Flavonoids

A MAP kinase inhibitor 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.

(-)-Liquiritigenin analytical standard provided with w/w absolute assay, to be used for quantitative titration.

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

Oxygen-heterocyclic compound

6,4'-Dihydroxy-7-methoxyflavanone is a naturally occurring flavanone compound, which is typically derived from various plant sources known for their rich polyphenolic content. This compound is characterized by its unique chemical structure, including hydroxyl and methoxy functional groups, contributing to its bioactivity. The mode of action of 6,4'-Dihydroxy-7-methoxyflavanone involves its ability to scavenge free radicals and its potential to modulate enzymatic activity, leading to an enhancement of the cellular antioxidant defense system. Such mechanisms are critical in mitigating oxidative stress, which is implicated in numerous pathological conditions. The uses and applications of 6,4'-Dihydroxy-7-methoxyflavanone are predominantly within the realm of biochemical and pharmacological research, where it is explored for its antioxidant properties. Investigations often focus on its potential as a therapeutic agent in diseases characterized by oxidative damage, such as neurodegenerative disorders and cardiovascular diseases. Additionally, this flavanone is of interest in the development of nutraceuticals and functional foods aimed at promoting health and preventing disease through natural antioxidants.

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

Oxygen-heterocyclic compound

Oxygen-heterocyclic compound

Natural glycoside

Luteolin is a flavonoid compound, which is a naturally occurring substance found predominantly in various fruits, vegetables, and medicinal herbs. Its sources are diverse, including parsley, artichokes, celery, and chamomile tea, where it is accumulated as a secondary metabolite. The mode of action of luteolin primarily involves the inhibition of key enzymes and pathways that lead to oxidative stress and inflammation, including but not limited to the cyclooxygenase and lipoxygenase pathways. This inhibition results in its strong antioxidant and anti-inflammatory properties. The applications of luteolin are extensive, particularly in biomedical research where it is studied for its potential roles in cancer prevention, neuroprotection, and the mitigation of cardiovascular diseases. Luteolin has also garnered interest due to its ability to modulate cell signaling pathways and gene expression. Its effectiveness in scavenging reactive oxygen and nitrogen species further underscores its significance in therapeutic research. Scientists are continuously exploring its pharmacokinetics and bioavailability to better understand its clinical relevance and potential health benefits.

6-Hydroxyflavone is a flavonoid compound, which is a type of secondary metabolite derived from plants. It is commonly found in various plant species and is known for its diverse array of biological activities. The mode of action of 6-Hydroxyflavone involves its interaction with various enzymatic systems and receptors, including modulation of signaling pathways and antioxidant activity. This compound acts primarily through the inhibition of enzymes such as phosphodiesterases and by exhibiting potential neuroprotective effects through GABAergic and serotonergic systems. The uses and applications of 6-Hydroxyflavone are deeply rooted in its pharmacological properties. It is actively researched for its potential therapeutic benefits, particularly in the treatment of neurological disorders, due to its capacity to cross the blood-brain barrier and exert effects within the central nervous system. Additionally, its antioxidant properties are of significant interest to those studying oxidative stress-related conditions. Current research continues to explore its potential in anti-inflammatory, anti-cancer, and anti-diabetic applications, making it a focal point for scientists seeking to develop novel therapeutic strategies.

Izalpinin is a specialized phytochemical compound, specifically a flavonoid, which is derived from various plant sources. It exhibits a range of bioactive properties due to its complex chemical structure. The primary mode of action of Izalpinin involves modulation of cellular signaling pathways and inhibition of specific enzymatic activities, which underpins its diverse pharmacological effects. The applications of Izalpinin are extensive in the field of medical research due to its anti-inflammatory, antioxidant, and potential anti-cancer activities. Researchers have been exploring its therapeutic potential in chronic diseases where oxidative stress and inflammatory processes play a crucial role. Additionally, its ability to interact with cellular targets makes it a compound of interest for further drug discovery and development efforts. Izalpinin is a subject of ongoing studies, which aim to elucidate its mechanisms and optimize its efficacy and safety profiles for potential clinical use.

