Thể loại: Bài báo quốc tế

Tác giả: M H T Tung, H V Duc, T T Huong, N T Duong, D T Phuong, D T Thao, B H Tai, Y H Kim, T T Bach, N M Cuong

Đơn vị: Phòng Thử nghiệm sinh học

Đăng tại: Sci Pharm.Published Online December 31st, 2012;


Số ISBN:

Năm: 2013


Liên kết:

Số lần xem: 2715

Review

Viết bởiThu nghiem SH

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, compounds3and5showed 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.

Keywords

Brucea mollis• Cytotoxicity • Quassinoids • Alkaloids • Triterpenoids

ReceivedJune 3rd, 2012 |AcceptedDecember 31st, 2012 |Published OnlineDecember 31st, 2012

http://dx.doi.org/10.3797/scipharm.1206-02

Ngày cập nhật: Thứ hai, 10 Tháng 11 2014