Flavonoids

Natural glycoside

4,7-Dihydroxy-2'-methoxyisoflavan is a naturally occurring isoflavan compound, which is typically extracted from various plant sources known for their medicinal properties. These sources include legumes and other plant families rich in phytoestrogens and related secondary metabolites. As an isoflavan, 4,7-Dihydroxy-2'-methoxyisoflavan exhibits significant antioxidant activity. This mode of action involves the scavenging of free radicals and reduction of oxidative stress within biological systems, potentially inhibiting cellular damage caused by reactive oxygen species. Its chemical structure allows it to interact with target molecules in a way that neutralizes these reactive species, thereby contributing to cellular protection. The uses and applications of 4,7-Dihydroxy-2'-methoxyisoflavan are of considerable interest in the fields of pharmacology and nutraceuticals, particularly regarding its potential role in the prevention and treatment of diseases linked to oxidative stress, such as cardiovascular diseases and certain types of cancer. Additionally, its presence in plant-derived foods or supplements makes it a subject of study for its benefits in human health and disease prevention.

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

From seeds of Karanja tree; insecticidal, acaricidal & fungicidal properties

5,2',3'-Trimethoxyflavanone is a specialized methoxyflavanone, which is a derivative of flavanone compounds. This compound is typically sourced from naturally occurring flavonoids found in various plant species. Its structure incorporates methoxy groups that contribute to its distinct chemical properties and potential biological activity. The mode of action of 5,2',3'-Trimethoxyflavanone involves modulation of various biochemical pathways. These mechanisms can include antioxidant activity, enzyme inhibition, or interactions with specific receptors in biological systems, contributing to its utility in scientific research. Due to these interactions, it holds potential for investigation in various bioactivities and pharmacological responses. The uses and applications of 5,2',3'-Trimethoxyflavanone are predominantly centered around research on its biochemical properties and effects. Scientists explore its possible roles in the study of cellular processes, potential therapeutic effects, and as a tool in understanding flavonoid-related pathways. Its value lies in contributing to the broader understanding of flavonoid function and the development of applications in health, medicine, and biotechnology.

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

5,2'-Dihydroxyflavone is a type of flavonoid, which is a class of polyphenolic compounds. These compounds are predominantly found in various plants, serving as part of their secondary metabolites. As a natural phytochemical, 5,2'-Dihydroxyflavone has garnered attention for its potential bioactive properties, particularly in the realm of neuroprotection. The compound's mode of action involves its ability to interact with a range of cellular pathways, including the modulation of enzyme activity and receptor binding. This includes potential antioxidant activity, which helps in mitigating oxidative stress by scavenging free radicals. Additionally, its potential to influence neurotrophic pathways suggests it may be beneficial in neuroprotection and neuroplasticity. Applications of 5,2'-Dihydroxyflavone span across various fields of research, particularly in the study of neurological disorders and cellular oxidative stress. Its ability to affect neuronal pathways makes it a subject of interest in exploring therapeutic avenues for conditions such as Alzheimer's disease, Parkinson's disease, and other neurodegenerative disorders. Although in vitro and in vivo studies continue to explore its efficacy, the compound remains a notable candidate for understanding the broader implications of flavonoids in health and disease management.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

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

Sinocrassoside C1 is a cycloartane triterpenoid, which is a class of chemical compounds. It is derived from the plant genus Sinocrassula, known for its traditional medicinal applications. The mode of action of Sinocrassoside C1 involves interactions with specific cellular targets, potentially influencing signal transduction pathways and modulating enzyme activities. These interactions may account for its reported bioactivities, including anti-inflammatory, anti-tumor, and neuroprotective effects. Research into Sinocrassoside C1 is centered on its potential applications in pharmacology, particularly its ability to inhibit certain cancer cell lines and reduce inflammation in animal models. Its potential as a lead compound for drug development underscores the interest in its comprehensive biological characterization and mechanism elucidation. Extensive studies are ongoing to further determine its therapeutic efficacy and safety profile. Scientists are particularly interested in its molecular interactions and potential for synergy with other compounds, aiming to leverage its properties in developing novel therapeutic agents.

2'-Methoxyflavone analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.