Paulete Romoff

Dr. Paulete Romoff


Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 March 2023 in Plants
Verified
Journal Article
Open access
PDF file
MRMarcela H. Retamozo
Marcela H. Retamozo
CSChristian C. Silva
Christian C. Silva
CTCinthia I. Tamayose
Cinthia I. Tamayose
JCJuliana Carvalho
Juliana Carvalho
PRPaulete Romoff
Paulete Romoff
MFMarcelo J. Pena Ferreira
Marcelo J. Pena Ferreira
Baccharis is one of the largest genera of Asteraceae and its species are used in folk medicine for several medicinal purposes due to the presence of bioactive compounds. We investigated the phytochemical composition of polar extracts of B. sphenophylla. Using chromatographic procedures, diterpenoids (ent-kaurenoic acid), flavonoids (hispidulin, eupafolin, isoquercitrin, quercitrin, biorobin, rutin, and vicenin-2), caffeic acid, and chlorogenic acid derivatives (5-O-caffeoylquinic acid and its methyl ester, 3,4-di-O-caffeoylquinic acid, 4,5-di-O-caffeoylquinic acid, and 3,5-di-O-caffeoylquinic acid and its methyl ester) were isolated from polar fractions and are described. The extract, polar fractions, and fifteen isolated compounds were evaluated in relation to radical scavenging activity using two assays. Chlorogenic acid derivatives and flavonols exhibited higher antioxidant effects, confirming that B. sphenophylla is an important source of phenolic compounds with antiradical properties.

3 September 2019 in Molecules
Verified
Journal Article
Open access
PDF file
PZPaulo R. F. Zampieri
Paulo R. F. Zampieri
CTCinthia I. Tamayose
Cinthia I. Tamayose
OFOriana A. Fávero
Oriana A. Fávero
PRPaulete Romoff
Paulete Romoff
MFMarcelo J. Pena Ferreira
Marcelo J. Pena Ferreira
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.