Flavonoids

Velutin is a natural flavonoid, which is derived from the leaves of certain plant species, specifically from the Asteraceae family. This compound demonstrates a unique mode of action by modulating various signaling pathways involved in inflammation and oxidative stress. Velutin effectively inhibits the activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and reduces the expression of pro-inflammatory cytokines, contributing to its anti-inflammatory properties.

Flavanone hydrazone (FH) is a natural compound that has been found to have antiviral activity against a number of viruses, including the papilloma virus and picornavirus. The antiviral activity of FH is due to its ability to inhibit the shikimate pathway, which is required for the synthesis of aromatic amino acids from chorismate. This inhibition prevents the production of viral proteins, leading to cell death. FH also has an inhibitory effect on hepatitis C virus and leukoplakia by inhibiting fatty acid synthesis. It may also be used in the treatment of inflammatory diseases such as rheumatoid arthritis and ulcerative colitis.

5,7,3'-Trihydroxyflavone is a flavonoid compound, which is a type of polyphenolic molecule found in plants. This compound is derived from various plant sources such as fruits, vegetables, and certain herbs, where it naturally occurs as part of the plant's secondary metabolites. It exhibits several biochemical actions, predominantly due to its antioxidant properties. This involves scavenging free radicals and chelating metal ions, which contribute to oxidative stress reduction. Additionally, it may influence various signaling pathways related to cell survival and inflammation.

Kaempferol 6-C-glucoside is a flavonoid glycoside, which is a natural compound found in various plant sources, particularly in leaves and fruits. It is a type of C-glycosyl flavonoid, where the glucose moiety is bound directly to the carbon atom of the flavonoid skeleton, differentiating it from the more common O-glycosides.

7-Hydroxy-2',4'-dimethoxyisoflavone is a synthetic isoflavone, which is derived from the structural modification of natural isoflavones found in various plants, such as soybeans and other legumes. It exerts its biological activity primarily through its interaction with cellular signaling pathways related to oxidative stress and inflammation. This compound functions by modulating enzyme activity, influencing the expression of genes involved in antioxidant defenses, and suppressing pro-inflammatory cytokines.

Hispidulin-7-O-glucoside analytical standard provided with w/w absolute assay, to be used for quantitative titration.

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

Prunetin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Nepetin-7-O-glucoside analytical standard provided with w/w absolute assay, to be used for quantitative titration.

Ipriflavone analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Quercetin-3-arabinofuranoside is a flavonoid, a type of plant-derived polyphenolic compound. It is sourced from various plant species, particularly fruits, vegetables, and grains, where it functions as a secondary metabolite. This compound acts primarily through antioxidant mechanisms, neutralizing free radicals and reducing oxidative stress in biological systems. Additionally, it may interact with various cellular signaling pathways, modulating enzyme activities and gene expression.

Pinostrobin is a natural flavonoid compound, which is derived primarily from the rhizomes of plants such as the fingerroot (Boesenbergia rotunda) and various species of the Pinus genus. Its mode of action involves potent antioxidant activity, where it scavenges free radicals, thus reducing oxidative stress. Additionally, Pinostrobin exhibits antimicrobial properties by disrupting microbial cell membranes and inhibiting essential microbial enzymes.

4'-O-Methylpunctatin is a specialized natural product, classified as a methoxyflavone, which is derived from specific plant sources known for their diverse phytochemical compositions. Structurally, it is a derivative of punctatin, modified through methylation, enhancing its biological properties and stability. This compound acts through various mechanisms, primarily influencing glucose metabolism pathways. It exhibits inhibitory effects on enzymes like α-glucosidase and provides antioxidant properties that protect pancreatic β-cells from oxidative stress.

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.

Cannflavin B is a specialized flavonoid compound, which is a secondary metabolite derived from Cannabis sativa. It exhibits a distinct mode of action as a potent anti-inflammatory agent. Cannflavin B exerts its effects through the inhibition of pro-inflammatory mediators such as prostaglandins and leukotrienes. These biochemical pathways are typically linked with the cyclooxygenase (COX) and lipoxygenase (LOX) enzymes, and Cannflavin B effectively interferes with these enzymatic processes to reduce inflammation at the molecular level.

