Flavonoids

5,7-Diacetoxy-8-methoxyflavone is derived from the roots of Scutellaria baicalensis and inhibits cAMP phosphodiesterase.

7,2'-Dibenzyloxy-8,4'-dimethoxyisoflavone is a complex flavonoid derivative, which is a synthetic isoflavone compound with potential applications in medical and biochemical research. It is derived from the modification of naturally occurring isoflavones, typically found in various plants, including soybeans. Isoflavones like this compound are of significant interest due to their estrogenic activities, as they can mimic or influence estrogen action in biological systems. The mode of action of 7,2'-Dibenzyloxy-8,4'-dimethoxyisoflavone involves binding to estrogen receptors, which can affect gene expression and cell signaling pathways. This action provides a model for understanding estrogenic interactions and the development of estrogen-related therapies. Its unique structural modifications enhance its binding affinity and selectivity, offering insights into the structural biology of receptor interactions. In terms of uses and applications, this compound is primarily utilized in research settings to study hormonal activities and potential therapeutic effects in estrogen-responsive conditions. It serves as a valuable tool in the investigation of endocrine modulation, offering a platform for developing novel therapeutics for conditions like osteoporosis, hormone-dependent cancers, and menopausal symptoms.

Scutellarin methylester is a flavonoid derivative, which is a modified form of the naturally occurring compound scutellarin. It originates from plant sources, notably from species within the *Scutellaria* genus. The modification to a methyl ester potentially increases its bioavailability and modifies its pharmacokinetic properties. The mode of action of scutellarin methylester involves several biochemical pathways. It is known to exhibit antioxidant activity, which helps in reducing oxidative stress by neutralizing free radicals. Scutellarin may also interact with various cellular signaling pathways, influencing processes such as inflammation and neuronal protection, possibly via modulating enzyme functions or receptor activities. This compound is of interest in diverse scientific fields due to its potential applications. It could serve in research focused on neuroprotection, cardiovascular health, and anti-inflammatory effects. Its ability to combat oxidative stress makes it a candidate for exploring therapies related to neurodegenerative diseases, ischemic stroke, and other conditions where oxidative damage is implicated.

Fisetin analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Oxygen-heterocyclic compound

Orobol 7,3',4'-trimethyl ether is a synthetic flavonoid compound, which is derived from the chemical modification of natural flavonoids. These modifications involve methylation, specifically at the 7, 3', and 4' positions of the flavone structure. This chemical derivation allows for enhanced stability and solubility compared to its natural counterparts. The mode of action of Orobol 7,3',4'-trimethyl ether involves the modulation of various biological pathways. As a flavonoid, it may interact with multiple cell signaling pathways, potentially affecting processes such as apoptosis, cell proliferation, and inflammation. Its methylation allows for specific binding affinities and cellular uptake, potentially enhancing its biological efficacy. In terms of uses and applications, Orobol 7,3',4'-trimethyl ether is primarily of interest in the fields of pharmacology and medicinal chemistry as a compound with potential therapeutic benefits. Research is ongoing to explore its efficacy as an anti-cancer, anti-inflammatory, and antioxidant agent. Its role in modulating cellular pathways makes it a promising candidate for drug development and a subject of study in biochemical research.

Isorhamnetin-3-O-rhamnoside analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Robinin is a flavonoid glycoside, which is a naturally occurring phytochemical compound. It is derived from plant sources, particularly within the Fabaceae family, such as Robinia pseudoacacia. The mode of action of Robinin involves its interaction with various cellular and molecular pathways, exhibiting properties such as antioxidant and anti-inflammatory effects. Robinin's uses and applications are of significant interest to researchers due to its potential therapeutic roles. It is explored in the context of cardiovascular health, as well as in the modulation of oxidative stress-related disorders. Additionally, its anti-inflammatory properties make it a candidate for studying its effects on chronic inflammatory conditions. The various biological activities of Robinin allow it to be a subject of study in pharmacognosy and therapeutic applications, though further research is needed to fully elucidate its potential benefits and mechanisms of action.

Natural glycoside

Natural glycoside