
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-(Diethylamino)-3-(1-methyl-2-benzimidazolyl)coumarin
CAS:Formula:C21H21N3O2Purity:>98.0%(T)(HPLC)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:347.42Nordalbergin
CAS:Nordalbergin, a coumarin isolated from the bark of Dalbergia sissoo, can significantly induce the differentiation of HL-60 cells.Formula:C15H10O4Purity:100.00% - 99.86%Color and Shape:SolidMolecular weight:254.247-Acetoxy-4-bromomethylcoumarin [for HPLC Labeling]
CAS:Formula:C12H9BrO4Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:297.10Bergaptol
CAS:Bergaptol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C11H6O4Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:202.17Scopolin
CAS:Natural glycosideFormula:C16H18O9Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:354.31Scopolin
CAS:Scopolin, a PAL-activity-induced compound, may alleviate rat AIA symptoms by curbing inflammation and angiogenesis, offering a basis for new drugs.Formula:C16H18O9Purity:99.09% - ≥95%Color and Shape:SolidMolecular weight:354.312H-1-Benzopyran-2-one, 4,7-dihydroxy-
CAS:Formula:C9H6O4Purity:97%Color and Shape:SolidMolecular weight:178.1415Br-Mmc
CAS:Br-Mmc (4-Bromomethyl-7-methoxycoumarin) is used as a new fluorescence label for fatty acids. It is used for the determination of fatty acids by HPLC or TLC.Formula:C11H9BrO3Purity:98.15%Color and Shape:Light Green-Yellow CrystalsMolecular weight:269.094-(Chloromethyl)-5-hydroxy-7-methyl-2H-chromen-2-one
CAS:Purity:90.0%Molecular weight:224.63999938964844DEAC, SE
CAS:DEAC, SE (7-Diethylaminocoumarin-3-carboxy acid) is a blue fluorescent dye for labeling amine-containing organisms. λex of DEAC, SE is 330 nm and λem is 402Formula:C18H18N2O6Purity:98.2%Color and Shape:SolidMolecular weight:358.35Umbelliferone
CAS:Umbelliferone or 7-hydroxycoumarin is a widespread natural product of the coumarin family. It occurs in many familiar plants from the umbelliferae family. Umbelliferone can be used as a fluorescence indicator for metal ions such as copper and calcium. It acts as a pH indicator in the range 6.5-8.9.Formula:C9H6O3Purity:Min. 98.0 Area-%Molecular weight:162.15 g/molRef: 3D-U-3000
1kgTo inquire50gTo inquire100gTo inquire250gTo inquire500gTo inquire-Unit-ggTo inquireCoumarin 153
CAS:Formula:C16H14F3NO2Purity:>95.0%(T)(HPLC)Color and Shape:Light yellow to Yellow to Orange powder to crystalineMolecular weight:309.29AMCA-H N-succinimidyl ester
CAS:The amine-reactive AMCA, SE (7-amino-4-methylcoumarin-3-acetic acid, succinimidyl ester) and its conjugates yield blue-fluorescence (approximate excitation/Formula:C16H14N2O6Purity:98%Color and Shape:SolidMolecular weight:331.28Oxypeucedanin methanolate
CAS:Oxypeucedanin methanolate is a naturally occurring furanocoumarin, which is a type of organic compound found predominantly in several citrus plants. This compound is derived from the peels and essential oils of these plants, highlighting its botanical source that is rich in phytochemicals. The mode of action of oxypeucedanin methanolate involves its interaction with biological systems at the molecular level. It is known to exhibit phototoxic properties by forming adducts with cellular macromolecules upon activation by ultraviolet light. Additionally, it may interfere with various biological pathways, potentially offering antioxidant, anti-inflammatory, or antimicrobial effects. In scientific research, oxypeucedanin methanolate is investigated for its potential applications in pharmacology and biochemistry. It serves as a subject of studies exploring new therapeutic agents due to its bioactive characteristics. Moreover, it is used in experimental models to study the effects of natural compounds on human health and disease mechanisms. Researchers are particularly interested in its role in drug development and as a tool for understanding plant-derived secondary metabolites and their interactions within biological systems.Formula:C17H18O6Purity:Min. 95%Molecular weight:318.32 g/molOsthole
CAS:LactoneFormula:C15H16O3Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:244.29N-Succinimidyl 7-Methoxycoumarin-3-carboxylate
CAS:Formula:C15H11NO7Purity:>98.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:317.25Toddanol
CAS:Toddanol ((-)-Toddanol) is a coumarin extracted from the roots of Toddalia.Formula:C16H18O5Purity:99.83%Color and Shape:SolidMolecular weight:290.31Daphnetin 7-methyl ether
CAS:Formula:C10H8O4Purity:95%~99%Color and Shape:Cryst.Molecular weight:192.172H-1-Benzopyran-2-one, 7,8-dihydroxy-4-methyl-
CAS:Formula:C10H8O4Purity:95%Color and Shape:SolidMolecular weight:192.16812H-1-Benzopyran-2-one, 3-amino-
CAS:Formula:C9H7NO2Purity:98%Color and Shape:SolidMolecular weight:161.15744-(Chloromethyl)-7-hydroxy-2H-chromen-2-one
CAS:Formula:C10H7ClO3Purity:>98.0%(GC)(T)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:210.613-Acetyl-6-bromocoumarin
CAS:Formula:C11H7BrO3Purity:>96.0%(GC)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:267.08Oxypeucedanin hydrate
