>>Signaling Pathways>> Obesity, Appetite Control & Diabetes>> Obesity>>Remogliflozin A

Remogliflozin A (Synonyms: GSK189074)

Catalog No.GC18762

레모글리플로진 A는 인간 및 쥐 SGLT2에 대해 각각 12.4 및 26nM의 Kis를 갖는 SGLT2(나트륨-포도당 공동수송체 2)의 강력하고 선택적인 억제제입니다.

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Remogliflozin A Chemical Structure

Cas No.: 329045-45-6

Size 가격 재고 수량
500μg
US$40.00
재고 있음
1mg
US$75.00
재고 있음
5mg
US$352.00
재고 있음
10mg
US$630.00
재고 있음

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products
Remogliflozin A is a potent inhibitor of sodium-glucose transporter 2 (SGLT2; Kis = 12.4 and 26 nM for human and rat SGLT2, respectively). It is selective for SGLT2 over SGLT1 (Kis = 4,520 and 997 nM for human and rat SGLT1, respectively). Following administration of a prodrug, remogliflozin etabonate, that is rapidly converted to remogliflozin A in vivo, rat urinary glucose excretion increases and plasma glucose and insulin concentrations decrease. Similar effects are observed following oral administration of remogliflozin etabonate to rats with diabetes induced by streptozotocin and db/db mice with hyperinsulinemia and obesity.

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Average Rating: 5 ★★★★★ (Based on Reviews and 38 reference(s) in Google Scholar.)

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