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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC2571 | Hmk-32 | Irriversible inhibitor of GSK3 |
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| DCC2572 | Hm-mc4-ppea | Potent inhibitor of nicotinamide phosphoribosyltransferase (Nampt) |
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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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| DCC2574 | Hmr1426 | Novel food intake-reducing agent |
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| DCC2575 | Hmr-1566 | Potent and selective I ks channel blocker |
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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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| DCC2577 | Hmref-ßglcnac | Novel Hexosaminidase-Targeting Fluorescence Probe for Visualizing Human Colorectal Cancer. |
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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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| DCC2579 | Hms-i2 | Novel chemical probe for heterochromatin formation and function, disrupting of heterochromatin-mediated transcriptional gene silencing |
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| DCC2580 | Hmsir-tubulin | Novel Blinking Fluorescent Probe for Tubulin Nanoscopy in Living and Fixed Cells |
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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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| DCC2582 | Hnpc-a3066 | Novel strobilurin acaricide, exhibiting larvicidal and ovicidal activities against various acarids |
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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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| DCC2584 | Hoechst-3325 | Fluorescent indicator of apoptosis, binding the minor groove of DNA at A and T rich regions |
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| DCC2585 | Hoi-07 | Novel specific Aurora B inhibitor |
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| DCC2586 | Holomycin | Antibiotic |
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| DCC2587 | Holothurin A | Natural inhibitor of dietary fat absorption and showing strong anti-obesity activity |
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| DCC2588 | Homochlorcyclizine Dihydrochloride | Histamine H1 receptor antagonist |
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| DCC2589 | Homovanillyl Sinapate | Novel c-Met inhibitor, markedly reducing tumor growth, showing excellent pharmacodynamics, and suppressing cell proliferation and microvessel density in an orthotopic model of triple negative breast cancer |
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| DCC2590 | Hpta-1 | Novel highly selective switch-on fluorescence sensor, targeting telomeric dimeric G-quadruplex, discriminating the telomeric dimeric G-quadruplex TTA45 against other types of DNA structures accompanied by a drastic enhancement of the emission intensity wi |
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| DCC2591 | Hpxr-agonist-28 | Novel silanol-based human pregnane X receptor (PXR) agonist |
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| DCC2592 | Hr1405-01 | Loxoprofen active metabolite, acting as a safe intravenous NSAID with superior anti-inflammatory and analgesic activities |
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| DCC2593 | Hras-1y I-motif Probe-1 | Novel Probe of the hras-1Y i-motif , selectively and directly interacting with the hras-1Y i-motif. |
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| DCC2594 | Hrv-14 Inhibitor 3v | Inhibitor of human rhinoviruses serotype 14 (HRV-14) |
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| DCC2595 | Hs-438 | Novel inhibitor of imatinib-resistant BCR-ABL T315I mutation in chronic myeloid leukemia |
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| DCC2596 | Hs-731 | μ-Opioid Receptor Agonist |
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| DCC2597 | Hsa-5b | Novel anticancer Gold(III) agent with remarkable cytotoxicity to gastric cancer cells |
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| DCC2598 | Hsd1237 | Novel potent inhibitor of the recombinant FLT3 kinase and its mutant forms, blocking the proliferation of AML cell lines, harboring oncogenic FLT3-ITD mutations with remarkable IC50 values, which were comparable to the approved FLT3 inhibitor quizartinib, |
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| DCC2599 | Hsgn-94 | Novel inhibitor of lipoteichoic acid (LTA) biosynthesis, potently inhibiting S. aureus and E. faecalis growth and biofilm formation |
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| DCC2600 | Hsk21542 | Novel Peripherally-Restricted Kappa Opioid Receptor (KOR) Agonist with Antinociceptive and Antipruritic Effects |
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