Pterocarpan

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

Erybraedin is a natural compound, which is an isoflavonoid derived from the root of plants belonging to the genus *Erythrina*. This compound exhibits a range of biological activities through its role as a phytoestrogen and inhibitor of key enzymes such as topoisomerases. Its mode of action includes interference with cellular processes like DNA replication and transcription, primarily by stabilizing the DNA-topoisomerase complex. This results in the inhibition of enzyme activity, preventing the re-ligation of DNA strands and ultimately leading to cell cycle arrest. Erybraedin's applications are diverse due to its multifaceted biological effects, including potential roles in anticancer therapies, owing to its ability to induce apoptosis in cancer cells. Additionally, its estrogenic properties are under investigation for implications in hormone-related disorders. Detailed exploration of its pharmacodynamics and pharmacokinetics continues to provide insight into its therapeutic potential, highlighting its significance in natural product research and drug discovery.

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

(±)-Neorautenane is an alkaloid compound, which is a naturally occurring product found in certain plant species. This product is derived from natural botanical sources, specifically plants that belong to particular genera known for their medicinal properties. The mode of action of (±)-Neorautenane involves interaction with specific biological pathways, potentially affecting neurobiological functions due to its structure and properties typical of alkaloids. (±)-Neorautenane is primarily studied for its pharmacological properties, including potential neuroprotective and analgesic effects. Its applications are predominantly within the field of biochemical and pharmacological research where it is used to explore its effects on cellular processes and its potential therapeutic benefits. The compound's intricate mode of bioactivity makes it a subject of interest for investigating novel treatments for neurological conditions. Scientists are particularly interested in understanding its mechanism to harness possible therapeutic applications that could benefit various medical fields. The ongoing research focuses on isolating and characterizing its effects to elucidate the full scope of its potential uses.

(+)-Medicarpin is a natural phytoalexin, which is a type of compound produced by plants as part of their defense mechanism against pathogens. It is primarily derived from species within the Fabaceae family, such as Medicago and Glycyrrhiza. As a specialized metabolite, (+)-Medicarpin plays a crucial role in plant resistance, accumulating in response to biotic stress. Its mode of action involves the disruption of fungal cell membranes and the inhibition of microbial growth, making it an effective antifungal agent. Additionally, (+)-Medicarpin exhibits significant anti-inflammatory properties through the modulation of inflammatory pathways and the reduction of pro-inflammatory mediators. The uses and applications of (+)-Medicarpin are extensive in scientific research. It is studied for its potential in developing new antifungal therapies and elucidating plant defense mechanisms. Moreover, its anti-inflammatory action makes it a valuable compound in exploring treatments for inflammatory diseases. Ongoing research aims to further understand its molecular interactions and broaden its utility in pharmacological and agricultural industries.

(-)-Maackiain is a naturally occurring isoflavonoid, which is a compound derived from the leguminous plant family, particularly in species like Maackia amurensis. It exhibits its bioactivity through its antifungal action, which involves the disruption of microbial cell membranes and inhibition of fungal enzyme systems, ultimately leading to impaired growth of pathogenic fungi. The compound has been extensively studied for its role in plant defense mechanisms as a phytoalexin, a substance produced in response to pathogen attack. Consequently, (-)-Maackiain has applications in agricultural biotechnology for developing disease-resistant crops. Additionally, its phytochemical properties have generated interest in pharmaceutical research where it is investigated for potential therapeutic uses, including cancer treatment and neuroprotection, due to its ability to modulate various biological pathways. Both its ecological and medicinal relevance make it a subject of interest for ongoing scientific investigations.

