In this work, two new flavonoids, oblongifolioside A (1) and oblongifolioside B (2), along with e... more In this work, two new flavonoids, oblongifolioside A (1) and oblongifolioside B (2), along with eight known compounds (3–10), are isolated from the leaves of Baccharis oblongifolia (Asteraceae). The new structures are established through spectroscopic data and the known compounds are identified by comparison with data reported in the literature. The compounds (1–10) are evaluated in relation to their antiradical properties. Compounds 1 and 2 are found to exhibit high antiradical activity compared to their respective non-acylated flavonoids.
Baccharis retusa, a medicinal Brazilian plant from Asteraceae, has been used in Brazilian folk me... more Baccharis retusa, a medicinal Brazilian plant from Asteraceae, has been used in Brazilian folk medicine to treatment of several illnesses, including parasitic diseases. Bioactivity-guided fractionation of the n-hexane extract from the aerial parts of B. retusa resulted in the isolation and characterization of three active related diterpenes: ent-15β-senecioyl-oxy-kaur-16-en-19-oic acid (1), ent-kaur-16-en-19-oic (2) and ent-16-oxo-17-nor-kauran-19-oic (3) acids. The structures of isolated compounds were defined by spectroscopic analysis, including NMR and HRESIMS. Antitrypanosomal activity of 1-3 was performed against cell-derived trypomastigotes using the colorimetric resazurin assay. The obtained results demonstrated that isolated compounds displayed a reduced toxicity against NCTC cells and were effective against the trypomastigote forms of T. cruzi with IC values of 3.8μM (1), 75.3μM (2) and 44.2μM (3). Additionally, compound 3 displayed activity against amastigote forms of T. c...
This paper describes a screening method for antioxidant potential determination based on luminol/... more This paper describes a screening method for antioxidant potential determination based on luminol/hemin/hydrogen peroxide chemiluminescence. The emission depletion, caused by an antiradical compound added during the chemiluminescence decay, is proportional to the number of reactive species trapped. Therefore, the difference between the areas of the emission decay curves, obtained in the absence and in the presence of the potential antioxidant, is a measure for the antiradical capacity of the sample. The technique has been applied to measure the antiradical capacity of pure compounds and complex mixtures from natural origin, providing reliable results that indicate the method's feasibility.
The Journal of Essential Oil Research, May 1, 2008
The essential oils from leaves of Eugenia brasiliensis and Eugenia sp. collected bimonthly during... more The essential oils from leaves of Eugenia brasiliensis and Eugenia sp. collected bimonthly during one year (four times in the 15 day of January, March, May, July, September, and November 2004) were subjected to GC-FID and GC/MS analysis. The obtained data showed a significant variation in the proportions of the components, which could be associated to climatic parameters in each
ABSTRACT The trunk wood of the central Brazilian Ocotea aciphylla contains two hydrobenzofuranoid... more ABSTRACT The trunk wood of the central Brazilian Ocotea aciphylla contains two hydrobenzofuranoid and three bicyclo[3.2.1]octanoid neolignans. The former comprise a novel representative of the rare ferrearin (3a-allyl-2-aryl-7a-hydroxy-3-methyl-2,3,3a,4,7,7a-hexahydro-7-oxobenzofuran) type.
Bioassay-guided fractionation of the EtOH extract of the aerial parts of Baccharis uncinella C. D... more Bioassay-guided fractionation of the EtOH extract of the aerial parts of Baccharis uncinella C. DC. (Asteraceae) led to identification of two cinnamic acid derivatives (caffeic and ferulic acids), two flavones (hispidulin and pectolinaringenin) and a mixture of three chlorogenic acids (3,4-, 3,5- and 4,5-O-dicaffeoylquinic acids), which displayed in vitro anti-trypanosomal activity. Pectolinaringenin, hispidulin and caffeic acid showed activity against trypomastigotes of Trypanosoma cruzi, exhibiting 50% inhibitory concentration (IC50) values of 52, 81 and 56 microg/mL, respectively, while the chlorogenic acid mixture showed an IC50 value of 61 microg/mL. The flavonoids and cinnamic acid derivatives were evaluated for cytotoxicity against NCTC cells resulting in a 50% cytotoxic concentration (CC50) ranging from 33.82 to 129.1 microg/mL while the chlorogenic acids did not display cytotoxicity (CC50 >150 microg/mL). This is the first report of anti-trypanosomal activity of compound...
The aim of this paper was to investigate the effect of chlorogenic acid (5-caffeoylquinic acid, 5... more The aim of this paper was to investigate the effect of chlorogenic acid (5-caffeoylquinic acid, 5CQA), isolated from Baccharis oxyodonta, on the structure and pharmacological effect of secretory phospholipase A2 (sPLA2) from Crotalus durissus terrificus. All in vitro and in vivo experiments were conducted using a purified sPLA2 compared under the same experimental conditions with sPLA2 : 5CQA. 5CQA induced several discrete modifications in the secondary structure and the hydrophobic characteristics of native sPLA2 that induced slight changes in the α-helical content, increase in the random coil structure, and decrease of fluorescence of native sPLA2. Moreover, 5CQA significantly decreased the enzymatic activity and the oedema and myonecrosis induced by native sPLA2. As the catalytic activity of sPLA2 plays an important role in several of its biological and pharmacological properties, antibacterial activity was used to confirm the decrease in its enzymatic activity by 5CQA, which ind...
