Flavonoids

5,7,4’-Trihydroxy-8-methylflavanone is a flavanone, which is a type of flavonoid compound. Flavonoids are secondary metabolites commonly found in plants and are responsible for a variety of biological activities. This particular compound can be sourced from various plant species known for their rich content of natural phenolic substances. The mode of action of 5,7,4’-Trihydroxy-8-methylflavanone primarily involves its role as an antioxidant. It functions by scavenging free radicals, thereby reducing oxidative stress within cells. This activity is pivotal in protecting cellular components from damage and plays a role in maintaining cellular homeostasis. The applications of 5,7,4’-Trihydroxy-8-methylflavanone span multiple scientific fields. In pharmacology, its potential therapeutic benefits are explored, particularly in relation to its antioxidant properties. Researchers also investigate its role in food sciences as a natural additive aiming to preserve food quality and nutritional value. Furthermore, the compound is studied for its prospective use in cosmetics, leveraging its free radical-scavenging ability to mitigate skin aging and damage.

Kaempferol-3-rutinoside-7-rhamnoside is a flavonoid glycoside, which is an organic compound derived from specific plant species like tea, onions, and broccoli. It primarily exists as a complex molecule formed by the bonding of kaempferol with sugar moieties-rutinoside and rhamnoside. This compound functions by modulating various cellular signaling pathways, including those involved in oxidation-reduction processes, apoptosis, and inflammation. It combats oxidative stress by scavenging free radicals, thereby providing a protective effect against cellular damage. The uses and applications of Kaempferol-3-rutinoside-7-rhamnoside are predominantly in the domain of biomedical research, where it is studied for its potential therapeutic effects. There is significant interest in its role as a potential candidate for cancer prevention, cardiovascular health, and neuroprotection due to its bioactivity. Moreover, its anti-inflammatory properties make it a subject of investigation in inflammatory diseases. The compound's bioavailability and metabolic pathways are also vital areas of research, aiding in understanding its full potential and efficacy in therapeutic settings.

Myricetin is used as an antioxidant. It is a cell-permeable flavonoid used in inflammatory, diabetes, and cancer studies. It is effective in protecting neurons against oxidative stresses. Further, it inhibits yeast alfa-glucosidase,1 glyoxalase I in vitro and bovine milk xanthine oxidase. 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.

Glycitein-7-O-methyl ether is an isoflavone derivative, which is a type of flavonoid. It is primarily sourced from soybean and other leguminous plants, where it is present as a minor phytoestrogen. The mode of action of Glycitein-7-O-methyl ether involves mimicking estrogenic activity, binding to estrogen receptors, which could potentially affect various physiological processes. Additionally, it may exhibit antioxidant properties, scavenging free radicals and thereby influencing oxidative stress-related pathways. The uses and applications of Glycitein-7-O-methyl ether are predominantly in the field of biochemical research, where it is studied for its potential effects on hormone-related conditions and its role as an antioxidant. In particular, it holds interest for its potential implications in cardiovascular health, bone density preservation, and postmenopausal therapy. Moreover, its role in cancer research is being explored due to its ability to interact with signaling pathways involving estrogen receptors, which could influence cancer cell proliferation. As such, it offers intriguing possibilities for developing future therapeutic strategies.

Polyphenolic compound from green tea. Possesses free-radical scavenging ability 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.

Ketone phenol

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

Applications (S)-Hesperetin is the aglucon of Hesperidin (H281185), a flavanone found in citrus fruits. References Tsujimoto, M., et al.: Biol. Pharm. Bull., 32, 671 (2009), Wang, H., et al.: J. Pharm. Biomed. Anal., 49, 1157 (2009), Lee, S,. et al.: Bioorg. Med. Chem. Lett., 19, 2116 (2009)

