Graduate School of Pharmaceutical Sciences, Tokushima University , Tokushima 770-8505, Japan.
Graduate School of Bioscience and Bioindustry, Tokushima University , Tokushima 770-8513, Japan.
Org Lett. 2016 Oct 21;18(20):5360-5363. doi: 10.1021/acs.orglett.6b02725. Epub 2016 Sep 28.
Two novel prenylated benzophenone related meroterpenes, hypatulins A (1) and B (2), were isolated from the leaves of Hypericum patulum. The structures of 1 and 2 were assigned by spectroscopic analysis, chemical conversion, and calculations of the ECD (electron circular dichroism) spectra. Hypatulin A (1) had a unique densely substituted tricyclic octahydro-1,5-methanopentalene core, while hypatulin B (2) possessed a bicyclo[3.2.1]octane moiety. Hypatulin A (1) exhibited antimicrobacterial activity against Bacillus subtilis. A possible biogenetic pathway of the new meroterpenes 1 and 2 from a prenylated benzophenone was presented.
从贯叶连翘的叶子中分离得到了两个新型的prenylated benzophenone 相关的 meroterpenes,hypatulins A(1)和 B(2)。通过光谱分析、化学转化和ECD(电子圆二色性)光谱计算确定了 1 和 2 的结构。Hypatulin A(1)具有独特的密集取代的三环八氢-1,5-甲烷并戊烯核心,而 Hypatulin B(2)则具有二环[3.2.1]辛烷部分。Hypatulin A(1)对枯草芽孢杆菌具有抗菌活性。提出了新的 meroterpenes 1 和 2 从 prenylated benzophenone 生物合成的可能途径。