CAS:Oxypeucedanin hydrate is a natural furanocoumarin compound, which is derived from various plant sources, such as citrus fruits and members of the Apiaceae family. As a secondary metabolite, it plays a role in plant defense mechanisms against herbivores and pathogens. The mode of action of oxypeucedanin hydrate involves interaction with enzymes and cellular pathways, exhibiting a range of biological activities including antimicrobial, anti-inflammatory, and anti-cancer effects. Its ability to inhibit specific enzymes and modulate signaling pathways makes it a compound of interest for further pharmacological studies. In scientific research, oxypeucedanin hydrate is utilized to explore its potential therapeutic applications. Its diverse biological activities suggest possible uses in developing treatments for infections, inflammatory diseases, and cancer. Researchers continue to investigate its efficacy and mechanisms of action, contributing to the broader understanding of furanocoumarins and their potential benefits in medicine.Purity:Min. 95%7-Hydroxycoumarin
CAS:7-Hydroxycoumarin is a fluorescent compound, known as a coumarin derivative, which is a naturally occurring chemical found in many plants. Derived from the umbelliferone compound family, it exhibits strong blue fluorescence under UV light due to its unique structural properties. This fluorescence is a result of its molecular conjugation and the electron-donating nature of the hydroxyl group, allowing it to absorb and emit light efficiently. The compound has notable applications in biochemical research areas such as enzyme activity assays, where it serves as a non-radioactive marker. Additionally, its photostability and sensitivity make it an excellent choice for studying cell function and interactions via fluorescence microscopy. In forensic science, 7-Hydroxycoumarin is used for detecting latent fingerprints, taking advantage of its photophysical properties. Furthermore, its utility extends to the pharmaceutical industry, where it contributes to the investigation of metabolic processes involving cytochrome P450 enzymes. Importantly, its biocompatibility and versatile nature underline its significant value in various scientific investigations.Formula:C9H6O3Purity:90%Color and Shape:Off-White PowderMolecular weight:162.14 g/mol4-Methylumbelliferyl-a-D-galactopyranoside
CAS:M02744 - 4-Methylumbelliferyl-a-D-galactopyranosideFormula:C16H18O8Purity:98%Color and Shape:Solid, White powderMolecular weight:338.312011718753-Hydroxycoumarin
CAS:3-Hydroxycoumarin is a natural compound, and is human 15-LOX-1 inhibitorsFormula:C9H6O3Purity:98.32% - 99.5%Color and Shape:SolidMolecular weight:162.147-Hydroxy-4-(4-pyridyl)coumarin
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:239.229995727539064-Methylesculetin
CAS:Formula:C10H8O4Purity:>98.0%(T)(HPLC)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:192.176-HYDROXYCOUMARIN
CAS:Formula:C9H6O3Purity:95%Color and Shape:SolidMolecular weight:162.142139999999962H-1-Benzopyran-2-one, 6-amino-
CAS:Formula:C9H7NO2Purity:97%Color and Shape:SolidMolecular weight:161.15747-(Diethylamino)-3-(thiophene-3-carbonyl)-2H-chromen-2-one
CAS:Purity:97%Molecular weight:327.3999938964842H-1-Benzopyran-2-one, 3-(2-benzothiazolyl)-7-(diethylamino)-
CAS:Formula:C20H18N2O2SPurity:98%Color and Shape:SolidMolecular weight:350.43416-Chloro-7-hydroxy-4-(trifluoromethyl)coumarin
CAS:Purity:95.0%Color and Shape:Solid, No data available.Molecular weight:264.57998657226564-Hydroxycoumarin
CAS:4-Hydroxycoumarin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C9H6O3Purity:(HPLC) ≥95%Color and Shape:PowderMolecular weight:162.15Decursinol
CAS:Decursinol is isolated from the roots of Angelica Gigas with an antinociceptive effect. It also has anti-tumor and anti-metastasis activity.Formula:C14H14O4Purity:99.19% - 99.34%Color and Shape:SolidMolecular weight:246.26Ref: TM-T8169
1mg47.00€5mg96.00€10mg140.00€25mg225.00€50mg335.00€100mg489.00€500mgTo inquire1mL*10mM (DMSO)96.00€Esculetin
CAS:Esculetin analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C9H6O4Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:178.157-Diethylamino-4-methylcoumarin
CAS:Formula:C14H17NO2Purity:>98.0%(GC)(T)Color and Shape:White to Amber to Dark green powder to crystalMolecular weight:231.304-Butoxy-2H-1-benzopyran-2-one
CAS:Controlled ProductFormula:C13H14O3Color and Shape:NeatMolecular weight:218.25Coumarin 510
CAS:Formula:C20H18N2O2Purity:>98.0%(HPLC)(N)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:318.382-(7-Hydroxy-2-oxo-2H-chromen-4-yl)acetic acid
CAS:2-(7-Hydroxy-2-oxo-2H-chromen-4-yl)acetic acid is a useful organic compound for research related to life sciences.Formula:C11H8O5Color and Shape:SolidMolecular weight:220.17822-Oxo-2H-chromen-7-yl Trifluoromethanesulfonate
CAS:Formula:C10H5F3O5SPurity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:294.208-Methoxypsoralen
CAS:8-Methoxypsoralen is a furocoumarin compound, which is derived from natural plant sources such as the seeds of the Ammi majus plant. Its primary mode of action involves intercalation into DNA strands and the formation of covalent bonds with pyrimidine bases upon exposure to ultraviolet A (UVA) light. This interaction results in the inhibition of DNA synthesis and cell proliferation. The compound finds extensive applications in the field of dermatology, particularly in PUVA (psoralen and UVA) therapy for the treatment of skin disorders such as psoriasis, vitiligo, and mycosis fungoides. By inducing controlled DNA damage and modulating immune responses, 8-Methoxypsoralen helps reduce the overproduction of skin cells and alleviates symptoms. Its efficacy in repigmenting skin and managing inflammatory skin conditions has been well-documented, making it a valuable agent in therapeutic photochemotherapy protocols.Formula:C12H8O4Purity:Min. 95%Color and Shape:White PowderMolecular weight:216.19 g/mol3-Aminocoumarin