Vestitol is a naturally occurring flavonoid, which is a bioactive compound derived from various plant species. As a flavonoid, vestitol is synthesized by plants during their metabolic processes and is found predominantly in legumes such as red clover. Its biochemical mode of action includes modulation of reactive oxygen species (ROS) and interactions with cellular signaling pathways that regulate oxidative stress. By scavenging free radicals, vestitol contributes to the protection of cellular structures and biomolecules from oxidative damage. Vestitol exhibits a range of biological activities that make it relevant in scientific research, particularly in the fields of pharmacology and biochemistry. Studies have demonstrated its anti-inflammatory and antimicrobial properties, alongside its role in modulating immune responses. Consequently, vestitol is investigated for its potential applications in the development of therapeutic agents targeting inflammatory diseases and related disorders. Additionally, its antioxidative characteristics present interest in exploring vestitol's role in preventing oxidative stress-related diseases. Research into vestitol's mechanism of action continues to expand the understanding of its potential benefits and applications in human health and disease.

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

Natural glycoside

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

Oxygen-heterocyclic compound

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. Hinokiflavone pentamethyl ether exhibits its mode of action primarily through the modulation of enzymatic pathways and interactions with cellular receptors. Its structure allows it to interact with specific biological targets, potentially influencing pathways involved in oxidative stress, inflammation, and cellular proliferation. The uses and applications of Hinokiflavone pentamethyl ether are primarily within the realm of scientific research, where it is employed in studies aiming to understand its pharmacological potential. Researchers investigate its capabilities for modulating cellular pathways, with implications for cancer, inflammation, and neuroprotection research. The compound serves as a valuable tool for elucidating the structure-activity relationships of flavonoid derivatives and exploring novel therapeutic approaches.

Hibifolin is a flavonol glycoside natural product,is a potential inhibitor of adenosine deaminase (Ki of 49.92 μM).

Applications 4'-O-Methyl-d3 Quercetin is the labeled analogue of 4'-O-Methyl Quercetin (M326580), a major metabolite of the flavanoid Quercetin (Q509500) with antioxidant properties. It helps to protect H9c2 cardiomyoblasts against H2O2-induced oxidative stress via the modulation of PI3K/Akt and ERK1/2 signaling pathways. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Duenas, M. et al.: Eur. Food Res. Technol., 232, 103 (2011); Ameho, C.K. et al.: J. Nutrit. Biochem., 19, 467 (2008); Angeloni, C. et al.: Biochimie, 89, 73 (2007)

Natural glycoside

Please enquire for more information about Erythrisenegalone including the price, delivery time and more detailed product information at the technical inquiry form on this page

Dihydrodaidzein ((±)-Dihydrodaidzein)-producing bacteria might lead to clarification of some of the mechanisms regulating the production of equol by fecal

3-Hydroxy-5,2',3'-trimethoxyflavone is a naturally occurring flavone, which is a type of polyphenolic compound found in various plants. This compound is derived from natural sources and is often isolated from specific plant species such as certain herbs and fruits. The mode of action of 3-Hydroxy-5,2',3'-trimethoxyflavone often involves interaction with biological pathways at the cellular level, potentially including antioxidant activity, modulation of enzyme function, and influence on signal transduction pathways. Due to its structural properties, this flavone is being studied for a range of biological activities, including its potential anti-inflammatory, anticancer, and neuroprotective effects. Research is ongoing to explore its efficacy and mechanisms in various in vitro and in vivo models. Its applications could extend to pharmaceuticals, nutraceuticals, and functional foods, assuming sufficient efficacy and safety can be demonstrated through rigorous scientific investigation. Scientists are actively investigating this compound to better understand its properties and potential benefits in both clinical and laboratory settings.

