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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 58 In Stock
2MG 33 In Stock
5MG 52 In Stock
10MG 85 In Stock
25MG 155 In Stock
50MG 245 In Stock
100MG 398 In Stock
200MG 579 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CDN1163
  • Note
    Research use only, not for human use.
  • Brief Description
    CDN1163 (CDN-1163) is a small molecule, allosteric activator of SERCA2.
  • Description
    CDN1163 (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.
  • In Vitro
    CDN1163 (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.
  • In Vivo
    CDN1163 (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.
  • Synonyms
    CDN 1163 | CDN-1163
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    892711-75-0
  • Formula Weight
    320.392
  • Molecular Formula
    C20H20N2O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO : 50 mg/mL 156.06 mM; H2O : < 0.1 mg/mL
  • SMILES
    O=C(NC1=C2N=C(C)C=CC2=CC=C1)C3=CC=C(OC(C)C)C=C3
  • Chemical Name
    4-(1-Methylethoxy)-N-(2-methyl-8-quinolinyl)benzamide

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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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