Identification of Novel GPR55 Modulators Using Cell-Impedance-Based Label-Free Technology

Author:

Morales Paula1,Whyte Lauren S.2,Chicharro Roberto1,Gómez-Cañas María345,Pazos M. Ruth345,Goya Pilar1,Irving Andrew J.6,Fernández-Ruiz Javier345,Ross Ruth A.2,Jagerovic Nadine1

Affiliation:

1. Instituto de Química Médica, CSIC, Calle Juan de la Cierva, 3, 28006 Madrid, Spain

2. Department of Pharmacology and Toxicology, Medical Sciences Building, University of Toronto, 1 King’s College Circle, Toronto, Ontario M5S 1A8, Canada

3. Departamento de Bioquímica y Biología Molecular, Facultad de Medicina, Universidad Complutense de Madrid, 28040 Madrid, Spain

4. Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), 28040 Madrid, Spain

5. Instituto Ramón y Cajal de Investigaciones Sanitarias (IRYCIS), 28034 Madrid, Spain

6. School of Biomolecular and Biomedical Science, University College Dublin, Dublin D4, Ireland

Funder

University of Toronto

Consejo Superior de Investigaciones Cient?ficas

Ministerio de Econom?a y Competitividad

European Social Fund

Comunidad de Madrid

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Reference61 articles.

1. Identification and cloning of three novel human G protein-coupled receptor genes GPR52, ΨGPR53 and GPR55: GPR55 is extensively expressed in human brain

2. Drmota, T.; Greasley, P.; Groblewski, T.(AstraZeneca) Screening assays for cannabinoid- ligand-type modulators of GPR55., WO2004/0748844, 2004.

3. Brown, A. J.; Wise, A.(Glaxosmithkline) Identification of modulators of GPR55 activity, WO2001/86305A2, 2001.

4. GPR55 and GPR35 and their relationship to cannabinoid and lysophospholipid receptors

5. The therapeutic potential of orphan GPCRs, GPR35 and GPR55

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