Departments of Chemistry and Earth, Oceans & Atmospheric Sciences, University of British Columbia , 2036 Main Mall, Vancouver, British Columbia, Canada V6T 1Z1.
Faculty of Health Sciences, Simon Fraser University , Burnaby, British Columbia, Canada V5A 1S6.
J Org Chem. 2016 Nov 18;81(22):11324-11334. doi: 10.1021/acs.joc.6b02312. Epub 2016 Nov 4.
Eight new sesterterpenoids, alotaketals D (8) and E (9), ansellones D (10), E (11), F (12), and G (13), and anvilones A (14) and B (15), have been isolated from extracts of the marine sponge Phorbas sp. collected in Howe Sound British Columbia, and their structures have been elucidated by analysis of NMR and MS data. Ansellone F (12) contains a rare 1,2-3,4-bis-epoxydecalin substructure. Anvilones A (14) and B (15) have an unprecedented tetracylic anvilane terpenoid carbon skeleton. Using a cell culture model of latent HIV-1 infection, ansellone A (3), alotaketal D (8), and anvilone A (14) were found to induce HIV proviral gene expression similar to the control compound prostratin (1), while the known sesterterpenoid alotaketal C (2), isolated from the same extract, was more potent and gave a stronger response than prostratin (1). Like prostratin (1), all of the Phorbas sesterterpenoids with latency reversal agent properties appear to activate protein kinase C signaling.
从在不列颠哥伦比亚豪湾采集的海绵 Phorbas sp. 的提取物中分离得到了 8 种新的倍半萜类化合物,分别为 alotaketals D(8)和 E(9)、ansellones D(10)、E(11)、F(12)和 G(13)以及 anvilones A(14)和 B(15),并通过 NMR 和 MS 数据分析阐明了它们的结构。Ansellone F(12)含有罕见的 1,2-3,4-双环氧癸烷亚结构。Anvilones A(14)和 B(15)具有前所未有的四环 anvilane 萜类碳骨架。在潜伏性 HIV-1 感染的细胞培养模型中,发现 ansellone A(3)、alotaketal D(8)和 anvilone A(14)诱导 HIV 前病毒基因表达类似于对照化合物 prostratin(1),而从同一提取物中分离得到的已知倍半萜类化合物 alotaketal C(2)比 prostratin(1)更有效,产生的反应更强。与 prostratin(1)一样,所有具有潜伏逆转剂特性的 Phorbas 倍半萜类化合物似乎都能激活蛋白激酶 C 信号转导。