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

(+/-)-Medicarpin is a natural isoflavonoid compound, which is derived from various leguminous plants, such as Medicago species. It functions as a phytoalexin, a type of antimicrobial and often antioxidative substance synthesized by plants as part of their defense mechanism against pathogens. The mode of action of (+/-)-Medicarpin involves disruption of the cellular processes of fungi, particularly by inhibiting the biosynthesis of ergosterol, a critical component of fungal cell membranes. This inhibition can lead to increased membrane permeability and subsequent cell death. (+/-)-Medicarpin has been extensively studied for its potential uses in agriculture and medicine. In agriculture, it serves as a natural fungicide to protect crops against fungal infections, thereby reducing the reliance on synthetic pesticides. In the medical field, its antifungal properties are being explored for therapeutic applications against pathogenic fungi affecting humans. Additionally, its role in modulating biological pathways has sparked interest in research on promoting bone health and possible anti-inflammatory effects. The multidisciplinary utility of (+/-)-Medicarpin underscores its significance in both academic research and practical applications.

8-Hydroxy-3,4,9,10-tetramethoxypterocarpan is a naturally occurring isoflavonoid, which is derived from the roots of certain plant species within the Fabaceae family. The compound is primarily isolated through extraction and purification processes that leverage its natural abundance in these botanical sources. This compound exhibits its mode of action through a range of biochemical interactions, including antioxidant and antimicrobial activities. Its antioxidant properties are attributed to the ability to scavenge free radicals, thereby mitigating oxidative stress at the cellular level. The antimicrobial activity is believed to stem from the disruption of microbial cell membrane integrity, leading to potential inhibitory effects on bacterial growth. 8-Hydroxy-3,4,9,10-tetramethoxypterocarpan has garnered attention in research for its potential applications in pharmacology and therapeutics. Studies are exploring its role in developing novel treatments for oxidative stress-related diseases and its efficacy as a natural antimicrobial agent. This compound is of particular interest in the fields of biochemistry and pharmacognosy, where its molecular interactions are elucidated for potential drug development.

2,8-Dihydroxy-3,9-dimethoxypterocarpan is a naturally occurring pterocarpan derivative, which is a type of phytochemical. This compound is typically sourced from various leguminous plants, where it serves as a phytoalexin. Phytoalexins are antimicrobial and often antioxidative substances synthesized de novo by plants in response to pathogen attack. The mode of action for 2,8-Dihydroxy-3,9-dimethoxypterocarpan includes disrupting microbial cell membranes and interfering with cellular metabolic processes, thereby inhibiting the growth of pathogens. Its antioxidant activity also helps in scavenging free radicals, which further contributes to its protective roles in plants. In scientific research, this compound is of interest due to its potential applications in agriculture as a natural pesticide alternative, aiding in the control of plant diseases. Additionally, it is investigated for possible therapeutic uses in humans, including antimicrobial and antioxidative health benefits. Continued study of 2,8-Dihydroxy-3,9-dimethoxypterocarpan could provide insights into new antimicrobial agents or plant protection strategies.

Demethylmedicarpin is a phytoalexin, which is a naturally occurring antimicrobial compound. It is typically derived from leguminous plants, such as alfalfa and other species within the Fabaceae family. The plant synthesizes this compound as a defense mechanism in response to pathogen attack, environmental stress, or injury. The mode of action of demethylmedicarpin involves the disruption of microbial cell processes, including inhibition of fungal and bacterial growth. It acts by interfering with the cell membrane integrity and cellular metabolism of pathogenic organisms, thereby halting their proliferation and mitigating infection spread. In scientific research, demethylmedicarpin is extensively studied for its potential applications in sustainable agriculture and plant protection. Its ability to enhance plant resistance without resorting to synthetic pesticides makes it an attractive candidate for developing eco-friendly pest management strategies. Moreover, insights into its biochemistry are valuable for advancing the understanding of plant-microbe interactions and could lead to advancements in crop resilience technologies.

