Discovery of Nanomolar Melanocortin-3 Receptor (MC3R)-Selective Small Molecule Pyrrolidine Bis-Cyclic Guanidine Agonist Compounds Via a High-Throughput "Unbiased" Screening Campaign

被引:6
作者
Doering, Skye R. [1 ,2 ]
Freeman, Katie [1 ,2 ]
Debevec, Ginamarie [3 ]
Geer, Phaedra [3 ]
Santos, Radleigh G. [4 ]
Lavoi, Travis M. [3 ]
Giulianotti, Marc A. [3 ]
Pinilla, Clemencia [3 ]
Appel, Jon R. [3 ]
Houghten, Richard A. [3 ]
Ericson, Mark D. [1 ,2 ]
Haskell-Luevano, Carrie [1 ,2 ]
机构
[1] Univ Minnesota, Dept Med Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Inst Translat Neurosci, Minneapolis, MN 55455 USA
[3] Florida Int Univ, Port St Lucie, FL 34987 USA
[4] Nova Southeastern Univ, Ft Lauderdale, FL 33314 USA
关键词
MELANOCYTE-STIMULATING HORMONE; SOLID-PHASE SYNTHESIS; MINIMAL ACTIVE SEQUENCE; ALPHA-MELANOTROPIN; COMBINATORIAL LIBRARIES; FRAMESHIFT MUTATION; MC4R AGONIST; FOOD-INTAKE; IN-VIVO; POTENT;
D O I
10.1021/acs.jmedchem.0c02041
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The central melanocortin-3 and melanocortin-4 receptors (MC3R, MC4R) are key regulators of body weight and energy homeostasis. Herein, the discovery and characterization of first-in-class small molecule melanocortin agonists with selectivity for the melanocortin-3 receptor over the melanocortin-4 receptor are reported. Identified via "unbiased" mixture-based high-throughput screening approaches, pharmacological evaluation of these pyrrolidine bis-cyclic guanidines resulted in nanomolar agonist activity at the melanocortin-3 receptor. The pharmacological profiles at the remaining melanocortin receptor subtypes tested indicated similar agonist potencies at both the melanocortin-1 and melanocortin-5 receptors and antagonist or micromolar agonist activities at the melanocortin-4 receptor. This group of small molecules represents a new area of chemical space for the melanocortin receptors with mixed receptor pharmacology profiles that may serve as novel lead compounds to modulate states of dysregulated energy balance.
引用
收藏
页码:5577 / 5592
页数:16
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