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ChemicalBook--->CAS DataBase List--->2083618-79-3

2083618-79-3

2083618-79-3 Structure

2083618-79-3 Structure
IdentificationBack Directory
[Name]

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
[Synonyms]

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-
[Molecular Formula]

C28H26N8O4
[MOL File]

2083618-79-3.mol
[Molecular Weight]

538.56
Chemical PropertiesBack Directory
[density ]

1.53±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

10.11±0.70(Predicted)
[color ]

White to off-white
Hazard InformationBack Directory
[Description]

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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