Mastering tricyclic ring systems for desirable functional cannabinoid activity

Autores
Petrov, Ravil R.; Knight, Lindsay; Chen, Shao Rui; Wager Miller, Jim; McDaniel, Steven W.; Diaz, Fanny; Barth, Francis; Pan, Hui Lin; Mackie, Ken; Cavasotto, Claudio Norberto; Diaz, Philippe
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
There is growing interest in using cannabinoid receptor 2 (CB2) agonists for the treatment of neuropathic pain and other indications. In continuation of our ongoing program aiming for the development of new small molecule cannabinoid ligands, we have synthesized a novel series of carbazole and γ-carboline derivatives. The affinities of the newly synthesized compounds were determined by a competitive radioligand displacement assay for human CB2 cannabinoid receptor and rat CB1 cannabinoid receptor. Functional activity and selectivity at human CB1 and CB2 receptors were characterized using receptor internalization and [35S]GTP-γ-S assays. The structure–activity relationship and optimization studies of the carbazole series have led to the discovery of a non-selective CB1 and CB2 agonist, compound 4. Our subsequent research efforts to increase CB2 selectivity of this lead compound have led to the discovery of CB2 selective compound 64, which robustly internalized CB2 receptors. Compound 64 had potent inhibitory effects on pain hypersensitivity in a rat model of neuropathic pain. Other potent and CB2 receptor–selective compounds, including compounds 63 and 68, and a selective CB1 agonist, compound 74 were also discovered. In addition, we identified the CB2 ligand 35 which failed to promote CB2 receptor internalization and inhibited compound CP55,940-induced CB2 internalization despite a high CB2 receptor affinity. The present study provides novel tricyclic series as a starting point for further investigations of CB2 pharmacology and pain treatment.
Fil: Petrov, Ravil R.. University Of Montana; Estados Unidos
Fil: Knight, Lindsay. Indiana University; Estados Unidos
Fil: Chen, Shao Rui. University Of Texas; Estados Unidos
Fil: Wager Miller, Jim. Indiana University; Estados Unidos
Fil: McDaniel, Steven W.. University Of Montana; Estados Unidos
Fil: Diaz, Fanny. University Of Montana; Estados Unidos
Fil: Barth, Francis. Sanofi-aventis R&D; Francia
Fil: Pan, Hui Lin. University Of Texas; Estados Unidos
Fil: Mackie, Ken. Indiana University; Estados Unidos
Fil: Cavasotto, Claudio Norberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires; Argentina
Fil: Diaz, Philippe. University Of Montana; Estados Unidos
Materia
Cannabinoid Receptor
Tricycling Ring System
Homology Modelling
Flexible Docking
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/12302

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network_name_str CONICET Digital (CONICET)
spelling Mastering tricyclic ring systems for desirable functional cannabinoid activityPetrov, Ravil R.Knight, LindsayChen, Shao RuiWager Miller, JimMcDaniel, Steven W.Diaz, FannyBarth, FrancisPan, Hui LinMackie, KenCavasotto, Claudio NorbertoDiaz, PhilippeCannabinoid ReceptorTricycling Ring SystemHomology ModellingFlexible Dockinghttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1There is growing interest in using cannabinoid receptor 2 (CB2) agonists for the treatment of neuropathic pain and other indications. In continuation of our ongoing program aiming for the development of new small molecule cannabinoid ligands, we have synthesized a novel series of carbazole and γ-carboline derivatives. The affinities of the newly synthesized compounds were determined by a competitive radioligand displacement assay for human CB2 cannabinoid receptor and rat CB1 cannabinoid receptor. Functional activity and selectivity