Nitrated and Brominated Narcotine and its Cleaved Adduct as Butyrylcholinesterase Inhibitors

M. Abbasi, Aziz‐ur‐Rehman, M. Qureshi, M. Shahid, S. Rasool, M. Ashraf
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引用次数: 2

Abstract

Narcotine is a very antitussive agent and its modification may lead to some more biological activities. In this presented paper, narcotine (1) was first subjected to nitration and bromination to yield nitrated narcotine (2) and brominated narcotine (3). It was further made to react with phenylchloroformate (6) to give a cleaved addition product 4. This adduct 4 was further nitrated and brominated to yield substituted derivatives 5 and 6, respectively. The structure elucidation of the synthesized compounds was processed via IR, EI-MS and 1 H-NMR spectra. These were also screened against butyrylcholinesterase enzyme and were found to the moderate inhibitors of butyrylcholinesterase except nitrated product, 2, of narcotine (1).
硝化和溴化纳可汀及其裂解加合物作为丁酰胆碱酯酶抑制剂
纳可汀是一种非常好的止咳剂,它的修饰可能会导致更多的生物活性。在本文中,首先对纳可汀(1)进行硝化和溴化,得到硝化纳可汀(2)和溴化纳可汀(3)。然后将其与氯甲酸苯酯(6)反应,得到裂解加成产物4。该加合物4进一步硝化和溴化,分别得到取代衍生物5和6。通过IR、EI-MS和1h - nmr对合成的化合物进行了结构分析。这些也筛选了丁基胆碱酯酶,发现除了硝化产物,2,纳可汀(1),是丁基胆碱酯酶的中度抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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