TY - JOUR
T1 - Antimycobacterial flavonoids from the leaf extract of Galenia africana
AU - Mativandlela, Sannah P.N.
AU - Muthivhi, Tshilidzi
AU - Kikuchi, Haruhisa
AU - Oshima, Yoshiteru
AU - Hamilton, Chris
AU - Hussein, Ahmed A.
AU - Van Der Walt, Martha L.
AU - Houghton, Peter J.
AU - Lall, Namrita
PY - 2009/12/28
Y1 - 2009/12/28
N2 - The bioassay-guided fractionation of the EtOH extract of the leaves of Galenia africana led to the isolation of three known flavonoids, (2S)-5,7,2′-trihydroxyflavanone (1), (E)-3,2′,4′- trihydroxychalcone (2), and (E)-2′,4′-dihydroxychalcone (3), and the new (E)-3,2′,4′-trihydroxy-3′-methoxychalcone (4). Compounds 1 and 3 exhibited moderate antituberculosis activity. During synergistic studies, a combination of compound 4 and an existing antituberculosis drug, isoniazid, reduced their original MICs 4-fold, resulting in a fractional inhibitory concentration of 0.50. The most pronounced effect was demonstrated by compound 1 and isoniazid reducing their MICs 16-fold and resulting in an FIC of 0.12. Both EtOH extract and isolated compounds failed to exhibit any NADPH oxidase activity at 800.0 μM concentrations, indicating that mycothiol disulfide reductase is not the target for their antituberculosis activity.
AB - The bioassay-guided fractionation of the EtOH extract of the leaves of Galenia africana led to the isolation of three known flavonoids, (2S)-5,7,2′-trihydroxyflavanone (1), (E)-3,2′,4′- trihydroxychalcone (2), and (E)-2′,4′-dihydroxychalcone (3), and the new (E)-3,2′,4′-trihydroxy-3′-methoxychalcone (4). Compounds 1 and 3 exhibited moderate antituberculosis activity. During synergistic studies, a combination of compound 4 and an existing antituberculosis drug, isoniazid, reduced their original MICs 4-fold, resulting in a fractional inhibitory concentration of 0.50. The most pronounced effect was demonstrated by compound 1 and isoniazid reducing their MICs 16-fold and resulting in an FIC of 0.12. Both EtOH extract and isolated compounds failed to exhibit any NADPH oxidase activity at 800.0 μM concentrations, indicating that mycothiol disulfide reductase is not the target for their antituberculosis activity.
UR - http://www.scopus.com/inward/record.url?scp=74049164200&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=74049164200&partnerID=8YFLogxK
U2 - 10.1021/np800778b
DO - 10.1021/np800778b
M3 - Article
C2 - 20035557
AN - SCOPUS:74049164200
SN - 0163-3864
VL - 72
SP - 2169
EP - 2171
JO - Journal of Natural Products
JF - Journal of Natural Products
IS - 12
ER -