The chemical substance known as "(2R,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside," with the CAS number 80443-12-5, is a complex organic compound characterized by its polyphenolic structure, which includes a chromenone core and a sugar moiety. This compound features multiple hydroxyl groups, contributing to its potential antioxidant properties and biological activity. The presence of the 6-deoxy-alpha-L-mannopyranoside unit suggests that it may exhibit glycosidic characteristics, influencing its solubility and interaction with biological systems. The stereochemistry indicated by the (2R,3R) configuration is crucial for its biological function, as it may affect the compound's binding affinity to various biological targets. Overall, this substance may be of interest in pharmacological research, particularly in the context of its potential health benefits and applications in natural product chemistry. Further studies would be necessary to elucidate its specific biological activities and mechanisms of action.

(2R,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside

80443-12-5: The chemical substance known as "(2R,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside," with the CAS number 80443-12-5, is a complex organic compound characterized by its polyphenolic structure, which includes a chromenone core and a sugar moiety. This compound features multiple hydroxyl groups, contributing to its potential antioxidant properties and biological activity. The presence of the 6-deoxy-alpha-L-mannopyranoside unit suggests that it may exhibit glycosidic characteristics, influencing its solubility and interaction with biological systems. The stereochemistry indicated by the (2R,3R) configuration is crucial for its biological function, as it may affect the compound's binding affinity to various biological targets. Overall, this substance may be of interest in pharmacological research, particularly in the context of its potential health benefits and applications in natural product chemistry. Further studies would be necessary to elucidate its specific biological activities and mechanisms of action.

<p>AChE/BChE-IN-11, natural from artichoke leaves, inhibits AChE and BChE (IC50: 70/71 μM) for Alzheimer's research.</p>

CAS 80443-12-5

(2R,3R)-5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 6-deoxy-alpha-L-mannopyranoside

AChE/BChE-IN-11

Ref: TM-T75544