Antibacterial constituents from Melodinus suaveolens

被引:11
作者
Li Jiang-Ling [1 ,2 ]
Lunga, Paul-Keilah [1 ,3 ]
Zhao Yun-Li [1 ]
Qin Xu-Jie [1 ,2 ]
Yang Xing-Wei [1 ,2 ]
Liu Ya-Ping [1 ]
Luo Xiao-Dong [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Univ Yaounde I, Fac Sci, Dept Biochem, Lab Phytobiochem & Med Plants Study, Yaounde, Cameroon
关键词
Melodinus suaveolens; Apocynaceae; Non-alkaloidal chemical constituents; Meningitis; Antibacterial activity; ALKALOIDS; TRITERPENOIDS; OXIDATION; LEAVES;
D O I
10.1016/S1875-5364(15)30020-0
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
To investigate the non-alkaloidal chemical constituents of the stems and leaves of Melodinus suaveolens and their antibacterial activities. Compounds were isolated and purified by repeated silica gel, Sephadex LH-20, RP18, and preparative HPLC. Their structures were elucidated by comparison with published spectroscopic data, as well as on the basis of extensive spectroscopic analysis. The antibacterial screening assays were performed by the dilution method. Fourteen compounds were isolated, and identified as lycopersene (1), betulinic aldehyde (2), 3 beta-acetoxy-22,23,24,25,26,27-hexanordammaran-20-one (3), 3a-acetyl-2, 3, 5-trimethy1-7a-hydroxy-5-(4,8,12-trimethy1-tridecany1)-1,3a,5,6,7,7a-hexahydro-4-oxainden-l-one (4), 3 beta-hydroxy-28-norlup-20(29)-ene-17 beta-hydroperoxide (5), 3 beta-hydroxy-28-norlup-20(29)-ene-17 alpha-hydroperoxide (6), beta-sitosterol (7), 28-nor-urs-12-ene-3 beta, 17 beta-diol (8), alpha-amyrin (9), ergosta-4,6,8(14),22-tetraen-3-one (10), 3 beta-hydroxy-urs-11-en-28,13 beta-olide (11), betulin (12), obtusalin (13), and ursolic acid (14). Among the isolates, compounds 1, 2, 6, 8, 10, and 14 showed potent antibacterial activities against the four bacteria. This is the first report of the antibacterial activity of the constituents of Melodinus suaveolens.
引用
收藏
页码:307 / 310
页数:4
相关论文
共 26 条
  • [1] A NEW ANTIBIOTIC
    AU, KS
    GRAY, DE
    [J]. BIOCHEMICAL PHARMACOLOGY, 1969, 18 (11) : 2673 - &
  • [2] Antiproliferative Triterpenes from Melaleuca ericifolia
    Bar, Fatma M. Abdel
    Zaghloul, Ahmed M.
    Bachawal, Sunitha V.
    Sylvester, Paul W.
    Ahmad, Kadria F.
    El Sayed, Khalid A.
    [J]. JOURNAL OF NATURAL PRODUCTS, 2008, 71 (10): : 1787 - 1790
  • [3] Cladocalol, a pentacyclic 28-nor-triterpene from Eucalyptus cladocalyx with cytotoxic activity
    Benyahia, S
    Benayache, S
    Benayache, F
    León, F
    Quintana, J
    López, M
    Hernández, JC
    Estévez, F
    Bermejo, J
    [J]. PHYTOCHEMISTRY, 2005, 66 (06) : 627 - 632
  • [4] Caffeoyl Triterpenes from Pear (Pyrus pyrifolia Nakai) Fruit Peels and Their Antioxidative Activities against Oxidation of Rat Blood Plasma
    Cho, Jeong-Yong
    Kim, Chan Mi
    Lee, Hyoung Jae
    Lee, Sang-Hyun
    Cho, Jeong-An
    Kim, Wol-Soo
    Park, Keun-Hyung
    Moon, Jae-Hak
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2013, 61 (19) : 4563 - 4569
  • [5] HE X, 1992, ACTA CHIM SINICA, V50, P96
  • [6] TRITERPENOIDS OF PAEONIA-JAPONICA CALLUS-TISSUE
    IKUTA, A
    ITOKAWA, H
    [J]. PHYTOCHEMISTRY, 1988, 27 (09) : 2813 - 2815
  • [7] International Symposium of Plant Diversity and Conservation in China, 1977, FLORA OF CHINA, P22
  • [8] International Symposium of Plant Diversity and Conservation in China, 1977, FLORA OF CHINA, P17
  • [9] Enterococcus faecalis tropism for the kidneys in the urinary tract of C57BL/6J mice
    Kau, AL
    Martin, SM
    Lyon, W
    Hayes, E
    Caparon, MG
    Hultgren, SJ
    [J]. INFECTION AND IMMUNITY, 2005, 73 (04) : 2461 - 2468
  • [10] Kitajima J, 1998, CHEM PHARM BULL, V46, P1647, DOI 10.1248/cpb.46.1647