In this work, two new flavonoids, oblongifolioside A (1) and oblongifolioside B (2), along with e... more In this work, two new flavonoids, oblongifolioside A (1) and oblongifolioside B (2), along with eight known compounds (3–10), are isolated from the leaves of Baccharis oblongifolia (Asteraceae). The new structures are established through spectroscopic data and the known compounds are identified by comparison with data reported in the literature. The compounds (1–10) are evaluated in relation to their antiradical properties. Compounds 1 and 2 are found to exhibit high antiradical activity compared to their respective non-acylated flavonoids.
Baccharis retusa, a medicinal Brazilian plant from Asteraceae, has been used in Brazilian folk me... more Baccharis retusa, a medicinal Brazilian plant from Asteraceae, has been used in Brazilian folk medicine to treatment of several illnesses, including parasitic diseases. Bioactivity-guided fractionation of the n-hexane extract from the aerial parts of B. retusa resulted in the isolation and characterization of three active related diterpenes: ent-15β-senecioyl-oxy-kaur-16-en-19-oic acid (1), ent-kaur-16-en-19-oic (2) and ent-16-oxo-17-nor-kauran-19-oic (3) acids. The structures of isolated compounds were defined by spectroscopic analysis, including NMR and HRESIMS. Antitrypanosomal activity of 1-3 was performed against cell-derived trypomastigotes using the colorimetric resazurin assay. The obtained results demonstrated that isolated compounds displayed a reduced toxicity against NCTC cells and were effective against the trypomastigote forms of T. cruzi with IC values of 3.8μM (1), 75.3μM (2) and 44.2μM (3). Additionally, compound 3 displayed activity against amastigote forms of T. c...
This paper describes a screening method for antioxidant potential determination based on luminol/... more This paper describes a screening method for antioxidant potential determination based on luminol/hemin/hydrogen peroxide chemiluminescence. The emission depletion, caused by an antiradical compound added during the chemiluminescence decay, is proportional to the number of reactive species trapped. Therefore, the difference between the areas of the emission decay curves, obtained in the absence and in the presence of the potential antioxidant, is a measure for the antiradical capacity of the sample. The technique has been applied to measure the antiradical capacity of pure compounds and complex mixtures from natural origin, providing reliable results that indicate the method's feasibility.
The Journal of Essential Oil Research, May 1, 2008
The essential oils from leaves of Eugenia brasiliensis and Eugenia sp. collected bimonthly during... more The essential oils from leaves of Eugenia brasiliensis and Eugenia sp. collected bimonthly during one year (four times in the 15 day of January, March, May, July, September, and November 2004) were subjected to GC-FID and GC/MS analysis. The obtained data showed a significant variation in the proportions of the components, which could be associated to climatic parameters in each
ABSTRACT The trunk wood of the central Brazilian Ocotea aciphylla contains two hydrobenzofuranoid... more ABSTRACT The trunk wood of the central Brazilian Ocotea aciphylla contains two hydrobenzofuranoid and three bicyclo[3.2.1]octanoid neolignans. The former comprise a novel representative of the rare ferrearin (3a-allyl-2-aryl-7a-hydroxy-3-methyl-2,3,3a,4,7,7a-hexahydro-7-oxobenzofuran) type.
Bioassay-guided fractionation of the EtOH extract of the aerial parts of Baccharis uncinella C. D... more Bioassay-guided fractionation of the EtOH extract of the aerial parts of Baccharis uncinella C. DC. (Asteraceae) led to identification of two cinnamic acid derivatives (caffeic and ferulic acids), two flavones (hispidulin and pectolinaringenin) and a mixture of three chlorogenic acids (3,4-, 3,5- and 4,5-O-dicaffeoylquinic acids), which displayed in vitro anti-trypanosomal activity. Pectolinaringenin, hispidulin and caffeic acid showed activity against trypomastigotes of Trypanosoma cruzi, exhibiting 50% inhibitory concentration (IC50) values of 52, 81 and 56 microg/mL, respectively, while the chlorogenic acid mixture showed an IC50 value of 61 microg/mL. The flavonoids and cinnamic acid derivatives were evaluated for cytotoxicity against NCTC cells resulting in a 50% cytotoxic concentration (CC50) ranging from 33.82 to 129.1 microg/mL while the chlorogenic acids did not display cytotoxicity (CC50 >150 microg/mL). This is the first report of anti-trypanosomal activity of compound...
The aim of this paper was to investigate the effect of chlorogenic acid (5-caffeoylquinic acid, 5... more The aim of this paper was to investigate the effect of chlorogenic acid (5-caffeoylquinic acid, 5CQA), isolated from Baccharis oxyodonta, on the structure and pharmacological effect of secretory phospholipase A2 (sPLA2) from Crotalus durissus terrificus. All in vitro and in vivo experiments were conducted using a purified sPLA2 compared under the same experimental conditions with sPLA2 : 5CQA. 5CQA induced several discrete modifications in the secondary structure and the hydrophobic characteristics of native sPLA2 that induced slight changes in the α-helical content, increase in the random coil structure, and decrease of fluorescence of native sPLA2. Moreover, 5CQA significantly decreased the enzymatic activity and the oedema and myonecrosis induced by native sPLA2. As the catalytic activity of sPLA2 plays an important role in several of its biological and pharmacological properties, antibacterial activity was used to confirm the decrease in its enzymatic activity by 5CQA, which ind...
Uploads
Papers by Paulete Romoff