3-Hydroxy-6,3',4',5'-tetramethoxyflavone is a naturally occurring flavonoid, which is derived from various plant sources, including certain species of the genus Chromolaena. It belongs to a class of polyphenolic compounds known for their potential biological activities. This flavonoid acts primarily through antioxidant mechanisms, where it scavenges free radicals and inhibits oxidative stress pathways. Additionally, it can modulate various signaling pathways, implicating roles in anti-inflammatory processes and cellular protection. Its uses and applications are predominantly in the field of biochemical research, where it serves as a model compound for studying flavonoid interactions and activities. It provides insights into polyphenolic behavior in biological systems and assists in understanding their therapeutic potential. Research into its efficacy and mechanisms continues to expand, with potential implications for developing new strategies in managing oxidative stress-related conditions. This compound is of significant interest due to its unique structural components, allowing for distinct interactions within biological environments, making it a valuable tool in the advancement of scientific knowledge regarding natural antioxidants.

Please enquire for more information about Milldurone including the price, delivery time and more detailed product information at the technical inquiry form on this page

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Rhamnocitrin can enhance the immune function, improve the formation of spleen cells of mice serum hemolysin of chicken red blood cell immune.

Picoxystrobin is a strobilurin fungicide, which is derived from natural fungal compounds. This compound is synthesized to mimic the mode of action found in fungi of the Strobilurus species. Picoxystrobin acts by inhibiting mitochondrial respiration in fungal cells. Specifically, it disrupts the electron transport chain by competitively binding to the Qo site of cytochrome b, effectively halting ATP production and leading to cell death. This fungicide is utilized primarily in agricultural settings to protect crops against a range of pathogenic fungi. It is applied to crops such as cereals, fruits, and vegetables to manage diseases caused by fungal pathogens. The systemic and protective properties of Picoxystrobin allow it to be absorbed by plant tissues and transported throughout the plant, providing defense against existing infections and new fungal attacks. Its role in integrated pest management strategies is critical due to its broad spectrum efficacy and ability to enhance crop yield quality by safeguarding plant health.

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

Oxygen-heterocyclic compound

3-(3-Hydroxyphenyl)propionic Acid (m-Hydroxyphenylpropionic acid) is one of the major metabolites of ingested caffeic acid.it inhibited osteoclastogenesis.

Bavachinin (Bavachinin A)(7-O-Methylbavachin) is a natural compound isolated from the Chinese herb Fructus Psoraleae with potent anti-angiogenic activity.

Rhusflavanone is a flavanone compound, which is a type of polyphenolic molecule found in certain medicinal plants. It is derived primarily from the Rhus genus, known for its rich content of bioactive compounds. The mode of action of Rhusflavanone involves the modulation of inflammatory pathways, as it exhibits inhibition of pro-inflammatory enzymes such as cyclooxygenase (COX) and lipoxygenase (LOX). Additionally, it shows potential in scavenging free radicals, contributing to its antioxidant capabilities. Rhusflavanone is being studied for its anti-inflammatory, antioxidant, and potential anticancer properties. Its applications are explored in therapeutic contexts, particularly in the development of treatments targeting inflammatory disorders and oxidative stress-related conditions. Researchers are investigating its effectiveness as a natural, plant-derived agent that can complement or provide alternatives to conventional synthetic pharmaceuticals. Continued studies focus on its bioavailability, safety, and efficacy in various in vitro and in vivo models to better understand its potential in clinical settings.

A natural product from green tea that induces apoptosis 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.

Luteolin-7-rutinoside is a flavonoid glycoside, which is typically sourced from various plant species, including Japanese honeysuckle and passionflower. This compound is known for its strong antioxidant and anti-inflammatory activities. The mode of action of Luteolin-7-rutinoside involves the modulation of several signaling pathways and inhibition of oxidative stress at the molecular level. This is achieved by scavenging free radicals and reducing the expression of pro-inflammatory cytokines. As a result, it can mitigate cellular damage and inflammation. The uses and applications of Luteolin-7-rutinoside are primarily in research settings where its effects on chronic inflammatory conditions, neurodegenerative diseases, and certain cancers are being explored. Additionally, due to its bioactive properties, it is studied for its potential therapeutic benefits in modulating immune responses and protecting against oxidative stress-related cellular damage. Researchers are particularly interested in its capacity to contribute to the development of treatments for inflammatory disorders and as a candidate for natural antioxidant therapies.