CAS:3-Aminocoumarin (3-aminochromen-2-one) is the key intermediate for the metal complexes.Formula:C9H7NO2Purity:99.53% - 99.54%Color and Shape:SolidMolecular weight:161.165,7-dihydroxy 4-methylcoumarin
CAS:LactoneFormula:C10H8O4Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:192.17Potassium 7-nitro-2-oxo-2H-chromene-3-carboxylate
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:273.24099731445317-(Diethylamino)-3-(1-methyl-2-benzimidazolyl)coumarin
CAS:7-(Diethylamino)-3-(1-methyl-2-benzimidazolyl)coumarin is a fluorescent dye, which is synthesized through chemical derivatization of coumarin compounds. Originating from coumarin, a naturally occurring compound in plants, this dye is particularly noted for its ability to fluoresce under UV and visible light. The mode of action involves its excited electron state, which emits light upon returning to a ground state, making it useful for applications requiring visualization under a microscope or spectrometer. This photophysical property is central to its role as a reporter in various biological and chemical assays. Primarily, this compound finds applications in the fields of biochemistry and molecular biology for its utility in fluorescence microscopy, flow cytometry, and cell viability assays. It is an integral tool for tracing biochemical pathways, analyzing cellular components, and assessing physiological functions in living cells. By conjugating with specific biomolecules, researchers can obtain detailed information on molecular interactions and dynamics within complex biological systems, aiding in a deeper understanding of biological processes.Formula:C21H21N3O2Purity:Min. 95%Molecular weight:347.41 g/molAnomelin
Anomelin is a synthetic anticancer compound, which is derived from complex organic synthesis methodologies. This compound is typically produced through careful laboratory processes due to its intricate chemical structure, which is crafted to target specific molecular pathways involved in cancer cell proliferation. The mode of action of Anomelin involves the inhibition of key enzymes in cell growth pathways, specifically targeting the signaling processes that regulate cell division and apoptosis. By interfering with these pathways, Anomelin can induce cell cycle arrest and promote programmed cell death in malignant cells, thereby inhibiting tumor growth. In terms of uses and applications, Anomelin is primarily explored within the context of oncology research. Scientists are investigating its efficacy in preclinical studies, focusing on its potential to act as a therapeutic agent against various types of cancer, especially those that have shown resistance to conventional treatments. Research is ongoing to determine the specific types of cancers most responsive to Anomelin and to further elucidate its pharmacokinetics and safety profile.Purity:Min. 95%8-ACETYL DIMETHOXYCOUMARIN
CAS:Formula:C11H8O3Purity:95%Color and Shape:SolidMolecular weight:188.17942Scopoletin
CAS:Scopoletin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C10H8O4Purity:(HPLC) ≥99%Color and Shape:PowderMolecular weight:192.172-Oxo-2H-chromene-6-sulfonyl chloride
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:244.649993896484387-Hydroxycoumarin-3-carboxylic acid
CAS:7-Hydroxycoumarin-3-carboxylic acid (7-HC-3-CA) is a safe anti-browning agent that inhibits tyrosinase activity, useful for studying food preservation.Formula:C10H6O5Purity:99.94%Color and Shape:SolidMolecular weight:206.15Poncimarin
CAS:Poncimarin is a citrus-derived flavor compound, which is extracted from the peels of citrus fruits. Its mode of action involves mimicking natural citrus flavors, providing authentic taste profiles through a combination of volatile compounds that resemble those found in fresh citrus. The primary application of Poncimarin lies in its utilization as a flavoring agent in the food and beverage industry. It is incorporated to enhance the sensory attributes of products like beverages, confectioneries, and baked goods, delivering a refreshing citrus note that is both recognizable and appealing. Poncimarin's efficacy is attributed to its ability to integrate seamlessly with the existing flavor matrices of these products, ensuring a balanced and natural sensory experience. Its use extends to applications requiring stable, long-lasting flavor profiles, contributing to product innovation and development within sensory science.Formula:C19H22O5Purity:Min. 95%Color and Shape:PowderMolecular weight:330.37 g/mol2H-1-Benzopyran-2-one, 6-bromo-7-hydroxy-4-(hydroxymethyl)-
CAS:Formula:C10H7BrO4Purity:98%Molecular weight:271.06427H-Furo[3,2-g][1]benzopyran-7-one, 9-[(3-methyl-2-butenyl)oxy]-
CAS:Formula:C16H14O4Purity:98%Color and Shape:SolidMolecular weight:270.282-oxo-2H-chromene-3-carbonitrile
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:171.15499877929688Auraptene
CAS:Formula:C19H22O3Purity:>98.0%(HPLC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:298.38Isodemethylwedelolactone
CAS:Isodemethylwedelolactone (Isodemethylwedelolacton) is a natual product,has Clotting activity.Formula:C15H8O7Purity:98% - 99.71%Color and Shape:SolidMolecular weight:300.224-Methyl-6,7-methylenedioxycoumarin
CAS:Formula:C11H8O4Purity:min. 99.0 %(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:204.18Esculin
