
Lactones
Les lactones sont une classe d'esters caractérisés par une structure cyclique formée par l'estérification intramoléculaire des acides hydroxyliques. Ces composés sont connus pour leurs structures annulaires distinctives, qui peuvent varier de trois à sept membres ou plus. Les lactones sont largement utilisées dans l'industrie des arômes et des parfums en raison de leurs arômes agréables, ainsi que dans les produits pharmaceutiques et agrochimiques pour leurs diverses activités biologiques. Chez CymitQuimica, nous proposons une sélection complète de lactones de haute qualité pour soutenir vos applications de recherche et industrielles, garantissant des performances fiables et efficaces dans vos projets.
490 produits trouvés pour "Lactones"
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Oroselol
CAS :<p>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.</p>Formule :C14H12O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :244.24 g/mol7-Hydroxycoumarin
CAS :<p>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.</p>Formule :C9H6O3Degré de pureté :90%Couleur et forme :Off-White PowderMasse moléculaire :162.14 g/mol5-Methoxypsoralen
CAS :<p>5-Methoxypsoralen is a light-activated compound, which is a naturally derived organic substance found in certain plants, particularly from the Apiaceae family. This compound functions as a furocoumarin that interacts with DNA through photoactivation, forming cross-links upon exposure to ultraviolet A (UVA) light. These cross-links disrupt DNA replication, ultimately inhibiting cell proliferation.</p>Formule :C12H8O4Degré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :216.19 g/mol(-)-Oxypeucedanin
CAS :<p>(-)-Oxypeucedanin is a natural furanocoumarin, which is a type of organic compound. Furanocoumarins are derived from specific plants and are known for their complex structures and biological activities. (-)-Oxypeucedanin is sourced primarily from plants belonging to the Apiaceae family, such as Peucedanum species.</p>Formule :C16H14O5Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :286.28 g/mol8-Geranyloxypsoralen
CAS :<p>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.</p>Formule :C21H22O4Degré de pureté :Min. 95 Area-%Couleur et forme :Off-White PowderMasse moléculaire :338.4 g/molApterin
CAS :<p>Apterin is a naturally occurring compound, classified as a coumarin derivative, which is isolated from members of the Apiaceae family. Its source is primarily derived from plant species known for their therapeutic properties.</p>Formule :C20H24O10Degré de pureté :Min. 95 Area-%Couleur et forme :White PowderMasse moléculaire :424.4 g/molAngelicin
CAS :<p>Angelicin is a furanocoumarin compound, which is derived from various plant sources, particularly within the Apiaceae family. The source of angelicin is often linked to traditional medicinal plants, where it is extracted and subsequently isolated for scientific investigation. Angelicin's mode of action involves intercalating within DNA strands, thereby affecting transcription and replication processes. This action is understood to be primarily photoactivated, leading to the formation of covalent bonds with DNA upon exposure to ultraviolet light, which can result in cross-linking.</p>Formule :C11H6O3Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :186.16 g/mol8-Hydroxy-7-methoxycoumarin
CAS :<p>8-Hydroxy-7-methoxycoumarin is a fluorescent compound, which is a derivative of the coumarin family. This compound is typically sourced through synthetic organic chemistry processes involving the modification of natural coumarin compounds. Its mode of action involves the ability to absorb ultraviolet light and re-emit it as visible light, a characteristic feature of fluorescent molecules. This property makes it particularly useful in scientific research.</p>Formule :C10H8O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :192.17 g/mol6,7,8-Trimethoxycoumarin
CAS :<p>6,7,8-Trimethoxycoumarin is a methoxylated coumarin compound, which is a derivative of the natural product coumarin. It is primarily sourced from certain plant species where methoxylation occurs naturally as part of plant secondary metabolism. The compound exhibits interesting properties due to its structural modifications, particularly in its potential interactions with biological molecules.</p>Formule :C12H12O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :236.22 g/mol5-Geranyloxy-7-methoxycoumarin
CAS :<p>5-Geranyloxy-7-methoxycoumarin is a naturally occurring compound known as a coumarin derivative, which is primarily sourced from specific plant species such as those within the Rutaceae family. This compound is characterized by its unique chemical structure that incorporates both geranyloxy and methoxy functional groups, conferring specific biological activities.</p>Formule :C20H24O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :328.4 g/mol4-Hydroxycoumarin
