Page Banner

United States Department of Agriculture

Agricultural Research Service

Title: Antimicrobial, Antiparasitic and Cytotoxic Spermine Alkaloids from Albizia schimperiana)

Author
item Samoylenko, Volodymyr
item Jacob, Melissa
item Khan, Shabana
item Zhao, Jianping
item Tekwani, Babu
item Midiwo, Jacob
item Walker, Larry
item Muhammad, Ilias

Submitted to: Natural Product Communications
Publication Type: Peer reviewed journal
Publication Acceptance Date: 3/31/2009
Publication Date: 6/3/2009
Citation: Samoylenko, V., Jacob, M.R., Khan, S.I., Zhao, J., Tekwani, B.L., Midiwo, J.O., Walker, L.A., Muhammad, I. 2009. Antimicrobial, Antiparasitic and Cytotoxic Spermine Alkaloids from Albizia schimperiana. Natural Product Communications. 4(6):791-796.

Interpretive Summary: Bioassay guided isolation of the Albizia schimperiana Oliv. (Leguminosae) extract afforded the new macrocyclic spermine alkaloid, 5,14-dimethylbudmunchiamine L1 (1), and three known budmunchiamine analogs (2-4). Compounds 1 and 3 exhibited significant in vitro antimicrobial activity against C. neoformans, methicillin-resistant S. aureus, E. coli, M. intracellulare, and A. fumigatus. In addition, they demonstrated strong in vitro antimalarial activities against CQ-susceptible (D6) and -resistant (W2) strains of Plasmodium falciparum (IC50 = 120-270 ng/mL), and cytotoxicity against human cancer cell lines and mammalian VERO cells. It was observed that hydroxyl substitution of the side chain of the budmunchiamines dramatically reduced the cytotoxicity and antimicrobial activity of the alkaloids (2 and 4) without decreasing antimalarial activity.

Technical Abstract: Albizia schimperiana Oliv. (Leguminosae) is a tree distributed in the highland of Kenya, where it is used as a traditional medicine for the treatment of bacterial and parasitic infections, notably pneumonia and malaria, respectively. Bioassay guided isolation of the CH2Cl2–MeOH 1:1/ MeOH-H2O 9:1 (mixed) extract of A. schimperiana afforded the new bioactive macrocyclic spermine alkaloid, namely 5,14-dimethylbudmunchiamine L1 (1), and three known budmunchiamine analogs 2-4. The structures of the compounds 1-4 were determined by 1D and 2D NMR data, including COSY, HMQC, and HMBC experiments, and ESI-HRMS. Compounds 1 and 3 exhibited significant in vitro antimicrobial activity against a panel of microorganisms, including C. neoformans, methicillin-resistant S. aureus, E. coli, M. intracellulare, A. fumigatus. In addition, they demonstrated strong in vitro antimalarial activities against chloroquine-susceptible (D6) and -resistant (W2) strains of Plasmodium falciparum with IC50s ranging from 120-270 ng/mL. Compounds 1-4 were also evaluated for cytotoxic activity against selected human cancer cell lines and mammalian kidney fibroblasts (VERO cells). It was observed that hydroxyl substitution of the side chain of the budmunchiamines dramatically reduced the cytotoxicity and antimicrobial activity of the alkaloids (2 and 4) without decreasing antimalarial activity.

Last Modified: 8/24/2016
Footer Content Back to Top of Page