Discovery of highly potent and selective orexin 1 receptor antagonists (1-SORAs) suitable for in vivo interrogation of orexin 1 receptor pharmacology

被引:13
作者
Stump, Craig A. [1 ]
Cooke, Andrew J. [1 ]
Bruno, Joseph [4 ]
Cabalu, Tamara D. [3 ]
Gotter, Anthony L. [2 ]
Harell, C. Meacham [2 ]
Kuduk, Scott D. [1 ]
McDonald, Terrence P. [2 ]
O'Brien, Julie [4 ]
Renger, John J. [2 ]
Williams, Peter D. [1 ]
Winrow, Christopher J. [2 ]
Coleman, Paul J. [1 ]
机构
[1] Merck Res Labs, Discovery Chem, West Point, PA 19486 USA
[2] Merck Res Labs, Neurosci, West Point, PA 19486 USA
[3] Merck Res Labs, Pharmacokinet Pharmacodynam & Drug Metab, West Point, PA 19486 USA
[4] Merck Res Labs, Vitro Pharmacol, West Point, PA 19486 USA
关键词
Selective orexin receptor antagonist (SORA); Dual orexin receptor antagonist (DORA); Orexin-1; Suvorexant; Filorexant; HUMAN NARCOLEPSY; SLEEP; INSOMNIA;
D O I
10.1016/j.bmcl.2016.10.019
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
While a correlation between blockade of the orexin 2 receptor (OX2R) with either a dual orexin receptor antagonist (DORA) or a selective orexin 2 receptor antagonist (2-SORA) and a decrease of wakefulness is well established, less is known about selective blockade of the orexin 1 receptor (OX1R). Therefore, a highly selective orexin 1 antagonist (1-SORA) with suitable properties to allow in vivo interrogation of OX1R specific pharmacology in preclinical species remains an attractive target. Herein, we describe the discovery of an optimized 1-SORA series in the piperidine ether class. Notably, a 4,4-difluoropiperidine core coupled with a 2-quinoline ether linkage provides OX1R selective compounds. The combination with an azabenzimidazole or imidazopyridine amide substituent leads to analogs 47 and 51 with > 625-fold functional selectivity for OX1R over OX2R in rat. Compounds 47 and 51 possess clean off-target profiles and the required pharmacokinetic and physical properties to be useful as 1-SORA tool compounds. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5809 / 5814
页数:6
相关论文
共 23 条
[1]  
[Anonymous], 2014, Patent Application WO, Patent No. [2014/113303 A1, 2014113303]
[2]   Narcolepsy in orexin knockout mice:: Molecular genetics of sleep regulation [J].
Chemelli, RM ;
Willie, JT ;
Sinton, CM ;
Elmquist, JK ;
Scammell, T ;
Lee, C ;
Richardson, JA ;
Williams, SC ;
Xiong, YM ;
Kisanuki, Y ;
Fitch, TE ;
Nakazato, M ;
Hammer, RE ;
Saper, CB ;
Yanagisawa, M .
CELL, 1999, 98 (04) :437-451
[3]   Discovery of [(2R,5R)-5-{[(5-Fluoropyridin-2-yl)oxy]methyl}-2-methylpiperidin-1-yl][5-methyl-2-(pyrimidin-2-yl)phenyl]methanone (MK-6096): A Dual Orexin Receptor Antagonist with Potent Sleep-Promoting Properties [J].
Coleman, Paul J. ;
Schreier, John D. ;
Cox, Christopher D. ;
Breslin, Michael J. ;
Whitman, David B. ;
Bogusky, Michael J. ;
McGaughey, Georgia B. ;
Bednar, Rodney A. ;
Lemaire, Wei ;
Doran, Scott M. ;
Fox, Steven V. ;
Garson, Susan L. ;
Gotter, Anthony L. ;
Harrell, C. Meacham ;
Reiss, Duane R. ;
Cabalu, Tamara D. ;
Cui, Donghui ;
Prueksaritanont, Thomayant ;
Stevens, Joanne ;
Tannenbaum, Pamela L. ;
Ball, Richard G. ;
Stellabott, Joyce ;
Young, Steven D. ;
Hartman, George D. ;
Winrow, Christopher J. ;
Renger, John J. .
CHEMMEDCHEM, 2012, 7 (03) :415-424
[4]   Discovery of the Dual Orexin Receptor Antagonist [(7R)-4-(5-Chloro-1,3-benzoxazol-2-yl)-7-methyl-1,4-diazepan-1-yl][5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone (MK-4305) for the Treatment of Insomnia [J].