Phaseollin is a phytoalexin, which is a naturally occurring antifungal compound. It is derived from Phaseolus vulgaris, commonly known as the common bean. This compound is synthesized by the plant in response to pathogenic attack, serving as a critical component of the plant's innate defense system. The mode of action of phaseollin involves disrupting fungal cell processes. This disruption leads to the inhibition of fungal growth and prevents further colonization of the plant tissues. The biosynthesis of phaseollin is typically triggered by the presence of fungal pathogens, indicating its role as an inducible resistance factor within plant defense mechanisms. Phaseollin is primarily studied in the context of plant-pathogen interactions. It serves as a model compound in the study of phytoalexin production and the broader field of plant immunity. Understanding the pathways and regulatory mechanisms involved in phaseollin biosynthesis can contribute to enhancing crop resistance to fungal infections, potentially leading to more resilient agricultural systems.

Homopterocarpin is a naturally occurring flavonoid, which is an isoflavonoid compound found primarily in the heartwood of Pterocarpus species. These trees, belonging to the Leguminosae family, are indigenous to tropical regions and have been utilized in traditional medicine for their bioactive properties. Homopterocarpin operates through various biochemical pathways, notably by exhibiting antioxidant and anti-inflammatory effects. Its mode of action involves the modulation of inflammatory cytokines and the scavenging of reactive oxygen species, contributing to its potential efficacy in managing oxidative stress-related disorders. In scientific applications, Homopterocarpin is explored for its potential in treating conditions such as cancer, cardiovascular diseases, and neurodegenerative disorders, where its ability to mitigate inflammation and oxidative damage is especially valuable. Additionally, it serves as a candidate in pharmacological studies aiming to develop novel therapeutic agents. Its efficacy, biodistribution, and metabolic stability remain areas of active research, as scientists aim to elucidate its full potential and mechanism of action in various biological contexts.

Pterocarpan is a natural phytochemical compound, which is a type of isoflavonoid derived from plants, particularly leguminous species. These compounds are part of the plant’s secondary metabolite arsenal, produced as a response to environmental stressors or pathogenic attacks. The mode of action of pterocarpans involves interaction with microbial cell membranes, leading to disruption and inhibition of pathogen growth, and the scavenging of free radicals, thereby exerting antioxidant effects. Pterocarpans are recognized for their role in the plant's defense mechanism, with applications in both agricultural and medical fields. In agriculture, they are explored for use as biopesticides, aiming to naturally protect crops against fungal and bacterial pathogens. In medical research, pterocarpans are investigated for their potential health benefits, including antimicrobial, anticancer, and neuroprotective effects. The continued exploration of these compounds underscores their significance in developing sustainable agricultural practices and novel therapeutic agents.

Pisatin is an isoflavonoid compound, which is a type of phytoalexin commonly found in leguminous plants, particularly in peas. It is synthesized by these plants as a natural defense mechanism. In terms of its mode of action, Pisatin inhibits fungal growth by disrupting the integrity of fungal cell membranes, thereby interfering with the pathogen's cellular processes. Pisatin plays a crucial role in the plant's immune response, especially when the plant is under attack by fungal pathogens. Its production is triggered by microbial infection or environmental stress, acting swiftly to deter further invasion. This makes it an important subject of study for scientists interested in plant pathology and natural plant defense systems. Research into Pisatin not only enhances the understanding of plant immunity but also offers potential applications in agriculture. By studying Pisatin and its biosynthetic pathways, scientists can explore new methods for improving crop resistance against fungal diseases, ultimately aiding in the development of more resilient leguminous crops.

Trifolirhizin is a flavonoid compound, which is derived from the roots of licorice, an herb widely used in traditional medicine. This bioactive compound is known for its pharmacological properties, primarily acting through modulation of inflammatory pathways. Trifolirhizin exerts its effects by inhibiting the activity of pro-inflammatory cytokines and enzymes, thereby reducing oxidative stress and inflammation at the cellular level. The compound is extensively studied for its potential applications in treating inflammatory conditions. Its ability to modulate immune responses has made it a subject of interest in research focused on diseases such as arthritis and inflammatory bowel disease. Further investigations are also exploring its antiviral and hepatoprotective effects, expanding its potential therapeutic uses. Trifolirhizin's significance in medicinal chemistry lies in its contributions to understanding the flavonoid class of compounds and their interactions within biological systems, offering promising avenues for the development of novel therapeutic agents.

