【结 构 式】 |
【药物名称】 【化学名称】3,5-Dibenzoyl-4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine 【CA登记号】359764-00-4 【 分 子 式 】C27H22ClNO2 【 分 子 量 】427.93489 |
【开发单位】Albert Szent-Györgyi Medical Univ. (Originator), Humboldt-Universität zu Berlin (Originator), Josai University (Originator), Meiji Pharmaceutical University (Originator), Saurashtra University (Originator) 【药理作用】Antibacterial Activity Enhancers, Antibacterial Drugs, ANTIINFECTIVE THERAPY, Modulators of the Therapeutic Activity of Antineoplastic Agents, Multidrug Resistance Modulators, ONCOLYTIC DRUGS, P-Glycoprotein (MDR-1) Inhibitors |
合成路线1
The title dihydropyridine is prepared by condensation of benzoylacetone (I) with 3-chlorobenzaldehyde (II) in the presence of aqueous ammonia, following a variation of the Hantzsch reaction.