The chemical substance known as "8H-Purin-8-one, 7,9-dihydro-7-methyl-2-[(7-methyl-6-quinoxalinyl)amino]-9-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-" with CAS number 2719736-43-1 is a complex organic compound characterized by its purine structure, which is a fundamental component of nucleic acids. This compound features multiple functional groups, including a quinoxaline moiety and a bicyclic structure, contributing to its potential biological activity. The presence of nitrogen atoms in the purine and quinoxaline rings suggests possible interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound's unique bicyclic structure may influence its pharmacokinetic properties, such as solubility and permeability. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and its potential applications could range from pharmaceuticals to biochemical research. However, specific biological activities, toxicity, and therapeutic potential would require further investigation through experimental studies.

8H-Purin-8-one, 7,9-dihydro-7-methyl-2-[(7-methyl-6-quinoxalinyl)amino]-9-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-

2719736-43-1: The chemical substance known as "8H-Purin-8-one, 7,9-dihydro-7-methyl-2-[(7-methyl-6-quinoxalinyl)amino]-9-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-" with CAS number 2719736-43-1 is a complex organic compound characterized by its purine structure, which is a fundamental component of nucleic acids. This compound features multiple functional groups, including a quinoxaline moiety and a bicyclic structure, contributing to its potential biological activity. The presence of nitrogen atoms in the purine and quinoxaline rings suggests possible interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound's unique bicyclic structure may influence its pharmacokinetic properties, such as solubility and permeability. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and its potential applications could range from pharmaceuticals to biochemical research. However, specific biological activities, toxicity, and therapeutic potential would require further investigation through experimental studies.

<p>DNA-PK-IN-5: potent DNA-PK inhibitor, reduces tumor repair, induces apoptosis, enhances radiotherapy, overcomes resistance.</p>

CAS 2719736-43-1

8H-Purin-8-one, 7,9-dihydro-7-methyl-2-[(7-methyl-6-quinoxalinyl)amino]-9-(8-oxa-3-azabicyclo[3.2.1]oct-3-yl)-

DNA-PK-IN-5

Ref: TM-T62191