1-Pentyl-3-phenylacetylindoles, a new class of cannabimimetic indoles

被引:98
作者
Huffman, JW [1 ]
Szklennik, PV
Almond, A
Bushell, K
Selley, DE
He, HJ
Cassidy, MP
Wiley, JL
Martin, BR
机构
[1] Clemson Univ, Howard L Hunter Lab, Clemson, SC 29634 USA
[2] Virginia Commonwealth Univ, Dept Pharmacol & Toxicol, Richmond, VA 23298 USA
关键词
cannabinoids; structure-activity relationships; cannabinoid receptors; aminoalkylindole;
D O I
10.1016/j.bmcl.2005.06.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A new class of cannabimimetic indoles, with 3-phenylacetyl or substituted 3-phenylacetyl substituents, has been prepared and their affinities for the cannabinoid CB1 and CB2 receptors have been determined. In general those compounds with a 2-substituted phenylacetyl group have good affinity for both receptors. The 4-substituted analogs have little affinity for either receptor, while the 3-substituted compounds are intermediate in their affinities. Two of these compounds, 1-pentyl-3-(2-methylphenylacetyl)indole (JWH-251) and 1-pentyl-3-(3-methoxyphenylacetyl)indole (JWH-302), have 5-fold selectivity for the CB1 receptor with modest affinity for the CB2 receptor. GTP gamma S determinations indicate that both compounds are highly efficacious agonists at the CB1 receptor and partial agonists at the CB2 receptor. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4110 / 4113
页数:4
相关论文
共 13 条
[1]   Influence of the N-1 alkyl chain length of cannabimimetic indoles upon CB1 and CB2 receptor binding [J].
Aung, MM ;
Griffin, G ;
Huffman, JW ;
Wu, MJ ;
Keel, C ;
Yang, B ;
Showalter, VM ;
Abood, ME ;
Martin, BR .
DRUG AND ALCOHOL DEPENDENCE, 2000, 60 (02) :133-140
[2]  
COMPTON DR, 1993, J PHARMACOL EXP THER, V265, P218
[3]   AMINOALKYLINDOLES - STRUCTURE-ACTIVITY-RELATIONSHIPS OF NOVEL CANNABINOID MIMETICS [J].
EISSENSTAT, MA ;
BELL, MR ;
DAMBRA, TE ;
ALEXANDER, EJ ;
DAUM, SJ ;
ACKERMAN, JH ;
GRUETT, MD ;
KUMAR, V ;
ESTEP, KG ;
OLEFIROWICZ, EM ;
WETZEL, JR ;
ALEXANDER, MD ;
WEAVER, JD ;
HAYCOCK, DA ;
LUTTINGER, DA ;
CASIANO, FM ;
CHIPPARI, SM ;
KUSTER, JE ;
STEVENSON, JI ;
WARD, SJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (16) :3094-3105
[4]  
Huffman JW, 1999, CURR MED CHEM, V6, P705
[5]   Structure-activity relationships for 1-alkyl-3-(l-naphthoyl)indoles at the cannabinoid CB1 and CB2 receptors:: steric and electronic effects of naphthoyl substituents.: New highly selective CB2 receptor agonists [J].
Huffman, JW ;
Zengin, G ;
Wu, MJ ;
Lu, JZ ;
Hynd, G ;
Bushell, K ;
Thompson, ALS ;
Bushell, S ;
Tartal, C ;
Hurst, DP ;
Reggio, PH ;
Selley, DE ;
Cassidy, MP ;
Wiley, JL ;
Martin, BR .
BIOORGANIC & MEDICINAL CHEMISTRY, 2005, 13 (01) :89-112
[6]   3-indolyl-1-naphthylmethanes:: New cannabimimetic Indoles provide evidence for aromatic stacking interactions with the CB1 cannabinoid receptor [J].
Huffman, JW ;
Mabon, R ;
Wu, MJ ;
Lu, JZ ;
Hart, R ;
Hurst, DP ;
Reggio, PH ;
Wiley, JL ;
Martin, BR .
BIOORGANIC & MEDICINAL CHEMISTRY, 2003, 11 (04) :539-549
[7]   DESIGN, SYNTHESIS AND PHARMACOLOGY OF CANNABIMIMETIC INDOLES [J].
HUFFMAN, JW ;
DAI, D ;
MARTIN, BR ;
COMPTON, DR .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (04) :563-566
[8]   The search for selective ligands for the CB2 receptor [J].
Huffman, JW .
CURRENT PHARMACEUTICAL DESIGN, 2000, 6 (13) :1323-1337
[9]   A general method for acylation of indoles at the 3-position with acyl chlorides in the presence of dialkylaluminum chloride [J].
Okauchi, T ;
Itonaga, M ;
Minami, T ;
Owa, T ;
Kitoh, K ;
Yoshino, H .
ORGANIC LETTERS, 2000, 2 (10) :1485-1487
[10]   The bioactive conformation of aminoalkylindoles at the cannabinoid CB1 and CB2 receptors: Insights gained from (E)- and (Z)-naphthylidene indenes [J].
Reggio, PH ;
Basu-Dutt, S ;
Barnett-Norris, J ;
Castro, MT ;
Hurst, DP ;
Seltzman, HH ;
Roche, MJ ;
Gilliam, AF ;
Thomas, BF ;
Stevenson, LA ;
Pertwee, RG ;
Abood, ME .
JOURNAL OF MEDICINAL CHEMISTRY, 1998, 41 (26) :5177-5187