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MBX-2982

    
≥98%

MBX-2982

源葉(MedMol)
S81786 一鍵復制產(chǎn)品信息
1037792-44-1
C22H24N8OS
448.54
MBX 2982; UNII-B5TRY67L51; CS-0745;
貨號 規(guī)格 價格 上海 北京 武漢 南京 購買數(shù)量
S81786-5mg ≥98% ¥457.00 10 - - -
S81786-10mg ≥98% ¥800.00 10 - - -
S81786-25mg ≥98% ¥1640.00 10 - - -
S81786-50mg ≥98% ¥2200.00 4 - - -
產(chǎn)品介紹 參考文獻 質(zhì)檢證書(COA) 摩爾濃度計算器 相關產(chǎn)品

產(chǎn)品介紹

MBX-2982 is a selective, orally-available G protein-coupled receptor 119 (GPR119) agonist.

產(chǎn)品描述: MBX-2982 is a selective, orally-available G protein-coupled receptor 119 (GPR119) agonist.
靶點: GPR119;GPR
體內(nèi)研究: To examine whether the observations in GLUTag and the primary intestinal cells has physiological relevance, C57BL/6 mice are treated with the GPR119 agonist MBX-2982 at a dose of 10 mg/kg. Note that in order to examine a direct GPR119 effect, no DPP-IV inhibitor is co-administered in this experiment, but a DPP-IV inhibitor is used to preserve active GLP-1 in the blood samples. The plasma GLP-1 levels from the mice dosed with MBX-2982 are increased without a glucose load, indicating that GPR119-mediated GLP-1 secretion is not dependent on glucose
參考文獻: 1. Hothersall JD, et al. Sustained wash-resistant receptor activation responses of GPR119 agonists. Eur J Pharmacol. 2015 Sep 5;762:430-42. 2. Lan H, et al. Agonists at GPR119 mediate secretion of GLP-1 from mouse enteroendocrine cells through glucose-independent pathways. Br J Pharmacol. 2012 Apr;165(8):2799-807. 3. Yang JW, et al. GPR119: a promising target for nonalcoholic fatty liver disease. FASEB J. 2016 Jan;30(1):324-35.
溶解性: Soluble  in  DMSO
保存條件: -20℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 2.229 ml 11.147 ml 22.295 ml
5 mM 0.446 ml 2.229 ml 4.459 ml
10 mM 0.223 ml 1.115 ml 2.229 ml
50 mM 0.045 ml 0.223 ml 0.446 ml
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參考文獻

質(zhì)檢證書(COA)

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摩爾濃度計算器

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