Department of Organic Chemistry, Faculty of Science, University of Yaoundé 1, Yaoundé P.O. Box 812, Cameroon.
Organic and Bioorganic Chemistry, Department of Chemistry, Bielefeld University, 33501 Bielefeld, Germany.
Molecules. 2022 Feb 7;27(3):1104. doi: 10.3390/molecules27031104.
The chemical investigation of the total alkaloid extract (TAE) of the stem bark of (Rutaceae) afforded an unreported indolopyridoquinazoline (compound ) along with nine previously known alkaloids -. In addition, six semi-synthetic derivatives -, , and were prepared by allylation and acetonidation of soyauxinium nitrate (), edulinine (), ribalinine () and arborinine (). The structures and spectroscopic data of five of them are reported herein for the first time. The suggested mechanism for the formation of the new -allylindolopyridoquinazoline is presented. The structures of natural and derived compounds were determined employing extensive NMR and MS techniques. The absolute configuration of stereogenic centers in compounds - were determined using NOESY technique and confirmed by the single-crystal X-ray diffraction (SC-XRD) technique. The use of SC-XRD further enabled us to carry out a structural revision of soyauxinium chloride recently isolated from the same plant to soyauxinium nitrate (). The TAE, fractions, compounds - and , and semi-synthetic derivatives -, , and were evaluated for their cytotoxic activity towards the cervix carcinoma cell line KB-3-1. No significant activity was recorded for most of the compounds except for , which showed moderate activity against the tested cancer cell lines.
从 (Rutaceae)茎皮的总生物碱提取物(TAE)中进行的化学研究得到了一种未报道的吲哚并吡啶并喹唑啉(化合物 ),以及另外 9 种先前已知的生物碱-。此外,通过硝酸()、埃杜林碱()、里巴林碱()和阿伯林碱()的烯丙基化和乙酰胺化,制备了 6 种半合成衍生物-、、、、。本文首次报道了其中 5 种的结构和光谱数据。提出了形成新的-烯丙基吲哚并吡啶并喹唑啉的建议机制。采用广泛的 NMR 和 MS 技术确定了天然和衍生化合物的结构。通过 NOESY 技术确定了化合物-中立体中心的绝对构型,并通过单晶 X 射线衍射(SC-XRD)技术进行了确认。SC-XRD 的使用还使我们能够对最近从同一植物中分离出的硝酸()进行结构修订,得到氯化()。TAE、馏分、化合物-和-以及半合成衍生物-、、和-都被评估了对宫颈癌细胞系 KB-3-1 的细胞毒性活性。除了-之外,大多数化合物都没有表现出显著的活性,而-对测试的癌细胞系表现出中等活性。