Heterociclos com Oxigénio (O)

Please enquire for more information about (2Z)-6-Hydroxy-2-(3-methoxybenzylidene)-7-methyl-1-benzofuran-3(2H)-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

N-[(8-Fluoro-2,3-Dihydro-1-Methyl-5-Phenyl-1H-1,4-Benzodiazepin-2-Yl)Methyl]-3-Furancarboxamide is a hydrophobic, implanting drug with an iontophoresis device. It has been shown to have therapeutic effects in cancer. The drug is a targetable molecule that can be used for diagnostic purposes and the treatment of various cancers. N-[(8-Fluoro-2,3-Dihydro-1,5 -Phenyl 1H -1,4 Benzodiazepin 2 Yl) Methyl] 3 Furancarboxamide has been shown to inhibit cell proliferation by blocking the synthesis of proteins required for DNA replication and also inhibits the activity of protein kinase C.

Benzofuran-7-carboxylic acid is a growth factor that stimulates the release of human growth hormone. It also has been shown to stimulate the release of tryptophan and 5-hydroxytryptamine in humans. Benzofuran-7-carboxylic acid binds to receptors on gland cells, leading to increased production of peptide hormones such as ACTH. This compound can be used diagnostically for detecting the levels of camp in humans or other animals, or as a diagnostic agent for identifying human pathogens.

Please enquire for more information about 2-Methyl-N-methyltetrahydro-2-furanmethanamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

[(1S,3S)-3-[[4-Methoxy-3-(3-methoxypropoxy)phenyl]methyl]-4-methyl-1-[(2S, 4S)-tetrahydro-4-(1-methylethyl)-5-oxo-2-furanyl]pentyl]car bamic acid 1,1-tert-butyl ester is a chiral building block that has been used in the scalable synthesis of various pharmaceuticals. The synthesis begins with ammonolysis of an amino chloride and chloroacetate. This reaction is followed by acetate extraction to yield the desired product. This process can be optimized by ring opening, magnesium removal and alkylation of aromatic hydrocarbons. The final reaction is the Suzuki coupling reaction with chromatographic purification.