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Dapagliflozin, 461432-26-8
  • 品牌:爱必信(absin)
  • 产地:中国
  • 货号:abs813289
  • cas:461432-26-8
  • 价格: ¥798/瓶
  • 发布日期: 2022-04-07
  • 更新日期: 2025-09-19
产品详请
产地 中国
品牌 爱必信(absin)
货号 abs813289
用途 见爱必信官网
英文名称 见爱必信官网
包装规格 5mg,5mg,5mg,10mg,10mg,10mg,50mg,50mg,50mg
纯度 >98%%
CAS编号 461432-26-8
别名 达格列净;达格列嗪;BMS-512148
是否进口

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抑制剂描述:

产品名称:Dapagliflozin

产品别名:见爱必信官网

英文别名:Dapagliflozin

靶点:SGLT

CAS:461432-26-8

纯度:>98%

外观:见爱必信官网

保存方法:Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.

描述:

Dapagliflozin是一种有效的,选择性的hSGLT2抑制剂,EC50为1.1 nM,比作用于hSGLT1选择性高1200倍。Dapagliflozin对hSGLT1不敏感,IC50是hSGLT2的1200倍。 Dapagliflozin作用于hSGLT2比Phlorizin效果高32倍。作用于hSGLT1比Phlorizin效果低4倍。

溶解性:DMSO : ≥ 100 mg/mL (244.58 mM)

体外研究:

Dapagliflozin is not sensitive to hSGLT1 with a 1200-fold IC50. Dapagliflozin is 32-fold more potent than phlorizin against hSGLT2 but 4-fold less than phlorizin against hSGLT1. Dapagliflozin is highly selective versus GLUT transporters and displays 8–9% inhibition in protein-free buffer at 20 μM and virtually no inhibition in the presence of 4% bovine serum albumin. Dapagliflozin has good permeability across Caco-2 cell membranes and is a substrate for P-glycoprotein (P-gp) but not a significant P-gp inhibitor. Dapagliflozin is stable in rat, dog, monkey, and human serum at 10 μM. Dapagliflozin shows no inhibitory responses or induction to human P450 enzymes. The in vitro metabolic pathways Dapagliflozin are glucuronidation, hydroxylation, and O-deethylation.

体内研究:Dapagliflozin reduces blood glucose levels by 55% after 0.1 mg/kg oral dose in hyperglycemic streptozotocin (STZ) rats, which is in part to the metabolic stability conferred by the C-glucoside linkage. Dapagliflozin displays a favorable absorption, distribution, metabolism, and excretion (ADME) profile and is orally bioavailable. Dapagliflozin (1 mg/kg) causes significant dose-dependent glucosuria and increase in urine volume in normal rats over 24 hours post-dose. Dapagliflozin induces increase in urine glucose and urine volume excretion at 6 hours post-dose in Zucker diabetic fatty (ZDF) rats. Dapagliflozin lowers fasting and fed glucose levels in ZDF rats even by 2 weeks of treatment, without any marker of renal or liver toxicity. Dapagliflozin significantly reduces the development of hyperglycaemia, with lowered blood glucose. Dapagliflozin could improve the insulin sensitivity, reduce β-cell mass and the development of impaired pancreatic function.

产品信息订购:

  产品货号   产品名称   规格 价格 大包装及货期
  abs813289   Dapagliflozin   5mg   798.00   立即咨询
  abs813289   Dapagliflozin   10mg   1161.00   立即咨询
  abs813289   Dapagliflozin   50mg   2787.00   立即咨询

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