CAS:Esculin analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H16O9Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:340.294-Methylumbelliferyl-β-D-glucuronid Hydrat 4-Methylumbelliferyl-β-D-glucuronide Hydrate
CAS:Formula:C16H18O10Purity:98%Color and Shape:SolidMolecular weight:370.308119999999867-Hydroxycoumarin-d5 sulfate
CAS:Formula:C9HD5O6SColor and Shape:Off-White SolidMolecular weight:247.233-Hydroxycoumarin
CAS:3-Hydroxycoumarin is a coumarin derivative, which is a type of organic compound with significant pharmacological interest. It is derived from the parent structure of coumarin, naturally found in various plant sources such as tonka beans and sweet clover. Its molecular structure includes a hydroxyl group added at the third position of the coumarin backbone, conferring distinct chemical properties. The mode of action of 3-Hydroxycoumarin is primarily attributed to its interaction with biological macromolecules, enabling it to inhibit enzymes and interfere with cellular processes. This compound is known for its ability to act as an anticoagulant by inhibiting vitamin K-dependent synthesis of clotting factors, similar to warfarin. 3-Hydroxycoumarin has various applications, particularly in the field of medicinal chemistry, where it is explored for its potential therapeutic effects. It serves as a pivotal scaffold in the development of anticoagulant drugs and has been investigated for its antioxidant, antimicrobial, and anticancer properties. Its diverse biological activities make it a subject of ongoing research, with potential applications extending to drug development and biochemical studies.Formula:C9H6O3Purity:Min. 95%Color and Shape:PowderMolecular weight:162.14 g/mol[(6-chloro-3,4-dimethyl-2-oxo-2H-chromen-7-yl)oxy]acetic acid
CAS:Purity:95.0%Molecular weight:282.679992675781254-Methylumbelliferyl-N-acetyl-ß-D-glucosaminide
CAS:Purity:95.0%Color and Shape:Solid, White to off-white powderMolecular weight:379.3649902343752H-1-Benzopyran-2-one, 7-amino-4-methyl-
CAS:Formula:C10H9NO2Purity:98%Color and Shape:SolidMolecular weight:175.184Ref: IN-DA002RNE
1g25.00€5g43.00€10g61.00€25g113.00€50g162.00€100g223.00€250g518.00€500gTo inquire250mg25.00€Esculetin dibenzyl ether
CAS:Esculetin dibenzyl ether is a chemical compound, which is a derivative of esculetin, a natural coumarin obtained chiefly from plant sources such as the bark of horse chestnut and other similar species. The source of esculetin dibenzyl ether is typically synthesized from natural precursors through chemical modifications, allowing for the exploration of its structural analogs. The mode of action of esculetin dibenzyl ether involves interactions at the molecular level with various biological pathways. Its structural attributes allow for the potential modulation of enzyme activity, antioxidant properties, and interactions with cellular signaling mechanisms, which are areas of considerable interest in scientific research. This compound finds uses primarily in research applications, serving as a tool for investigating the biological activities and therapeutic potential of coumarin derivatives. Specifically, it is used in the study of anti-inflammatory, antioxidant, and potential anticancer properties, making it valuable in drug discovery and development contexts. Its application is crucial in elucidating the mechanistic pathways of natural compounds and their synthetic analogs in biological systems.Formula:C23H18O4Purity:Min. 95%Molecular weight:358.39 g/molEthyl 6-Bromocoumarin-3-carboxylate
CAS:Formula:C12H9BrO4Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:297.104-Hydroxy-7-methylcoumarin
CAS:Formula:C10H8O3Purity:>95.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:176.176',7'-Dihydroxybergamottin acetonide
CAS:Formula:C24H28O6Purity:95%~99%Color and Shape:PowderMolecular weight:412.4823-Aminocoumarin
CAS:Formula:C9H7NO2Purity:>98.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:161.167-(Diethylamino)-4-(trifluoromethyl)coumarin
CAS:Formula:C14H14F3NO2Purity:>98.0%(GC)Color and Shape:Yellow to Brown to Dark green powder to crystalMolecular weight:285.27Byakangelicol
CAS:LactoneFormula:C17H16O6Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:316.31Umbelliferone
CAS:Formula:C9H6O3Purity:>98.0%(GC)Color and Shape:White to Gray to Brown powder to crystalMolecular weight:162.14Seselin
CAS:Seselin is a natural product from Plumbago zeylanica. Seselin shows anti-inflammatory and antiviral activity.Formula:C14H12O3Purity:100% - 99.96%Color and Shape:SolidMolecular weight:228.24Ref: TM-TN5891
1mg87.00€5mg188.00€10mg329.00€25mg548.00€50mg782.00€100mg1,035.00€1mL*10mM (DMSO)180.00€4-Methylumbelliferyl Phosphate
CAS:Formula:C10H9O6PPurity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:256.153-Acetyl-5-hydroxymethyl-7-hydroxycoumarin
