Norwegian College of Fishery Science, University of Tromsø , Breivika N-9037, Tromsø, Norway.
J Nat Prod. 2014 Feb 28;77(2):364-9. doi: 10.1021/np401002s. Epub 2014 Feb 18.
Pulmonarins A and B are two new dibrominated marine acetylcholinesterase inhibitors that were isolated and characterized from the sub-Arctic ascidian Synoicum pulmonaria collected off the Norwegian coast. The structures of natural pulmonarins A and B were tentatively elucidated by spectroscopic methods and later verified by comparison with synthetically prepared material. Both pulmonarins A and B displayed reversible, noncompetitive acetylcholinesterase inhibition comparable to several known natural acetylcholinesterase inhibitiors. Pulmonarin B was the strongest inhibitor, with an inhibition constant (Ki) of 20 μM. In addition to reversible, noncompetitive acetylcholinesterase inhibition, the compounds displayed weak antibacterial activity but no cytotoxicity or other investigated bioactivities.
肺囊素 A 和 B 是两种新型海洋二溴化乙酰胆碱酯酶抑制剂,从采集自挪威海岸的亚北极区 Ascidian Synoicum pulmonaria 中分离并鉴定得到。天然肺囊素 A 和 B 的结构通过光谱方法初步阐明,并通过与合成制备的材料进行比较得到进一步验证。肺囊素 A 和 B 均表现出与几种已知天然乙酰胆碱酯酶抑制剂相当的可逆、非竞争性乙酰胆碱酯酶抑制作用。肺囊素 B 是最强的抑制剂,其抑制常数(Ki)为 20 μM。除了可逆、非竞争性乙酰胆碱酯酶抑制作用外,这些化合物还表现出较弱的抗菌活性,但没有细胞毒性或其他研究的生物活性。