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Design, synthesis and in vivo Iin vitro screening of novel chlorokojic acid derivatives

机译:新型氯杂酸衍生物的设计,合成和体外筛选

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摘要

A series of novel Mannich bases of chlorokojic acid (2-chloromethyl-5-hydroxy-4H-pyran-4-one) were synthesized and their biological activities were investigated. Anticonvulsant activity results according to phase-l tests of Antiepileptic Drug Development (ADD) Program revealed that compound 13 was the most effective one at 4h against subcutaneous pentylenetetrazole (scPTZ)-induced seizure test. Antimicrobial activities were evaluated in vitro against bacteria and fungi by using broth microdilution method.The antitubercular activities against Mycobocterium tuberculosis and M. avium were discussed with Resazurin microplate assay (REMA).The antimicrobial activity results indicated that compounds , 12 (MIC: 8-16 ug/mL) showed higher activity against Gram negative bacteria while compound 12 had MIC: 4-16 ug/mL against Gram positive bacteria. Compound 1 was the most active one with MIC values of 8-32 ug/mL against fungi. Mannich bases also exhibit significant antitubercular activity in a MIC range of 4 to 32 ug/mL, especially compound 18 against M. avium.
机译:合成了一系列新型氯己酸(2-氯甲基-5-羟基-4-吡喃-4-一)的曼尼希碱,研究了它们的生物活性。根据抗癫痫药物开发的相 - L试验(添加)程序的抗惊厥活性结果显示,化合物13在皮下五苯乙烯丁唑(SCPTZ)诱导的癫痫发作试验中是最有效的。通过使用肉汤微量稀释方法对细菌和真菌进行体外进行抗菌活性。用丙蛋白微孔板测定(Rema)讨论了对霉菌霉菌结核菌和M.Avium的抗细胞活性。抗微生物活性结果表明化合物12(MIC:8- 16 ug / ml)显示对革兰根阴性细菌的较高活性,而化合物12具有麦克风:4-16μg/ ml对革兰氏阳性细菌。化合物1是最活跃的,具有8-32ug / mL对抗真菌的MIC值。 Mannich碱还在麦克风范围内表现出显着的抗细胞活性,麦克风范围为4至32ug / ml,特别是化合物18对抗M. Avium。

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