Glyceollin IV is a specialized phytoalexin, which is a type of naturally occurring compound produced by plants as a response to stress or pathogen attack, such as soybeans. This compound is derived from the isoflavonoid metabolic pathway and is part of a group of glyceollins known for their bioactive properties. Glyceollin IV operates primarily through mechanisms involving the modulation of cellular stress responses and inhibition of certain enzymatic pathways that contribute to its antimicrobial, antioxidant, and antitumor activities. Research into Glyceollin IV has unveiled its promising applications in various fields such as oncology, where it has been observed to interfere with cancer cell proliferation and promote apoptosis. Additionally, its antioxidant properties render it a valuable candidate for further exploration in the context of oxidative stress-related disorders. The antibacterial and antifungal effects also suggest potential uses in agricultural biotechnology to enhance crop resistance to pathogens. As studies continue, Glyceollin IV’s multifaceted bioactivities underscore its potential as a significant compound in scientific research aimed at developing novel therapeutic and protective strategies.

(-)-Medicarpin is a phytoalexin, which is a type of natural antimicrobial compound. It is derived from leguminous plants, including certain species of Medicago, where it plays a crucial role in plant defense mechanisms. This compound is biosynthesized in response to pathogenic attack, particularly fungal infections, thereby enhancing the plant's resistance to such threats. The mode of action of (-)-Medicarpin primarily involves its interaction with cellular structures of invading fungi, disrupting their growth and viability. Additionally, it exhibits estrogenic activity by binding to estrogen receptors, influencing various biological processes. This dual functionality makes (-)-Medicarpin of considerable interest in both agricultural and biomedical research. In practical applications, (-)-Medicarpin is studied for its potential use in developing eco-friendly fungicides and as a model compound for understanding plant immunity. In biomedicine, its estrogenic properties are explored for potential therapeutic uses, such as in the management of osteoporosis and hormone-related conditions. However, much of its application remains in the exploratory and experimental phases, warranting further research to understand its full potential and limitations in both agricultural and medical contexts.

6a-Hydroxymaackiain is a naturally occurring phytoalexin, which is an antimicrobial compound produced by plants as part of their defense mechanisms against pathogens. This particular compound is typically sourced from leguminous plants, where it is synthesized in response to external stressors such as microbial infection. The mode of action of 6a-Hydroxymaackiain involves disrupting the cell membranes of invading microorganisms, thereby inhibiting their ability to grow and proliferate. This defense strategy allows the plant to resist infection and maintain its overall health. The uses and applications of 6a-Hydroxymaackiain are primarily in the field of plant pathology and agricultural research, where it is studied for its role in enhancing disease resistance in crops. Additionally, its antimicrobial properties make it an interesting candidate for exploration in developing natural plant protection agents. Its ability to inhibit harmful microorganisms without damaging the plant itself signifies its potential in sustainable agriculture practices, contributing to the reduction of chemical pesticide usage and promoting environmental health.

Methylnissolin is a synthetic antimicrobial agent, which is developed from chemically modified natural peptides. This compound operates by interfering with microbial cell wall synthesis, leading to structural instability and eventual cell lysis. Methylnissolin’s precise mode of action allows for targeted disruption of bacterial cell processes without affecting mammalian cells, which makes it a compelling choice for therapeutic applications. Methylnissolin is primarily utilized in biomedical research as a model compound to explore mechanisms of bacterial resistance and to develop new antimicrobial therapies. Its efficacy against a range of gram-positive and gram-negative bacteria enables its widespread application in both laboratory studies and potential clinical developments. Furthermore, its unique mode of action opens avenues for exploring synergistic effects with other antibiotics, thereby enhancing the overall antibiotic arsenal. Its role is crucial in the ongoing quest to address antibiotic resistance, representing a significant advancement in the design of next-generation antimicrobials.