TY - JOUR
T1 - Antioxidant and antimutagenic polyisoprenylated benzophenones and xanthones from Rheedia acuminata
AU - Almanza Vega, Giovanna Rocio Almanza Vega
AU - Quispe, Rauĺ
AU - Mollinedo Portugal, Patricia Andrea
AU - Rodrigo, Gloria
AU - Fukushima, Odette
AU - Villagomez, Rodrigo
AU - Akesson, Bjorn
AU - Sterner, Olov
PY - 2011/9
Y1 - 2011/9
N2 - Dichloromethane extract of the stem bark of Rheedia acuminata yielded three benzophenones with antioxidant activity, the new one named acuminophenone A (1), guttiferone K (2) and isoxanthochymol (3), along with the known xanthones formoxanthone C (4) and macluraxanthone (5). The structures were established through interpretation of their spectroscopic data, the stereochemistry of compounds (1) and (2) were resolved by experimental and computational experiments and their antioxidant activities were measured using the DPPH, ABTS and TEAC assays. The antioxidant results showed that metabolites 1, 4 and 5 had a better antioxidant activity than the reference compound quercetin. In addition, we evaluate the mutagenicity and antimutagenicity of the CH2Cl2 extract as well as of the free radical scavenger compounds 1, 4 and 5 by the AMES Salmonella/microsomal test. No mutagenicity was found in the CH 2Cl2 extract using Salmonella typhimurium strains TA98, TA100, TA102, TA1537 and TA1538, with or without S9 metabolic activation. The pure compounds neither showed mutagenicity in TA 102 strain and the most important result was the strong reduction of mutagenic effect induced by hydrogen peroxide in S. typhimurium TA 102, with or without S9, showed by the compounds 1 (more than 93%) and 4 (more than 88%) at 0.02 μg/plate.
AB - Dichloromethane extract of the stem bark of Rheedia acuminata yielded three benzophenones with antioxidant activity, the new one named acuminophenone A (1), guttiferone K (2) and isoxanthochymol (3), along with the known xanthones formoxanthone C (4) and macluraxanthone (5). The structures were established through interpretation of their spectroscopic data, the stereochemistry of compounds (1) and (2) were resolved by experimental and computational experiments and their antioxidant activities were measured using the DPPH, ABTS and TEAC assays. The antioxidant results showed that metabolites 1, 4 and 5 had a better antioxidant activity than the reference compound quercetin. In addition, we evaluate the mutagenicity and antimutagenicity of the CH2Cl2 extract as well as of the free radical scavenger compounds 1, 4 and 5 by the AMES Salmonella/microsomal test. No mutagenicity was found in the CH 2Cl2 extract using Salmonella typhimurium strains TA98, TA100, TA102, TA1537 and TA1538, with or without S9 metabolic activation. The pure compounds neither showed mutagenicity in TA 102 strain and the most important result was the strong reduction of mutagenic effect induced by hydrogen peroxide in S. typhimurium TA 102, with or without S9, showed by the compounds 1 (more than 93%) and 4 (more than 88%) at 0.02 μg/plate.
KW - Acuminophenone A
KW - Antimutagenicity
KW - Antioxidant capacity
KW - Formoxanthone C
KW - Guttiferone K
KW - Isoxanthochymol
KW - Macluraxanthone
KW - Mutagenicity
KW - Polyisoprenylated benzophenones
KW - Prenylated xanthones
KW - Rheedia acuminata
UR - http://www.scopus.com/inward/record.url?scp=80155169009&partnerID=8YFLogxK
U2 - 10.1177/1934578x1100600916
DO - 10.1177/1934578x1100600916
M3 - Artículo
C2 - 21941896
AN - SCOPUS:80155169009
VL - 6
SP - 1269
EP - 1274
JO - Natural Product Communications
JF - Natural Product Communications
SN - 1934-578X
IS - 9
ER -