Natural glycoside

3,5,7,2',6'-Pentahydroxyflavanone is a flavonoid derivative, which is a type of polyphenolic compound known for its potential health benefits. Typically sourced from various plants, flavonoids like 3,5,7,2',6'-Pentahydroxyflavanone are abundant in fruits, vegetables, and certain medicinal herbs. The mode of action of this compound primarily involves its ability to exert antioxidant and anti-inflammatory effects. It achieves this by scavenging free radicals and modulating pathways associated with oxidative stress and inflammation. The uses and applications of 3,5,7,2',6'-Pentahydroxyflavanone are primarily in research focused on understanding and harnessing the benefits of natural compounds in pharmacology and nutrition science. It is often investigated for its role in potentially preventing or managing conditions related to oxidative stress, such as cardiovascular diseases and certain chronic inflammatory conditions. Moreover, due to its antioxidant capabilities, it is also a point of interest in studies aiming to develop dietary supplements and functional foods that can contribute to health maintenance and disease prevention.

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

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

Luteolin-6-C-glucoside has antioxidant activity.

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

Isoglabrone is a flavonoid compound, which is derived primarily from certain plant species known for their medicinal properties. As a plant-derived compound, isoglabrone is part of a broader class of natural products that are the focus of extensive research due to their diverse biological activities. The mode of action of isoglabrone involves the modulation of various signaling pathways, which may include antioxidant, anti-inflammatory, and anticancer activities. These actions are mediated through interactions with cellular receptors and enzyme systems, altering gene expression and cellular responses. The uses and applications of isoglabrone are primarily centered around its potential in the pharmaceutical and nutraceutical fields. Scientific investigations are ongoing to explore its efficacy in the treatment or management of various conditions, such as cancer, cardiovascular diseases, and inflammatory disorders. Due to its promising bioactivity, isoglabrone is a subject of considerable interest in drug discovery and development, as researchers aim to harness its potential as a therapeutic agent.

Neoisoliquiritigenin is a flavonoid compound, which is a phytoestrogen derived from the root of Glycyrrhiza glabra, commonly known as licorice. Its mode of action primarily involves modulation of various cellular signaling pathways, including its notable antioxidant and anti-inflammatory effects. This compound exhibits a significant capability to scavenge free radicals and to inhibit pro-inflammatory mediators, thereby impacting oxidative stress and inflammatory responses at the cellular level. The uses and applications of Neoisoliquiritigenin are diverse in the realm of biomedical research. It is extensively studied for its potential therapeutic effects in chronic inflammatory diseases, cancer prevention, and neuroprotection. Additionally, there is ongoing research to evaluate its role in metabolic syndrome management due to its ability to influence lipid and glucose metabolism. As an interesting compound in the pharmacological landscape, Neoisoliquiritigenin offers promising insights into the development of novel therapeutics targeting oxidative and inflammatory pathways.

Oxygen-heterocyclic compound

Conrauinone A is a naturally derived compound, which is a specialized natural product extracted from a specific plant source. This compound is known for its unique structural properties and potential biological activities. Conrauinone A functions primarily through a mode of action that involves interaction with specific cellular targets, leading to modulation of biochemical pathways that are crucial for certain cellular processes. The uses and applications of Conrauinone A are primarily focused on its potential therapeutic benefits. Research has indicated that it might have significant roles in the development of treatments for specific diseases, particularly those involving dysregulation of cellular mechanisms. Its applications extend into the fields of pharmacology, where it is being investigated for its efficacy and safety in various preclinical and possibly clinical studies. The ongoing scientific exploration aims at understanding its complete pharmacodynamic and pharmacokinetic profiles, which are essential for advancing its potential medical applications.

