Youssef Diaa T A, Yamaki Rodney K, Kelly Michelle, Scheuer Paul J
Department of Pharmacognosy, Faculty of Pharmacy, Suez Canal University, Ismailia 41522, Egypt.
J Nat Prod. 2002 Jan;65(1):2-6. doi: 10.1021/np0101853.
The lipophilic partition of a methanol extract of the Red Sea sponge Hyrtios erecta yielded a novel pentacyclic sesterterpene ester salmahyrtisol A (1), three new scalarane-type sesterterpenes, 3-acetyl sesterstatin 1 (3), 19-acetyl sesterstatin 3 (4), and salmahyrtisol B (5), together with the previously reported sesterterpenes hyrtiosal (2), scalarolide (6), and salmahyrtisol C (7). The structure determination was based on extensive NMR studies and high-resolution mass spectral measurements. In addition, salmahyrtisol A has a previously unknown pentacyclic carbon skeleton. The new compounds show significant cytotoxicity to murine leukemia (P-388), human lung carcinoma (A-549), and human colon carcinoma (HT-29). A biosynthetic relationship between 1 and 2 is briefly discussed.
红海海绵直立希氏海绵甲醇提取物的亲脂性部分产生了一种新型五环倍半萜酯salmahyrtisol A(1)、三种新的鲨烷型倍半萜3-乙酰基倍半他汀1(3)、19-乙酰基倍半他汀3(4)和salmahyrtisol B(5),以及先前报道的倍半萜hyrtiosal(2)、scalarolide(6)和salmahyrtisol C(7)。结构鉴定基于广泛的核磁共振研究和高分辨率质谱测量。此外,salmahyrtisol A具有先前未知的五环碳骨架。这些新化合物对小鼠白血病(P-388)、人肺癌(A-549)和人结肠癌(HT-29)显示出显著的细胞毒性。简要讨论了1和2之间的生物合成关系。