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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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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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| DCC1554 | cpu-0213 |
Novel endothelin receptor antagonist, suppressing the upregulation of matrix metalloproteinases and connexin 43 in hyperthyroid myocardium
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| DCC1553 | Cpr005231 |
Novel inhibitor of death-associated protein kinase 1 (DAPK1), also inhibiting VEGF-receptor 2 and tyrosine-protein kinase SRC
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| DCC1552 | Cppz-2c |
Novel positive allosteric modulator (PAM) of metabotropic glutamate receptor 5 (mGlu5)
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| DCC1551 | Cpp11h |
Novel selective NADPH oxidase 2 (Nox2) inhibitor, attenuating endothelial cell inflammation and vessel dysfunction and restoring mouse hind-limb flow
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| DCC1550 | Cpp11g |
Novel selective NADPH oxidase 2 (Nox2) inhibitor, attenuating endothelial cell inflammation and vessel dysfunction and restoring mouse hind-limb flow
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| DCC1549 | Cpimpdh-in-c64 |
Novel CpIMPDH inhibitor
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| DCC1548 | Cpi-7c |
Unique inhibitor of MDM2, inhibiting MDM2-p53 interaction and promoting MDM2 degradation
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| DCC1547 | Cpi098 |
Novel selective inhibitor of the CREB binding protein (CBP)
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| DCC1546 | Cpfikk-in-4b |
Novel potent inhibitor of CpFIKK catalytic activity
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| DCC1545 | Cpd7 Hydrochloride |
Novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein
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| DCC1544 | Cpd118 |
Novel inhibitor of against human liver FBPase (IC50, 0.029±0.006 μM) and high selectivity relative to the other six AMP-binding enzymes, producing significant glucose-lowering effects on both type 2 diabetic KKAy mice and ZDF rats
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| DCC1543 | Cp-94707 |
Novel nonnucleoside reverse transcriptase inhibitor (NNRTI)
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| DCC1542 | Cp-868388 |
Potent PPARα agonist with a Ki of 10.8 nM
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| DCC1541 | Cp-615003 |
Novel Mdr1 P-glycoprotein substrate
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| DCC1540 | Cp-457920 |
Novel selective α5 GABA A receptor agonist
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| DCC1539 | Cp-339818 |
Inhibitor of Kv1.3 potassium ion channels
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| DCC1538 | Cp-320626 |
Inhibitor of glycogen phosphorylase; Antidiabetic
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| DCC1537 | Cp-281384 |
Novel potent and selective p38alpha inhibitor
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| DCC1536 | Cp-195543 |
Potent and selective leukotriene B4 antagonist
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| DCC1535 | Covidcil-19 |
Novel viral propagation inhibitor, binding to the revised attenuator hairpin structure of the SARS-CoV-2 frameshifting element (FSE), stabilizing the hairpin's folded state and reducing frameshifting efficiency in cells
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| DCC1534 | Coupy-15 |
Novel Potent Mitochondria-Targeted Photodynamic Therapy Anticancer Agent
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| DCC1533 | Coum-tac |
Novel Dual Covalent Inhibitor and Potential Fluorescent Label of HadA in Mycobacterium tuberculosis
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