The chemical substance known as (4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)methyl beta-D-allopyranoside, with the CAS number 29010-56-8, is a glycoside derivative of anthraquinone. This compound features a complex structure that includes an anthracene core substituted with hydroxyl and carbonyl functional groups, contributing to its potential reactivity and biological activity. The presence of the beta-D-allopyranoside moiety indicates that it is a sugar derivative, which may enhance its solubility and interaction with biological systems. Such compounds are often studied for their potential applications in pharmaceuticals, particularly due to their ability to interact with biological targets. The hydroxyl groups can participate in hydrogen bonding, influencing the compound's solubility and stability. Additionally, the dioxo groups may contribute to redox activity, making it of interest in studies related to oxidative stress and cellular signaling. Overall, this compound exemplifies the intersection of organic chemistry and biochemistry, with implications for drug development and therapeutic applications.

Aloe-emodin-glucoside is a stimulant-laxative which has been shown to enhance colonic membrane permeability of water-soluble and poorly permeable compounds.

(4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)methyl beta-D-allopyranoside

29010-56-8: The chemical substance known as (4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)methyl beta-D-allopyranoside, with the CAS number 29010-56-8, is a glycoside derivative of anthraquinone. This compound features a complex structure that includes an anthracene core substituted with hydroxyl and carbonyl functional groups, contributing to its potential reactivity and biological activity. The presence of the beta-D-allopyranoside moiety indicates that it is a sugar derivative, which may enhance its solubility and interaction with biological systems. Such compounds are often studied for their potential applications in pharmaceuticals, particularly due to their ability to interact with biological targets. The hydroxyl groups can participate in hydrogen bonding, influencing the compound's solubility and stability. Additionally, the dioxo groups may contribute to redox activity, making it of interest in studies related to oxidative stress and cellular signaling. Overall, this compound exemplifies the intersection of organic chemistry and biochemistry, with implications for drug development and therapeutic applications.

CAS 29010-56-8

(4,5-dihydroxy-9,10-dioxo-9,10-dihydroanthracen-2-yl)methyl beta-D-allopyranoside

Aloe-emodin-glucoside

Ref: BP-BP3954