7-Hydroxy-2',4',5'-trimethoxyisoflavone is a naturally occurring flavonoid, which is commonly isolated from various plant sources, including legumes and other flavonoid-rich botanical species. This compound exhibits a unique structural configuration characterized by hydroxyl and methoxy functional groups, contributing to its notable bioactivity.

Hinokiflavone pentamethyl ether is a synthetic flavonoid derivative, which is a chemically modified compound sourced from the natural biflavonoid, hinokiflavone. It is characterized by the methylation of phenolic hydroxyl groups, enhancing its stability and solubility. This compound can be derived through organic synthesis techniques involving the catalytic methylation of hinokiflavone.

Quercetin-3-arabinoside is a flavonoid glycoside, which is a naturally occurring compound found in various plants including fruits and vegetables. It is derived from quercetin, a flavonoid widely distributed in the plant kingdom. The arabinoside component is a sugar moiety that enhances the solubility and stability of the compound. Quercetin-3-arabinoside exerts its effects through antioxidant activity, where it scavenges free radicals and chelates metal ions, thus protecting cells from oxidative stress and potential damage.

6,7-Dimethoxy-2',4'-dihydroxyisoflavone is a naturally occurring isoflavone, which is typically derived from various plant sources, such as legumes or medicinal herbs. It belongs to a class of polyphenolic compounds known for their antioxidative capabilities. This compound acts primarily by scavenging free radicals and reducing oxidative stress, thus protecting cellular structures from damage. Its mode of action involves the modulation of cellular antioxidant pathways and potential interaction with estrogen receptors, contributing to its biological effects.

4'-Methoxyflavone is a synthetic flavonoid, which is derived from modifications of naturally occurring flavonoid structures. It is synthesized through chemical processes involving the methoxylation of flavonoids, commonly found in plants. The compound exhibits its mode of action primarily through antioxidant activity. By scavenging free radicals, 4'-Methoxyflavone helps to prevent oxidative stress at the cellular level, which can damage DNA, proteins, and lipids.

7,2',4'-Tribenzyloxyisoflavone is a synthetic compound, which is a derivative of isoflavones, known for its potential role in biochemical and pharmacological research. This compound is primarily sourced through chemical synthesis involving the modification of the isoflavone structure by introducing benzyloxy groups, which alters its physicochemical properties and enhances its stability and solubility for research purposes.

3'-Benzyloxy-4',5,6,7-tetramethoxyflavone is a synthetic flavone derivative, which is structurally modified from naturally occurring flavonoids. These compounds are often sourced from various plant species or created synthetically to mimic the beneficial components found in plant matter. The mode of action of this compound primarily hinges on its ability to interact with cellular pathways due to its polyphenolic structure. Such interactions may include the inhibition of certain enzymes, modulation of receptor activities, or altering oxidative states within cells.

3,3',4',7-Tetrahydroxyflavanone is a flavanone compound, which is a type of polyphenolic molecule. This compound is primarily derived from various plant sources, where it occurs naturally in fruits, vegetables, and certain herbs. Its structure is characterized by its multiple hydroxyl groups, which contribute to its chemical reactivity and biological interactions.

7,2'-Dibenzyloxy-4'-methoxyisoflavone is a synthetic isoflavone compound, which is derived from chemical synthesis processes rather than natural sources. Isoflavones are a class of flavonoids often studied for their diverse biological activities, including antioxidant, anti-inflammatory, and potential anticancer properties. This compound is characterized by its unique chemical structure that incorporates benzyl and methoxy groups, possibly enhancing its pharmacokinetic profile and efficacy.

Silicristin is a flavonolignan compound, which is derived from the seeds of the milk thistle plant, Silybum marianum. This compound is one of the key constituents of silymarin, a complex group of flavonolignans used extensively in herbal medicine. Silicristin is isolated through advanced chromatographic techniques, ensuring high purity and specificity for research applications.

5-Methyl 7-methoxyisoflavone is a synthetic isoflavone derivative, which is typically sourced in the laboratory through chemical synthesis processes involving the modification of plant-derived isoflavones. This compound is structurally similar to certain natural flavonoids but is characterized by the addition of the methyl and methoxy groups, which are not found in its natural counterparts.

