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Cat. No. Product Name Field of Application Chemical Structure
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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DCC2537 Hi-346
Potent inhibitor of multidrug-resistant human immunodeficiency virus-1 (HIV-1)
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DCC2536 Hi-253
Potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus (HIV)
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DCC2535 Hi-207
Non-nucleoside reverse transcriptase inhibitor
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DCC2534 Clomethiazole Edisylate
Positive allosteric modulator at the barbiturate/picrotoxin site of the GABAA receptor
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DCC2533 Hhs-465
Novel sulfur-triazole exchange (SuTEx) covalent probe with ~5-fold enhanced chemoselectivity for tyrosines over other nucleophilic amino acids
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DCC2532 Hgh Fragment 177-191 (tfa Salt)
Fragment 177-191 of human growth hormone, regulating fat metabolism but without the adverse effects on blood sugar or growth, stimulating lipolysis (the breakdown or destruction of fat) and inhibiting lipogenesis (the transformation of nonfat food materia
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DCC2531 Hg-7-85-01
Novel type II inhibitor of wild-type and gatekeeper mutants of BCR-ABL, PDGFRalpha, Kit, and Src kinases
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DCC2530 Hfi-142
Insulin-regulated aminopeptidase (IRAP) inhibitor, mprovin memory in control and memory-deficient mice models
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DCC2529 Hexyl-acrdim
Potent inducer of oxidative stress as well as cell cycle arrest in the S-phase, significantly decreasing intracellular ATP level
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