Recent developments in cannabinoid ligands

被引:42
作者
Padgett, LW [1 ]
机构
[1] Clemson Univ, Howard L Hunter Chem Lab, Clemson, SC 29634 USA
关键词
cannabinoid; structure-activity relationship; pyrazole; aminoalkylindole;
D O I
10.1016/j.lfs.2005.05.020
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Over the past 40 years, much research has been carried out directed toward the characterization of the cannabinergic system. With the identification of two G-protein coupled receptors and the endogenous ligand, anandamide, pharmacological targets have expanded to encompass hydrolase and transport proteins as well as novel classes of cannabinoid ligands. Those ligands that demonstrate high affinity for the receptors and good biological efficacy are tied together through lipophilic regions repeatedly demonstrated necessary for activity. This review presents recent developments in the structure-activity relationships of several classes of cannabinoid ligands. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1767 / 1798
页数:32
相关论文
共 78 条
  • [11] ISOLATION AND STRUCTURE OF A BRAIN CONSTITUENT THAT BINDS TO THE CANNABINOID RECEPTOR
    DEVANE, WA
    HANUS, L
    BREUER, A
    PERTWEE, RG
    STEVENSON, LA
    GRIFFIN, G
    GIBSON, D
    MANDELBAUM, A
    ETINGER, A
    MECHOULAM, R
    [J]. SCIENCE, 1992, 258 (5090) : 1946 - 1949
  • [12] Potent imidazole and triazole CB1 receptor antagonists related to SR141716
    Dyck, B
    Goodfellow, VS
    Phillips, T
    Grey, J
    Haddach, M
    Rowbottom, M
    Naeve, GS
    Brown, B
    Saunders, J
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (05) : 1151 - 1154
  • [13] EDERY J, 1972, ARZNEIMITTEL-FORSCH, V22, P1995
  • [14] Synthesis and biological evaluation of 1,8-naphthyridin-4(1H)-on-3-carboxamide derivatives as new ligands of cannabinoid receptors
    Ferrarini, PL
    Calderone, V
    Cavallini, T
    Manera, C
    Saccomanni, G
    Pani, L
    Ruiu, S
    Gessa, GL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2004, 12 (08) : 1921 - 1933
  • [15] Synthesis and structure-activity relationships of amide and hydrazide analogues of the cannabinoid CB1 receptor antagonist N-(piperidinyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide (SR141716)
    Francisco, MEY
    Seltzman, HH
    Gilliam, AF
    Mitchell, RA
    Rider, SL
    Pertwee, RG
    Stevenson, LA
    Thomas, BF
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2002, 45 (13) : 2708 - 2719
  • [16] ISOLATION, STRUCTURE, AND PARTIAL SYNTHESIS OF AN ACTIVE CONSTITUENT OF HASHISH
    GAONI, Y
    MECHOULAM, R
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (08) : 1646 - +
  • [17] 4-aryl/cycloalkyl-5-phenyloxazole derivatives as selective COX-2 inhibitors
    Hashimoto, H
    Maeda, K
    Ozawa, K
    Haruta, J
    Wakitani, K
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (01) : 65 - 68
  • [18] The CB1 cannabinoid receptor in the brain
    Howlett, AC
    [J]. NEUROBIOLOGY OF DISEASE, 1998, 5 (06) : 405 - 416
  • [19] HOWLETT AC, 1988, MOL PHARMACOL, V33, P297
  • [20] International Union of Pharmacology. XXVII. Classification of cannabinoid receptors
    Howlett, AC
    Barth, F
    Bonner, TI
    Cabral, G
    Casellas, P
    Devane, WA
    Felder, CC
    Herkenham, M
    Mackie, K
    Martin, BR
    Mechoulam, R
    Pertwee, RG
    [J]. PHARMACOLOGICAL REVIEWS, 2002, 54 (02) : 161 - 202