Oxygen-heterocyclic compound

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

(-)-Butin (Butin) has antioxidant activity, can protect cells against H2O2-induced apoptosis, oxidative DNA damage and oxidative mitochondrial dysfunction; it

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.

7-Benzyloxy-4'-methoxyisoflavone is a synthetic isoflavone derivative, which is meticulously designed with specific substituents to enhance its bioactivity. This compound is derived from isoflavones, a class of naturally occurring polyphenolic compounds found predominantly in soy products and other plants. Isoflavones are known for their diverse biological activities, including antioxidant and anti-inflammatory properties. The compound’s mode of action involves modulation of enzymatic pathways, interaction with cellular receptors, and influence on oxidative stress markers. It is believed to interact with estrogen receptors and other cellular pathways, potentially influencing hormonal and metabolic processes. 7-Benzyloxy-4'-methoxyisoflavone has been explored for its applications in health sciences, particularly in research related to metabolic health, muscle growth, and age-related conditions. Its potential to promote anabolic activities without the androgenic effects traditionally associated with such activities makes it a subject of interest in muscle physiology studies. Additionally, owing to its antioxidative properties, it may play a role in mitigating oxidative damage, thus representing a potential adjunct in nutritional and therapeutic formulations.

Homoeriodictyol, a naturally occurring, bitter-masking flavanone, as a promising agent to increase appetite and food intake.

Applications A hyponotic-anaesthetic agent. References Gyermek, et al.: J. Med. Chem., 11, 117 (1968)

Icariin (Ieariline) is a flavonol glycoside that inhibits PDE5 and PDE4 activity and is a PPARα activator. Cost-effective and quality-assured.

5,7-Dimethoxy-4'-hydroxyflavanone is a synthetic flavonoid compound, which is derived from the structural modification of naturally occurring flavonoids found in plants. Alterations in its chemical structure provide enhanced properties for various scientific applications. The mode of action of this compound primarily involves its ability to act as a potent antioxidant. By scavenging free radicals, it protects biological systems from oxidative stress, thereby playing a pivotal role in cellular protection and homeostasis. The applications of 5,7-Dimethoxy-4'-hydroxyflavanone are diverse and widely explored in biochemical and pharmacological research. Its antioxidant capabilities make it a subject of interest in studies related to cellular aging, neuroprotection, and cardiovascular health. Furthermore, its effects are being evaluated in the context of anti-cancer research, where its potential to modulate signaling pathways and inhibit tumor growth is under scrutiny. The compound's unique properties expand the horizons of flavonoid research, offering potential new avenues for therapeutic development.

Oxygen-heterocyclic compound

5-Hydroxy-4'-methoxyflavone is a naturally occurring flavone, which is a type of polyphenolic compound found in various plants. It is derived from natural sources such as fruits, vegetables, and certain herbs. This compound is part of the larger class of flavonoids, which are known for their various biological activities and potential health benefits. The mode of action of 5-Hydroxy-4'-methoxyflavone involves multiple biochemical pathways. It may exert antioxidative properties by scavenging free radicals and modulating oxidative stress. Additionally, it could influence signaling pathways related to inflammation, cell cycle regulation, and apoptosis, although the precise mechanisms may vary depending on the specific cellular context and concentration. Research into the applications of 5-Hydroxy-4'-methoxyflavone is ongoing, with studies exploring its potential roles in pharmacological and nutraceutical contexts. It is being investigated for its possible effects on chronic conditions where oxidative stress and inflammation play a critical role. Furthermore, its potential neuroprotective, cardioprotective, and anticancer properties are subjects of scientific interest, making it a candidate for further detailed studies aimed at therapeutic development.