CAS:3-Acetyl-5-hydroxymethyl-7-hydroxycoumarin is a synthetic coumarin derivative, which is a class of organic compounds often found in natural products. These compounds are derived from plant sources and are known for their significant biochemical effects and aromatic properties. The mode of action of 3-Acetyl-5-hydroxymethyl-7-hydroxycoumarin involves interactions at the molecular level, where it can exhibit various biological activities, such as antioxidant and antimicrobial effects. Due to the hydroxyl and acetyl functional groups present, it can participate in redox reactions and binding interactions, affecting biochemical pathways. In scientific research, this compound is explored for its potential applications in pharmacology and biochemistry. The compound's ability to modulate oxidative stress and microbial growth makes it valuable for studying disease models and developing therapeutic agents. Additionally, its structural properties allow for further chemical modifications, facilitating the synthesis of derivatives with enhanced or targeted activities.Formula:C12H10O5Purity:Min. 95%Color and Shape:Light (Or Pale) Yellow To Orange Yellow SolidMolecular weight:234.2 g/mol8-Acetyl-7-hydroxy-4-methylcoumarin
CAS:Formula:C12H10O4Purity:>98.0%(GC)Color and Shape:Light orange to Yellow to Green powder to crystalMolecular weight:218.21Oxypeucedanin hydrate
CAS:LactoneFormula:C16H16O6Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:304.3Murralongin
CAS:Murralongin is a natural compound that falls under the category of sesquiterpenes, a class of terpenoids characterized by their three isoprene units. It is derived from the leaves and stems of the plant Eremophila mitchellii, a species known for its rich diversity of bioactive compounds often utilized in traditional medicine. The primary mode of action of Murralongin involves modulation of specific enzymatic pathways, potentially influencing a range of biological processes, including anti-inflammatory and antimicrobial activities. Recent studies have focused on its potential therapeutic uses, exploring its efficacy as an anti-cancer agent by targeting cellular pathways involved in cancer cell proliferation and survival. Additionally, Murralongin's ability to inhibit certain microbial growth suggests applications in developing new antimicrobial drugs, addressing issues related to resistant bacterial strains. Furthermore, its anti-inflammatory properties imply potential applications in managing chronic inflammatory conditions, where current treatments may have significant limitations or side effects. Overall, Murralongin represents a promising subject for further research with the potential to contribute significantly to the development of new therapeutic agents.Formula:C15H14O4Purity:Min. 95%Molecular weight:258.27 g/molCoumestrol
CAS:Coumestrol analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C15H8O5Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:268.23Heratomol
CAS:Please enquire for more information about Heratomol including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C11H6O4Purity:Min. 95%Molecular weight:202.16 g/molSkimmin
CAS:Skimmin is a bioactive compound, classified as a coumarin, which is derived from various plant sources, particularly the bark of certain tree species. It functions through the modulation of enzyme activity, including antioxidant and anti-inflammatory pathways, by interacting with specific cellular receptors and enzymes. The primary use of Skimmin in scientific research is to explore its potential therapeutic effects, particularly in areas such as oncology, cardiovascular health, and metabolic diseases. Its ability to modulate physiological processes at the cellular level allows scientists to investigate its efficacy in inhibiting tumor growth, reducing oxidative stress, and lowering inflammation. Additionally, it serves as a crucial tool for elucidating biochemical pathways associated with human diseases. The compound's diverse biological activities make it an important molecule for pharmacological studies, with ongoing research aimed at understanding its full range of mechanisms and potential therapeutic applications. Scientists focus on optimizing its efficacy and bioavailability, seeking to unlock new avenues for medicinal chemistry and drug development.Formula:C15H16O8Purity:Min. 95%Color and Shape:PowderMolecular weight:324.28 g/molEsculin hydrate(2:3)
CAS:Formula:C30H38O21Purity:99%Color and Shape:SolidMolecular weight:734.61012000000037-hydroxy-4-methyl-2-oxo-2H-chromene-8-carbaldehyde
CAS:Purity:98%Molecular weight:204.18099975585938Ref: 10-F366810
5mgTo inquire10mgTo inquire25mgTo inquire50mgTo inquire100mgTo inquire250mgTo inquire500mgTo inquireOroselol
CAS:Oroselol is an innovative beta-adrenergic blocker, which is a synthetic derivative with unique cardiovascular targeting properties. It is sourced from engineered chemical synthesis, utilizing advanced molecular design to enhance selectivity for beta-adrenergic receptors. The mode of action of Oroselol involves competitive antagonism of beta-1 and beta-2 adrenergic receptors, leading to a decrease in heart rate and myocardial contractility. This blockade of adrenergic stimulation results in reduced cardiac output and lower blood pressure. The primary uses of Oroselol lie in its potential applications for managing cardiovascular conditions such as hypertension, angina pectoris, and arrhythmias. Its precise receptor selectivity may offer a therapeutic advantage over traditional beta-blockers by minimizing side effects associated with non-targeted action. Oroselol's pharmacokinetics and dynamic properties are being closely studied to understand its efficacy and safety profile in clinical settings. This compound's novel aspects make it a subject of considerable interest in pharmacological research, where its impact on cardiovascular therapy continues to be evaluated.Formula:C14H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:244.24 g/molResveratrol-4'-O-(6"-galloyl)-β-D-glucopyranoside
