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In vitro bioassay guided anti-dermatophyte and cytotoxic activities from Piper umbellatum L. Miq. led to 4-nerolidylcatechol

dc.contributor.authorFreitas, Jolindo A. [UNESP]
dc.contributor.authorSorrechia, Rodrigo [UNESP]
dc.contributor.authorPoliti, Flávio A. S. [UNESP]
dc.contributor.authorSantos, André G. [UNESP]
dc.contributor.authorRodrigues, Edvânio R. [UNESP]
dc.contributor.authorSantos, Lourdes C. [UNESP]
dc.contributor.authorFusco-Almeida, Ana M. [UNESP]
dc.contributor.authorOliveira, Andrew A.
dc.contributor.authorGuido, Rafael V. C.
dc.contributor.authorPietro, Rosemeire C. L. R. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2021-06-25T10:33:09Z
dc.date.available2021-06-25T10:33:09Z
dc.date.issued2020-01-01
dc.description.abstractDermatophytosis is a dermic disease caused by fungi. The aim of this study was to search anti-dermatophyte bioactive compounds in Piper umbellatum leaves. Cytotoxicity evaluation was performed against MRC-5 and HepG2 as a selectivity parameter. Crude ethanol extract presented MIC value of 39.1 μg/mL against M. canis and no cytotoxicity to Hep G2 (human liver cancer) and MRC-5 (normal lung fibroblast). 4-nerolydilcatechol was isolated from P. umbellatum ethanolic extract. MIC values for 4-NC were 7.6μM to M. canisand 15.6μM to Trichophyton rubrum. 4-NC presented activity against M. canis14 times lower than to MRC-5 (non-tumoral human cell line), which suggest selective activity for this fungus. Molecular modeling suggests 4-NC could bind to CYP51, present in lanosterol synthesis, blocking fungi development. In conclusion, P. umbellatum crude ethanol extract and 4-NC demonstrated high and selective in vitro antifungal activity. (Figure presented.).en
dc.description.affiliationSchool of Pharmaceutical Sciences Department of Drugs and Medicines São Paulo State University(UNESP)
dc.description.affiliationSchool of Pharmaceutical Sciences Department of Natural Principles and Toxicology São Paulo State University (UNESP)
dc.description.affiliationInstitute of Chemistry Department of Organic Chemistry São Paulo State University (UNESP)
dc.description.affiliationSchool of Pharmaceutical Sciences Department of Clinical Analysis São Paulo State University(UNESP)
dc.description.affiliationSão Carlos Institute of Physics University of São Paulo (USP)
dc.description.affiliationJolindo A. Freitas School of Pharmaceutical Sciences of Ribeirão Preto University of São Paulo
dc.description.affiliationUnespSchool of Pharmaceutical Sciences Department of Drugs and Medicines São Paulo State University(UNESP)
dc.description.affiliationUnespSchool of Pharmaceutical Sciences Department of Natural Principles and Toxicology São Paulo State University (UNESP)
dc.description.affiliationUnespInstitute of Chemistry Department of Organic Chemistry São Paulo State University (UNESP)
dc.description.affiliationUnespSchool of Pharmaceutical Sciences Department of Clinical Analysis São Paulo State University(UNESP)
dc.format.extent3423-3427
dc.identifierhttp://dx.doi.org/10.1080/14786419.2019.1569656
dc.identifier.citationNatural Product Research, v. 34, n. 23, p. 3423-3427, 2020.
dc.identifier.doi10.1080/14786419.2019.1569656
dc.identifier.issn1478-6427
dc.identifier.issn1478-6419
dc.identifier.scopus2-s2.0-85087863549
dc.identifier.urihttp://hdl.handle.net/11449/206494
dc.language.isoeng
dc.relation.ispartofNatural Product Research
dc.sourceScopus
dc.subject4-Nerolidylcatechol
dc.subjectantifungal
dc.subjectcytotoxicity
dc.subjectdermatophytes;Piper umbellatum
dc.titleIn vitro bioassay guided anti-dermatophyte and cytotoxic activities from Piper umbellatum L. Miq. led to 4-nerolidylcatecholen
dc.typeArtigo
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentAnálises Clínicas - FCFpt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentPrincípios Ativos Naturais e Toxicologia - FCFpt
unesp.departmentQuímica Orgânica - IQARpt

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