at human CB1 and CB2 receptors were characterized using receptor internalization and [35S]GTP-γ-S assays. The structure–activity relationship and optimization studies of the carbazole series have led to the discovery of a non-selective CB1 and CB2 agonist, compound 4. Our subsequent research efforts to increase CB2 selectivity of this lead compound have led to the discovery of CB2 selective compound 64, which robustly internalized CB2 receptors. Compound 64 had potent inhibitory effects on pain hypersensitivity in a rat model of neuropathic pain. Other potent and CB2 receptor–selective compounds, including compounds 63 and 68, and a selective CB1 agonist, compound 74 were also discovered. In addition, we identified the CB2 ligand 35 which failed to promote CB2 receptor internalization and inhibited compound CP55,940-induced CB2 internalization despite a high CB2 receptor affinity. The present study provides novel tricyclic series as a starting point for further investigations of CB2 pharmacology and pain treatment.Fil: Petrov, Ravil R.. University Of Montana; Estados UnidosFil: Knight, Lindsay. Indiana University; Estados UnidosFil: Chen, Shao Rui. University Of Texas; Estados UnidosFil: Wager Miller, Jim. Indiana University; Estados UnidosFil: McDaniel, Steven W.. University Of Montana; Estados UnidosFil: Diaz, Fanny. University Of Montana; Estados UnidosFil: Barth, Francis. Sanofi-aventis R&D; FranciaFil: Pan, Hui Lin. University Of Texas; Estados UnidosFil: Mackie, Ken. Indiana University; Estados UnidosFil: Cavasotto, Claudio Norberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires; ArgentinaFil: Diaz, Philippe. University Of Montana; Estados UnidosElsevier Masson2013-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/12302Petrov, Ravil R.; Knight, Lindsay; Chen, Shao Rui; Wager Miller, Jim; McDaniel, Steven W.; et al.; Mastering tricyclic ring systems for desirable functional cannabinoid activity; Elsevier Masson; European Journal Of Medical Chemistry; 69; 11-2013; 881-9070223-5234enginfo:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0223523413006193info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ejmech.2013.09.038info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T09:36:16Zoai:ri.conicet.gov.ar:11336/12302instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 09:36:16.77CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Mastering tricyclic ring systems for desirable functional cannabinoid activity
title Mastering tricyclic ring systems for desirable functional cannabinoid activity
spellingShingle Mastering tricyclic ring systems for desirable functional cannabinoid activity
Petrov, Ravil R.
Cannabinoid Receptor
Tricycling Ring System
Homology Modelling
Flexible Docking
title_short Mastering tricyclic ring systems for desirable functional cannabinoid activity
title_full Mastering tricyclic ring systems for desirable functional cannabinoid activity
title_fullStr Mastering tricyclic ring systems for desirable functional cannabinoid activity
title_full_unstemmed Mastering tricyclic ring systems for desirable functional cannabinoid activity
title_sort Mastering tricyclic ring systems for desirable functional cannabinoid activity
dc.creator.none.fl_str_mv Petrov, Ravil R.
Knight, Lindsay
Chen, Shao Rui
Wager Miller, Jim
McDaniel, Steven W.
Diaz, Fanny
Barth, Francis
Pan, Hui Lin
Mackie, Ken
Cavasotto, Claudio Norberto
Diaz, Philippe
author Petrov, Ravil R.
author_facet Petrov, Ravil R.
Knight, Lindsay
Chen, Shao Rui
Wager Miller, Jim
McDaniel, Steven W.
Diaz, Fanny
Barth, Francis
Pan, Hui Lin
Mackie, Ken
Cavasotto, Claudio Norberto
Diaz, Philippe
author_role author
author2 Knight, Lindsay
Chen, Shao Rui
Wager Miller, Jim
McDaniel, Steven W.
