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Dapagliflozin (2S)-1,2-propanediol hydrate

CAS No. 960404-48-2

Dapagliflozin (2S)-1,2-propanediol hydrate( BMS-512148 | BMS512148 | BMS 512148 )

Catalog No. M16859 CAS No. 960404-48-2

A potent, selective, orally active hSGLT2 inhibitor with EC50 of 1.12 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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5MG 39 In Stock
10MG 55 In Stock
25MG 67 In Stock
50MG 84 In Stock
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500MG 255 In Stock
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Biological Information

  • Product Name
    Dapagliflozin (2S)-1,2-propanediol hydrate
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective, orally active hSGLT2 inhibitor with EC50 of 1.12 nM.
  • Description
    A potent, selective, orally active hSGLT2 inhibitor with EC50 of 1.12 nM; displays >300-fold selectivity over hSGLT1 (EC50=330 nM), highly selectivity versus GLUT transporters; also is a potent selective inhibitor of rSGLT2 (EC50=3 nM), with 200-fold selectivity versus rSGLT1; significantly improves glucose homeostasis, reduces blood glucose levels in hyperglycemic streptozotocin (STZ) rats.Diabetes Approved(In Vitro):Dapagliflozin ((2S)-1,2-propanediol, hydrate) (0-10 μM; 24 hours) significantly increases the cell survival in hypoxic HK2 cell in a dose-dependent manner.Dapagliflozin ((2S)-1,2-propanediol, hydrate) (0-10 μM; 2 hours) increases the HIF1 expression, increases AMPK and EKR phosphorylation in hypoxic HK2 cells, but shows no effect on the phosphorylation of AMPK and ERK in normoxic HK2 cells.
  • In Vitro
    Dapagliflozin ((2S)-1,2-propanediol, hydrate) (0-10 μM; 24 hours) significantly increases the cell survival in hypoxic HK2 cell in a dose-dependent manner.Dapagliflozin ((2S)-1,2-propanediol, hydrate) (0-10 μM; 2 hours) increases the HIF1 expression, increases AMPK and EKR phosphorylation in hypoxic HK2 cells, but shows no effect on the phosphorylation of AMPK and ERK in normoxic HK2 cells. Cell Viability Assay Cell Line:Hypoxic HK2 cell Concentration:0 μM, 1 μM, 2 μM, 5 μM, 10 μM Incubation Time:24 hours Result:Improved the cell viability in a dose-dependent manner compared with control cells.Western Blot Analysis Cell Line:Hypoxic HK2 cell, Normoxic HK2 cells Concentration:0 μM, 1 μM, 2 μM, 5 μM, 10 μM Incubation Time:24 hours Result:Induced HIF1 expression in hypoxic and normoxic HK2 cells.
  • In Vivo
    ——
  • Synonyms
    BMS-512148 | BMS512148 | BMS 512148
  • Pathway
    GPCR/G Protein
  • Target
    SGLT
  • Recptor
    SGLT2
  • Research Area
    Metabolic Disease
  • Indication
    Diabetes

Chemical Information

  • CAS Number
    960404-48-2
  • Formula Weight
    502.9823
  • Molecular Formula
    C24H35ClO9
  • Purity
    >98% (HPLC)
  • Solubility
    10 mM in DMSO
  • SMILES
    CCOC1=CC=C(C=C1)CC2=C(C=CC(=C2)C3C(C(C(C(O3)CO)O)O)O)Cl.CC(CO)O.O
  • Chemical Name
    D-Glucitol, 1,5-anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-, (1S)-, compd. with (2S)-1,2-propanediol, hydrate (1:1:1)

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Meng W, et al. J Med Chem. 2008 Mar 13;51(5):1145-9. 2. Han S, et al. Diabetes. 2008 Jun;57(6):1723-9. 3. Wilson C. Nat Rev Endocrinol. 2010 Oct;6(10):531. 4. Komoroski B, et al. Clin Pharmacol Ther. 2009 May;85(5):513-9.
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