Lead Discovery and Rapid Structure Elucidation Group, Sequoia Sciences, Inc. , 1912 Innerbelt Business Center Drive, St. Louis, Missouri 63114, USA.
J Nat Prod. 2012 Jul 27;75(7):1319-25. doi: 10.1021/np300241d. Epub 2012 Jul 3.
High-throughput natural products chemistry methods have facilitated the isolation of eight new (1-8) and two known (9 and 10) beilschmiedic acid derivatives from the leaves of a Gabonese species of Beilschmiedia. Compounds 3-10 were isolated in microgram quantities, and the NMR data for structure elucidation and dereplication were acquired utilizing a Bruker BioSpin TCI 1.7 mm MicroCryoProbe. All of the compounds were screened for cytotoxic and antibacterial activity against NCI-H460 human lung cancer cells and a clinical isolate of methicillin-resistant Staphylococcus aureus, respectively. This is the first report of cytotoxic activity for the endiandric/beilschmiedic acid class of compounds.
高通量天然产物化学方法促进了从加蓬贝氏木属植物叶片中分离出 8 个新的(1-8)和 2 个已知(9 和 10)贝氏酸衍生物。化合物 3-10 以微克量分离,结构鉴定和去重的 NMR 数据利用布鲁克 BioSpin TCI 1.7 毫米 MicroCryoProbe 获取。所有化合物均针对 NCI-H460 人肺癌细胞和耐甲氧西林金黄色葡萄球菌的临床分离株进行了细胞毒性和抗菌活性筛选。这是首例报道内二萜/贝氏酸类化合物具有细胞毒性活性。