详细信息
文献类型:期刊文献
中文题名:一种噻唑类衍生物的合成及应用研究
英文题名:Synthesis and Application of the Thiazole Derivative
作者:黑延琳[1,2];于绪平[1];金剑炜[1];宋少奇[1];商甜波[2,3];罗艳娟[2,3];潘晓军[1];陈龙[1];徐慧婷[2,3]
机构:[1]浙江医药股份有限公司,浙江绍兴312000;[2]脂溶性维生素浙江省工程研究中心(绍兴文理学院),浙江绍兴312000;[3]浙江绍兴文理学院化学化工学院,浙江绍兴312000
年份:2022
卷号:51
期号:14
起止页码:14
中文期刊名:山东化工
外文期刊名:Shandong Chemical Industry
语种:中文
中文关键词:噻唑;合成;药理活性;阿尔兹海默症
外文关键词:thiazole;synthesis;pharmacological activity;alzheimer’s disease;
中文摘要:噻唑类化合物在抗菌、抗结核、抗癌、抗神经衰退性疾病等方面展现着巨大的用途。以对甲基苯酚为原料,通过取代、重排等过程合成目标化合物2-(4-甲基苯氧甲基)-4-(N-异丁基-N-乙酰基-氨甲基)-噻唑,并通过核磁等表征确认结构。同时,对该化合物的药理活性进行了研究,结果表明其对丁酰胆碱酯酶(BuChE)有较强的抑制活性,为开发新型阿尔兹海默症的治疗药物提供了思路。
外文摘要:Thiazole compounds have shown great uses in antibacterial,anti-tuberculosis,anti-cancer,and anti-neurodegenerative diseases.In this paper,the target compound 2-(4-Methylphenoxymethyl)-4-(N-isobutyl-N-acetyl-aminomethyl)-thiazole was synthesized by p-cresol through substitution,rearrangement and other reactions and the structure was confirmed by NMR.At the same time,the pharmacological activity of the compound was studied,and the results showed that it has a strong inhibitory activity on Bu Ch E,which provides ideas for the development of new therapeutic drugs for AD.
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