The chemical substance with the name "7-(2-{[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione - 7-(2-{[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione (1:1)" and CAS number 8004-31-7 is a complex organic compound characterized by its purine structure, which includes multiple functional groups such as amino, hydroxy, and methyl groups. This compound is likely to exhibit properties typical of purine derivatives, including potential biological activity, as purines are fundamental components of nucleic acids and play critical roles in cellular processes. The presence of hydroxy groups suggests it may have enhanced solubility in polar solvents and could participate in hydrogen bonding. Additionally, the stereochemistry indicated by the (1S,2R) configuration may influence its interaction with biological targets, potentially affecting its pharmacological profile. Overall, this compound's intricate structure suggests it may have applications in medicinal chemistry or biochemistry, although specific biological activities would require further investigation.

7-(2-{[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione - 7-(2-{[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione (1:1)

8004-31-7: The chemical substance with the name "7-(2-{[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione - 7-(2-{[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione (1:1)" and CAS number 8004-31-7 is a complex organic compound characterized by its purine structure, which includes multiple functional groups such as amino, hydroxy, and methyl groups. This compound is likely to exhibit properties typical of purine derivatives, including potential biological activity, as purines are fundamental components of nucleic acids and play critical roles in cellular processes. The presence of hydroxy groups suggests it may have enhanced solubility in polar solvents and could participate in hydrogen bonding. Additionally, the stereochemistry indicated by the (1S,2R) configuration may influence its interaction with biological targets, potentially affecting its pharmacological profile. Overall, this compound's intricate structure suggests it may have applications in medicinal chemistry or biochemistry, although specific biological activities would require further investigation.

<p>Acrinor is a adrenergic beta receptor agonist.</p>

CAS 8004-31-7

7-(2-{[(1S,2R)-2-hydroxy-1-methyl-2-phenylethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione - 7-(2-{[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino}ethyl)-1,3-dimethyl-3,7-dihydro-1H-purine-2,6-dione (1:1)

Acrinor

Ref: TM-T25003