The Discovery and Development of the N-Substituted trans-3,4-Dimethyl-4-(3′-hydroxyphenyl)piperidine Class of Pure Opioid Receptor Antagonists

被引:17
|
作者
Carroll, F. Ivy [1 ]
Dolle, Roland E. [2 ]
机构
[1] Res Triangle Inst, Ctr Organ & Med Chem, Res Triangle Pk, NC 27709 USA
[2] Cubist Pharmaceut, Lexington, MA 02421 USA
关键词
alvimopan; drug design; JDTic; medicinal chemistry; opioid antagonists; CARBOXAMIDO-BIARYL ETHERS; SELECTIVE ANTAGONISTS; INVERSE AGONISTS; COCAINE ABUSERS; KAPPA; RATS; POTENT; IDENTIFICATION; SEEKING; CONFORMATION;
D O I
10.1002/cmdc.201402142
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
N-Substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidines are a class of pure opioid receptor antagonists with a novel pharmacophore. This opioid receptor antagonist pharmacophore was used as a lead structure to design and develop several interesting and useful opioid receptor antagonists. In this review we describe: 1) early SAR studies that led to the discovery of LY255582 and analogues that are nonselective opioid receptor antagonists developed for the treatment of obesity; 2) the discovery and commercialization of LY246736 (alvimopan; ENTEREG (R)), a peripherally selective opioid receptor antagonist that accelerates the time to upper and lower GI recovery following surgeries that include partial bowel resection with primary anastomosis; and 3) the discovery and development of the potent and selective kappa opioid receptor antagonist JDTic and analogues as potential pharmacotherapies for treating depression, anxiety, and substance abuse (nicotine, alcohol, and cocaine). In addition, the use of JDTic for obtaining the X-ray structure of the human kappa opioid receptor is discussed.
引用
收藏
页码:1638 / 1654
页数:17
相关论文
共 50 条
  • [1] Elucidation of the bioactive conformation of the N-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine class of μ-opioid receptor antagonists
    Le Bourdonnec, Bertrand
    Goodman, Allan J.
    Michaut, Mathieu
    Ye, Hai-Fen
    Graczyk, Thomas M.
    Belanger, Serge
    Herbertz, Torsten
    Yap, Glenn P. A.
    DeHaven, Robert N.
    Dolle, Roland E.
    JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (25) : 7278 - 7289
  • [2] Novel trans-3,4-dimethyl-4-(3-hydroxyphenyl) piperidines as μ opioid receptor antagonists with improved opioid receptor selectivity profiles
    Le Bourdonnec, Bertrand
    Barker, William M.
    Belanger, Serge
    Wiant, Daniel D.
    Conway-James, Nathalie C.
    Cassel, Joel A.
    O'Neill, Timothy J.
    Little, Patrick J.
    DeHaven, Robert N.
    DeHaven-Hudkins, Diane L.
    Dolle, Roland E.
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (06) : 2006 - 2012
  • [3] Stereocontrolled synthesis of the trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonist alvimopan.
    Le Bourdonnec, B
    Dolle, RE
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2002, 224 : U195 - U195
  • [4] Stereocontrolled synthesis of the trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonist alvimopan.
    Le Bourdonnec, B
    Dolle, RE
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 228 : U33 - U33
  • [5] Synthesis and structure activity relationship of a series of 2-and 6-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonists
    Goodman, AJ
    Michaut, M
    Ye, HF
    Graczyk, TM
    Belanger, S
    DeHaven, RN
    Dolle, RE
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U2569 - U2570
  • [6] trans-3,4-Dimethyl-4-(3-carboxamidophenyl)piperidines:: A novel class of μ-selective opioid antagonists
    Le Bourdonnec, B
    Belanger, S
    Cassel, JA
    Stabley, GJ
    DeHaven, RN
    Dolle, RE
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2003, 13 (24) : 4459 - 4462
  • [7] Synthesis and structure activity relationship of a series of 2-and 6-substituted trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonists.
    Goodman, AJ
    Le Bourdonnec, B
    Michaut, M
    Ye, HF
    Belanger, S
    Cassel, JA
    DeHaven, RN
    Dolle, RE
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 229 : U118 - U118
  • [8] DISCOVERY OF A POTENT, PERIPHERALLY SELECTIVE TRANS-3,4-DIMETHYL-4-(3-HYDROXYPHENYL)PIPERIDINE OPIOID ANTAGONIST FOR THE TREATMENT OF GASTROINTESTINAL MOTILITY DISORDERS
    ZIMMERMAN, DM
    GIDDA, JS
    CANTRELL, BE
    SCHOEPP, DD
    JOHNSON, BG
    LEANDER, JD
    JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (15) : 2262 - 2265
  • [9] STRUCTURE-ACTIVITY-RELATIONSHIPS OF TRANS-3,4-DIMETHYL-4-(3-HYDROXYPHENYL)PIPERIDINE ANTAGONISTS FOR MU-OPIOID AND KAPPA-OPIOID RECEPTORS
    ZIMMERMAN, DM
    LEANDER, JD
    CANTRELL, BE
    REEL, JK
    SNODDY, J
    MENDELSOHN, LG
    JOHNSON, BG
    MITCH, CH
    JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (20) : 2833 - 2841
  • [10] Synthesis of trans-3,4-dimethyl-4-(3-hydroxyphenyl)piperidine opioid antagonists: Application of the cis-thermal elimination of carbonates to alkaloid synthesis
    Werner, JA
    Cerbone, LR
    Frank, SA
    Ward, JA
    Labib, P
    TharpTaylor, RW
    Ryan, CW
    JOURNAL OF ORGANIC CHEMISTRY, 1996, 61 (02): : 587 - 597