Amentoflavone is a biflavonoid compound, which is a naturally occurring substance found in various plants such as Ginkgo biloba and Hypericum perforatum. Its molecular structure consists of two flavonoid units joined together, contributing to its unique biochemical characteristics. The source of amentoflavone spans across several medicinal plants, where it plays roles in the plants’ defense mechanisms.

Vicenin III is a natural flavonoid compound, which is a type of polyphenolic metabolite commonly found in various plant species. It is primarily extracted from herbaceous plants and certain fruits and vegetables, where it acts as a secondary metabolite contributing to the plant's defense mechanisms. The compound exerts its effects through antioxidant properties, which involve scavenging free radicals and reducing oxidative stress at the cellular level. Additionally, it demonstrates anti-inflammatory activity by modulating key signaling pathways and inhibiting pro-inflammatory mediators.

8-Prenylgenistein is a prenylated isoflavone, which is a type of naturally occurring polyphenolic compound. It is primarily sourced from plants, particularly legumes, and is a derivative of genistein, an isoflavone commonly found in soy products. The addition of a prenyl group distinguishes 8-prenylgenistein from its parent compound, potentially enhancing its bioactivity and pharmacokinetics.

4'-Geranyloxyisoliquiritigenin is a prenylated chalcone, which is naturally derived from certain plants, especially those belonging to the Fabaceae family. It is a bioactive compound that emerges from the prenylation of isoliquiritigenin, a chalcone found in licorice root. This modification enhances the lipophilicity and bioavailability of the molecule.

Kaempferol 3-O-neohesperidoside is a flavonoid glycoside, which is a plant-derived secondary metabolite. It is commonly found in various fruits, vegetables, and herbs, including citrus fruits and certain medicinal plants. The compound consists of the flavonoid kaempferol linked to a neohesperidose sugar moiety.

3,3',4',5,5',8-Hexahydroxyflavone is a naturally occurring flavonoid, which is a type of polyphenolic compound. It is derived from various plant sources, including fruits, vegetables, and certain medicinal herbs. The compound is characterized by its chemical structure, which includes multiple hydroxyl groups, contributing to its biological activity.

The mode of action of 3,3',4',5,5',8-Hexahydroxyflavone involves its interaction with various cellular pathways and enzymes. Primarily, it is known for its antioxidant properties, where it scavenges free radicals and reactive oxygen species, thereby reducing oxidative stress. Additionally, it may exhibit anti-inflammatory effects by modulating signaling pathways involved in inflammation.

In terms of uses and applications, 3,3',4',5,5',8-Hexahydroxyflavone is primarily explored in scientific research focusing on its potential health benefits. Studies investigate its role in disease prevention, particularly conditions associated with oxidative stress and inflammation, such as cardiovascular diseases and neurodegenerative disorders. While it holds promise in these areas, further research is necessary to fully understand its mechanisms and therapeutic potential.

Phaseollinisoflavan is a naturally occurring isoflavone compound, which is derived from the legume plant, Phaseolus vulgaris, commonly known as the common bean. Its mode of action primarily involves the inhibition of enzymatic activity, particularly affecting pathways related to oxidative stress and various metabolic processes. This isoflavone exerts its effects by modulating signal transduction pathways, which are critical in cellular response mechanisms.

Dillenetin is a flavonoid compound, which is derived from natural plant sources, particularly found in the genus Dillenia. It exhibits significant bioactivity with a mode of action primarily involving the modulation of cell signaling pathways. Dillenetin is known to bind to specific enzymes and receptors, influencing cellular processes such as proliferation, apoptosis, and oxidative stress responses.

7-O-Methyl quercetin is a flavonoid derivative, which is a naturally occurring compound found in several plant species, often referred to as a methylated form of the flavonoid quercetin. It is primarily sourced from plants such as onion, green tea, and various berries, where it serves diverse ecological roles, including defense mechanisms against herbivores and pathogens.

Beta-Naphthoflavone is a synthetic polycyclic aromatic compound, which is a laboratory-created substance designed to mimic naturally occurring compounds. It is a model compound widely used in scientific research due to its ability to induce specific enzyme pathways. Beta-Naphthoflavone primarily affects the aryl hydrocarbon receptor (AhR) pathway. Upon binding to this receptor, it modulates the expression of genes involved in xenobiotic metabolism, particularly influencing the cytochrome P450 enzymes. These enzymes play a crucial role in the metabolism of various xenobiotics and endogenous compounds.