5-lipoxygenase inhibitors with histamine H1 receptor antagonist activity

被引:33
作者
Lewis, TA [1 ]
Bayless, L [1 ]
Eckman, JB [1 ]
Ellis, JL [1 ]
Grewal, G [1 ]
Libertine, L [1 ]
Nicolas, JM [1 ]
Scannell, RT [1 ]
Wels, BF [1 ]
Wenberg, K [1 ]
Wypij, DM [1 ]
机构
[1] UCB Res, Cambridge, MA 02139 USA
关键词
D O I
10.1016/j.bmcl.2004.02.005
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel compounds with both 5-lipoxygenase (5-LO) inhibitory and histamine H-1 receptor antagonist activity were designed for the treatment of asthma. These dual-function compounds were made by connecting 5-LO and H-1 pharmacophores, N-hydroxyureas and benzhydryl piperazines, respectively. A range of in vitro activities was observed, with the furan analog 10 demonstrating both activities in an animal model. The activities observed were compared to single-function drugs. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2265 / 2268
页数:4
相关论文
共 21 条
[1]  
Barnes PJ, 1998, PHARMACOL REV, V50, P515
[2]  
BERNSTEIN PR, 1997, BURGERS MED CHEM DRU, V5, P405
[3]   Dual acting anti-inflammatory drugs: A reappraisal [J].
Bertolini, A ;
Ottani, A ;
Sandrini, M .
PHARMACOLOGICAL RESEARCH, 2001, 44 (06) :437-450
[4]   (R)-(+)-N-[3-[5-[(4-FLUOROPHENYL)METHYL]-2-THIENYL]-1-METHYL-2-PROPYNYL]-N-HYDROXYUREA (ABT-761), A 2ND-GENERATION 5-LIPOXYGENASE INHIBITOR [J].
BROOKS, CDW ;
STEWART, AO ;
BASHA, A ;
BHATIA, P ;
RATAJCZYK, JD ;
MARTIN, JG ;
CRAIG, RA ;
KOLASA, T ;
BOUSKA, JB ;
LANNI, C ;
HARRIS, RR ;
MALO, PE ;
CARTER, GW ;
BELL, RL .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (24) :4768-4775
[5]   SUBSTITUTION-REACTIONS OF 2-BENZENESULFONYL CYCLIC ETHERS WITH CARBON NUCLEOPHILES [J].
BROWN, DS ;
BRUNO, M ;
DAVENPORT, RJ ;
LEY, SV .
TETRAHEDRON, 1989, 45 (13) :4293-4308
[6]  
CARTER GW, 1991, J PHARMACOL EXP THER, V256, P929
[7]   Binding characteristics of cetirizine and levocetirizine to human H1 histamine receptors:: Contribution of Lys191 and Thr194 [J].
Gillard, M ;
Van Der Perren, C ;
Moguilevsky, N ;
Massingham, R ;
Chatelain, P .
MOLECULAR PHARMACOLOGY, 2002, 61 (02) :391-399
[8]   A novel and simple asymmetric synthesis of CMI-977 (LDP-977): a potent anti-asthmatic drug lead [J].
Gurjar, MK ;
Murugaiah, AMS ;
Radhakrishna, P ;
Ramana, CV ;
Chorghade, MS .
TETRAHEDRON-ASYMMETRY, 2003, 14 (10) :1363-1370
[9]   A study of novel antiallergic agents with eosinophilic infiltration inhibiting action [J].
Kawasaki, N ;
Miyataka, H ;
Matsumoto, H ;
Yamashita, N ;
Sakane, T ;
Mizushima, Y ;
Satoh, T .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1999, 9 (01) :19-24
[10]  
KONSETT H, 1940, ARCH EXP PATHOL PH, V195, P71