Thienopyrimidine Derivatives as GPR55 Receptor Antagonists: Insight into Structure–Activity Relationship

Author:

Figuerola-Asencio Laura1,Morales Paula1ORCID,Zhao Pingwei2,Hurst Dow P.3,Sayed Sommayah S.3,Colón Katsuya L.3,Gómez-Cañas María4,Fernández-Ruiz Javier4ORCID,Croatt Mitchell P.3ORCID,Reggio Patricia H.3,Abood Mary E.2,Jagerovic Nadine1ORCID

Affiliation:

1. Instituto de Química Médica, Consejo Superior de Investigaciones Científicas, 28006Madrid, Spain

2. Center for Substance Abuse Research, Temple University, Philadelphia, Pennsylvania19122, United States

3. Center for Drug Discovery, Department of Chemistry and Biochemistry, University North Carolina, Greensboro, North Carolina27599, United States

4. Department of Biochemistry and Molecular Biology, Faculty of Medicine, Complutense University, CIBERNED and IRYCIS, 28040Madrid, Spain

Funder

Consejo Superior de Investigaciones Cient?ficas

Comunidad de Madrid

Ministerio de Ciencia, Innovaci?n y Universidades

National Institute on Drug Abuse

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Effects of a Novel GPR55 Antagonist on the Arachidonic Acid Cascade in LPS-Activated Primary Microglial Cells

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

3. Wise, A.; Brown, A. J.Identification of Modulators of GPR55. WO200186305, 2001.

4. Drmota, T.; Greasley, P.; Groblewski, T.; Drmota, P.; Greasley, P.; Groblewski, T.Screening Assays for Cannabinoid- Ligand Type Modulators. WO2004074844, 2004.

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