TY  - JOUR
A1  - Chepkirui, Carolyne
A1  - Ochieng, Purity J.
A1  - Sarkar, Biswajyoti
A1  - Hussain, Aabid
A1  - Pal, Chiranjib
A1  - Yang, Li Jun
A1  - Coghi, Paolo
A1  - Akala, Hoseah M.
A1  - Derese, Solomon
A1  - Ndakala, Albert
A1  - Heydenreich, Matthias
A1  - Wong, Vincent K. W.
A1  - Erdelyi, Mate
A1  - Yenesew, Abiy
T1  - Antiplasmodial and antileishmanial flavonoids from Mundulea sericea
JF  - Fitoterapia
N2  - Five known compounds (1-5) were isolated from the extract of Mundulea sericea leaves. Similar investigation of the roots of this plant afforded an additional three known compounds (6-8). The structures were elucidated using NMR spectroscopic and mass spectrometric analyses. The absolute configuration of 1 was established using ECD spectroscopy. In an antiplasmodial activity assay, compound 1 showed good activity with an IC50 of 2.0 mu M against chloroquine-resistant W2, and 6.6 mu M against the chloroquine-sensitive 3D7 strains of Plasmodium falciparum. Some of the compounds were also tested for antileishmanial activity. Dehydrolupinifolinol (2) and sericetin (5) were active against drug-sensitive Leishmania donovani (MHOM/IN/83/AG83) with IC50 values of 9.0 and 5.0 mu M, respectively. In a cytotoxicity assay, lupinifolin (3) showed significant activity on BEAS-2B (IC50 4.9 mu M) and HePG2 (IC50 10.8 mu M) human cell lines. All the other compounds showed low cytotoxicity (IC50 > 30 mu M) against human lung adenocarcinoma cells (A549), human liver cancer cells (HepG2), lung/bronchus cells (epithelial virus transformed) (BEAS-2B) and immortal human hepatocytes (LO2)
KW  - Mundulea sericea
KW  - leguminosae
KW  - flavanonol
KW  - flavonol
KW  - antiplasmodial
KW  - antileishmanial
KW  - cytotoxicity
Y1  - 2020
U6  - https://doi.org/10.1016/j.fitote.2020.104796
SN  - 0367-326X
SN  - 1873-6971
VL  - 149
PB  - Elsevier
CY  - Amsterdam
ER  - 
TY  - JOUR
A1  - Adem, Fozia A.
A1  - Kuete, Victor
A1  - Mbaveng, Armelle T.
A1  - Heydenreich, Matthias
A1  - Koch, Andreas
A1  - Ndakala, Albert
A1  - Irungu, Beatrice
A1  - Yenesew, Abiy
A1  - Efferth, Thomas
T1  - Cytotoxic flavonoids from two Lonchocarpus species
JF  - Natural Product Research
N2  - A new isoflavone, 4′-prenyloxyvigvexin A (1) and a new pterocarpan, (6aR,11aR)-3,8-dimethoxybitucarpin B (2) were isolated from the leaves of Lonchocarpus bussei and the stem bark of Lonchocarpus eriocalyx, respectively. The extract of L. bussei also gave four known isoflavones, maximaisoflavone H, 7,2′-dimethoxy-3′,4′-methylenedioxyisoflavone, 6,7,3′-trimethoxy-4′,5′-methylenedioxyisoflavone, durmillone; a chalcone, 4-hydroxylonchocarpin; a geranylated phenylpropanol, colenemol; and two known pterocarpans, (6aR,11aR)-maackiain and (6aR,11aR)-edunol. (6aR,11aR)-Edunol was also isolated from the stem bark of L. eriocalyx. The structures of the isolated compounds were elucidated by spectroscopy. The cytotoxicity of the compounds was tested by resazurin assay using drug-sensitive and multidrug-resistant cancer cell lines. Significant antiproliferative effects with IC50 values below 10 μM were observed for the isoflavones 6,7,3′-trimethoxy-4′,5′-methylenedioxyisoflavone and durmillone against leukemia CCRF-CEM cells; for the chalcone, 4-hydroxylonchocarpin and durmillone against its resistant counterpart CEM/ADR5000 cells; as well as for durmillone against the resistant breast adenocarcinoma MDA-MB231/BCRP cells and resistant gliobastoma U87MG.ΔEGFR cells.
KW  - Lonchocarpus bussei
KW  - Lonchocarpus eriocalyx
KW  - Leguminosae
KW  - isoflavone
KW  - pterocarpan
KW  - cytotoxicity
Y1  - 2019
U6  - https://doi.org/10.1080/14786419.2018.1462179
SN  - 1478-6419
SN  - 1478-6427
VL  - 33
IS  - 18
SP  - 2609
EP  - 2617
PB  - Routledge, Taylor & Francis Group
CY  - Abingdon
ER  -