Scientia Pharmaceutica (Sep 2016)

Cytotoxic Compounds from Brucea mollis

  • Mai Hung Thanh TUNG,
  • Ho Viet ĐUC,
  • Tran Thu HUONG,
  • Nguyen Thanh DUONG,
  • Do Thi PHUONG,
  • Do Thi THAO,
  • Bui Huu TAI,
  • Young Ho KIM,
  • Tran The BACH,
  • Nguyen Manh CUONG

DOI
https://doi.org/10.3797/scipharm.1206-02
Journal volume & issue
Vol. 81, no. 3
pp. 819 – 832

Abstract

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Ten compounds, including soulameanone (1), isobruceine B (2), 9-methoxy-canthin-6-one (3), bruceolline F (4), niloticine (5), octatriacontan-1-ol (6), bombiprenone (7), α-tocopherol (8), inosine (9), and apigenin 7-O-β-D-glucopyranoside (10), were isolated from the leaves, stems, and roots of Brucea mollis Wall. ex Kurz. Their structures were determined using one- and two-dimensional NMR spectroscopy and mass spectrometry. All compounds were evaluated for their cytotoxic activity against KB (human carcinoma of the mouth), LU-1 (human lung adenocarcinoma), LNCaP (human prostate adeno-carcinoma), and HL-60 (human promyelocytic leukemia) cancer cell lines. Compound 2 showed significant cytotoxic activity against KB, LU-1, LNCaP, and HL-60 cancer cells with IC50 values of 0.39, 0.40, 0.34, and 0.23 μg/mL, respectively. In addition, compounds 3 and 5 showed significant cytotoxic activity against KB, LU-1, LNCaP, and HL-60 cancer cells with IC50 values around 1–4 μg/mL. Compounds 9-methoxycanthin-6-one (3) and niloticine (5) have been discovered for the first time from the Brucea genus.

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