Pratensein 7-O-glucoside is a naturally occurring flavonoid glucoside, which is extracted from various plant sources such as red clover, Trifolium pratense. This compound is formed when the flavonoid pratensein is glycosylated at the 7th position with glucose. As a member of the isoflavone group, Pratensein 7-O-glucoside may exert its effects primarily through antioxidant mechanisms, neutralizing reactive oxygen species and reducing oxidative stress. Given its potential antioxidant properties, Pratensein 7-O-glucoside is investigated for applications in fields such as pharmacology and nutraceuticals. It might contribute to the mitigation of oxidative damage in cells, thus playing a role in the study of aging, cancer, and cardiovascular diseases. In addition, its phytoestrogenic activity suggests possible uses in hormonal therapies, particularly for conditions related to estrogen deficiency. Further research is essential to fully characterize its bioactivity and therapeutic potential in clinical settings.

6,2'-Dimethoxyflavone is a flavonoid compound, which is a type of secondary metabolite commonly found in plants. This compound is derived from various plant sources, where it acts as a natural antioxidant. The mode of action of 6,2'-Dimethoxyflavone includes modulation of signaling pathways involved in inflammation and cell proliferation. It influences the activity of specific enzymes and receptors, such as kinases and growth factor receptors, thereby affecting cellular responses. In scientific research, 6,2'-Dimethoxyflavone is studied for its potential applications in pharmacology. It has been explored for its anti-inflammatory, neuroprotective, and anticancer properties. Researchers are particularly interested in its ability to modulate pathways that are crucial in the pathogenesis of various diseases. Moreover, its antioxidant properties contribute to its therapeutic potential, helping to combat oxidative stress. Due to these characteristics, 6,2'-Dimethoxyflavone is considered a promising candidate for further study in the development of novel therapeutic agents targeting critical biological pathways.

Gossypin is a flavonoid compound, which is a type of polyphenol found in various natural sources, such as plants. It is primarily isolated from the flowers of Hibiscus species. The mode of action of gossypin involves various biochemical pathways, including its role as a free-radical scavenger and modulator of several enzymes. It exhibits antioxidant, anti-inflammatory, and neuroprotective properties through interactions with cellular receptors and signaling pathways. Gossypin is studied for its potential in various scientific applications. It has shown promise in preclinical studies for treating conditions such as cancer, diabetes, and neurodegenerative diseases. Researchers are investigating its ability to inhibit tumor growth and metastasis, as well as its potential to enhance insulin sensitivity and protect neuronal cells. The compound’s multifaceted mechanisms make it a subject of interest in pharmacological and biochemical research, with ongoing studies to further elucidate its therapeutic potential.

Baicalin 7-b-D-glucuronide is a flavonoid metabolite, which is primarily derived from the root of the plant *Scutellaria baicalensis*, commonly known as Chinese skullcap. This compound occurs as part of the extensive array of flavonoids in traditional medicinal plants used in various ethnic medicine systems. Baicalin 7-b-D-glucuronide exerts its biological effects through multiple mechanisms of action, primarily involving its interaction with cellular pathways related to inflammation and oxidative stress. It is known to inhibit the production of pro-inflammatory cytokines and enzymes by modulating signaling pathways such as NF-κB and MAPK. Additionally, it has been shown to scavenge free radicals, thereby exerting antioxidant effects. The primary applications of Baicalin 7-b-D-glucuronide are in research related to its potential therapeutic uses, including its roles in anti-inflammatory, antioxidant, and neuroprotective strategies. It holds promise in the investigation of treatments for conditions such as inflammatory diseases, neurodegenerative disorders, and potentially in oncology, due to its ability to influence cellular homeostasis and prevent oxidative damage. As such, it serves as a significant compound of interest in the development of novel therapeutic agents.

