1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea (AR9281) as a potent, selective, and orally available soluble epoxide hydrolase inhibitor with efficacy in rodent models of hypertension and dysglycemia

被引:67
|
作者
Anandan, Sampath-Kumar [1 ]
Webb, Heather Kay [1 ]
Chen, Dawn [1 ]
Wang, Yi-Xin [1 ]
Aavula, Basker R. [1 ]
Cases, Sylvaine [1 ]
Cheng, Ying [1 ]
Do, Zung N. [1 ]
Mehra, Upasana [1 ]
Vinh Tran [1 ]
Vincelette, Jon [1 ]
Waszczuk, Joanna [1 ]
White, Kathy [1 ]
Wong, Kenneth R. [1 ]
Zhang, Le-Ning [1 ]
Jones, Paul D. [2 ,3 ]
Hammock, Bruce D. [2 ,3 ]
Patel, Dinesh V. [1 ]
Whitcomb, Randall [1 ]
MacIntyre, D. Euan [1 ]
Sabry, James [1 ]
Gless, Richard [1 ]
机构
[1] Arete Therapeut Inc, San Francisco, CA 94080 USA
[2] Univ Calif Davis, Dept Entomol, Davis, CA 95616 USA
[3] Univ Calif Davis, UCD Canc Ctr, Davis, CA 95616 USA
关键词
sEH inhibitor; AR9281; Efficacy; DIO model; AngII hypertension model; Diabetes; EPOXYEICOSATRIENOIC ACIDS; INSULIN-RESISTANCE; 12-(3-ADAMANTAN-1-YL-UREIDO)DODECANOIC ACID; VASCULAR INFLAMMATION; BLOOD-PRESSURE; HIGHLY POTENT; PHARMACOKINETICS; METABOLISM; DISCOVERY; ATHEROSCLEROSIS;
D O I
10.1016/j.bmcl.2010.12.042
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
1-(1-Acetyl-piperidin-4-yl)-3-adamantan-1-yl-urea 14a (AR9281), a potent and selective soluble epoxide hydrolase inhibitor, was recently tested in a phase 2a clinical setting for its effectiveness in reducing blood pressure and improving insulin resistance in pre-diabetic patients. In a mouse model of diet induced obesity, AR9281 attenuated the enhanced glucose excursion following an intraperitoneal glucose tolerance test. AR9281 also attenuated the increase in blood pressure in angiotensin-II-induced hypertension in rats. These effects were dose-dependent and well correlated with inhibition of the sEH activity in whole blood, consistent with a role of sEH in the observed pharmacology in rodents. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:983 / 988
页数:6
相关论文
共 15 条
  • [11] (2S,4S)-1-[2-(1,1-Dimethyl-3-oxo-3-pyrrolidin-1-yl-propylamino)acetyl]-4-fluoro-pyrrolidine-2-carbonitrile: A potent, selective, and orally bioavailable dipeptide-derived inhibitor of dipeptidyl peptidase IV
    Yeh, Teng-Kuang
    Tsai, Ting-Yueh
    Hsu, Tsu
    Cheng, Jai-Hong
    Chen, Xin
    Song, Jen-Shin
    Shy, Horng-Shing
    Chiou, Mei-Chun
    Chien, Chia-Hui
    Tseng, Ya-Ju
    Huang, Chung-Yu
    Yeh, Kai-Chia
    Huang, Yu-Lin
    Huang, Chih-Hsiang
    Huang, Yu-Wen
    Wang, Min-Hsien
    Tang, Hung-Kuan
    Chao, Yu-Sheng
    Chen, Chiung-Tong
    Jiaang, Weir-Torn
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (12) : 3596 - 3600
  • [12] Pharmacological characterization of a novel, potent, selective, and orally active fatty acid amide hydrolase inhibitor, PKM-833 [(R)-N-(pyridazin-3-yl)-4-(7-(trifluoromethyl)chroman-4-yl)piperazine-1-carboxamide] in rats: Potential for the treatment of inflammatory pain
    Endo, Toshiya
    Takeuchi, Takashi
    Maehara, Shunsuke
    PHARMACOLOGY RESEARCH & PERSPECTIVES, 2020, 8 (02):
  • [13] Identification of 1-(3-(6,7-Dimethoxyquinazolin-4-yloxy)phenyl)-3-(5-(1,1,1-trifluoro-2-methylpropan-2-yl)isoxazol-3-yl)urea Hydrochloride (CEP-32496), a Highly Potent and Orally Efficacious Inhibitor of V-RAF Murine Sarcoma Viral Oncogene Homologue B1 (BRAF) V600E
    Rowbottom, Martin W.