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

Eupatorin 5-methyl ether is a bioactive compound, which is a naturally occurring flavonoid found in certain plant species. This compound is derived from various plants, including those in the Asteraceae family. Eupatorin 5-methyl ether functions primarily through modulating various biochemical pathways, exhibiting anti-inflammatory, antioxidant, and anticancer activities. The specific mode of action involves the inhibition of enzymes and modulation of signaling pathways that are pivotal in the proliferation and survival of cancer cells. It impedes key growth factor receptors and kinases, thereby regulating the cell cycle and promoting apoptosis in malignant cells. Additionally, its antioxidant properties play a crucial role in reducing oxidative stress, a known contributor to numerous chronic diseases. Eupatorin 5-methyl ether is explored extensively in pharmacological and biochemical studies for its potential therapeutic effects. Its applications range across various disciplines, including oncology, where it is evaluated for its efficacy in inhibiting tumor growth, and in chronic disease management due to its anti-inflammatory properties. Researchers continue to investigate its full potential and applicability in the development of new therapeutic agents.

7-O-Methyl-liquiritigenin is a flavonoid that has been shown to have anticarcinogenic properties. It has been studied in human studies and shown to be safe for use in cancer patients. 7-O-Methyl-liquiritigenin inhibits the growth of cancer cells by inhibiting cell proliferation, inducing apoptosis, and arresting the cell cycle at G2/M phase. 7-O-Methyl-liquiritigenin also inhibits the production of cyclooxygenase 2 (COX2) and prostaglandin E2 (PGE2), which have been linked to tumor promotion. 7-O-Methyl-liquiritigenin has been shown to inhibit the growth of human colon cancer cells in vitro, as well as in vivo when injected into mice. This compound also inhibits PIM1, an oncogene that regulates cellular proliferation, differentiation, tumor progression, angiogenesis, and metast

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

Oxygen-heterocyclic compound

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

Pomiferin-3',4'-dimethylether is a natural flavonoid compound, which is isolated from plants such as the Osage orange (Maclura pomifera). This compound is derived through meticulous extraction techniques that preserve its bioactive properties. As a methylated derivative of pomiferin, it exhibits a unique mode of action characterized by its interaction with various cellular pathways. These interactions enable it to exert antioxidant, anti-inflammatory, and potential antimicrobial effects, making it a subject of significant interest in medicinal chemistry and pharmacognosy. The study of pomiferin-3',4'-dimethylether focuses on its potential applications in enhancing health through its innate ability to modulate oxidative stress and inflammatory responses. Current research explores its applicability in developing therapeutic interventions for conditions linked to oxidative damage and chronic inflammation. Scientists are particularly keen on understanding its molecular mechanisms to harness its capabilities in creating novel pharmaceuticals or nutraceuticals, emphasizing its role in contributing to health and disease prevention strategies.

Flavone is a type of flavonoid, which is a naturally occurring compound found in various plant sources. As a subgroup of polyphenolic compounds, flavones are primarily derived from the leaves, stems, and seeds of plants like parsley, thyme, and celery. The mode of action of flavones involves their ability to act as antioxidant agents, scavenging free radicals and reducing oxidative stress in biological systems. This mechanism plays a crucial role in protecting cells from damage and maintaining cellular integrity. In scientific research, flavones are extensively studied for their potential applications in health and disease prevention. They have been investigated for their anti-inflammatory, anticancer, and neuroprotective effects, among others. Flavones have shown promise in modulating signaling pathways and influencing the expression of genes related to cell proliferation and apoptosis. These attributes make them of significant interest in the development of therapeutic agents and nutritional supplements aimed at promoting health and mitigating disease processes, especially those related to oxidative stress and inflammation.

Cochliophilin A is a specialized secondary metabolite, which is isolated from certain fungal species, notably of the genus *Cochliobolus*. This compound is known for its role as a self-germination and tropic factor, meaning it can influence both the germination and directional growth of fungal spores. The mechanism of action involves its binding to specific receptors on the spore surface, triggering intracellular pathways that promote germination under suitable environmental conditions. Furthermore, it can induce directed growth responses, facilitating interactions between fungi and host organisms in nature. In terms of applications, Cochliophilin A is primarily utilized as a tool in scientific research to investigate fungal biology and ecology, offering insights into plant-pathogen interactions and fungal development. Its unique properties make it an intriguing subject for studies on signal transduction and chemotropism in fungal species. As it modulates key biological processes, Cochliophilin A holds potential utility in agricultural science for the development of strategies to manage fungal plant diseases by influencing spore germination and growth patterns.