Myricetin trimethyl ether is a flavonoid derivative, which is a metabolite of myricetin, a naturally occurring flavonoid found in various fruits, vegetables, and herbs. This compound is of significant interest due to its potential bioactive properties. It is commonly studied within the context of its antioxidative mechanisms, where it functions by neutralizing free radicals and attenuating oxidative stress, a key factor implicated in the pathogenesis of numerous chronic diseases. The mode of action of myricetin trimethyl ether involves electron donation to free radicals, which stabilizes these reactive species and prevents cellular damage. Additionally, it may modulate signaling pathways related to inflammation and apoptosis, offering a broad spectrum of biological activities. This renders it a promising candidate for investigating therapeutic strategies against cancer, cardiovascular diseases, and neurodegenerative disorders. Applications of myricetin trimethyl ether predominantly focus on its potential in pharmacological research. Scientists examine its role as a protective agent in cellular models of disease, aiming to elucidate its efficacy and safety profile. Furthermore, it serves as a lead compound in the development of novel therapeutic agents, highlighting the growing interest in flavonoid derivatives within medicinal chemistry and drug discovery domains.

Naringin hydrate is a flavonoid compound, which is found predominantly in citrus fruits such as grapefruits. This compound is a glycoside, sourced primarily from the peels and seeds of these fruits, playing a role as a natural constituent of the fruit's phytonutrient profile. The mode of action of naringin hydrate involves its ability to modulate a variety of biological pathways. It exhibits antioxidant properties by scavenging free radicals and enhancing the body’s endogenous antioxidant enzymes. Additionally, naringin hydrate demonstrates anti-inflammatory actions through the inhibition of pro-inflammatory cytokines and the modulation of signaling pathways such as NF-kB and MAPK. Naringin hydrate has been extensively researched for its potential therapeutic applications. Its antioxidant properties make it a subject of interest in preventing oxidative stress-related diseases, including cardiovascular diseases and cancers. The anti-inflammatory benefits of naringin hydrate are being explored for conditions like arthritis and metabolic disorders. Moreover, studies suggest its potential role in neuroprotection and improving lipid metabolism, highlighting its promise in dietary and pharmacological interventions.

4'-Methoxyflavanone is a methoxy-substituted flavanone, which is a specialized class of flavonoids. These compounds are primarily derived from plant sources and are known for their diverse biological activities. The modification of the flavanone structure with a methoxy group can significantly influence its biochemical interactions and properties. As a naturally sourced compound, 4'-Methoxyflavanone exhibits its mode of action through potential antioxidative mechanisms. This involves the scavenging of free radicals and the inhibition of oxidative stress pathways, which are key processes implicated in cellular damage and various pathologies. The compound's uses and applications include studies focused on its potential therapeutic roles in mitigating oxidative stress-related conditions. Researchers are particularly interested in its pharmacological profile, which may contribute to the development of novel antioxidant therapies. Additionally, 4'-Methoxyflavanone serves as an important chemical scaffold in medicinal chemistry for the synthesis of analogs with enhanced biological activities. Its roles in laboratory research extend to elucidating the structure-activity relationships within the flavonoid class of compounds.

Natural glycoside

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

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

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

3',4',7-Trimethoxyquercetin (3,5-Dihydroxy-7,3',4'-trimethoxyflavone) is a polymethoxyquercetin isolated from Scutellaria baicalensis with antioxidant activity.

Oxygen-heterocyclic compound

Procyanidin A1 analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Hydroxygenkwanin is a type of flavonoid, which is a natural compound extracted from various plant sources, particularly those within the Asteraceae family. It functions predominantly through its ability to modulate multiple signaling pathways, including antioxidant, anti-inflammatory, and apoptosis-inducing activities. Hydroxygenkwanin acts by influencing cellular signaling cascades, enhancing or inhibiting the expression of specific proteins and genes related to cell cycle regulation and immune response. The compound is used primarily in research settings to explore its potential therapeutic applications. Due to its bioactive properties, it is being studied for its anti-cancer, anti-inflammatory, and neuroprotective effects. Investigations are ongoing to determine its efficacy and safety in modulating biological responses, particularly in the context of cancer treatment and neurology. The understanding of Hydroxygenkwanin’s mechanisms could contribute to the development of novel therapeutic strategies targeting oxidative stress and inflammation-related diseases.

