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Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening

AIM: The transient receptor potential vanilloid type 1 (TRPV1) is responsible for pain perception in the peripheral nervous system (PNS). TRPV1 is thus considered a versatile target for development of non-opioid analgesics. RESULTS: Pharmacophore-based clustering of a publicly available data set of...

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Detalles Bibliográficos
Autores principales: Goldmann, Daria, Pakfeifer, Peter, Hering, Steffen, Ecker, Gerhard F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422283/
https://www.ncbi.nlm.nih.gov/pubmed/25826358
http://dx.doi.org/10.4155/fmc.14.168
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author Goldmann, Daria
Pakfeifer, Peter
Hering, Steffen
Ecker, Gerhard F
author_facet Goldmann, Daria
Pakfeifer, Peter
Hering, Steffen
Ecker, Gerhard F
author_sort Goldmann, Daria
collection PubMed
description AIM: The transient receptor potential vanilloid type 1 (TRPV1) is responsible for pain perception in the peripheral nervous system (PNS). TRPV1 is thus considered a versatile target for development of non-opioid analgesics. RESULTS: Pharmacophore-based clustering of a publicly available data set of TRPV1 antagonists revealed a set of models, which were validated with data sets of inactive compounds, decoys and known drug candidates. The top ranked pharmacophore models were subsequently used for virtual screening. Based on a unique in-house protocol, a set of compounds was selected and biologically tested for modulation of TRPV1 in a voltage-clamp model. CONCLUSION: Pharmacophore models extracted from large public data sets are a valuable source for identification of novel scaffolds for TRPV1 receptor modulation.
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spelling pubmed-64222832019-03-18 Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening Goldmann, Daria Pakfeifer, Peter Hering, Steffen Ecker, Gerhard F Future Med Chem Article AIM: The transient receptor potential vanilloid type 1 (TRPV1) is responsible for pain perception in the peripheral nervous system (PNS). TRPV1 is thus considered a versatile target for development of non-opioid analgesics. RESULTS: Pharmacophore-based clustering of a publicly available data set of TRPV1 antagonists revealed a set of models, which were validated with data sets of inactive compounds, decoys and known drug candidates. The top ranked pharmacophore models were subsequently used for virtual screening. Based on a unique in-house protocol, a set of compounds was selected and biologically tested for modulation of TRPV1 in a voltage-clamp model. CONCLUSION: Pharmacophore models extracted from large public data sets are a valuable source for identification of novel scaffolds for TRPV1 receptor modulation. 2015 /pmc/articles/PMC6422283/ /pubmed/25826358 http://dx.doi.org/10.4155/fmc.14.168 Text en http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Goldmann, Daria
Pakfeifer, Peter
Hering, Steffen
Ecker, Gerhard F
Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title_full Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title_fullStr Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title_full_unstemmed Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title_short Novel scaffolds for modulation of TRPV1 identified with pharmacophore modeling and virtual screening
title_sort novel scaffolds for modulation of trpv1 identified with pharmacophore modeling and virtual screening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6422283/
https://www.ncbi.nlm.nih.gov/pubmed/25826358
http://dx.doi.org/10.4155/fmc.14.168
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