
Lactones
Lactones are a class of esters characterized by a cyclic structure formed through the intramolecular esterification of hydroxy acids. These compounds are known for their distinct ring structures, which can range from three to seven or more members. Lactones are widely utilized in the flavor and fragrance industry due to their pleasant aromas, as well as in pharmaceuticals and agrochemicals for their diverse biological activities. At CymitQuimica, we offer a comprehensive selection of high-quality lactones to support your research and industrial applications, ensuring reliable and effective performance in your projects.
Products of "Lactones"
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Heraclenol 3'-O-β-D-apiofuranosyl-(1→6)-β-D-glucopyranoside
CAS:Formula:C27H34O15Purity:95%~99%Color and Shape:PowderMolecular weight:598.554Columbianadin
CAS:LactoneFormula:C19H20O5Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:328.367-Prenyloxycoumarin
CAS:7-Prenyloxycoumarin (Nsc267697) is a natural product from Heracleum dissectum,and possess preventive and therapeutic effects on breast cancer.Formula:C14H14O3Purity:99.50% - ≥95%Color and Shape:SolidMolecular weight:230.26Osthole
CAS:Formula:C15H16O3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:244.294-Hydroxy-6-methylcoumarin
CAS:4-Hydroxy-6-methylcoumarin (4-HMC), a natural anti-inflammatory and anti-tumor agent, is used in food as a flavor, preservative, and antioxidant.Formula:C10H8O3Purity:99.92% - 99.95%Color and Shape:White PowderMolecular weight:176.17Seselin
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:353.332H-1-Benzopyran-2-one, 7-hydroxy-6-methoxy-
CAS:Formula:C10H8O4Purity:98%Color and Shape:SolidMolecular weight:192.1681Coumarin
CAS:Coumarin is an organic chemical compound, which is a naturally occurring substance found in various plants, including tonka beans, sweet clover, and cinnamon. Structurally, it is a benzopyrone, characterized by a benzene ring fused to a lactone. Coumarin acts primarily as an anticoagulant by inhibiting the synthesis of vitamin K-dependent clotting factors in the liver. This mode of action disrupts the coagulation cascade, reducing the blood’s ability to clot effectively. In scientific research, Coumarin’s applications extend beyond its anticoagulant properties. It is utilized in the study of plant-microbe interactions due to its role in plant defense mechanisms. Additionally, Coumarin derivatives are investigated for their potential anticancer and antifungal activities, providing valuable insights into therapeutic development. Its aromatic properties also make it a subject of interest in the synthesis of fragrance and flavor compounds, though its use in consumable products is regulated due to potential hepatotoxicity. Understanding Coumarin’s diverse mechanisms and applications contributes significantly to various fields, including pharmacology, agronomy, and materials science.Formula:C9H6O2Purity:Min. 95%Color and Shape:White PowderMolecular weight:146.14 g/mol(+)-praeruptorin a
CAS:LactoneFormula:C21H22O7Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:386.46-Hydroxy-7-methoxy-4-phenylcoumarin
CAS:6-Hydroxy-7-methoxy-4-phenylcoumarin is a synthetic chemical compound classified as a coumarin derivative. Derived from natural coumarin structures, this compound is often synthesized through organic chemistry techniques involving the hydroxylation and methoxylation of coumarin backbones, with the addition of a phenyl group. Its mode of action is primarily attributed to its potential interactions with various biological pathways, including enzyme inhibition or modulation of signaling cascades. The structural configuration allows it to engage in hydrogen bonding and pi-pi interactions, facilitating its activity within biological systems. Applications of 6-Hydroxy-7-methoxy-4-phenylcoumarin are primarily in biochemical research and pharmacological studies. It is investigated for its potential roles in modulating biological processes such as inflammation, oxidative stress, and cellular signaling pathways. Moreover, its structural backbone makes it a candidate for drug development research, exploring its efficacy and mechanism of action compared to similar coumarin-based compounds.Formula:C16H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:268.26 g/mol7-Ethoxy-4-methyl-2H-chromen-2-one
CAS:Formula:C12H12O3Purity:98%Color and Shape:SolidMolecular weight:204.22188000000003Psoralidin
CAS:Psoralidin inhibits Akt phosphorylation and phosphatidylinositol 3-kinase activation and transcriptionally.Formula:C20H16O5Purity:98% - 98.75%Color and Shape:SolidMolecular weight:336.34Angelicin
CAS:Angelicin is a furocoumarin found in Psoralea corylifolia L. fruit, can block the phosphorylation of IκBα, NFκBp65, p38 MAPK, and JNK in lipopolysaccharide-induced acute lung injury model, suggests that angelicin was potentially advantageous to prevent inflammatory diseases by inhibiting NF-κB and MAPK pathways, it might be a potential new agent for prevention of inflammatory reactions and diseases in the clinic.Formula:C11H6O3Purity:95%~99%Color and Shape:PowderMolecular weight:186.166prim-O-Glucosylcimifugin
CAS:Formula:C22H28O11Purity:>97.0%(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:468.46