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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DCC2588 | Homochlorcyclizine Dihydrochloride |
Histamine H1 receptor antagonist
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| DCC2587 | Holothurin A |
Natural inhibitor of dietary fat absorption and showing strong anti-obesity activity
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| DCC2586 | Holomycin |
Antibiotic
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| DCC2585 | Hoi-07 |
Novel specific Aurora B inhibitor
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| DCC2584 | Hoechst-3325 |
Fluorescent indicator of apoptosis, binding the minor groove of DNA at A and T rich regions
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| DCC2583 | Hocpca |
Highly potent and selective ligand for the GHB binding sites, binding with 27 times better affinity than GHB itself and acrossing the blood brain barrier in vitro and in vivo
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| DCC2582 | Hnpc-a3066 |
Novel strobilurin acaricide, exhibiting larvicidal and ovicidal activities against various acarids
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| DCC2581 | Hn-cbl |
Novel selective inhibitor of the lymphocytic leukemia (LL) cell survival , Selectively Enhancing the Killing Effect through STAT3 Binding on Lymphocytic Leukemia Cells In Vitro and In Vivo
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| DCC2580 | Hmsir-tubulin |
Novel Blinking Fluorescent Probe for Tubulin Nanoscopy in Living and Fixed Cells
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| DCC2579 | Hms-i2 |
Novel chemical probe for heterochromatin formation and function, disrupting of heterochromatin-mediated transcriptional gene silencing
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| DCC2578 | Hms-i1 |
Novel chemical probe for heterochromatin formation and function, disrupting of heterochromatin-mediated transcriptional gene silencing
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| DCC2577 | Hmref-ßglcnac |
Novel Hexosaminidase-Targeting Fluorescence Probe for Visualizing Human Colorectal Cancer.
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| DCC2576 | Hmref-s-neu5ac |
Novel sialidase-activatable fluorescence probe with improved stability for the sensitive detection of sialidase
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| DCC2575 | Hmr-1566 |
Potent and selective I ks channel blocker
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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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