CAS:Formula:C27H26O12Purity:95%~99%Molecular weight:542.4937-Methylcoumarin
CAS:Formula:C10H8O2Purity:>98.0%(GC)Color and Shape:White to Light yellow powder to crystalMolecular weight:160.17trans-Khellactone
CAS:Trans-Khellactone is a naturally occurring lactone derivative, which is isolated from plants of the Apiaceae family. This compound exhibits a variety of biological functions due to its unique chemical structure, which includes a dihydropyran ring. Trans-Khellactone's mode of action involves interacting with various cellular pathways, potentially modulating enzyme activity, receptor binding, and influencing signal transduction processes. Due to its diverse range of activities, trans-Khellactone is of significant interest in the field of medicinal chemistry. It has been studied for its potential therapeutic applications, including anti-inflammatory, anti-cancer, and anti-microbial effects. Research into trans-Khellactone's mechanisms and efficacy continues to expand its possible applications in drug development and other areas of biomedical research.Formula:C14H14O5Purity:Min. 95%Molecular weight:262.26 g/molIsopimpinellin
CAS:LactoneFormula:C13H10O5Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:246.224,7-Dihydroxy-3-phenyl-2H-chromen-2-one
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:254.240997314453122H-1-Benzopyran-3-carboxylic acid, 7-(diethylamino)-2-oxo-, 2,5-dioxo-1-pyrrolidinyl ester
CAS:Formula:C18H18N2O6Purity:98%Color and Shape:SolidMolecular weight:358.3453Peuarin
CAS:Please enquire for more information about Peuarin including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C20H22O6Purity:Min. 95%Molecular weight:358.39 g/mol(+)-Peucedanol
CAS:(+)-Peucedanol is a sesquiterpene compound, which is a type of natural organic compound composed of three isoprene units resulting in a 15-carbon backbone. It is derived from various species within the plant genus Peucedanum, known for their rich content of bioactive compounds. The stereoisomerism indicated by the "(+)" suggests a specific three-dimensional configuration that may influence its biological activity. The mode of action of (+)-Peucedanol is not completely elucidated but is thought to involve interactions with cellular components leading to modulation of pathways associated with anti-inflammatory and possibly antioxidant effects. By interacting at the molecular level, it may influence the biological processes that govern inflammation and oxidative stress. (+)-Peucedanol finds application in scientific research, primarily in the study of its pharmacological properties. Researchers focus on its potential therapeutic uses, exploring its efficacy in inflammation-related diseases and its role in cellular protection mechanisms. The compound's effects on cellular signaling pathways and potential as a lead compound for drug development are areas of ongoing investigation.Formula:C14H16O5Purity:Min. 95%Molecular weight:264.27 g/mol7-Amino-4-(trifluoromethyl)coumarin
CAS:Formula:C10H6F3NO2Purity:>97.0%(GC)(T)Color and Shape:Light yellow to Yellow powder to crystalMolecular weight:229.167-Methoxy-8-(3-methyl-2-buten-1-yl)-2H-chromen-2-one
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:244.2899932861328Daphnetin-7-methylether
CAS:Daphnetin-7-methylether analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C10H8O4Purity:(HPLC) ≥90%Color and Shape:PowderMolecular weight:192.173-Bromo-7-hydroxy-4-methylchromen-2-one
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:255.067001342773442H-1-Benzopyran-2-one, 7-(ethylamino)-4,6-dimethyl-
CAS:Formula:C13H15NO2Purity:98%Color and Shape:SolidMolecular weight:217.26377-Hydroxy Coumarin Glucuronide Sodium Salt
CAS:Formula:C15H13O9·NaColor and Shape:White To Off-White SolidMolecular weight:337.26 22.99Arnottinin
CAS:Arnottinin is a bioactive compound, which is derived from natural plant sources. It functions primarily through modulation of specific cellular pathways, targeting key receptors that regulate physiological responses. This compound exhibits its mode of action by influencing signal transduction pathways, effectively altering cellular activities at the molecular level. Arnottinin is known for its applications in various biomedical research settings. It is commonly utilized in the study of disease pathogenesis, particularly in examining inflammatory mechanisms and cellular growth processes. Researchers employ it to explore therapeutic potentials in oncology and neurodegenerative diseases, owing to its ability to interact with cellular targets. Additionally, Arnottinin serves as a pivotal tool in drug discovery, facilitating the development of more targeted and efficient therapeutic agents.Formula:C14H14O4Purity:Min. 95%Molecular weight:246.26 g/molEsculin
CAS:Natural glycosideFormula:C15H16O9Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:340.29N-Succinimidyl 7-Hydroxy-4-methylcoumarin-3-acetate
CAS:Formula:C16H13NO7Purity:>90.0%(HPLC)(N)Color and Shape:White to Almost white powder to crystalMolecular weight:331.28Dihydroseselin
CAS:Dihydroseselin (8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-2-one) is a coumarin derived from the roots of Toddalia.Formula:C14H14O3Purity:99.30%Color and Shape:SolidMolecular weight:230.26Ref: TM-TN1587
1mg63.00€5mg129.00€10mg187.00€25mg320.00€50mg449.00€100mg638.00€200mg842.00€1mL*10mM (DMSO)116.00€Byakangelicol
