Nakao Y, Oku N, Matsunaga S, Fusetani N
Laboratory of Aquatic Natural Products Chemistry, Graduate School of Agricultural and Life Science, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan.
J Nat Prod. 1998 May;61(5):667-70. doi: 10.1021/np970544n.
Two new potent serine protease inhibitors, cyclotheonamides E2 (3) and E3 (4), have been isolated from a marine sponge of the genus Theonella. Their structures were determined by interpretation of spectral data and chemical degradation studies. They are closely related to the previously reported cyclotheonamide E, from which they differ in the N-acyl group of the alanyl side chain. Cyclotheonamides E, E2, and E3 were more active against thrombin than against trypsin.
从西奥海绵属的一种海洋海绵中分离出了两种新的强效丝氨酸蛋白酶抑制剂,环西奥酰胺E2(3)和E3(4)。通过光谱数据分析和化学降解研究确定了它们的结构。它们与先前报道的环西奥酰胺E密切相关,只是在丙氨酰侧链的N-酰基上有所不同。环西奥酰胺E、E2和E3对凝血酶的活性比对胰蛋白酶的活性更强。