
Coumarins
Coumarins are a class of polycyclic aromatic compounds consisting of a benzene ring fused to a pyrone ring. These compounds are widely used as fragrances, flavoring agents, and in the synthesis of pharmaceuticals and agrochemicals. Coumarins exhibit various biological activities, including anticoagulant, anti-inflammatory, and antimicrobial properties. At CymitQuimica, we provide a wide selection of high-quality coumarins for your research and industrial applications.
Products of "Coumarins"
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7-(Dimethylamino)-4-methylcoumarin (purified by sublimation)
CAS:Formula:C12H13NO2Purity:>99.0%(GC)(T)Color and Shape:White to Green to Brown powder to crystalMolecular weight:203.24Coumestrol
CAS:Controlled ProductApplications This compound has estrogenic activity. It exhibits bright blue fluorescence in neutral or acid solution, and greenish-yellow fluorescence in strong alkali solution. References Wolfbeis, O.S. & K. Schaffner: Photochem. Photobiol., 32, 143(1980), Bickoff et al.: J.Am. Chem Soc. 80, 3969 (1958)Formula:C15H8O5Color and Shape:NeatMolecular weight:268.227-Hydroxycoumarin-3-carboxylic Acid
CAS:Formula:C10H6O5Purity:>98.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:206.15Marmin
CAS:Marmin is a natural bioactive compound, which is a type of limonoid. It is primarily sourced from citrus fruits, especially those belonging to the Rutaceae family, such as lemons and oranges. The compound exhibits a range of biological activities due to its multifaceted mode of action. Marmin functions as a calcium antagonist, which contributes to its vasodilatory effects, improving blood circulation and exhibiting potential cardiovascular benefits. Additionally, it shows anti-inflammatory and antioxidant properties, making it relevant in the context of oxidative stress-related conditions. Its action may influence pathways involved in inflammation and cellular damage, thus highlighting its therapeutic potential. The compound’s uses extend to various applications in pharmacological research. Scientists are exploring its potential roles in preventing cardiovascular diseases, reducing inflammatory responses, and managing oxidative stress. The ongoing studies aim to elucidate its efficacy and safety profile, providing insights into possible therapeutic applications. Marmin's bioactivity makes it an intriguing subject for further investigation in both fundamental research and potential clinical settings.Formula:C19H24O5Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:332.39 g/mol3-Chloro-7-hydroxy-4-methylcoumarin
CAS:Formula:C10H7ClO3Purity:>98.0%(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:210.61Isoscopoletin
CAS:LactoneFormula:C10H8O4Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:192.17ETHYL 3-COUMARINCARBOXYLATE
CAS:Purity:97.0%Color and Shape:Solid, CrystallineMolecular weight:218.207992553710944-Hydroxy-6-methylcoumarin
CAS:Formula:C10H8O3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:176.17Fraxinol
CAS:Fraxinol is a natural lignan, which is a small class of polyphenols, derived from the inner bark of the Ash tree (Fraxinus species). Its primary action is believed to involve antioxidant and anti-inflammatory pathways, where it scavenages reactive oxygen species and modulates cytokine production. This activity suggests potential modulation of cellular oxidative stress responses, contributing to its therapeutic interest. The compound is being studied extensively for its potential medicinal applications. These include its use as a supplement in the management of inflammatory conditions and as an adjunct in therapies addressing oxidative stress-related diseases. Additionally, due to its bioactivity, Fraxinol is being explored in various experimental setups to elucidate its full pharmacological spectrum, particularly in relation to its impact on cellular signaling and gene expression modification pathways. These studies aim to uncover new insights into its possible application in clinical settings.Purity:Min. 95%Seselin
CAS:Seselin is a furanocoumarin, a type of organic compound, which is typically sourced from various plant species, particularly those in the Apiaceae family. This compound is characterized by a furan ring fused with a coumarin core, contributing to its unique chemical structure. The mode of action of Seselin involves interactions at the molecular level that can influence various biochemical pathways. This includes potential binding to proteins, modulation of enzyme activities, and interactions with cellular receptors, making it a compound of interest in the study of biochemical signaling and regulation. In terms of applications, Seselin is primarily used in scientific research. Its potential biological activities, such as antimicrobial, anti-inflammatory, and anticancer properties, are subjects of extensive study. Researchers explore its interactions and effects in cell culture models and preclinical studies to better understand its mechanisms and potential therapeutic uses. Seselin's complex structure and bioactivity make it a valuable compound for experimental investigations aimed at elucidating how natural compounds can be utilized in developing new treatments or understanding biological processes.Formula:C14H12O3Purity:Min. 95%Molecular weight:228.24 g/molDaphnetin-8-methyl ether
CAS:Daphnetin-8-methyl ether is a naturally derived coumarin compound, which is predominantly sourced from the Daphne genus of plants, among other botanical species known for their therapeutic potential. This compound is recognized for its biochemical interaction with key cellular pathways, particularly through the modulation of enzymes and receptors associated with inflammatory and oxidative stress responses. The mode of action involves the inhibition of specific kinase pathways, which plays a crucial role in reducing inflammatory mediators and oxidative damage at the cellular level. This precise interaction highlights its potential utility in therapeutic research, particularly concerning inflammatory diseases and oxidative stress-related conditions. In scientific research, Daphnetin-8-methyl ether is explored for its applications in pharmacological studies focusing on chronic inflammation, neuroprotection, and other health conditions where oxidative stress is a contributing factor. Given its origin and biological activity, this compound serves as a pivotal subject for biochemical investigations aiming to elucidate novel therapeutic approaches and drug development pathways.Formula:C10H8O4Purity:Min. 95%Molecular weight:192.17 g/molAcenocoumarol
CAS:Formula:C19H15NO6Purity:>98.0%(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:353.332-(7-Methoxy-2-oxo-2H-chromen-4-yl)acetic acid
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:234.20700073242188