Dihydrodaidzein-7,4'-dimethylether is a synthetic compound that falls under the category of isoflavone derivatives. Isoflavones are naturally occurring compounds typically sourced from soybeans and other legumes. Their structural similarity to estrogen allows them to exert estrogenic or anti-estrogenic effects, depending on the context and biological system. This compound operates by interacting with estrogen receptors, impacting various signaling pathways. Its ability to modulate these receptors offers insights into its potential roles in biological mechanisms including antioxidation, anti-inflammation, and possibly cancer inhibition. Due to its unique chemical structure, it may have distinct properties compared to its non-methylated counterparts, affecting its bioavailability and metabolism. Dihydrodaidzein-7,4'-dimethylether is primarily used in scientific research to explore the influences of isoflavone derivatives on cellular and molecular processes. Understanding its mode of action can provide valuable insights into the development of therapeutic agents, particularly those targeting hormone-dependent conditions. Research applications may include studies on cellular signaling, metabolism, and the development of novel pharmacological interventions.

Hesperetin is a flavonoid compound, which is naturally derived from citrus fruits such as oranges and lemons. As a notable bioactive molecule, its mode of action primarily involves the modulation of oxidative stress and inflammatory pathways. Hesperetin exerts its effects by scavenging free radicals and inhibiting the activation of inflammatory cytokines, making it a compound of significant interest in the biochemical and pharmacological sectors. The uses and applications of hesperetin are diverse, encompassing research into cardiovascular health, cancer prevention, and protection against neurodegenerative disorders. It is frequently investigated for its potential to improve vascular function, reduce blood pressure, and lower cholesterol levels. Furthermore, its anti-inflammatory effects are studied in the context of arthritis and other inflammatory diseases. Hesperetin's neuroprotective properties also suggest potential therapeutic applications in conditions such as Alzheimer's and Parkinson’s disease, where oxidative stress plays a critical pathological role.

(+/-)-Dihydrokaempferol analytical standard provided with w/w absolute assay, to be used for quantitative titration.

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

Natural glycoside

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

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. The compound's uses and applications are notably centered around its potential therapeutic effects. It has been the subject of research for its anti-cancer properties, attributed to its ability to induce apoptosis in cancer cells and inhibit tumor growth. Additionally, Dillenetin is studied for its antioxidant effects, making it a candidate for investigations into mitigating oxidative stress-related disorders. Its role in modulating inflammatory pathways also suggests further applications in managing chronic inflammatory conditions. Given its diverse bioactivities, Dillenetin remains a compound of interest in pharmacological research and drug development.

3',4'-Dihydroxyflavanone is a type of flavonoid, which is a class of polyphenolic compounds known for diverse biological activities. This compound is primarily sourced from various plants, where it plays a role in plant defense mechanisms due to its antioxidant properties. The mode of action of 3',4'-Dihydroxyflavanone involves the scavenging of free radicals, thereby mitigating oxidative stress at the cellular level. This activity is facilitated by its dihydroxy structure, which allows it to donate hydrogen atoms to neutralize reactive oxygen species. In scientific research, 3',4'-Dihydroxyflavanone is extensively studied for its potential applications in pharmacology and nutraceuticals. It is investigated for its role in modulating oxidative stress-related pathways, which are implicated in various diseases, including cancer, cardiovascular disorders, and neurodegenerative conditions. Moreover, its ability to influence signaling pathways makes it a candidate for developing therapeutic agents aimed at reducing inflammation and enhancing cellular resilience. As researchers continue to explore the biochemical interactions of flavonoids, 3',4'-Dihydroxyflavanone remains a compound of interest due to its promising biological activities.

Iriskashmirianin is a naturally occurring flavonoid derivative, which is isolated from specific plant sources. It belongs to the broader class of flavonoids, compounds known for their bioactive properties. The mode of action of Iriskashmirianin involves its interaction with cellular pathways, where it functions primarily as an antioxidant and anti-inflammatory agent. It neutralizes free radicals and modulates inflammatory responses by influencing various signaling pathways at the molecular level. This compound is utilized in scientific research focused on understanding oxidative stress-related conditions and inflammatory diseases. It is also studied for its potential therapeutic applications, given its ability to modulate biological processes. Researchers explore its use in pharmaceuticals or nutraceuticals aimed at preventing or treating conditions linked to oxidative damage and inflammation. The continued investigation into Iriskashmirianin may further elucidate its potential in developing novel therapeutic strategies for managing chronic diseases.