Oxygen-heterocyclic compound

4'-Hydroxywogonin is a bioactive flavonoid, which is derived primarily from the roots of the plant *Scutellaria baicalensis*. This compound is a naturally occurring flavone, a subclass of flavonoids, known for its potential therapeutic properties. The mode of action of 4'-Hydroxywogonin involves its ability to modulate various cellular signaling pathways. It is particularly noted for its anti-inflammatory and antioxidant effects, which are mediated through the inhibition of pro-inflammatory cytokines and the scavenging of free radicals, respectively. The applications of 4'-Hydroxywogonin are being explored in a variety of biomedical research fields. It has shown promise in preclinical studies related to the treatment of inflammatory disorders, neurodegenerative diseases, and certain types of cancer. Researchers are particularly interested in its potential to modulate immune responses and protect against oxidative stress-related cell damage. Further studies are necessary to fully elucidate its mechanisms and efficacy in clinical settings, but its natural origin and bioactivity make it a compound of significant interest in pharmacological research.

2′,4,4′,6′-Tetrahydroxychalcone (Isosalipurpol) has antiallergic activity, and suppresses asthmatic symptoms by inhibiting Th2 cytokine from CD4 T cells.

Lupinalbin B is a bioactive compound, specifically classified as an alkaloid, which is derived from the seeds of the Lupinus plant species. These plants, commonly known as lupins, are a part of the legume family and are cultivated primarily for their seeds that contain high protein content. The presence of alkaloids like Lupinalbin B in lupin seeds is a result of the plant's secondary metabolism, which serves various ecological functions, including defense against herbivores. The mode of action of Lupinalbin B involves interaction with specific biological pathways, often exerting inhibitory effects on enzyme activity that can affect cellular processes. Such actions make Lupinalbin B a compound of interest in pharmacological research, particularly in the study of its potential therapeutic applications. Lupinalbin B is being actively researched for its potential applications in medicine, including its role as an anti-inflammatory and anticancer agent. Its ability to modulate biological pathways and enzyme functions makes it a promising candidate for further drug development studies aimed at treating chronic diseases. Additionally, its natural occurrence in lupin seeds adds a layer of interest to its ecological and agricultural roles.

Oxygen-heterocyclic compound

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

A citrus bioflavanoid that inhibits cytochrome P-450 monooxygenase activityNaringin is used to prepare naringin dihydrochalcone, which is about 300-1800 times sweeter than sugar. It is a citrus bioflavonoid reported to inhibit cytochrome P450 monooxygenase activity. It also acts as an inhibitor of cytochrome P450 enzymes. It is employed as an antioxidant, lipid lowering and anticancer agent. In addition to this, it is used in a study to assess aldosterone production by a human adrenocortical cell line and to improve cognitive deficits of Alzheimer's disease. 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.

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

7,2'-Dihydroxy-4',5'-methylenedioxyisoflavone is a naturally occurring isoflavone compound, which is typically isolated from various plant sources. This compound is a secondary metabolite, often found in plants known for their therapeutic properties. Isoflavones are well-recognized for their potential bioactivity, acting as phytoestrogens due to their structural similarity to estrogen. The mode of action of 7,2'-Dihydroxy-4',5'-methylenedioxyisoflavone involves interaction with estrogen receptors, where it can exhibit either estrogenic or anti-estrogenic effects depending on the target tissue. This dual activity allows it to modulate hormone-related pathways, which can influence cellular processes such as proliferation and apoptosis. The uses and applications of this compound span across pharmacological and nutraceutical fields. Research suggests potential roles in managing hormone-related disorders, cancer chemoprevention, and cardiovascular health. Its bioactive profile makes it a subject of interest in the development of therapeutic agents and functional foods aimed at promoting health and preventing disease. Ongoing studies are essential to fully elucidate its mechanisms and efficacy in different biological systems.

Oxygen-heterocyclic compound

Phytoalexin isolated from the fungus-inoculated leaflets of Lotus angustissimus