Chowdhury Nargis Sultana, Sohrab Md Hossain, Rana Md Sohel, Hasan Choudhury Mahmood, Jamshidi Shirin, Rahman Khondaker Miraz
Pharmaceutical Sciences Research Division (PSRD), BCSIR Laboratories, Dhaka , Dr. Qudrat-I-Khuda Road, Dhanmondi, Dhaka, Bangladesh.
Department of Pharmacy, Manarat International University , Dhaka, Bangladesh.
J Nat Prod. 2017 Apr 28;80(4):1173-1177. doi: 10.1021/acs.jnatprod.6b00610. Epub 2017 Mar 3.
Bioactivity-guided fractionation of the ethyl acetate extract obtained from the culture of the endophytic fungus Fusarium solani resulted in the isolation of one new naphthoquinone, 9-desmethylherbarine (1), and two azaanthraquinone derivatives, 7-desmethylscorpinone (2) and 7-desmethyl-6-methylbostrycoidin (3), along with four known compounds. Their structures were elucidated by spectral analysis, as well as a direct comparison of spectral data with those of known compounds. Azaanthraquinones 2 and 3 showed cytotoxic activity against four human tumor cell lines, MDA MB 231, MIA PaCa2, HeLa, and NCI H1975. A molecular docking study suggested DNA interactions as the mode of action of these naphthoquinones and azaanthraquinones.
对从内生真菌茄病镰刀菌培养物中获得的乙酸乙酯提取物进行生物活性导向分离,得到了一种新的萘醌,9-去甲基草杆菌素(1),以及两种氮杂蒽醌衍生物,7-去甲基蝎毒素(2)和7-去甲基-6-甲基波斯特曲菌素(3),同时还得到了四种已知化合物。通过光谱分析以及将光谱数据与已知化合物的数据进行直接比较,阐明了它们的结构。氮杂蒽醌2和3对四种人类肿瘤细胞系MDA MB 231、MIA PaCa2、HeLa和NCI H1975显示出细胞毒性活性。分子对接研究表明,DNA相互作用是这些萘醌和氮杂蒽醌的作用方式。