
Flavonoids
Flavonoids are a group of plant metabolites with antioxidant properties that contribute to the color of fruits and flowers. They play a significant role in protecting plants from UV radiation and pathogens. Flavonoids are studied for their potential health benefits, including anti-inflammatory, antiviral, and anticancer properties. They are widely researched in the fields of pharmacology, nutrition, and molecular biology.
Subcategories of "Flavonoids"
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Rhoifolin
CAS:Rhoifolin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C27H30O14Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:578.53Panicolin
CAS:Oxygen-heterocyclic compoundFormula:C17H14O6Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:314.29Calycosin
CAS:Oxygen-heterocyclic compoundFormula:C16H12O5Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:284.275-demethylnobiletin
CAS:Oxygen-heterocyclic compoundFormula:C20H20O8Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:388.37Lupinisoflavone A
CAS:Lupinisoflavone A is a naturally occurring bioactive compound, specifically an isoflavone, which is extracted from the seeds and other parts of lupine plants. The lupine species are known for their rich phytochemical profile, which includes various bioactive compounds with potential health benefits. Lupinisoflavone A is structurally characterized by its isoflavone backbone, contributing to its diverse biological effects. The mode of action of lupinisoflavone A involves modulating various cellular pathways, including those related to anti-inflammatory and antioxidant activities. It may exert its effects by interacting with specific cellular receptors or enzymes, potentially influencing gene expression and protein synthesis, which are crucial for maintaining cellular homeostasis. Lupinisoflavone A has captured scientific interest due to its potential applications in the fields of medicine and pharmacology. It is being studied for its therapeutic potential in managing conditions such as chronic inflammation and oxidative stress-related disorders. Researchers are also exploring its role in cancer prevention and treatment, given its possible ability to inhibit tumor cell proliferation and induce apoptosis. Its diverse range of biological activities suggests that lupinisoflavone A may be a valuable candidate for developing novel therapeutic agents.Formula:C20H16O6Purity:Min. 95%Molecular weight:352.34 g/molGallocatechin
CAS:Oxygen-heterocyclic compoundFormula:C15H14O7Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:306.27Xanthohumol
CAS:Ketone with other oxygen functionsFormula:C21H22O5Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:354.4rac-Tetrahydrodaidzein
CAS:rac-Tetrahydrodaidzein is a racemic compound, which is a mixture of two enantiomers. It is derived from the reduction of the isoflavone daidzein, primarily found in soybeans and other legumes. This compound exhibits interesting pharmacological properties due to its ability to interact with estrogen receptors, functioning as a modulator of estrogenic activity. Its mode of action involves binding to these receptors, potentially influencing various estrogen-mediated physiological processes. In research contexts, rac-Tetrahydrodaidzein is studied for its potential applications in fields such as oncology, osteoporosis, and cardiovascular health. It is of particular interest in cancer research due to its potential role in modulating pathways involved in cell proliferation and apoptosis. Additionally, its influence on bone density makes it a candidate for osteoporosis studies. The cardiovascular benefits are being explored in the context of its effects on lipid profiles and vascular function, making it a multifunctional compound with diverse implications for further scientific investigation.Formula:C15H14O4Purity:Min. 95%Color and Shape:PowderMolecular weight:258.27 g/mol3',4',5,7-Tetrahydroxyflavone
CAS:Formula:C15H10O6Purity:98%Color and Shape:SolidMolecular weight:286.23635-Hydroxy-7,8-dimethoxy (2R)-flavanone-5-o-beta-D-glucopyranoside
CAS:5-Hydroxy-7,8-dimethoxy (2R)-flavanone-5-o-beta-D-glucopyranoside is a flavanone glycoside, which is a type of naturally occurring polyphenolic compound. This compound is typically derived from various plant sources, particularly those used in traditional medicine. Flavanone glycosides are known for their antioxidant properties. They act by scavenging free radicals and inhibiting oxidative stress, thereby protecting cells from damage. The specific mode of action includes interaction with cellular pathways to enhance the natural defense mechanisms against oxidative damage. The applications of 5-Hydroxy-7,8-dimethoxy (2R)-flavanone-5-o-beta-D-glucopyranoside are broad and promising in the field of biomedical research. It is studied for its potential therapeutic effects, including anti-inflammatory and anticancer properties, contributing to its consideration in drug development and nutraceuticals. As an antioxidant, it holds potential in preventing or managing oxidative stress-related diseases, making it an attractive subject for further pharmacological research and development.Formula:C23H26O10Purity:Min. 95%Molecular weight:462.40 g/mol2',5,6',7-Tetraacetoxyflavanone
CAS:2',5,6',7-Tetraacetoxyflavanone is a flavanone derivative, which is a type of flavonoid compound primarily sourced from plants, particularly citrus fruits. Its structure consists of a flavanone backbone with acetoxy groups at specific positions, which may influence its biochemical activity. Flavanones like 2',5,6',7-Tetraacetoxyflavanone are of interest in the scientific community due to their potential biological activities, including antioxidant properties. The mode of action of 2',5,6',7-Tetraacetoxyflavanone involves scavenging free radicals and modulating oxidative stress pathways, which makes it a candidate for reducing oxidative damage in cells. This activity is particularly relevant in the context of preventing cellular aging and mitigating damage induced by environmental stressors or pathogenic processes. In terms of applications, 2',5,6',7-Tetraacetoxyflavanone is studied extensively within the fields of biochemistry and pharmacology. Researchers focus on its potential use in developing therapeutic agents for diseases where oxidative stress plays a pivotal role, such as cardiovascular diseases, cancer, and neurodegenerative disorders. While still primarily in the research phase, understanding its properties could lead to advances in health-related biotechnologies.Formula:C23H20O10Purity:Min. 95%Molecular weight:456.4 g/molAmaronol A
CAS:Amaronol A analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H12O8Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:320.265,6,7,8-Tetrahydroxyflavone
CAS:5,6,7,8-Tetrahydroxyflavone is a naturally derived flavonoid, which is isolated from various plants known for their rich polyphenolic content. This compound belongs to the broader class of flavonoids, compounds renowned for their antioxidative properties. Its mode of action involves modulation of various cellular pathways, including the inhibition of oxidative stress and modulation of enzyme activities, which are critical for cellular homeostasis and protection. Research into 5,6,7,8-Tetrahydroxyflavone suggests potential applications in pharmaceutical and nutraceutical fields due to its antioxidative and anti-inflammatory properties. It may have therapeutic potential in addressing oxidative stress-related conditions and could be explored for its benefits in chronic inflammatory diseases. Within the scientific community, its role in cellular protection mechanisms presents a valuable area of research for developing strategies in combating diseases linked to oxidative damage.Purity:Min. 95%