Oxygen-heterocyclic compound

Quercetagetin-7-O-glucoside is a flavonoid glycoside, which is a type of phytochemical compound. It is derived from various plant sources, notably plants in the Asteraceae family. The compound consists of the flavonoid quercetagetin and a glucose molecule, forming a glycoside linkage. Its mode of action primarily involves antioxidant activity, where it scavenges free radicals and chelates metal ions, thus potentially reducing oxidative stress in biological systems. Research into Quercetagetin-7-O-glucoside shows its promise in various applications, particularly in the fields of pharmacology and nutraceuticals. It has been explored for its anti-inflammatory, anticancer, and cardioprotective effects, largely attributed to its ability to modulate cellular signaling pathways and inhibit oxidative damage. While much of the investigation remains at the preclinical stage, it offers an intriguing prospect for inclusion in therapies aimed at managing oxidative stress-related conditions. Its biochemical interactions suggest potential utility in developing new therapeutic agents, with ongoing studies aiming to elucidate its full range of biological activities and efficacy in clinical settings.

Oxygen-heterocyclic compound

(+)-Taxifolin analytical standard provided with w/w absolute assay, to be used for quantitative titration.

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. The mode of action of Silicristin primarily involves modulation of oxidative stress and inhibition of lipid peroxidation. It exerts hepatoprotective effects by enhancing the activity of antioxidant enzymes and scavenging free radicals within hepatic cells. This biochemically protective role is facilitated through interaction with cellular components to stabilize cell membranes and prevent cellular damage. Silicristin is predominantly utilized in scientific research, specifically in exploring hepatoprotective mechanisms and the biochemical pathways involved in liver health. It serves as a tool in experimental models to elucidate the cellular and molecular responses to oxidative damage in hepatic tissues. Researchers employ Silicristin to better understand liver diseases and to develop potential therapeutic strategies and compounds related to liver function and detoxification processes.

Genistin is a naturally occurring isoflavone glycoside, which is derived primarily from soybeans and other legumes. It serves as a glycoside form of genistein, a well-known phytoestrogen. The mode of action of Genistin involves its bioconversion into genistein through hydrolysis. Once converted, it functions by binding to estrogen receptors, exhibiting estrogenic activity that can modulate various biological pathways. Genistin is important in scientific research due to its implications in health and disease prevention. It is studied extensively for its antioxidant, anti-inflammatory, and potential anticancer properties. Researchers are also exploring its role in reducing the risk of hormone-dependent cancers, cardiovascular diseases, and osteoporosis. Furthermore, Genistin is being investigated for its potential neuroprotective effects, offering insights into the management of neurodegenerative disorders. Its distinct endocrine modulating capabilities make it a valuable compound in understanding estrogen-related mechanisms within biological systems.

3-Hydroxy-7,8,2'-trimethoxyflavone is a specialized flavone compound, which is a naturally occurring polyphenolic product found in certain plants. It is derived from various botanical sources, where it functions as a secondary metabolite, contributing to the plant's defense mechanisms against pathogens and environmental stress. The mode of action of 3-Hydroxy-7,8,2'-trimethoxyflavone involves its role as an antioxidant. It effectively scavenges free radicals due to its polyphenolic structure, thus protecting cells from oxidative damage. This mechanism is crucial because it helps in mitigating oxidative stress, a key factor in numerous chronic diseases and aging processes. In terms of applications, 3-Hydroxy-7,8,2'-trimethoxyflavone is studied extensively for its potential health benefits. Its antioxidant properties make it a candidate for research in areas such as cancer prevention, cardiovascular health, and neuroprotection. Additionally, it is analyzed for its anti-inflammatory and anti-carcinogenic potential, offering a promising avenue for therapeutic developments. Current research focuses on elucidating its bioavailability and efficacy in various clinical models to further understand its role in human health.

