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Vildagliptin

CAS No. 274901-16-5

Vildagliptin ( LAF-237 )

产品货号. M13841 CAS No. 274901-16-5

维格列汀(Vildagliptin),原名LAF237,是新型二肽基肽酶4(DPP-4)抑制剂类药物的新型口服抗高血糖药(抗糖尿病药)。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥282 有现货
10MG ¥468 有现货
25MG ¥714 有现货
50MG ¥927 有现货
100MG ¥1251 有现货
500MG ¥2601 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥360 有现货

生物学信息

  • 产品名称
    Vildagliptin
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    维格列汀(Vildagliptin),原名LAF237,是新型二肽基肽酶4(DPP-4)抑制剂类药物的新型口服抗高血糖药(抗糖尿病药)。
  • 产品描述
    Vildagliptin, previously identified as LAF237, is a new oral anti-hyperglycemic agent (anti-diabetic drug) of the new dipeptidyl peptidase-4 (DPP-4) inhibitor class of drugs. Vildagliptin inhibits the inactivation of GLP-1 and GIP by DPP-4, allowing GLP-1 and GIP to potentiate the secretion of insulin in the beta cells and suppress glucaon release by the alpha cells of the islets of Langerhans in the pancreas. It is currently in clinical trials in the U.S. and has been shown to reduce hyperglycemia in type 2 diabetes mellitus. While the drug is still not approved for use in the US, it was approved in Feb 2008 by European Medicines Agency for use within the EU and is listed on the Australian PBS with certain restrictions. (In Vitro):Vildagliptin promotes beta cell survival by inhibiting cell apoptosis. Vildagliptin also promotes cell proliferation.(In Vivo):Vildagliptin (35 mg/kg; once daily by oral gavage) increases plasma active GLP-1 levels in islets of db/db mice.Vildagliptin (10 μmol/kg; orally) significantly decreases glucose excursions and stimulate insulin secretion in obese male Zucker rats.
  • 体外实验
    Vildagliptin promotes beta cell survival by inhibiting cell apoptosis. Vildagliptin also promotes cell proliferation.
  • 体内实验
    Vildagliptin (35 mg/kg; once daily by oral gavage) increases plasma active GLP-1 levels in islets of db/db mice.Vildagliptin (10 μmol/kg; orally) significantly decreases glucose excursions and stimulate insulin secretion in obese male Zucker rats. Animal Model:Male db/db mice (BKS) and wildtype mice Dosage:35 mg/kg Administration:Oral gavage; once daily; for 6 weeks Result:Increased plasma active GLP-1 levels (22.63±1.19 vs. 11.69±0.44).Animal Model:Obese male Zucker rats Dosage:10 μmol/kg (Pharmacokinetic Analysis)Administration:Orally Result:Significantly decreased glucose excursions and stimulate insulin secretion.
  • 同义词
    LAF-237
  • 通路
    Metabolic Enzyme/Protease
  • 靶点
    DPP
  • 受体
    DPP-4
  • 研究领域
    Metabolic Disease
  • 适应症
    ——

化学信息

  • CAS Number
    274901-16-5
  • 分子量
    303.4
  • 分子式
    C17H25N3O2
  • 纯度
    >98% (HPLC)
  • 溶解度
    Ethanol: 60 mg/mL (197.75 mM); Water: 60 mg/mL (197.75 mM); DMSO: 60 mg/mL (197.75 mM)
  • SMILES
    N#C[C@H]1N(C(CN[C@@]23C[C@@]4(O)C[C@](C3)([H])C[C@@](C4)([H])C2)=O)CCC1
  • 化学全称
    (S)-1-(2-(((1s,3R,5R,7S)-3-hydroxyadamantan-1-yl)amino)acetyl)pyrrolidine-2-carbonitrile

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Villhauer EB, et al. J Med Chem, 2003, 46(13), 2774-2789.
产品手册
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