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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/12302
Ver los metadatos del registro completo
id |
CONICETDig_8ad3a31f9b218648226957e264bebc29 |
---|---|
oai_identifier_str |
oai:ri.conicet.gov.ar:11336/12302 |
network_acronym_str |
CONICETDig |
repository_id_str |
3498 |
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 |
_version_ |
1844613136428040192 |
score |
13.070432 |