Highly efficient synthesis and characterization of the GPR30-selective agonist G-1 and related tetrahydroquinoline analogs†
Abstract
The GPR30
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* Corresponding authors
a Department of Chemistry and Biochemistry MSC 3C, New Mexico State University, P.O. Box 30001, Las Cruces, New Mexico
b Institute of Chemistry, Romanian Academy, Timisoara, Romania
c Division of Biocomputing, Department of Biochemistry & Molecular Biology, University of New Mexico Health Sciences Center, Albuquerque
d Cancer Research and Treatment Center, University of New Mexico Health Sciences Center, Albuquerque
e Department of Pathology, University of New Mexico Health Sciences Center, Albuquerque
f
Department of Cell Biology & Physiology, University of New Mexico Health Sciences Center, Albuquerque
E-mail:
jarterbu@nmsu.edu
The GPR30
R. Burai, C. Ramesh, M. Shorty, R. Curpan, C. Bologa, L. A. Sklar, T. Oprea, E. R. Prossnitz and J. B. Arterburn, Org. Biomol. Chem., 2010, 8, 2252 DOI: 10.1039/C001307B
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