The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins

Detalhes bibliográficos
Autor(a) principal: Santos, Marcelo H. dos
Data de Publicação: 2016
Outros Autores: Santos, Jorge A. N., Kondo, Márcia Y., Freitas, Renato F., Ramalho, Teodorico C., Assis, Diego M., Juliano, Luiz, Juliano, Maria A., Puzer, Luciano
Tipo de documento: Artigo
Idioma: eng
Título da fonte: LOCUS Repositório Institucional da UFV
Texto Completo: https://doi.org/10.1016/j.bmcl.2016.01.039
http://www.locus.ufv.br/handle/123456789/19688
Resumo: The human tissue kallikreins (KLK1–KLK15) comprise a family of 15 serine peptidases detected in almost every tissue of the human body and that actively participate in many physiological and pathological events. Some kallikreins are involved in diseases for which no effective therapy is available, as for example, epithelial disorders, bacterial infections and in certain cancers metastatic processes. In recent years our group have made efforts to find inhibitors for all kallikreins, based on natural products and synthetic molecules, and all the inhibitors developed by our group presented a competitive mechanism of inhibition. Here we describe fukugetin, a natural product that presents a mixed-type mechanism of inhibition against KLK1 and KLK2. This type of inhibitor is gaining importance today, especially for the development of exosite-type inhibitors, which present potential to selectively inhibit the enzyme activity only against specific substrate.
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spelling Santos, Marcelo H. dosSantos, Jorge A. N.Kondo, Márcia Y.Freitas, Renato F.Ramalho, Teodorico C.Assis, Diego M.Juliano, LuizJuliano, Maria A.Puzer, Luciano2018-05-18T12:17:21Z2018-05-18T12:17:21Z2016-03-010960894Xhttps://doi.org/10.1016/j.bmcl.2016.01.039http://www.locus.ufv.br/handle/123456789/19688The human tissue kallikreins (KLK1–KLK15) comprise a family of 15 serine peptidases detected in almost every tissue of the human body and that actively participate in many physiological and pathological events. Some kallikreins are involved in diseases for which no effective therapy is available, as for example, epithelial disorders, bacterial infections and in certain cancers metastatic processes. In recent years our group have made efforts to find inhibitors for all kallikreins, based on natural products and synthetic molecules, and all the inhibitors developed by our group presented a competitive mechanism of inhibition. Here we describe fukugetin, a natural product that presents a mixed-type mechanism of inhibition against KLK1 and KLK2. This type of inhibitor is gaining importance today, especially for the development of exosite-type inhibitors, which present potential to selectively inhibit the enzyme activity only against specific substrate.engBioorganic & Medicinal Chemistry Lettersv. 26, n. 5, p. 1485-1489, Março 2016Elsevier Ltdinfo:eu-repo/semantics/openAccessEnzymeSerine proteaseKallikreinInhibitorFlavoneMolecular dockingMolecular dynamic simulationThe natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreinsinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfreponame:LOCUS Repositório Institucional da UFVinstname:Universidade Federal de Viçosa (UFV)instacron:UFVORIGINALartigo.pdfartigo.pdftexto completoapplication/pdf1077203https://locus.ufv.br//bitstream/123456789/19688/1/artigo.pdf30059e4fdecf0e4efcc009bdbfa84ff4MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://locus.ufv.br//bitstream/123456789/19688/2/license.txt8a4605be74aa9ea9d79846c1fba20a33MD52THUMBNAILartigo.pdf.jpgartigo.pdf.jpgIM Thumbnailimage/jpeg6615https://locus.ufv.br//bitstream/123456789/19688/3/artigo.pdf.jpg78cea9297f3435789fa39ab739c3c15dMD53123456789/196882018-05-18 23:00:43.313oai:locus.ufv.br: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Repositório InstitucionalPUBhttps://www.locus.ufv.br/oai/requestfabiojreis@ufv.bropendoar:21452018-05-19T02:00:43LOCUS Repositório Institucional da UFV - Universidade Federal de Viçosa (UFV)false
dc.title.en.fl_str_mv The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
title The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
spellingShingle The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
Santos, Marcelo H. dos
Enzyme
Serine protease
Kallikrein
Inhibitor
Flavone
Molecular docking
Molecular dynamic simulation
title_short The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
title_full The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
title_fullStr The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
title_full_unstemmed The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
title_sort The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
author Santos, Marcelo H. dos
author_facet Santos, Marcelo H. dos
Santos, Jorge A. N.
Kondo, Márcia Y.
Freitas, Renato F.
Ramalho, Teodorico C.
Assis, Diego M.
Juliano, Luiz
Juliano, Maria A.
Puzer, Luciano
author_role author
author2 Santos, Jorge A. N.
Kondo, Márcia Y.
Freitas, Renato F.
Ramalho, Teodorico C.
Assis, Diego M.
Juliano, Luiz
Juliano, Maria A.
Puzer, Luciano
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Santos, Marcelo H. dos
Santos, Jorge A. N.
Kondo, Márcia Y.
Freitas, Renato F.
Ramalho, Teodorico C.
Assis, Diego M.
Juliano, Luiz
Juliano, Maria A.
Puzer, Luciano
dc.subject.pt-BR.fl_str_mv Enzyme
Serine protease
Kallikrein
Inhibitor
Flavone
Molecular docking
Molecular dynamic simulation
topic Enzyme
Serine protease
Kallikrein
Inhibitor
Flavone
Molecular docking
Molecular dynamic simulation
description The human tissue kallikreins (KLK1–KLK15) comprise a family of 15 serine peptidases detected in almost every tissue of the human body and that actively participate in many physiological and pathological events. Some kallikreins are involved in diseases for which no effective therapy is available, as for example, epithelial disorders, bacterial infections and in certain cancers metastatic processes. In recent years our group have made efforts to find inhibitors for all kallikreins, based on natural products and synthetic molecules, and all the inhibitors developed by our group presented a competitive mechanism of inhibition. Here we describe fukugetin, a natural product that presents a mixed-type mechanism of inhibition against KLK1 and KLK2. This type of inhibitor is gaining importance today, especially for the development of exosite-type inhibitors, which present potential to selectively inhibit the enzyme activity only against specific substrate.
publishDate 2016
dc.date.issued.fl_str_mv 2016-03-01
dc.date.accessioned.fl_str_mv 2018-05-18T12:17:21Z
dc.date.available.fl_str_mv 2018-05-18T12:17:21Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://doi.org/10.1016/j.bmcl.2016.01.039
http://www.locus.ufv.br/handle/123456789/19688
dc.identifier.issn.none.fl_str_mv 0960894X
identifier_str_mv 0960894X
url https://doi.org/10.1016/j.bmcl.2016.01.039
http://www.locus.ufv.br/handle/123456789/19688
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartofseries.pt-BR.fl_str_mv v. 26, n. 5, p. 1485-1489, Março 2016
dc.rights.driver.fl_str_mv Elsevier Ltd
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Elsevier Ltd
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Bioorganic & Medicinal Chemistry Letters
publisher.none.fl_str_mv Bioorganic & Medicinal Chemistry Letters
dc.source.none.fl_str_mv reponame:LOCUS Repositório Institucional da UFV
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