Cox, Christopher D. ;
Breslin, Michael J. ;
Whitman, David B. ;
Schreier, John D. ;
McGaughey, Georgia B. ;
Bogusky, Michael J. ;
Roecker, Anthony J. ;
Mercer, Swati P. ;
Bednar, Rodney A. ;
Lemaire, Wei ;
Bruno, Joseph G. ;
Reiss, Duane R. ;
Harrell, C. Meacham ;
Murphy, Kathy L. ;
Garson, Susan L. ;
Doran, Scott M. ;
Prueksaritanont, Thomayant ;
Anderson, Wayne B. ;
Tang, Cuyue ;
Roller, Shane ;
Cabalu, Tamara D. ;
Cui, Donahui ;
Hartman, George D. ;
Young, Steven D. ;
Koblan, Ken S. ;
Winrow, Christopher J. ;
Renger, John J. ;
Coleman, Paul J. .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (14) :5320-5332
[5]   The hypocretins: Hypothalamus-specific peptides with neuroexcitatory activity [J].
De Lecea, L ;
Kilduff, TS ;
Peyron, C ;
Gao, XB ;
Foye, PE ;
Danielson, PE ;
Fukuhara, C ;
Battenberg, ELF ;
Gautvik, VT ;
Bartlett, FS ;
Frankel, WN ;
van den Pol, AN ;
Bloom, FE ;
Gautvik, KM ;
Sutcliffe, JG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :322-327
[6]   The duration of sleep promoting efficacy by dual orexin receptor antagonists is dependent upon receptor occupancy threshold [J].
Gotter, Anthony L. ;
Winrow, Christopher J. ;
Brunner, Joseph ;
Garson, Susan L. ;
Fox, Steven V. ;
Binns, Jacquelyn ;
Harrell, Charles M. ;
Cui, Donghui ;
Yee, Ka Lai ;
Stiteler, Mark ;
Stevens, Joanne ;
Savitz, Alan ;
Tannenbaum, Pamela L. ;
Tye, Spencer J. ;
McDonald, Terrence ;
Yao, Leon ;
Kuduk, Scott D. ;
Uslaner, Jason ;
Coleman, Paul J. ;
Renger, John J. .
BMC NEUROSCIENCE, 2013, 14
[7]   International Union of Basic and Clinical Pharmacology. LXXXVI. Orexin Receptor Function, Nomenclature and Pharmacology [J].
Gotter, Anthony L. ;
Webber, Andrea L. ;
Coleman, Paul J. ;
Renger, John J. ;
Winrow, Christopher J. .
PHARMACOLOGICAL REVIEWS, 2012, 64 (03) :389-420
[8]   Novel Octahydropyrrolo[3,4-c]pyrroles Are Selective Orexin-2 Antagonists: SAR Leading to a Clinical Candidate [J].
Letavic, Michael A. ;
Bonaventure, Pascal ;
Carruthers, Nicholas I. ;
Dugovic, Christine ;
Koudriakova, Tatiana ;
Lord, Brian ;
Lovenberg, Timothy W. ;
Ly, Kiev S. ;
Mani, Neelakandha S. ;
Nepomuceno, Diane ;
Pippel, Daniel J. ;
Rizzolio, Michele ;
Shelton, Jonathan E. ;
Shah, Chandra R. ;
Shireman, Brock T. ;
Young, Lana K. ;
Yun, Sujin .
JOURNAL OF MEDICINAL CHEMISTRY, 2015, 58 (14) :5620-5636
[9]   The sleep disorder canine narcolepsy is caused by a mutation in the hypocretin (orexin) receptor 2 gene [J].
Lin, L ;
Faraco, J ;
Li, R ;
Kadotani, H ;
Rogers, W ;
Lin, XY ;
Qiu, XH ;
de Jong, PJ ;
Nishino, S ;
Mignot, E .
CELL, 1999, 98 (03) :365-376
[10]   The Dual Orexin Receptor Antagonist Almorexant Induces Sleep and Decreases Orexin-Induced Locomotion by Blocking Orexin 2 Receptors [J].
Mang, Geraldine M. ;
Duerst, Thomas ;
Buerki, Hugo ;
Imobersteg, Stefan ;
Abramowski, Dorothee ;
Schuepbach, Edi ;
Hoyer, Daniel ;
Fendt, Markus ;
Gee, Christine E. .
SLEEP, 2012, 35 (12) :1625-1635