Flavonoids

Ketone phenol

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. This compound's uses and applications are primarily centered in biochemical and pharmacological research. It is explored for its potential antioxidative, anti-inflammatory, and anticancer properties. As a flavone derivative, it is valuable in elucidating the structure-activity relationships inherent to flavonoids and could serve as a lead compound in the development of therapeutic agents. The study of 3'-Benzyloxy-4',5,6,7-tetramethoxyflavone adds to the broader understanding of flavonoid bioactivity and their possible applications in medicinal chemistry.

Luteolin-4'-O-glucoside analytical standard provided with w/w absolute assay, to be used for quantitative titration.

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

7-Benzyloxy-2',4',5'-trimethoxyisoflavone is a specialized type of isoflavone, which is a class of naturally occurring organic compounds related to flavonoids. It is typically derived from plant sources, showcasing the vast chemical diversity and potential bioactivity present in botanicals. This compound operates through various biochemical pathways, often interacting with specific cellular receptors or enzymes to exert its effects. Its mode of action can include antioxidant activity or modulation of signaling pathways, which are crucial for maintaining cellular homeostasis and function. The applications of 7-Benzyloxy-2',4',5'-trimethoxyisoflavone are primarily in the realm of pharmacological research, where it is explored for its potential therapeutic uses. It may be investigated for its roles in combating oxidative stress or influencing pathways associated with inflammation and cellular growth. científicos pursue its study to uncover new medical insights and develop novel therapeutic strategies.

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

Poncirin is a natural flavonoid glycoside, which is derived from the fruit of Poncirus trifoliata, commonly known as bitter orange. This compound is extracted from the plant materials using solvents followed by purification processes to isolate the active flavonoid. Poncirin exhibits various modes of action, including antioxidant and anti-inflammatory effects, likely due to its ability to scavenge free radicals and modulate signaling pathways involved in inflammation. Additionally, it has been studied for its potential to inhibit specific enzymes linked to disease processes, indicating a possible therapeutic role in metabolic and degenerative diseases. In scientific research, Poncirin is utilized for its potential applications in developing therapeutic agents. It is especially explored for its efficacy in targeting oxidative stress-related conditions and inflammation. Its bioactivity indicates potential utility in pharmaceutical formulations aimed at managing conditions such as cardiovascular diseases, certain types of cancer, and other inflammatory disorders. Ongoing studies continue to explore its pharmacokinetics and bioavailability to better understand its efficacy and therapeutic potential.

Herbacetin-8-glucoside is a flavonoid compound, which is a naturally occurring glucoside derived from various plant sources, predominantly found in flaxseed and some other plant species. The glycosidic linkage occurs at the 8th position on the herbacetin structure, contributing to its unique biochemical profile. Herbacetin-8-glucoside functions primarily through its potent antioxidant and anti-inflammatory mechanisms, effectively scavenging free radicals and modulating inflammatory pathways. Within scientific research, herbacetin-8-glucoside is utilized for its promising therapeutic potential, especially in the field of chronic inflammatory diseases and oxidative stress-related conditions. Its role in modulating key signaling pathways suggests potential applications in developing treatments for conditions like cardiovascular diseases, neurodegenerative disorders, and certain cancers. Researchers continue to explore its bioavailability and pharmacokinetics to better understand its efficacy in clinical settings.

Oxygen-heterocyclic compound

Pinocembrin dimethylether is a flavonoid derivative, which is synthesized from natural sources such as honey, propolis, and certain plants. It retains the core flavonoid structure while being modified to enhance its bioavailability and stability. This compound acts primarily as a neuroprotective agent through its antioxidative and anti-inflammatory properties. It interacts with various molecular pathways to mitigate oxidative stress and reduce neuroinflammation, contributing to cellular protection. Pinocembrin dimethylether has several potential applications in the biomedical field. It is being studied for its role in treating neurodegenerative diseases such as Alzheimer's and Parkinson's, where oxidative stress and inflammation are pivotal in disease progression. Additionally, its antioxidative properties make it a candidate for use in cardiovascular health, where it may help in reducing the risk of ischemic injury. Further research is exploring its applications in cancer therapies, given its ability to modulate signaling pathways involved in cell proliferation and survival.

Chrysoeriol is a flavonoid compound, which is derived from various plant sources, including many herbs and flowers such as chamomile and tarragon. It functions through inhibition of certain cellular pathways that lead to inflammation, such as the suppression of NF-kB and cyclooxygenase activity. Additionally, chrysoeriol exhibits antioxidative effects by scavenging free radicals and enhancing the body's natural antioxidant enzyme systems. In scientific applications, chrysoeriol is studied for its potential roles in anti-inflammatory and antioxidant therapies. Its ability to modulate inflammatory pathways makes it a candidate for research in conditions characterized by excessive inflammation, such as arthritis. Furthermore, owing to its antioxidative properties, it is of interest in studies on oxidative stress-related diseases, which include neurodegenerative disorders and cardiovascular diseases. Chrysoeriol is also explored in the context of cancer research, where its impact on cellular signaling and oxidative stress pathways is investigated.

Ampelopsin-3'-O-glucoside is a flavonoid glycoside, which is a compound derived from various plant sources, including members of the Vitaceae family. This compound is characterized by the attachment of a glucose molecule to the flavonoid ampelopsin, altering its solubility and bioavailability properties. Its mode of action is primarily through its antioxidant activity, involving the scavenging of free radicals and inhibition of oxidative stress pathways. These properties are of significant interest due to their potential in modulating the oxidative status in biological systems. The applications of Ampelopsin-3'-O-glucoside are mainly investigational and focused on exploring its biological effects in vitro and in vivo. Research is directed at understanding its potential role in mitigating conditions exacerbated by oxidative stress, such as chronic inflammation and certain metabolic disorders. Additionally, its utility as a biochemical probe for exploring cellular pathways regulated by oxidative states is being investigated. While promising, these applications remain largely confined to the research setting, necessitating further studies to ascertain its efficacy and safety in more applied contexts.

Natural glycoside

Isorhamnetin is a naturally occurring flavonoid, which is isolated from various plant sources such as fruits, vegetables, and medicinal herbs like Ginkgo biloba. As a member of the flavonoid family, it is primarily derived from the glycosylation and methylation of quercetin. The mode of action of isorhamnetin is mainly attributed to its potent antioxidant capabilities. It scavenges reactive oxygen species and inhibits oxidative stress, which may lead to beneficial effects in preventing cellular damage. Isorhamnetin is extensively used in scientific research due to its pharmacological properties. Studies investigate its potential applications in reducing inflammation, modulating enzyme activities, and its anticarcinogenic potentials. It is also explored for its role in protecting cardiovascular health by improving lipid profiles and enhancing endothelial function. Researchers are particularly interested in the compound's capability to regulate signaling pathways involved in cell proliferation and apoptosis, making it a subject of interest in cancer research. Thus, isorhamnetin presents a valuable compound for further exploration in the development of therapeutic strategies for various diseases.