Pharmacognosy Department, Faculty of Pharmacy, October 6 University, 6th of October City 12585, Egypt.
Biochemistry Department, Faculty of Pharmacy, October 6 University, 6th of October City 12585, Egypt.
Molecules. 2023 Dec 29;29(1):199. doi: 10.3390/molecules29010199.
is one of the oldest known medicinal plants and the largest genera of the Ephedraceae family. In vivo antitumor evaluation of revealed that ethyl acetate (EtOAc) was the most bioactive fraction. Bio-guided fractionation of EtOAc fraction afforded nine compounds isolated for the first time from the plant species. Macrocyclic spermine alkaloids (1,9), proanthocyanidins (2,4,5), quinoline alkaloids (7,8), phenolic (3), and nucleoside (6) were identified and elucidated by spectroscopic analyses including 1D and 2D NMR, ESI-MS-MS spectrometry. The tested compounds exhibited moderate anticancer activity, except for the kynurenic acid derivative (6-mKYNA) which showed significant cytotoxicity and remarkable inhibition of CA-19.9 and CA-125 tumor biomarkers. In-silico study was conducted to determine the anti-proliferative mechanism of 6-mKYNA by using the CK2 enzyme active site. Moreover, the ADME computational study suggested that 6-mKYNA is an effective candidate with a promising pharmacokinetic profile and therapeutic potential against various types of cancer.
是最古老的药用植物之一,也是麻黄科最大的属。体内抗肿瘤评价表明,乙酸乙酯(EtOAc)是最具生物活性的部分。EtOAc 部分的生物导向分离得到了从该植物种中首次分离出的九种化合物。大环腐胺生物碱(1、9)、原花青素(2、4、5)、喹啉生物碱(7、8)、酚类(3)和核苷(6)通过包括 1D 和 2D NMR、ESI-MS-MS 光谱在内的光谱分析进行了鉴定和阐明。除了色氨酸衍生物(6-mKYNA)外,测试的化合物表现出中等的抗癌活性,6-mKYNA 具有显著的细胞毒性和对 CA-19.9 和 CA-125 肿瘤标志物的显著抑制作用。通过使用 CK2 酶活性位点进行了计算机模拟研究,以确定 6-mKYNA 的抗增殖机制。此外,ADME 计算研究表明,6-mKYNA 是一种有效的候选药物,具有有前途的药代动力学特征和对各种类型癌症的治疗潜力。