antibiofim activity against Staphylococcus epidermidis
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| DCC2557 | Hjc05100 |
Novel apigenin analogue, suppressing pancreatic stellate cell proliferation
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| DCC2556 | Hjc0149 |
Novel potent orally bioavailable inhibitor of signal transducer and activator of transcription 3 (STAT3)
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| DCC2555 | Hjc0123 |
Novel orally bioavailable STAT3 inhibitor
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| DCC2554 | hjc0122 |
AMPA Receptor Positive Allosteric Modulator
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| DCC2553 | Hiv-1 Inhibitor 9d |
Novel highly potent HIV-1 inhibitor with broad-spectrum activity (EC50 = 2.0-57 nM) against resistant strains, exhibiting good solubility and safety profiles and a good PK profile with an oral bioavailability of 59% in rats
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| DCC2552 | Hiv-1 In Photoprobe |
Novel photoaffinity-labeled probe for full-length human immunodeficiency virus-1 integrase (HIV-1 IN)
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| DCC2551 | Histidyltyrosine |
Novel enhancer of catalytic efficiency of neurolysin
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| DCC2550 | Histidyl-histidine |
Novel enhancer of catalytic efficiency of neurolysin
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| DCC2549 | Histidine-proline |
Allosteric inhibitor of ATP phosphoribosyltransferase (ATPPRT), binding to the ATPPRT:ATP complex via a two-step binding mechanism, inhibiting ATPPRT competitively and likely uncompetitively, respectively, against PRPP and ATP
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| DCC2548 | Hippeastrine Hydrobromide |
Natural alkaloid, demonstrating significant cytotoxicity against a panel of human and murine tumor cell lines
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| DCC2547 | Hipk1/2-in-a64 |
Novel Potent Inhibitor of HIPK1/HIPK2 Kinase
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| DCC2546 | Himbacine |
Natural muscarinic receptor antagonist
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| DCC2545 | Hif-in-33 |
Novel HIF Pathway Inhibitor
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