The chemical substance with the name "[3,5-dihydroxy-2-methyl-6-(sulfanylmethyl)phenyl]carbonyl (3R)-3-hydroxy-L-prolyl-L-seryl-3-thioxo-L-alanyl-N-L-alanyl-L-alaninate" and CAS number "161161-54-2" is a complex organic compound characterized by its multi-functional groups, including hydroxyl, thio, and carbonyl moieties. This compound features a phenolic structure with dihydroxy substitutions, which can contribute to its potential antioxidant properties. The presence of sulfur in the sulfanylmethyl group suggests possible reactivity and interactions with other biomolecules, potentially influencing its biological activity. Additionally, the compound contains several amino acid residues, indicating that it may play a role in peptide synthesis or biological processes. Its stereochemistry, particularly the (3R) configuration, implies specific spatial arrangements that can affect its interaction with biological targets. Overall, this compound's unique structural features may confer specific pharmacological properties, making it of interest in medicinal chemistry and biochemistry research. Further studies would be necessary to elucidate its precise biological functions and potential applications.

[3,5-dihydroxy-2-methyl-6-(sulfanylmethyl)phenyl]carbonyl (3R)-3-hydroxy-L-prolyl-L-seryl-3-thioxo-L-alanyl-N-L-alanyl-L-alaninate

161161-54-2: The chemical substance with the name "[3,5-dihydroxy-2-methyl-6-(sulfanylmethyl)phenyl]carbonyl (3R)-3-hydroxy-L-prolyl-L-seryl-3-thioxo-L-alanyl-N-L-alanyl-L-alaninate" and CAS number "161161-54-2" is a complex organic compound characterized by its multi-functional groups, including hydroxyl, thio, and carbonyl moieties. This compound features a phenolic structure with dihydroxy substitutions, which can contribute to its potential antioxidant properties. The presence of sulfur in the sulfanylmethyl group suggests possible reactivity and interactions with other biomolecules, potentially influencing its biological activity. Additionally, the compound contains several amino acid residues, indicating that it may play a role in peptide synthesis or biological processes. Its stereochemistry, particularly the (3R) configuration, implies specific spatial arrangements that can affect its interaction with biological targets. Overall, this compound's unique structural features may confer specific pharmacological properties, making it of interest in medicinal chemistry and biochemistry research. Further studies would be necessary to elucidate its precise biological functions and potential applications.

<p>GR 122222X is an inhibitor of topoisomerase II.</p>

CAS 161161-54-2

[3,5-dihydroxy-2-methyl-6-(sulfanylmethyl)phenyl]carbonyl (3R)-3-hydroxy-L-prolyl-L-seryl-3-thioxo-L-alanyl-N-L-alanyl-L-alaninate

GR 122222X

Ref: TM-T24100