6,8-Diprenylnaringenin is a prenylated flavonoid, which is an organic compound predominantly derived from the hops plant, Humulus lupulus. This compound exhibits a unique mode of action owing to its interaction with estrogen receptors, where it acts as a phytoestrogen. Its chemical structure, characterized by the presence of prenyl groups, enhances its bioavailability and affinity for these receptors, suggesting its potential role in modulating estrogenic activity in biological systems. Within the scientific community, 6,8-Diprenylnaringenin is of interest due to its diverse applications, particularly in the study of hormonal regulation and potential therapeutic roles. Researchers have explored its application in areas such as the management of menopausal symptoms, osteoporosis, and hormone-dependent cancers. Its activity as a phytoestrogen positions it as a compound of interest for further research in endocrinology and pharmacology, aimed at understanding and harnessing its biological effects in clinical settings.

Furano(2,3:7,6)-4'-hydroxyflavanone is a sophisticated flavonoid compound, which is a type of polyphenolic molecule commonly found in various plant species. As a naturally derived substance, it originates from the complex biosynthetic pathways in plants, specifically contributing to their defense mechanisms and pigmentation. The mode of action of Furano(2,3:7,6)-4'-hydroxyflavanone involves its interaction with cellular processes, potentially exhibiting antioxidant properties by scavenging free radicals and modulating enzymatic activity related to oxidative stress pathways. The uses and applications of Furano(2,3:7,6)-4'-hydroxyflavanone encompass both research and potential therapeutic domains. In scientific research, it is studied for its biochemical interactions and effects on cell signaling pathways. Its ability to mitigate oxidative damage makes it a compound of interest in the investigation of age-related diseases and other conditions linked to oxidative stress. Additionally, its flavonoid structure could be explored for drug discovery efforts, examining its potential as a lead compound in pharmaceutical development targeting specific metabolic or inflammatory pathways.

Phytoestrogen; estrogen receptor agonist; PPARγ ligand

Cirsimarin (Cirsitakaoside) is a flavonoid isolated from Microtea debilis.

Ononin is an isoflavonoid glycoside, which is derived from various plant sources, including species of the genus Ononis. It is primarily sourced from the roots and aerial parts of these plants, where it occurs as a natural constituent. The mode of action of Ononin involves its hydrolysis to form its aglycone, formononetin, which is known to exhibit estrogenic activity due to its structural similarity to estrogenic compounds. In scientific research, Ononin is studied for its potential pharmacological properties, including anti-inflammatory, antioxidant, and anticancer activities. Its applications in medicine are explored through its ability to modulate hormone receptors and influence cellular pathways associated with oxidative stress and inflammation. Ononin’s investigation as a bioactive compound continues in the context of herbal medicine and its roles in traditional therapeutic practices. Ongoing studies aim to elucidate its mechanisms of action, bioavailability, and potential therapeutic index for applications in complex disease models.

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

Eucomol is a synthetic compound derived from plant-based sources, designed as an antioxidant agent. It functions by scavenging reactive oxygen species (ROS), thereby reducing oxidative stress in biological systems. Eucomol's mode of action involves donating electrons to neutralize free radicals, which prevents cellular damage and maintains cellular homeostasis. In the scientific research context, Eucomol is utilized for studying its effects on oxidative stress-related pathologies such as neurodegenerative diseases, cardiovascular disorders, and cancer. Its efficacy in neutralizing free radicals makes it a valuable tool in laboratory experiments aimed at understanding the molecular mechanisms of oxidative damage and the protective role of antioxidants. Researchers also explore its potential in therapeutic applications due to its ability to modulate redox signaling pathways. Eucomol's versatility in experimental settings underscores its importance in advancing the study of antioxidant therapeutics.