    Faraoni, Raffaella
    Chao, Qi
    Campbell, Brian T.
    Lai, Andiliy G.
    Setti, Eduardo
    Ezawa, Maiko
    Sprankle, Kelly G.
    Abraham, Sunny
    Lan Tran
    Struss, Brian
    Gibney, Michael
    Armstrong, Robert C.
    Gunawardane, Ruwanthi N.
    Nepomuceno, Ronald R.
    Valenta, Ianina
    Hua, Helen
    Gardner, Michael F.
    Cramer, Merry D.
    Gitnick, Dana
    Insko, Darren E.
    Apuy, Julius L.
    Jones-Bolin, Susan
    Ghose, Arup K.
    Herbertz, Torsten
    Ator, Mark A.
    Dorsey, Bruce D.
    Ruggeri, Bruce
    Williams, Michael
    Bhagwat, Shripad
    James, Joyce
    Holladay, Mark W.
    JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (03) : 1082 - 1105
  • [14] Identification of (R)-N-((4-Methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide (CPI-1205), a Potent and Selective Inhibitor of Histone Methyltransferase EZH2, Suitable for Phase I Clinical Trials for B-Cell Lymphomas
    Vaswani, Rishi G.
    Gehling, Victor S.
    Dakin, Les A.
    Cook, Andrew S.
    Nasveschuk, Christopher G.
    Duplessis, Martin
    Iyer, Priyadarshini
    Balasubramanian, Srividya
    Zhao, Feng
    Good, Andrew C.
    Campbell, Robert
    Lee, Christina
    Cantone, Nico
    Cummings, Richard T.
    Normant, Emmanuel
    Bellon, Steven F.
    Albrecht, Brian K.
    Harmange, Jean-Christophe
    Trojer, Patrick
    Audia, James E.
    Zhang, Ying
    Justin, Neil
    Chen, Shuyang
    Wilson, Jon R.
    Gamblin, Steven J.
    JOURNAL OF MEDICINAL CHEMISTRY, 2016, 59 (21) : 9928 - 9941
  • [15] 1-[3-aminobenzisoxazol-5′-yl]-3-trifluoromethyl-6-12′-(3-(R)-hydroxy-N-pyrrolidinyl)methyl-[1,1′]-biphen-4-yl]-1,4,5,6-tetrahydropyrazolo-13,4-c]-pyridin-7-one (BMS-740808) a highly potent, selective, efficacious, and orally bioavailable inhibitor of blood coagulation factor Xa 10.1016/j.bmel.2006.02.069
    Pinto, Donald J. P.
    Orwat, Michael J.
    Quan, Mimi L.
    Han, Qi
    Galemmo, Robert A., Jr.
    Amparo, Eugene
    Wells, Brian
    Ellis, Christopher
    He, Ming Y.
    Alexander, Richard S.
    Rossi, Karen A.
    Smallwood, Angela
    Wong, Pancras C.
    Luettgen, Joseph M.
    Rendina, Alan R.
    Knabb, Robert M.
    Mersinger, Lawrence
    Kettner, Charles
    Bal, Steven
    He, Kan
    Wexler, Ruth R.
    Lam, Patrick Y. S.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2006, 16 (15) : 4141 - 4147