Bioactivity | Danuglipron (PF-06882961) tromethamine is an orally active glucagon-like peptide-1 receptor (GLP-1R) agonist. Danuglipron tromethamine has the potential for type 2 diabetes research[1][2]. |
Invitro | Danuglipron (PF-06882961) tromethamine 在 cAMP 和 βArr 通路上均显示出激动剂活性。Danuglipron 是 CS cAMP 测定中的完全激动剂(EC50 为 13 nM)。Danuglipron tromethamine 是募集 βArr2 的部分激动剂(EC50 为 490 nM)[1]。 MCE has not independently confirmed the accuracy of these methods. They are for reference only. 0 --> Danuglipron tromethamine 相关抗体: |
In Vivo | Danuglipron(PF-06882961;10 mg/kg;口服;单剂量)tromethamine 可降低 hGLP-1R 小鼠模型腹膜内葡萄糖耐量试验 (IPGTT) 后的血糖水平[2]。Danuglipron 在雄性 Wistar 大鼠和雄性食蟹猴体内的药代动力学参数[1]。1.19 Species |
CAS | 2230198-03-3 |
Formula | C35H41FN6O7 |
Molar Mass | 676.73 |
Transport | Room temperature in continental US; may vary elsewhere. |
Storage | Please store the product under the recommended conditions in the Certificate of Analysis. |
Reference | [1]. David A Griffithm, et al. A Small-Molecule Oral Agonist of the Human Glucagon-like Peptide-1 Receptor. J Med Chem. 2022 Jun 23;65(12):8208-8226. [2]. W. GUO, et al. Preclinical pharmacology of low molecular weight GLP-1 receptor agonist XW014. |