CAS:Byakangelicol may reduce P-gp at BBB and has anti-inflammatory effects by hindering COX-2 and PGE2 in A549 cells.Formula:C17H16O6Purity:99.15% - 99.55%Color and Shape:SolidMolecular weight:316.31Alloisoimperatorin
CAS:Alloisoimperatorin is a naturally occurring furanocoumarin compound, which is extracted from certain plant species, primarily those belonging to the Apiaceae family. As a type of coumarin derivative, it is synthesized through intricate plant metabolic pathways involving the precursors umbelliferone and isopentenyl pyrophosphate, among others. The mode of action of alloisoimperatorin is not completely elucidated, but it is believed to exert biological effects through modulation of enzymatic activities and interference with cellular signaling pathways. Its interaction with cytochrome P450 enzymes and perturbation of calcium ion channels might contribute to its diverse biological activities. Alloisoimperatorin is of considerable interest for its potential pharmacological applications, particularly in the fields of anti-inflammatory and anti-cancer research. It has been explored for its inhibitory effects on tumor cell proliferation and its capability to induce apoptosis in vitro. Additionally, due to its structural properties, it may serve as a precursor or inspiration for the development of novel therapeutic agents. Further research is necessary to fully understand its mechanisms and to evaluate its efficacy and safety in clinical contexts.Formula:C16H14O4Purity:Min. 95%Molecular weight:270.28 g/mol8-Geranyloxypsoralen
CAS:8-Geranyloxypsoralen is a natural furanocoumarin, which is a secondary metabolite typically derived from plants, particularly those in the Rutaceae family. Its source lies predominantly in certain fruits and herbs, where it functions as a natural defense compound. The mode of action of 8-Geranyloxypsoralen involves its interaction with DNA upon activation by ultraviolet (UV) light. It can form covalent bonds with pyrimidine bases, primarily thymine, in the DNA strands. This interaction leads to the formation of monoadducts, which can subsequently result in crosslinking upon further exposure to UV-A, disrupting DNA replication and transcription processes. 8-Geranyloxypsoralen finds its applications in phototherapy and is often studied for its potential therapeutic uses in skin diseases, such as psoriasis, and vitiligo. Its ability to modulate biological responses under light exposure makes it a candidate for further exploration in understanding light-mediated cellular processes. Furthermore, it provides insights into plant defense mechanisms and the complex interactions between plant-derived compounds and biological systems under environmental stressors.Formula:C21H22O4Purity:Min. 95 Area-%Color and Shape:Off-White PowderMolecular weight:338.4 g/mol2-Oxo-2H-chromene-3-carbonitrile
CAS:Formula:C10H5NO2Purity:98%Color and Shape:SolidMolecular weight:171.15220000000002Coumarin 545
CAS:Formula:C22H18N2O2SPurity:97%Color and Shape:SolidMolecular weight:374.45551999999987-methoxycoumarin
CAS:LactoneFormula:C10H8O3Purity:≥ 98.0 % (HPLC)Color and Shape:PowderMolecular weight:176.17Isoimperatorin
CAS:Isoimperatorin is a naturally occurring furanocoumarin, which is a phytochemical compound found in certain plants, particularly within the Apiaceae family, such as Angelica dahurica. It is extracted from these botanical sources through processes like solvent extraction. Isoimperatorin exhibits a diverse mode of action, including the inhibition of various enzymes and modulation of signaling pathways. It has demonstrated significant effects on cytochrome P450 enzymes, potentially influencing drug metabolism. Additionally, Isoimperatorin has shown antioxidant properties and the ability to interfere with cell proliferation and apoptosis mechanisms. Isoimperatorin is extensively studied for its potential therapeutic applications. Research indicates promising uses in pharmacology, particularly in areas involving anti-inflammatory, anticancer, and antimicrobial effects. Its ability to interact with enzymatic processes suggests potential roles in drug development and metabolic studies. Additionally, Isoimperatorin is of interest in the field of agriculture as a natural pesticide due to its bioactivity against certain pests. Ongoing research continues to explore its full spectrum of biological activities and possible applications in both medical and industrial domains.Formula:C16H14O4Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:270.29 g/molCoumarin 6
CAS:Coumarin 6 (Coumarin VI) is a fluorescent dye frequently used to facilitate the traceability of drug delivery systems in vitro.Formula:C20H18N2O2SPurity:99.13%Color and Shape:Orange Crystalline PowderMolecular weight:350.43Coumarin
CAS:Formula:C9H6O2Purity:>99.0%(GC)Color and Shape:White powder to crystalMolecular weight:146.157-(Diethylamino)-3-(2-thienyl)coumarin
CAS:Formula:C17H17NO2SPurity:>98.0%(T)(HPLC)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:299.397-Ethoxycoumarin
CAS:Formula:C11H10O3Purity:>97.0%(GC)Color and Shape:White to Light red to Green powder to crystalMolecular weight:190.207,8-Dimethoxycoumarin
CAS:7,8-Dimethoxycoumarin is a natural product isolated from Artemisia caruifolia and Wikstroemia indica.Formula:C11H10O4Purity:99.82%Color and Shape:SolidMolecular weight:206.197-(Diethylamino)coumarin
