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Luseogliflozin hydrate (Synonyms: TS 071 hydrate)

Catalog No.GF10241

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Luseogliflozin hydrate Chemical Structure

Cas No.: 1152425-66-5

Taille Prix Stock
5mg
450,00 $US
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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products
Luseogliflozin (TS 071) hydrate is a selective potent and orally active second-generation sodium-glucose co-transporter 2 (SGLT2) inhibitor with an IC50鈥塷f鈥?.26 nM. Luseogliflozin hydrate can be used for the research of type 2 diabetes mellitus (T2DM).

Luseogliflozin can increase beta cell proliferation through the activation of the FoxM1/PLK1/CENP-A pathway via humoral factors thats act in an insulin/IGF-1 receptor-independent manner. Luseogliflozin increases beta cell proliferation in OSI-906-treated mice[2].

SGLT2 inhibition with Luseogliflozin (10 mg/kg/daily; oral gavage) significantly ameliorates hyperglycaemia, but not hyperinsulinaemia, in the OSI-906(45 mg/kg)-treated mice. Luseogliflozin ameliorates hyperglycaemia induced by OSI-906[2].

[1]. Anthony Markham,et al. Luseogliflozin: first global approval. Drugs. 2014 Jun;74(8):945-50. 

[2]. Jun Shirakawa,et al. Luseogliflozin increases beta cell proliferation through humoral factors that activate an insulin receptor- and IGF-1 receptor-independent pathway. Diabetologia. 2020 Mar;63(3):577-587. 

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