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Novel inhibitors

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Cat. No. Product Name Field of Application Chemical Structure
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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DCC2544 Hif-hydroxylase Modulator-ii
Novel hypoxia inducible factor hydroxylase modulator
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DCC2543 Hif-hydroxylase Modulator
Novel hypoxia inducible factor hydroxylase modulator
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DCC2542 Hif-1alpha-p300 Ppi Inhibitor-3
Novel HIF-1alpha-p300 Protein Protein Interaction inhibitor
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DCC2541 Hif-1alpha Inhibitor-1
Novel HIF-1alpha inhibitor
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DCC2540 Hie-124
CNS active anticonvulsant and ultra-short acting hypnotic
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DCC2539 Hiapp(23-27)
Pentapeptide sequences of hIAPP, being sufficient for the formation of beta-sheet-containing amyloid fibrils and self-assemble laterally into unusually broad ribbons
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DCC2538 Hiapp(22-27)
Hexapeptide sequences of hIAPP, being sufficient for the formation of beta-sheet-containing amyloid fibrils and coiling around each other in a typical amyloid fibril morphology
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