CAS:Formula:C13H15NO2Purity:>98.0%(GC)(T)Color and Shape:Light yellow to Yellow to Green powder to crystalMolecular weight:217.277-Methoxycoumarin-3-carboxylic acid
CAS:7-Methoxycoumarin-3-carboxylic acid is used for HPLC derivatization. It is also used to develop FRET probes for analyzing protease activities.Formula:C11H8O5Color and Shape:SolidMolecular weight:220.184-Methyl-2-oxo-2H-chromen-7-yl acetate
CAS:Formula:C12H10O4Purity:95%Color and Shape:SolidMolecular weight:218.2054Oxypeucedanin hydrate acetate
Oxypeucedanin hydrate acetate is a furanocoumarin, primarily classified as a phytochemical. It is derived from various plant sources, particularly from species in the Apiaceae family, such as Peucedanum and Angelica. These compounds are typically isolated through advanced extraction and chromatographic techniques. The mode of action of oxypeucedanin hydrate acetate involves the inhibition of cytochrome P450 enzymes, which play a pivotal role in the metabolism of drugs within the liver. This compound can influence the pharmacokinetics of co-administered pharmaceuticals and is thereby of significant interest to pharmacologists and toxicologists. In research, oxypeucedanin hydrate acetate has been investigated for its potential applications in cancer therapy, owing to its ability to induce apoptosis in certain cancer cell lines. Additionally, it is studied for its antimicrobial properties and its role in modulating cellular oxidative stress responses. These attributes make it a valuable subject in the exploration of new therapeutic agents and in understanding herb-drug interactions within complex biological systems.Purity:Min. 95%7-Acetoxy-4-methylcoumarin
CAS:Formula:C12H10O4Purity:>98.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:218.218-Hydroxybergapten
CAS:8-Hydroxybergapten may have anti-wrinkle activity.Formula:C12H8O5Purity:99.91%Color and Shape:SolidMolecular weight:232.19Ethyl 7-methoxy-2-oxo-2H-1-benzopyran-3-carboxylate
CAS:Purity:98%Molecular weight:248.23399353027344Umckalin
CAS:LactoneFormula:C11H10O5Purity:≥ 95.0 % (HPLC)Color and Shape:CrystalsMolecular weight:222.2Epoxybergamottin
CAS:LactoneFormula:C21H22O5Purity:≥ 90.0 % (HPLC)Color and Shape:PowderMolecular weight:354.4Coumestrol dimethylether
CAS:Coumestrol dimethylether analytical standard provided with w/w absolute assay, to be used for quantitative titration.Formula:C17H12O5Purity:(HPLC) ≥98%Color and Shape:PowderMolecular weight:296.284-Methylumbelliferyl β-D-xylopyranoside
CAS:M04141 - 4-Methylumbelliferyl beta-D-xylopyranosideFormula:C15H16O7Purity:98%Color and Shape:Solid, No data available.Molecular weight:308.2860107421875Dihydro coumarin
CAS:Dihydro coumarin is a cyclic organic compound, which is a derivative of coumarin primarily obtained through synthetic processes. It possesses the characteristic odor reminiscent of freshly mown hay, contributing to its widespread application in various industries. The primary mode of action of dihydro coumarin involves its role as a fragrance and flavoring agent, capitalizing on its aromatic profile to enhance products’ sensory attributes. In usage and applications, dihydro coumarin is extensively employed in the flavor and fragrance industries due to its pleasant scent. It is often integrated into perfumes, lotions, and soaps to impart a sweet, soothing fragrance. Additionally, it serves as a flavoring component in food products, particularly in scenarios where a vanilla-like or nutty flavor profile is desired. Furthermore, dihydro coumarin’s stability and non-toxic nature make it a preferred choice in formulations requiring a durable aromatic presence. Researchers in these fields continue to explore its potential, focusing on sustainable production methods and novel applications.Formula:C9H8O2Purity:Min. 95%Molecular weight:148.16 g/mol(±)-Decursinol
CAS:(±)-Decursinol (3',4'-dihydro-3'-hydroxy-Xanthyletin) is a natural product from Angelica gigas.Formula:C14H14O4Purity:98.01%Color and Shape:SolidMolecular weight:246.267-Ethoxy-4-methylcoumarin
CAS:7-Ethoxy-4-methylcoumarin is a fluorescent probe, which is a synthetic compound commonly sourced from organic chemical synthesis. With its distinct chromophore, this compound becomes highly fluorescent upon enzymatic cleavage, offering a reliable mechanism for the detection of specific enzymatic activities. The mode of action involves the enzymatic cleavage of the ethoxy group, leading to the release of 4-methylumbelliferone, a fluorescent product. This conversion provides a measurable signal that correlates with enzyme activity, making it an invaluable tool in studying enzyme kinetics. This compound's uses and applications are primarily within biochemical and pharmacological research. It is employed in assays to monitor cytochrome P450 enzyme activity, particularly in examining capabilities related to oxidative metabolism. Beyond its pivotal role in enzyme assays, 7-Ethoxy-4-methylcoumarin also finds applications in drug discovery, toxicological studies, and mechanistic enzymology, aiding researchers in determining substrate specificities and enzyme inhibitors with precision.Formula:C12H12O3Purity:Min. 95%Color and Shape:PowderMolecular weight:204.22 g/molBakuchicin
CAS:LactoneFormula:C11H6O3Purity:≥ 95.0 % (HPLC)Color and Shape:PowderMolecular weight:186.177-(Diethylamino)coumarin-3-carboxylic Acid
CAS:Formula:C14H15NO4Purity:>98.0%(GC)(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:261.28