4-Aminothieno[3,2-d]pyrimidine-7-carboxylic acid is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both a thieno and a pyrimidine ring. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), contributing to its potential as a bioactive molecule. The presence of these functional groups suggests that it may exhibit acidic properties and can participate in hydrogen bonding, making it of interest in medicinal chemistry and drug design. Its molecular structure allows for various interactions with biological targets, potentially influencing its pharmacological activity. Additionally, the compound's solubility and stability can be affected by the pH of the environment, which is crucial for its application in biological systems. As a member of the thienopyrimidine family, it may also share similar properties with other compounds in this class, such as acting as an enzyme inhibitor or modulating biological pathways. Overall, 4-aminothieno[3,2-d]pyrimidine-7-carboxylic acid presents a promising scaffold for further research and development in pharmaceutical applications.

4-aminothieno[3,2-d]pyrimidine-7-carboxylic acid

1318242-98-6: 4-Aminothieno[3,2-d]pyrimidine-7-carboxylic acid is a heterocyclic organic compound characterized by its unique bicyclic structure, which incorporates both a thieno and a pyrimidine ring. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), contributing to its potential as a bioactive molecule. The presence of these functional groups suggests that it may exhibit acidic properties and can participate in hydrogen bonding, making it of interest in medicinal chemistry and drug design. Its molecular structure allows for various interactions with biological targets, potentially influencing its pharmacological activity. Additionally, the compound's solubility and stability can be affected by the pH of the environment, which is crucial for its application in biological systems. As a member of the thienopyrimidine family, it may also share similar properties with other compounds in this class, such as acting as an enzyme inhibitor or modulating biological pathways. Overall, 4-aminothieno[3,2-d]pyrimidine-7-carboxylic acid presents a promising scaffold for further research and development in pharmaceutical applications.

Thieno[3,2-d]pyrimidine-7-carboxylic acid, 4-amino-

4-Aminothieno[3,2-d]pyrimidine-7-carboxylic acid

CAS 1318242-98-6

4-aminothieno[3,2-d]pyrimidine-7-carboxylic acid

Thieno[3,2-d]pyrimidine-7-carboxylic acid, 4-amino-

Ref: IN-DA000ZSL

4-Aminothieno[3,2-d]pyrimidine-7-carboxylic acid

Ref: 54-OR73052

4-AMINO-THIENO[3,2-D]PYRIMIDINE-7-CARBOXYLIC ACID

Ref: 10-F468123