Antiproliferative activity of stilbene derivatives and other constituents from the stem bark of Morus nigra L

  • Nat Prod Res. 2020 Dec;34(24):3506-3513. doi: 10.1080/14786419.2019.1573236.
Fatma M Abdel Bar  1  2 Ghada M Abbas  2  3 Ahmed A Gohar  2 Mohamed-Farid I Lahloub  2
Affiliations
  • 1. Department of Pharmacognosy, Faculty of Pharmacy, Prince Sattam Bin Abdulaziz University, Al-Kharj, Saudi Arabia.
  • 2. Department of Pharmacognosy, Faculty of Pharmacy, Mansoura University, Mansoura, Egypt.
  • 3. Pharmacognosy Department, Faculty of Pharmacy, Horus University- Egypt (HUE), Damietta, Egypt.
Abstract

The antiproliferative activities of 2',3,4',5,5'-pentahydroxy-cis-stilbene 1, resveratrol 2, oxyresveratrol 3, norartocarpetin 4, kuwanon C 5, morusin 6, cudraflavone A7, kuwanon G 8, albafuran C 9, mulberrofuran G 10, 3-acetyl-O-α-amyrin 11, 3-acetyl-O-β-amyrin 12, ursolic acid-3-O-acetate 13 and uvaol 14, previously identified from the barks of Morus nigra L., were investigated against HepG2 and MCF-7 cell lines. In addition, a series of methylated Stilbenes 15-19 were prepared using compounds 1-3 and their antiproliferative effects were similarly investigated. The structure of a new 2',3,4'-trimethoxy-5-hydroxy-trans-stilbene 19 was elucidated using spectroscopic techniques. It showed remarkable activity against MCF-7 cells with IC50 12.5 μM. However, kuwanon C (5) showed the highest antiproliferative activity with IC50 3.92 and 9.54 μM against MCF-7 and HepG2, respectively.

Keywords
Morus nigra; Diels-Alder adducts; antiproliferative activity; prenylated flavonoids; stilbenes.
Products