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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2541 | Hif-1alpha Inhibitor-1 | Novel HIF-1alpha inhibitor |
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| DCC2542 | Hif-1alpha-p300 Ppi Inhibitor-3 | Novel HIF-1alpha-p300 Protein Protein Interaction inhibitor |
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| DCC2543 | Hif-hydroxylase Modulator | Novel hypoxia inducible factor hydroxylase modulator |
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| DCC2544 | Hif-hydroxylase Modulator-ii | Novel hypoxia inducible factor hydroxylase modulator |
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| DCC2545 | Hif-in-33 | Novel HIF Pathway Inhibitor |
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| DCC2546 | Himbacine | Natural muscarinic receptor antagonist |
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| DCC2547 | Hipk1/2-in-a64 | Novel Potent Inhibitor of HIPK1/HIPK2 Kinase |
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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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| 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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| DCC2550 | Histidyl-histidine | Novel enhancer of catalytic efficiency of neurolysin |
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| DCC2551 | Histidyltyrosine | Novel enhancer of catalytic efficiency of neurolysin |
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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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| 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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| DCC2554 | hjc0122 | AMPA Receptor Positive Allosteric Modulator |
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| DCC2555 | Hjc0123 | Novel orally bioavailable STAT3 inhibitor |
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| DCC2556 | Hjc0149 | Novel potent orally bioavailable inhibitor of signal transducer and activator of transcription 3 (STAT3) |
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| DCC2557 | Hjc05100 | Novel apigenin analogue, suppressing pancreatic stellate cell proliferation |
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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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| DCC2559 | Hk2 Modulator-1 | Novel allosteric hexokinase 2 (HK2) modulator, selectively detaching HK2 from the mitochondria |
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| DCC2560 | hl010183 | Novel Metformin Derivative; Inhibitor of Proliferation and Invasion of Triple-Negative Breast Cancer Cells |
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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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| DCC2562 | hla20a | Selective Acetylcholinesterase Inhibitor |
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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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| DCC2564 | Hlcl-61 | First-in-class inhibitor of protein arginine methyltransferase 5 (PRMT5) |
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| DCC2565 | Hlö-7 Dimesylate | Novel Nerve Agent Reactivator |
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| DCC2566 | Hm-50316 | Potent and highly selective FABP4 inhibitor |
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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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| 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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| DCC2569 | Hmbpp Triammonium Salt | Potent stimulator of gamma delta T cells |
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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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