Composés polycycliques

Please enquire for more information about 2-(4-Hydroxyphenyl)-8-methylquinoline-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 1-Boc-4-bromo-1H-indazole including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-Bromo-7-methoxyquinoline including the price, delivery time and more detailed product information at the technical inquiry form on this page

2-Bromohypoxanthine is a fluorescent analogue of the naturally occurring nucleoside hypoxanthine. It is used as a marker for 2-bromoethoxyacetic acid (2BEA) in human serum and has been shown to be useful for prognosis of metastatic colorectal cancer. 2-Bromohypoxanthine binds to proteins that contain polyunsaturated fatty acids, such as leucovorin and fatty acids, and can be used as a diagnostic tool for detection of these proteins. 2-Bromohypoxanthine is also known to inhibit the proliferation of cancer cells by blocking the growth factor signaling pathway.

Please enquire for more information about 7-Chloro-8-methyl-2-(2-methylphenyl)quinoline-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 8-Chloro-2-(3,4-dichlorophenyl)quinoline-4-carbonyl chloride including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about 2'-Isobutyl-1'-oxo-1',4'-dihydro-2'H-spiro[cyclopentane-1,3'-isoquinoline]-4'-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

6-Chloro-5-azaindole is an organic compound that is classified as a benzyl derivative. It is used as a reagent for the synthesis of other compounds and as a chemical intermediate. 6-Chloro-5-azaindole can be synthesized by reacting benzaldehyde with hydroxyl in the presence of alkali. 6-Chloro-5-azaindole can also be obtained from chlorinated benzylic alcohols, such as 6-chloro-5-(2,4,6-trimethylbenzyl)pyridine. This compound has toxic effects and should be handled with care.

Please enquire for more information about 8-Chloro-1,2,3,4-tetrahydroisoquinoline hydrochloride 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-Methoxy-3,4-dihydroisoquinolin-1(2H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

3-Formyl-1H-indole-2-carboxylic acid is an organic compound that is a structural analog of indole. It can be used as a precursor in the synthesis of various heterocycles, such as indole, benzofuran and benzothiophene. 3-Formyl-1H-indole-2-carboxylic acid has low toxicity and can be used in catalytic reactions. The reactivity of 3-formylindoles is similar to that of 2,3,5,6 tetrahydrobenzo[b]thiophenes.

5,7-Dinitrooxindole is an oxindole that has been synthesized by the ring-opening of hydroxylated triazoles. It has a hydrophobic character due to the presence of two nitro groups in the molecule. This compound can be used as a synthetic precursor for other compounds with biological activity. 5,7-Dinitrooxindole can be oxidized with hydroxide ions to yield 7-hydroxy-5,6-dinitrooxindole, which is an optical isomer of the molecule. The conformation of 5,7-dinitrooxindole can be transferred to other molecules using amines and cyclic sulfoxides.

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.