Identification, synthesis, and biological evaluation of novel pyrazoles as low molecular weight luteinizing hormone receptor agonists

被引:31
|
作者
Jorand-Lebrun, Catherine
Brondyk, Bill
Lin, Jing
Magar, Sharad
Murray, Robert
Reddy, Adulla
Shroff, Hitesh
Wands, Greg
Weiser, Weishui
Xu, Qihong
McKenna, Sean
Brugger, Nadia
机构
[1] Merck Serono Geneva Res Ctr, CH-1211 Geneva, Switzerland
[2] EMD Serono Res Inst, Rockland, MA 02370 USA
关键词
gonadotropins; luteinizing hormone receptor agonist; regioselective; pyrazole synthesis;
D O I
10.1016/j.bmcl.2006.12.062
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the course of a high throughput screening, a series of pyrazole compounds were identified with luteinizing hormone receptor (LH-R) agonist activity. A focused pyrazole library was produced by solid-phase synthesis and key pyrazole regioisomers were obtained selectively in solution. Evaluation of those compounds in a cAMP assay in CHO cells transfected with h-LH receptor allowed us to propose a structure-activity relationship model for this series and led to the identification of the first low molecular weight molecule with in vitro activity in a Leydig cells assay (ED50 = 1.31 mu M) and in vivo in a model of testosterone induction in rats (significant effect at 32 mpk ip). (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2080 / 2085
页数:6
相关论文
共 50 条
  • [21] SYNTHESIS AND BIOLOGICAL EVALUATION OF SUPERACTIVE AGONISTS OF GROWTH HORMONE-RELEASING HORMONE
    IZDEBSKI, J
    PINSKI, J
    HORVATH, JE
    HALMOS, G
    GROOT, K
    SCHALLY, AV
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (11) : 4872 - 4876
  • [22] A signaling-selective, nanomolar potent allosteric low molecular weight agonist for the human luteinizing hormone receptor
    van Koppen, Chris J.
    Zaman, Guido J. R.
    Timmers, C. Marco
    Kelder, Jan
    Mosselman, Sietse
    van de Lagemaat, Ruud
    Smit, Martin J.
    Hanssen, Rob G. J. M.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2008, 378 (05) : 503 - 514
  • [23] Induction of ovulation by a potent, orally active, low molecular weight agonist (Org 43553) of the luteinizing hormone receptor
    van de Lagemaat, R.
    Timmers, C. M.
    Kelder, J.
    van Koppen, C.
    Mosselman, S.
    Hanssen, R. G. J. M.
    HUMAN REPRODUCTION, 2009, 24 (03) : 640 - 648
  • [24] A signaling-selective, nanomolar potent allosteric low molecular weight agonist for the human luteinizing hormone receptor
    Chris J. van Koppen
    Guido J. R. Zaman
    C. Marco Timmers
    Jan Kelder
    Sietse Mosselman
    Ruud van de Lagemaat
    Martin J. Smit
    Rob G. J. M. Hanssen
    Naunyn-Schmiedeberg's Archives of Pharmacology, 2008, 378 : 503 - 514
  • [25] Synthesis and biological evaluation of novel pyrazoles and indazoles as activators of the nitric oxide receptor, soluble guanylate cyclase
    Selwood, DL
    Brummell, DG
    Budworth, J
    Burtin, GE
    Campbell, RO
    Chana, SS
    Charles, IG
    Fernandez, PA
    Glen, RC
    Goggin, MC
    Hobbs, AJ
    Kling, MR
    Liu, Q
    Madge, DJ
    Meillerais, S
    Powell, KL
    Reynolds, K
    Spacey, GD
    Stables, JN
    Tatlock, MA
    Wheeler, KA
    Wishart, G
    Woo, CK
    JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (01) : 78 - 93
  • [26] Design, synthesis and biological evaluation of novel tetrahydroisoquinoline quaternary derivatives as peripheral κ-opioid receptor agonists
    Guo, Ting
    Gan, Zongjie
    Chen, Jie
    Wang, Dechuan
    He, Ling
    Song, Qiao
    Xu, Yungen
    BIOORGANIC & MEDICINAL CHEMISTRY, 2016, 24 (13) : 2964 - 2970
  • [27] Identification and synthesis of low-molecular weight cholecystokinin B receptor (CCKBR) agonists as mediators of long-term synaptic potentiation
    Zhang, Yanmei
    Wang, Yican
    Guo, Yiping
    Liao, Jinxi
    Tu, Zhengchao
    Lu, Yongzhi
    Ding, Ke
    Tortorella, Micky D.
    He, Jufang
    MEDICINAL CHEMISTRY RESEARCH, 2019, 28 (03) : 387 - 393
  • [28] Identification and synthesis of low-molecular weight cholecystokinin B receptor (CCKBR) agonists as mediators of long-term synaptic potentiation
    Yanmei Zhang
    Yican Wang
    Yiping Guo
    Jinxi Liao
    Zhengchao Tu
    Yongzhi Lu
    Ke Ding
    Micky D. Tortorella
    Jufang He
    Medicinal Chemistry Research, 2019, 28 : 387 - 393
  • [29] A low molecular weight agonist signals by binding to the transmembrane domain of thyroid-stimulating hormone receptor (TSHR) and luteinizing hormone/chorionic gonadotropin receptor (LHCGR)
    Jäschke, H
    Neumann, S
    Moore, S
    Thomas, CJ
    Colson, AO
    Costanzi, S
    Kleinau, G
    Jiang, JK
    Paschke, R
    Raaka, BM
    Krause, G
    Gershengorn, MC
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (15) : 9841 - 9844
  • [30] Synthesis and Biological Evaluation of a Series of Liver-Selective Phosphonic Acid Thyroid Hormone Receptor Agonists and Their Prodrugs
    Boyer, Serge H.
    Jiang, Hongjian
    Jacintho, Jason D.
    Reddy, Mali Venkat
    Li, Haiqing
    Li, Wenyu
    Godwin, Jennifer L.
    Schulz, William G.
    Cable, Edward E.
    Hou, Jinzhao
    Wu, Rongrong
    Fujitaki, James M.
    Hecker, Scott J.
    Erion, Mark D.
    JOURNAL OF MEDICINAL CHEMISTRY, 2008, 51 (22) : 7075 - 7093