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| Cat. No. | Product Name | Field of Application | Chemical Structure |
|---|---|---|---|
| DCC1584 | Csv0c018875 Hydrochloride |
Novel G9a (EHMT2) inhibitor, binding tightly inside the active site cavity of G9a, inhibiting the activity of G9a in both enzyme and cell based assays with much lesser toxicity than BIX-0129
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| DCC1583 | C-src-in-12 |
Novel substrate-competive c-Src inhibitor
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| DCC1582 | Csl-32 |
Novel modulator of PI3K and NF-κB activities, blocking migration and production of inflammatory mediators
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| DCC1581 | Cryptozepine-2 |
Novel photoisomerizable potent and selective M1 ligand, mimicing the tricyclic chemical structure and display reversibly controlled activity, showing stronger inhibition upon illumination both in vitro and in cardiac atria ex vivo
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| DCC1580 | Cryptopleurine |
Inhibitor of gene products associated with cell survival, proliferation, invasion, and angiogenesis, targeting NF-κB pathway, showing antiproliferative activity and unique mode of action
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| DCC1579 | Cryosim-3 |
Novel water-soluble, potent, and selective TRPM8 receptor agonist
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| DCC1578 | Cryosim-1 |
Novel TRPM8 agonist
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| DCC1577 | Crx-527 |
Novel potent powerful lipid A analogue as a conjugation-ready TLR4 ligand
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| DCC1576 | Crx-526 |
TLR4 antagonist, protecting against advanced diabetic nephropathy
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| DCC1575 | Crth2 Antagonist K117 |
Potent and selective CRTH2 antagonist
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| DCC1574 | Crt0093964 |
Potent and selective inhibitor of AKR1C3
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| DCC1573 | Crt0083914 |
Potent and selective inhibitor of AKR1C3
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| DCC1572 | Crs400393 |
Novel potent and mycobacteria-specific antimycobacterial agent, targeting MmpL3, a mycobacterial mycolic acid transporterr, demonstrating MIC = 0.03, 2, and ≤ 0.12 μg/mL against Mabs, Mycobacterium avium complex (MAC), and Mtb respectively
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| DCC1571 | Crs400359 |
Novel potent and mycobacteria-specific antimycobacterial agent, targeting MmpL3, improving the antimycobacterial activity and being also potent against Mtb
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| DCC1570 | Crom-2 |
Novel potent, selective, and reversible inhibitor of human monoamine oxidase B (hMAO-B)
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| DCC1569 | Crom-1 |
Novel potent, selective, and reversible inhibitor of human monoamine oxidase B (hMAO-B)
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| DCC1568 | Crl-40940 |
Selective dopaminergic reuptake inhibitor
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| DCC1567 | Cribrostatin 6 |
Antineoplastic and Antibacterial; Inducer of death in cancer cells through a reactive oxygen species (ROS)-mediated mechanism; Dark blue cancer cell growth inhibitor
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| DCC1566 | Cremastranone |
Natural antiangiogenic homoisoflavanone, inhibiting the proliferation, migration and tube formation ability of human retinal microvascular endothelial cells
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| DCC1565 | Crebbp-in-9 |
Novel CREBBP Bromodomain Inhibitor
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| DCC1564 | Creb Inhibitor 666-15 |
Novel potent and cell-permeable inhibitor of cAMP-response element binding protein (CREB)
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| DCC1563 | Creatine Phosphate Disodium Hydrate |
Substrate for the assay of creatine kinase, providing a quick source of energy for muscle fibers to contract when they need an initial burst of energy
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| DCC1562 | Cranad-5 |
Foster Resonance Energy Transfer (FRET) pair for Aβ40 aggregates
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| DCC1561 | Cranad-102 |
Novel probe for selectively detecting sAβ species in Alzheimer's disease (AD)
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| DCC1560 | Cra-19156 |
Novel potent HDAC8 inhibitor
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| DCC1559 | Cqs1000 |
Novel NIR-II probe, noninvasively and dynamically visualizing and monitoring many physiological and pathological conditions of circulatory systems, including lymphatic drainage and routing, angiogenesis of tumor, and vascular deformity such as arterial th
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| DCC1558 | Cqmu152 |
Novel RORγt inhibitor, suppressing Th17 cell differentiation, reducing the severity of experimental autoimmune disease models such as EAU, EAE, and type 1 diabetes
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| DCC1557 | Cqmu151 |
Novel RORγt inhibitor, suppressing Th17 cell differentiation, reducing the severity of experimental autoimmune disease models such as EAU, EAE, and type 1 diabetes
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| DCC1556 | Cpx-351 |
Liposomal-encapsulated combination of daunorubicin and cytarabine for the treatment of newly diagnosed tAML or AML with myelodysplasia-related changes (AML-MRCs)
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| DCC1555 | Cpu-l1 |
Novel potent and selective fluorescent inhibitor of glutaminase (GLS1)
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