TY  - JOUR
A1  - Omosa, Leonidah K.
A1  - Amugune, Beatrice
A1  - Ndunda, Beth
A1  - Milugo, Trizah K.
A1  - Heydenreich, Matthias
A1  - Yenesew, Abiy
A1  - Midiwo, Jacob O.
T1  - Antimicrobial flavonoids and diterpenoids from Dodonaea angustifolia
JF  - South African journal of botany : an international interdisciplinary journal for botanical sciences
KW  - Dodonaea angustifolia
KW  - Surface exudates
KW  - Flavone
KW  - Flavanone
KW  - Diterpenoid
KW  - Antimicrobial activities
Y1  - 2014
U6  - https://doi.org/10.1016/j.sajb.2013.11.012
SN  - 0254-6299
SN  - 1727-9321
VL  - 91
SP  - 58
EP  - 62
PB  - Elsevier
CY  - Amsterdam
ER  - 
TY  - GEN
A1  - Peter, Martin G.
A1  - Yenesew, Abiy
A1  - Twinomuhwezi, Hannington
A1  - Kabaru, Jacques M.
A1  - Akala, Hoseah M.
A1  - Kiremire, Bernard T.
A1  - Heydenreich, Matthias
A1  - Eyase, Fredrick
A1  - Waters, Norman C.
A1  - Walsh, Douglas S.
T1  - Antiplasmodial and larvicidal flavonoids from Derris trifoliata
N2  - From the dichloromethane-methanol (1:1) extract of the seed pods of Derris trifoliata, a new flavanone derivative (S)-lupinifolin 4´-methyl ether was isolated. In addition, the known flavonoids lupinifolin and rotenone were identified. The structures were determined on the basis of spectroscopic evidence. Lupinfolin showed moderate in vitro antiplasmodial activity against the D6 (chloroquine-sensitive) and W2 (chloroquineresistant) strains of Plasmodium falciparum. The different parts of this plant showed larvicidal activities against Aedes aegypti and rotenoids were identified as the active principles.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 121 
KW  - Derris trifoliata
KW  - Leguminosae
KW  - Flavanone
KW  - (S)-Lupinifolin 4´-methyl ether
KW  - Lupinifolin
Y1  - 2009
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-44614
ER  -