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2083618-79-3

中文名稱 化合物 PDZ1I
英文名稱 1H-Cyclopenta[d][1,2,4]triazolo[1,5-a]pyrimidine-2-carboxamide, N-[2,5-dimethyl-4-[[1-oxo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)propyl]amino]phenyl]-5,6,7,8-tetrahydro-8-oxo-
CAS 2083618-79-3
分子式 C28H26N8O4
分子量 538.56
MOL 文件 2083618-79-3.mol
更新日期 2024/12/05 21:11:27
2083618-79-3 結構式 2083618-79-3 結構式

基本信息

中文別名
化合物 PDZ1I
英文別名
PDZ1i
1H-Cyclopenta[d][1,2,4]triazolo[1,5-a]pyrimidine-2-carboxamide, N-[2,5-dimethyl-4-[[1-oxo-3-(5-phenyl-1,3,4-oxadiazol-2-yl)propyl]amino]phenyl]-5,6,7,8-tetrahydro-8-oxo-

物理化學性質

密度1.53±0.1 g/cm3(Predicted)
酸度系數(shù)(pKa)10.11±0.70(Predicted)
形態(tài)Solid
顏色White to off-white

應用領域

用途一
PDZ1i, also known as 113B7, is an inhibitor of MDA-9/Syntenin activity. PDZ1i radiosensitized GBM cells. PDZ1i inhibited crucial GBM signaling involving FAK and mutant EGFR, EGFRvIII, and abrogated gains in secreted proteases, MMP-2 and MMP-9, following radiation. In an in vivo glioma model, PDZ1i resulted in smaller, less invasive tumors and enhanced survival. When combined with radiation, survival gains exceeded radiotherapy alone.
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