Orforglipron (Synonyms: LY3502970; GLP-1 receptor agonist 1)
目录号: PL02012 纯度: ≥98%
CAS No. :2212020-52-3
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中文名称
Orforglipron
英文名称
Orforglipron
英文别名
GLP-1 receptor agonist 1;3-[(1S,2S)-1-[5-[(4S)-2,2-Dimethyloxan-4-yl]-2-[(4S)-2-(4-fluoro-3,5-dimethylphenyl)-3-[3-(4-fluoro-;3-[(1S,2S)-1-[5-[(4S)-2,2-Dimethyloxan-4-yl]-2-[(4S)-2-(4-fluoro-3,5-dimethylphenyl)-3-[3-(4-fluoro-1-methylindazol-5-yl)-2-oxoimidazol-1-yl]-4-methyl-6,7-dihydro-4H-pyrazolo[4,3-c]pyridine-5-carbonyl]indol-1-yl]-2-methylcyclopropyl]-1,2,4-oxadiazolidin-5-one
Cas No.
2212020-52-3
分子式
C48H50F2N10O5
分子量
884.97
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Orforglipron (LY3502970) (GLP-1 receptor agonist 1) 是一种胰高血糖素样肽 (GLP-1) 受体激动剂,详细信息请参考专利文献 WO2018056453A1 中的化合物 67。
生物活性
Orforglipron (LY3502970) (GLP-1 receptor agonist 1) is a GLP-1 receptor agonist extracted from patent WO2018056453A1, Compound 67.
性状
Solid
IC50 & Target[1][2]
GLP-1 receptor
体外研究(In Vitro)
Orforglipron is an incretin secreted from L cells of the small intestine when nutrients pass through the digestive tract, and glucose is transmitted via the GLP-1 receptor. Orforglipron exhibits various actions such as dependent gastric emptying delay, and feeding suppression. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Pyrazolopyridine derivative having glp-1 receptor agonist effect. WO2013046136A1.
[2]. Kawai T, Sun B, Yoshino H, et al. Structural basis for GLP-1 receptor activation by LY3502970, an orally active nonpeptide agonist. Proc Natl Acad Sci U S A. 2020;117(47):29959-29967.
溶解度数据
In Vitro: DMSO : 100 mg/mL (113.26 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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