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Novel inhibitors

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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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