The chemical substance with the name "(2R,3S)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl]-5-methoxy-2,3-dihydro-4H-chromen-4-one" and CAS number "101236-49-1" is a flavonoid compound, characterized by its complex polyphenolic structure. This compound features multiple hydroxyl groups, which contribute to its potential antioxidant properties, making it of interest in various biological and pharmacological studies. The presence of methoxy and hydroxy substituents enhances its solubility and reactivity, while the chromenone core is indicative of its classification within the flavonoid family. Its stereochemistry, denoted by the (2R,3S) configuration, suggests specific spatial arrangements that may influence its biological activity and interactions with other molecules. This compound may exhibit various biological activities, including anti-inflammatory and anticancer properties, although specific studies would be necessary to elucidate its mechanisms of action and therapeutic potential. Overall, its structural complexity and functional groups position it as a significant candidate for further research in medicinal chemistry and natural product studies.

(2R,3S)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl]-5-methoxy-2,3-dihydro-4H-chromen-4-one

101236-49-1: The chemical substance with the name "(2R,3S)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl]-5-methoxy-2,3-dihydro-4H-chromen-4-one" and CAS number "101236-49-1" is a flavonoid compound, characterized by its complex polyphenolic structure. This compound features multiple hydroxyl groups, which contribute to its potential antioxidant properties, making it of interest in various biological and pharmacological studies. The presence of methoxy and hydroxy substituents enhances its solubility and reactivity, while the chromenone core is indicative of its classification within the flavonoid family. Its stereochemistry, denoted by the (2R,3S) configuration, suggests specific spatial arrangements that may influence its biological activity and interactions with other molecules. This compound may exhibit various biological activities, including anti-inflammatory and anticancer properties, although specific studies would be necessary to elucidate its mechanisms of action and therapeutic potential. Overall, its structural complexity and functional groups position it as a significant candidate for further research in medicinal chemistry and natural product studies.

Kushenol K is a potent and Selective Inhibitor of cGMP Phosphodiesterase 5, it also has inhibitory effects on diacylglycerol acyltransferase (DGAT).

CAS 101236-49-1

(2R,3S)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl]-5-methoxy-2,3-dihydro-4H-chromen-4-one

Kushenol K

Ref: TM-TN1843