CAS :<p>4-Hydroxycoumarin is a synthetic organic compound, which is a derivative of coumarin. This compound derives from a benzopyrone structure, specifically known as a precursor in the synthesis of various anticoagulant agents. Its mode of action involves the inhibition of the enzyme vitamin K epoxide reductase. This inhibition subsequently decreases the synthesis of active clotting factors II, VII, IX, and X by preventing the regeneration of reduced vitamin K.</p>Formule :C9H6O3Degré de pureté :Min. 97.5 Area-%Couleur et forme :PowderMasse moléculaire :162.14 g/molOxypeucedanin
CAS :<p>Oxypeucedanin is a furanocoumarin compound, which is derived from various plant sources, most notably those in the Apiaceae family such as Peucedanum and Angelica species. It functions primarily as a photoreactive agent, capable of interacting with DNA under ultraviolet (UV) light through a process called photoactivation. Upon UV exposure, it forms covalent bonds with DNA, leading to cross-linking that can disrupt cellular functions.</p>Formule :C16H14O5Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :286.28 g/molIsoscopoletin
CAS :<p>Isoscopoletin is a naturally occurring coumarin derivative, which is typically sourced from various plants, including some medicinal herbs. This compound is found in a variety of plant species, where it plays a role in the plant's defense mechanisms against pathogens. It is known for its characteristic chemical structure that belongs to the coumarin family, which is widespread in the plant kingdom.</p>Formule :C10H8O4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :192.17 g/molBergaptol
CAS :<p>Bergaptol is a naturally occurring furanocoumarin, which is a compound derived from plants, particularly from the Rutaceae family such as bergamot and other citrus species. It is primarily characterized by its chemical structure containing a furan ring fused to a coumarin moiety. Bergaptol acts primarily through its interaction with biological systems by inhibiting certain enzymatic activities and interfering with the biological pathways that involve reactive oxygen species. This compound exhibits antioxidant properties, reducing oxidative stress by scavenging free radicals and thereby protecting cells from damage.</p>Formule :C11H6O4Degré de pureté :Min. 95%Couleur et forme :Off-White PowderMasse moléculaire :202.16 g/mol5,7-Dimethoxycoumarin
CAS :<p>5,7-Dimethoxycoumarin is a naturally occurring coumarin derivative, which is primarily sourced from various plant species, most notably those belonging to the Apiaceae and Rutaceae families. This compound is characterized by the presence of methoxy groups at the 5 and 7 positions on the coumarin core structure. These structural features contribute to its biological activity by influencing its interaction with various biomolecular targets.</p>Formule :C11H10O4Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :206.19 g/molPoncimarin
CAS :<p>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.</p>Formule :C19H22O5Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :330.37 g/mol4-Hydroxy-3-phenylcoumarin
CAS :<p>4-Hydroxy-3-phenylcoumarin is an organic compound, which is a derivative of coumarin. It is synthetically derived through chemical modification processes that introduce a hydroxy group and a phenyl ring to the coumarin core structure. Its mechanism of action involves the inhibition of vitamin K epoxide reductase, an enzyme critical for the cyclic conversion of vitamin K. This inhibition prevents the activation of vitamin K-dependent clotting factors, thereby exerting its anticoagulant effects.</p>Formule :C15H10O3Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :238.24 g/molGlycocoumarin - Glycyrrhiza uralensis (liquorice)
CAS :<p>Glycocoumarin is a phytochemical compound that is primarily categorized as a bioactive flavonoid. It is derived from Glycyrrhiza uralensis, commonly known as liquorice, a plant renowned for its diverse pharmacological properties. The mode of action of glycocoumarin involves the modulation of various biological pathways, including its potential to influence inflammatory responses and antioxidant activity. This compound is known to interact with cellular signaling mechanisms, which could mediate its effects on immune modulation and cellular protection.</p>Formule :C21H20O6Degré de pureté :Min. 98 Area-%Couleur et forme :PowderMasse moléculaire :368.38 g/molUmbelliferone
CAS :<p>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.</p>Formule :C9H6O3Degré de pureté :Min. 98.0 Area-%Masse moléculaire :162.15 g/molRef: 3D-U-3000
1kgÀ demander50gÀ demander100gÀ demander250gÀ demander500gÀ demander-Unit-ggÀ demanderPsoralen
CAS :<p>Psoralen is a naturally occurring furocoumarin compound, which is derived from various plants, including those in the Apiaceae family, such as parsley and celery. Its mode of action involves intercalating into DNA and forming covalent cross-links when activated by ultraviolet A (UVA) light. This photoreactivity enables it to modify the biological activity of nucleic acids, making it a valuable tool in both therapeutic and experimental settings.</p>Formule :C11H6O3Degré de pureté :Min. 98 Area-%Couleur et forme :White PowderMasse moléculaire :186.16 g/mol
