Robinson Sarah J, Hoobler Eric K, Riener Michelle, Loveridge Steven T, Tenney Karen, Valeriote Frederick A, Holman Theodore R, Crews Phillip
Department of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, California 95064, USA.
J Nat Prod. 2009 Oct;72(10):1857-63. doi: 10.1021/np900465e.
Enzyme screening of crude sponge extracts prioritized a 2005 Papua New Guinea collection of Hyrtios sp. for further study. The MeOH extract contained puupehenone and four puupehenone analogues (1, 2, 3, 5, and 7) along with a new diastereomer, 20-epi-hydroxyhaterumadienone (4), and a new analogue, 15-oxo-puupehenoic acid (6). The drimane terpene core of 4 and 6 was rapidly dereplicated, and the modified Mosher's method identified 4, while 1D and 2D NMR techniques were used to solve 6. These compounds plus noteworthy repository natural products and standards were tested against three lipoxygenase isozymes, human 5-, 12-, and 15-lipoxygenases. Significant potency and selectivity profiles were exhibited in the human 5-lipoxygenase assay by puupehenone (1) and jaspaquinol (9) and structural factors responsible for activity identified.
对海绵粗提物进行酶筛选后,2005年采集自巴布亚新几内亚的Hyrtios sp.样本被优先选作进一步研究对象。甲醇提取物中含有puupehenone及其四种类似物(1、2、3、5和7),还有一种新的非对映异构体20-表羟基海兔二烯酮(4)和一种新的类似物15-氧代-puupehenoic酸(6)。4和6的杜松烷萜烯核心结构很快被鉴定出来,采用改良的莫舍尔方法鉴定出了4,而通过一维和二维核磁共振技术解析出了6。将这些化合物以及值得注意的天然产物库中的天然产物和标准品针对三种脂氧合酶同工酶,即人5-、12-和15-脂氧合酶进行了测试。在人5-脂氧合酶测定中,puupehenone(1)和jaspaquinol(9)表现出显著的活性和选择性特征,并确定了其活性的结构因素。