9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4

9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4 is a stable isotope labeled compound that is commonly used in research laboratories for various purposes. This compound is a highly specialized derivative of 9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole, a heterocyclic organic molecule that is structurally related to indole and pyridine. The addition of four deuterium atoms to this molecule allows for more accurate and precise analysis in research applications. One of the main uses of 9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4 is in drug metabolism and pharmacokinetic studies. By using this labeled compound, researchers can track the movement and breakdown of drugs in the body with greater accuracy. This information can be used to optimize drug dosing and minimize potential side effects. In addition to its use in drug metabolism studies, 9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4 is also used in research on the mechanisms of DNA damage and repair. The compound has been shown to interact with DNA and induce damage, making it a valuable tool in studying these processes. Chemically, 9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4 is a heterocyclic compound with a molecular formula of C16H10D4N3. It has a molecular weight of 246.33 g/mol and a melting point of 205-210°C. The compound is soluble in organic solvents such as methanol and dimethyl sulfoxide. Overall, the use of 9-(4’-Aminophenyl)-9H-pyrido[3,4-b]indole-d4 in research applications is a valuable tool for understanding drug metabolism and DNA damage and repair mechanisms. Its stable isotope labeling allows for more accurate analysis and its unique chemical properties make it an important compound in the field of organic chemistry.