Department of Chemistry, Faculty of Science , University of Malaya , 50603 Kuala Lumpur , Malaysia.
Institute of Biological Sciences, Faculty of Science , University of Malaya , 50603 Kuala Lumpur , Malaysia.
J Nat Prod. 2019 Apr 26;82(4):850-858. doi: 10.1021/acs.jnatprod.8b00919. Epub 2019 Mar 14.
Examination of the EtOH extract of the leaves of the Malayan Tabernaemontana corymbosa resulted in the isolation of four new (1-4) and two known bisindole alkaloids (5, 6) of the Aspidosperma- Aspidosperma type. The structures of these alkaloids were determined based on analysis of the spectroscopic data (NMR and HRESIMS). X-ray diffraction analyses of the related bisindole alkaloids conophylline (5) and conophyllinine (6) established the absolute configurations. Treatment of the bisindole alkaloid conophylline (5) with benzeneselenic anhydride gave, in addition to the known bisindole polyervinine (7) previously isolated from another Malayan Tabernaemontana, another bisindole product, 8, an isolable tautomer of 7. X-ray diffraction analyses yielded the absolute configurations of both bisindoles and in addition showed that polyervinine (7) exists primarily as the neutral dione structure. The bisindoles (1-8) and the related conophylline-type bisindoles (9-13) showed pronounced in vitro growth inhibitory activity against an array of human cancer cell lines, including KB, vincristine-resistant KB, PC-3, LNCaP, MCF7, MDA-MB-231, A549, HT-29, and HCT 116 cells, with IC values for the active compounds in the 0.01-5 μM range.
对马来亚 Tabernaemontana corymbosa 叶片的 EtOH 提取物进行检查,结果分离得到了四个新的(1-4)和两个已知的 Aspidosperma-Aspidosperma 型双吲哚生物碱(5,6)。这些生物碱的结构是基于光谱数据分析(NMR 和 HRESIMS)确定的。相关双吲哚生物碱科罗菲林(5)和科罗菲宁(6)的 X 射线衍射分析确定了它们的绝对构型。用苯硒酸酐处理双吲哚生物碱科罗菲林(5),除了先前从另一种马来亚 Tabernaemontana 中分离得到的已知双吲哚多烯维宁(7)外,还得到了另一种双吲哚产物 8,它是 7 的可分离互变异构体。X 射线衍射分析确定了两种双吲哚的绝对构型,此外还表明多烯维宁(7)主要以中性二酮结构存在。双吲哚(1-8)和相关的科罗菲林型双吲哚(9-13)对一系列人类癌细胞系(包括 KB、长春新碱耐药 KB、PC-3、LNCaP、MCF7、MDA-MB-231、A549、HT-29 和 HCT 116 细胞)表现出显著的体外生长抑制活性,活性化合物的 IC 值在 0.01-5 μM 范围内。