
CDN1163
CAS No. 892711-75-0
CDN1163( CDN 1163 | CDN-1163 )
Catalog No. M16438 CAS No. 892711-75-0
CDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2.
Purity : >98% (HPLC)






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2MG | 34 | In Stock |
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5MG | 55 | In Stock |
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10MG | 80 | In Stock |
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25MG | 149 | In Stock |
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50MG | 266 | In Stock |
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100MG | 470 | In Stock |
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Biological Information
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Product NameCDN1163
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NoteResearch use only, not for human use.
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Brief DescriptionCDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2.
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DescriptionCDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2, dose-dependently increases the Vmax of SERCA2 Ca2+-ATPase activity in ER microsomes; increases Ca2+-ATPase activity and significantly enhances Ca2+ uptake into the ER, attenuates H2O2-stimulated cell death in HEK cells; improves glucose homeostasis and metabolic parameters, increases glucose tolerance in ob/ob mice; CDN1163 reduces lipid accumulation and decreases lipogenesis in obese mice livers.
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In VitroCDN1163 (10μM; 24 hours; rat cardiac myocyte cells) treatment reduces high glucose-induced resistin and nuclear NFATc expression and increases the phosphorylation of AMPKα in a time-dependent manner. Western Blot Analysis Cell Line:Rat cardiac myocyte cells (H9c2)Concentration:10?μM Incubation Time:24 hours Result:High glucose-induced resistin and nuclear NFATc expression are significantly reduced. The phosphorylation of AMPKα is increased in a time-dependent manner.
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In VivoCDN1163 (50 mg/kg; intraperitoneal injection; for 5 days; male ob/ob mice and lean ob/+ mice) increases SERCA2 Ca2+-ATPase activity, decreases endoplasmic reticulum (ER) stress-induced cell death in vitro and improves liver Ca2+ transport activity. CDN1163 reduces blood glucose levels and improves metabolic parameters and gluconeogenic gene expression, reverses hepatic steatosis, inhibits ER stress and ER stress-induced apoptosis, and improves mitochondrial efficiency in ob/ob mice in vivo. Animal Model:Male 8-10-week old ob/ob mice and lean ob/+ mice Dosage:50 mg/kg Administration:Intraperitoneal injection; for 5 days Result:Markedly lowered fasting blood glucose, improved glucose tolerance, and ameliorated hepatosteatosis but did not alter glucose levels or body weight. Increased expression of uncoupling protein 1 (UCP1) and UCP3 in brown adipose tissue and reduced the hepatic expression of genes involved in gluconeogenesis and lipogenesis, attenuated ER stress response and ER stress-induced apoptosis, and improved mitochondrial biogenesis, possibly through SERCA2-mediated activation of AMP-activated protein kinase pathway.
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SynonymsCDN 1163 | CDN-1163
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PathwayGPCR/G Protein
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TargetCalcium Channel
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RecptorCalcium Channel
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Research Area——
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Indication——
Chemical Information
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CAS Number892711-75-0
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Formula Weight320.392
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Molecular FormulaC20H20N2O2
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Purity>98% (HPLC)
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SolubilityDMSO : 50 mg/mL 156.06 mM; H2O : < 0.1 mg/mL
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SMILESO=C(NC1=C2N=C(C)C=CC2=CC=C1)C3=CC=C(OC(C)C)C=C3
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Chemical Name4-(1-Methylethoxy)-N-(2-methyl-8-quinolinyl)benzamide
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Krajnak K, et al. Bioorg Med Chem Lett. 2018 May 15;28(9):1591-1594.
2. Kang S, et al. J Biol Chem. 2016 Mar 4;291(10):5185-98.
3. Dahl R. Bioorg Med Chem. 2017 Jan 1;25(1):53-57.
4. Cornea RL, et al. J Biomol Screen. 2013 Jan;18(1):97-107.
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