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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC2528 | Hexim1 Inducer 4a1 |
Novel potent inducer of hexamethylene bis-acetamide inducible protein 1 (HEXIM1)
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| DCC2527 | Hexafluoro |
Novel inhibitor of the phosphorylation of DRP1, stimulating a phenotype suggestive of respiration through mitochondrial normalization and demonstrating activity in Vemurafenib-resistant melanoma in vivo
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| DCC2526 | Hetrombopag Olamine |
Novel orally bioavailable, non-peptide thrombopoietin (TPO) receptor agonist
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| DCC2525 | Heterotaxin |
Novel TGF-β Signaling Inhibitor
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| DCC2524 | Het-dpd-13a |
Novel LsrK inhibitor (ID 50 119 μM) agaist antimicrobial resistance (AMR)
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| DCC2523 | Hepta-histidine |
Novel inhibitor of Tau aggregation against Tau-related neurodegenerative diseases including Alzheimer's disease (AD)
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| DCC2522 | Hepcidin |
Master regulator of iron homeostasis, contributing to Swedish mutant APP-induced osteoclastogenesis and trabecular bone loss
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| DCC2521 | Heparin Disaccharide I-s Sodium Salt |
Heparin derivative for treatment of thrombotic diseases
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| DCC2520 | Hemisurfen |
Heparan sulfate antagonist
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| DCC2519 | Hemigossypol |
The biosynthetic precursor of gossypol
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| DCC2518 | Hemiasterlin |
Cytotoxic peptide, inducing mitotic arrest and abnormal spindle formation
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| DCC2517 | Helioxanthin |
Inhibitor of interleukin-1β-induced MIP-1β production
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| DCC2516 | Helenalin Methacrylate |
Natural anti-inflammatory and anti-cancer agent
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| DCC2515 | Helenalin Acetate |
Anti-inflammatory and anti-cancer agent, disrupting the cooperation of CCAAT-box/enhancer-binding protein beta (C/EBPß) and co-activator p300
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| DCC2514 | Hds029 |
Potent inhibitor of the ErbB receptor family (IC50 values are 0.3, 0.5 and 1.1 nM for ErbB1 (EGFR), ErbB4 and ErbB2 respectively)
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