Polycyclic Compounds

Please enquire for more information about 5-Bromo-1-methyl-1H-indole-3-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

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L-(2S,3aR,7aS)-Octahydroindole-2-carboxylic acid is an opioid drug that binds to the μ-opioid receptor. It is a synthetic compound with affinity for the opiate receptors in the brain and spinal cord, which leads to its analgesic effects. L-(2S,3aR,7aS)-Octahydroindole-2-carboxylic acid has been industrially produced by cyclizing the dimethyl ester of L-tryptophan. This synthesis process can be carried out by refluxing 3-hydroxy indole with acetic anhydride and hydrochloric acid in methanol at 60°C for about 16 hours. The resulting product is then heated with concentrated hydrochloric acid until it crystallizes. The resulting product can then be recrystallized from hot water or ethanol and dried over magnesium sulphate. L-(

Please enquire for more information about Ethyl 2-methyl-2H-indazole-7-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 6-Fluoro-3,4-dihydro-2h-isoquinolin-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

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.

Please enquire for more information about 1-N-Cbz-1,2-dihydro-1H-spiro[indole-3,4-piperidine]HCl including the price, delivery time and more detailed product information at the technical inquiry form on this page

(+)-Epicatechin (Dexepicatechin) is a natural product and an antioxidant agent.

7-Fluorooxindole is an alkylating agent that can be used in the synthesis of oxindoles. This compound can be prepared by aldol condensation reaction with butyllithium, followed by alkylation with bromides or iodides. The use of 7-fluorooxindole and its derivatives has been optimized to yield high yields. The optimal conditions for this reaction are deprotonation with an organometallic reagent, such as butyllithium, followed by alkylation with bromides or iodides.

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2-Hydroxy methyl imidazole is an organic compound that contains a reactive hydroxyl group. It is used as a sealant in the manufacturing of paper and textiles, as well as in the production of synthetic leather. The reaction mechanism of 2-hydroxy methyl imidazole involves the formation of an inorganic acid and copper complex. The conformational properties of 2-hydroxy methyl imidazole have been studied using covalent adducts, which are molecules with metal atoms bound to them. Magnetic resonance spectroscopy has been used to study the activation energies for 2-hydroxy methyl imidazole.

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(S)-(-)-6,7-Dimethoxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid hydrochloride is a synthetic chiral compound that is used to study the role of glyoxylate in biochemical reactions. This drug is an enolate and alkylating agent that can react with nucleophiles such as amines and thiols. It has been shown to be effective against perchlorates by hydrolyzing them into chlorine and oxygen gas. This drug has also been shown to inhibit the growth of Rhodobacter sphaeroides by inhibiting glyoxylate metabolism.