The natural flavone fukugetin as a mixed-type inhibitor for human tissue kallikreins
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , , |
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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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 |
format |
article |
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 |
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Elsevier Ltd |
eu_rights_str_mv |
openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
Bioorganic & Medicinal Chemistry Letters |
publisher.none.fl_str_mv |
Bioorganic & Medicinal Chemistry Letters |
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