Oxygen-heterocyclic compound

5,7-Dihydroxy-3',4',5'-trimethoxyflavanone analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

7-Hydroxyisoflavone-7-O-glucoside is a glucoside derivative of isoflavone, which is a naturally occurring flavonoid often sourced from plants such as legumes and soy. This compound is known for its biochemical properties, primarily its role as an antioxidant and its capacity to modulate inflammation. The mode of action of 7-Hydroxyisoflavone-7-O-glucoside involves the scavenging of free radicals and the inhibition of pro-inflammatory pathways, which contributes to its protective effects against oxidative stress and inflammatory damage. This glucoside derivative may also exert its effects through the modulation of signaling pathways that are crucial for cellular health. 7-Hydroxyisoflavone-7-O-glucoside is utilized largely in research settings to explore its potential therapeutic benefits. It holds promise in studying applications related to combating oxidative stress-related disorders, inflammation, and perhaps in the modulation of metabolic pathways. Researchers are particularly interested in its potential implications in the prevention or treatment of certain chronic diseases where oxidative stress and inflammation are contributing factors.

Eucomnalin is a synthetic compound, which is derived from a carefully controlled chemical synthesis process. Its mode of action involves modulation of specific biochemical pathways, targeting enzymes critical for cellular processes. This modulation allows it to influence various cellular functions, potentially rectifying imbalances or dysfunctions present in certain disease states. In terms of uses and applications, Eucomnalin shows promise in therapeutic contexts, particularly for its ability to intervene in metabolic or signaling pathways that are disrupted in certain pathological conditions. Ongoing research is exploring its efficacy and safety profile in preclinical models, seeking to ascertain its potential as a novel therapeutic agent. While further studies are required to fully understand its applications, Eucomnalin represents an intriguing candidate for future pharmacological developments in fields such as oncology or metabolic disorders, where precise intervention at the molecular level can have significant therapeutic benefits.

Corylin is a major bioactive compound isolated from Psoralea corylifolia L; it has the activity of antibiotic or anticancer.

7,2'-Dimethoxyflavone is a naturally occurring flavone compound, which is a type of phytochemical widely distributed in the plant kingdom. It is derived from various plant sources, particularly within species known for traditional medicinal uses. The compound exhibits multiple modes of action, primarily interacting with cellular pathways related to oxidative stress and enzyme modulation. It acts as an inhibitor of specific enzymatic processes, contributing to its potential therapeutic effects. In terms of applications, 7,2'-Dimethoxyflavone has been studied for its role in anti-inflammatory and anticancer activities. Its ability to modulate signaling pathways and reduce oxidative damage is of particular interest in pharmacological research. The compound is also being explored for neuroprotective effects, as it may influence pathways involved in neuronal health and resilience to injury. Researchers are keen on investigating its potential as a lead compound for drug development, targeting a variety of pathological conditions where inflammation and oxidative stress are central features. The ongoing study of 7,2'-Dimethoxyflavone illustrates the broader interest in flavonoids as promising candidates for developing novel therapeutic agents.

Azaleatin is a natural product from Rhododendron simsii.

Applications Procyanidin B2 3,3'-di-O-gallate is an important compound whose activity results in the inhibition of growth pertaining to human prostate carcinoma cell lines. Coming from the group of compounds known as flavonoids, Procyanidin B2 3,3'-di-O-gallate shows interesting biological activities relating to various human cancer diseases. References Saito, A. et al.: Heterocycles, 80, 1081 (2010); Shrestha, S.P. et al.: Pharm. Res., 29, 856 (2012);

8-Prenylquercetin is a prenylated flavonoid, a compound that belongs to the larger class of polyphenols. It is typically derived from various plant sources, often synthesized from quercetin, which is abundant in fruits and vegetables. The addition of a prenyl group is believed to enhance its biological activity and lipophilicity compared to non-prenylated flavonoids. As for its mode of action, 8-Prenylquercetin exhibits a range of biochemical interactions. It is known to affect cellular signaling pathways, potentially modulating enzyme activities and interacting with cellular receptors. This can lead to antioxidant, anti-inflammatory, and potential anti-cancer effects that are being actively researched. The applications of 8-Prenylquercetin are mainly in the field of biochemistry and pharmacology, where its unique properties are studied for therapeutic potential. Research is ongoing to explore its efficacy in various disease models, especially where oxidative stress and inflammation play a role. Scientists are particularly interested in its potential to enhance the efficacy of conventional drugs and its role in multi-target approaches in disease prevention and treatment.