Diaz, Fanny
Barth, Francis
Pan, Hui Lin
Mackie, Ken
Cavasotto, Claudio Norberto
Diaz, Philippe
author2_role author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Cannabinoid Receptor
Tricycling Ring System
Homology Modelling
Flexible Docking
topic Cannabinoid Receptor
Tricycling Ring System
Homology Modelling
Flexible Docking
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv There is growing interest in using cannabinoid receptor 2 (CB2) agonists for the treatment of neuropathic pain and other indications. In continuation of our ongoing program aiming for the development of new small molecule cannabinoid ligands, we have synthesized a novel series of carbazole and γ-carboline derivatives. The affinities of the newly synthesized compounds were determined by a competitive radioligand displacement assay for human CB2 cannabinoid receptor and rat CB1 cannabinoid receptor. Functional activity and selectivity at human CB1 and CB2 receptors were characterized using receptor internalization and [35S]GTP-γ-S assays. The structure–activity relationship and optimization studies of the carbazole series have led to the discovery of a non-selective CB1 and CB2 agonist, compound 4. Our subsequent research efforts to increase CB2 selectivity of this lead compound have led to the discovery of CB2 selective compound 64, which robustly internalized CB2 receptors. Compound 64 had potent inhibitory effects on pain hypersensitivity in a rat model of neuropathic pain. Other potent and CB2 receptor–selective compounds, including compounds 63 and 68, and a selective CB1 agonist, compound 74 were also discovered. In addition, we identified the CB2 ligand 35 which failed to promote CB2 receptor internalization and inhibited compound CP55,940-induced CB2 internalization despite a high CB2 receptor affinity. The present study provides novel tricyclic series as a starting point for further investigations of CB2 pharmacology and pain treatment.
Fil: Petrov, Ravil R.. University Of Montana; Estados Unidos
Fil: Knight, Lindsay. Indiana University; Estados Unidos
Fil: Chen, Shao Rui. University Of Texas; Estados Unidos
Fil: Wager Miller, Jim. Indiana University; Estados Unidos
Fil: McDaniel, Steven W.. University Of Montana; Estados Unidos
Fil: Diaz, Fanny. University Of Montana; Estados Unidos
Fil: Barth, Francis. Sanofi-aventis R&D; Francia
Fil: Pan, Hui Lin. University Of Texas; Estados Unidos
Fil: Mackie, Ken. Indiana University; Estados Unidos
Fil: Cavasotto, Claudio Norberto. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigación en Biomedicina de Buenos Aires; Argentina
Fil: Diaz, Philippe. University Of Montana; Estados Unidos
description There is growing interest in using cannabinoid receptor 2 (CB2) agonists for the treatment of neuropathic pain and other indications. In continuation of our ongoing program aiming for the development of new small molecule cannabinoid ligands, we have synthesized a novel series of carbazole and γ-carboline derivatives. The affinities of the newly synthesized compounds were determined by a competitive radioligand displacement assay for human CB2 cannabinoid receptor and rat CB1 cannabinoid receptor. Functional activity and selectivity at human CB1 and CB2 receptors were characterized using receptor internalization and [35S]GTP-γ-S assays. The structure–activity relationship and optimization studies of the carbazole series have led to the discovery of a non-selective CB1 and CB2 agonist, compound 4. Our subsequent research efforts to increase CB2 selectivity of this lead compound have led to the discovery of CB2 selective compound 64, which robustly internalized CB2 receptors. Compound 64 had potent inhibitory effects on pain hypersensitivity in a rat model of neuropathic pain. Other potent and CB2 receptor–selective compounds, including compounds 63 and 68, and a selective CB1 agonist, compound 74 were also discovered. In addition, we identified the CB2 ligand 35 which failed to promote CB2 receptor internalization and inhibited compound CP55,940-induced CB2 internalization despite a high CB2 receptor affinity. The present study provides novel tricyclic series as a starting point for further investigations of CB2 pharmacology and pain treatment.
publishDate 2013
dc.date.none.fl_str_mv 2013-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/12302
Petrov, Ravil R.; Knight, Lindsay; Chen, Shao Rui; Wager Miller, Jim; McDaniel, Steven W.; et al.; Mastering tricyclic ring systems for desirable functional cannabinoid activity; Elsevier Masson; European Journal Of Medical Chemistry; 69; 11-2013; 881-907
0223-5234
url http://hdl.handle.net/11336/12302
identifier_str_mv Petrov, Ravil R.; Knight, Lindsay; Chen, Shao Rui; Wager Miller, Jim; McDaniel, Steven W.; et al.; Mastering tricyclic ring systems for desirable functional cannabinoid activity; Elsevier Masson; European Journal Of Medical Chemistry; 69; 11-2013; 881-907
0223-5234
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0223523413006193
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ejmech.2013.09.038
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier Masson
publisher.none.fl_str_mv Elsevier Masson
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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