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5篇 您的检索式:作者名="Regasini"
    题名 作者 年代 出处 被引量
1Synthesis and evaluation of novel prenylated chalcone derivatives as anti-leishmanial and anti-trypanosomal compounds显示文摘Thais Gaban Passalacqua Luiz Antonio Dutra Letícia de Almeida Angela Maria Arenas Velásquez Fabio Aurelio Esteves Torres Paulo Renato Yamasaki Mariana Bastos dos Santos Luis Octavio Regasini Paul A.M. Michels Vanderlan da Silva Bolzani Marcia A.S. Graminh 2015Bioorganic & Medicinal Chemistry Letters2015,,:1
2Flavonols from Pterogyne nitens and their evaluation as myeloperoxidase inhibitors显示文摘Regasini L O Vellosa J C R Silva D H S 2008Phytochemistry2008,69,8:1
3Nitensidine A, a guanidine alkaloid from Pterogyne nitens , is a novel substrate for human ABC transporter ABCB1显示文摘Yasuhiro Tajima Hiroshi Nakagawa Ai Tamura Onat Kadioglu Kazuhiro Satake Yuji Mitani Hayato Murase Luis Octavio Regasini Vanderlan da Silva Bolzani Toshihisa Ishikawa Gert Fricker Thomas Efferth 2014Phytomedicine2014,,3:1
4Free radical scavenging activity of Kielmeyera variahilis (Clusiaceae) 显示文摘Coqueiro A Regasini LO Skrzek SC 2013Molecules2013,18,2:1
5Anti-Candida and anti-Cryptococcus evaluation of 15 non-alkaloidal compounds from Pterogyne nitens显示文摘Objective: To evaluate anti-Candida and anti-Cryptococcus activities of 15 nonalkaloidal compounds from Pterogyne nitens Tulasne(Leguminosae), a South American medicinal plant.Methods: Compounds were submitted to antifungal assays, using microdilution method described by Clinical and Laboratory Standards Institute document, with minor modifications. Five species of Candida and two species of Cryptococcus, including clinical isolates were screened. Antifungal activity was expressed by minimum inhibitory concentration(MIC). Amphotericin B and fluconazole were used as standard antifungal drugs.Results: Among tested compounds, six substances presented fungal growth inhibition(MIC < 31.2 mg/m L) [three flavone derivatives(1–3), a glycosylated flavonol derivative(5)and two phenolic acids(10 and 12)]. Sorbifolin(1), exhibited potent antifungal activity,demonstrating MIC value of 3.90 mg/m L against Candida glabrata ATCC 90030, Cryptococcus gattii 118 and fluconazole-resistant clinical isolate of Cryptococcus neoformans var. grubii. Pedalin(2) and nitensoside B(3), two glycosylated flavone derivatives, were active against Cryptococcus neoformans ATCC 90012(MIC = 7.80 mg/m L).Conclusions: Flavone derivatives from Pterogyne nitens can serve as prototypes for the design and development of innovative anti-Candida and anti-Cryptococcus hits.Caroline Sprengel Lima Carlos Roberto Polaquini Mariana Bastos dos Santos Fernanda Patricia Gullo Fernanda Sangalli Leite Liliane Scorzoni Vanderlan da Silva Bolzani Maria Jose Soares Mendes-Giannini Ana Marisa Fusco-Almeida Andréia Alves Rezende Luis Octavio Regasini 2016Asian Pacific Journal of Tropical Biomedicine2016,6,10:0
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