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 |
| 10MG | ¥316 | 有现货 |
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| 25MG | ¥405 | 有现货 |
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| 50MG | ¥494 | 有现货 |
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| 100MG | ¥689 | 有现货 |
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| 500MG | ¥948 | 有现货 |
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| 1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Vildagliptin
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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
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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)。
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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.
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体外实验Vildagliptin promotes beta cell survival by inhibiting cell apoptosis. Vildagliptin also promotes cell proliferation.
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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.
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同义词LAF-237
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通路Metabolic Enzyme/Protease
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靶点DPP
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受体DPP-4
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研究领域Metabolic Disease
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适应症——
化学信息
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CAS Number274901-16-5
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分子量303.4
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分子式C17H25N3O2
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纯度>98% (HPLC)
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溶解度Ethanol: 60 mg/mL (197.75 mM); Water: 60 mg/mL (197.75 mM); DMSO: 60 mg/mL (197.75 mM)
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SMILESN#C[C@H]1N(C(CN[C@@]23C[C@@]4(O)C[C@](C3)([H])C[C@@](C4)([H])C2)=O)CCC1
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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
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储存条件(-20℃)
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运输条件With Ice Pack
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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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