Four novel bis-(naphtho-γ-pyrones) isolated from Fusarium species as inhibitors of HIV-1 integrase

被引:44
作者
Singh, SB
Zink, DL
Bills, GF
Teran, A
Silverman, KC
Lingham, RB
Felock, P
Hazuda, DJ
机构
[1] Merck Res Labs, Rahway, NJ 07065 USA
[2] Merck Sharp & Dohme Espana SA, CIBE, Madrid 28027, Spain
[3] Merck Res Labs, West Point, PA 19486 USA
关键词
D O I
10.1016/S0960-894X(02)01057-0
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Integration of viral DNA into host cell DNA is an essential step in retroviral (HIV-1) replication and is catalyzed by HIV-1 integrase. HIV-1 integrase is a novel therapeutic target and is the focus of efforts to identify effective inhibitors that will prevent, or cure HIV infections, Four novel naphtho-gamma-pyrones belonging to the chaetochromin and ustilaginoidin family, were discovered as inhibitors of HIV-1 integrase from the screening Of fungal extracts using a recombinant in vitro assay. These compounds inhibit both the Coupled and strand transfer activity of HIV-1 integrase with IC50 values of 1-3 and 4-12 muM respectively. The discovery structure elucidation chemical modification and the structure-activity relationship of these compounds are described. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:713 / 717
页数:5
相关论文
共 19 条
[1]   HIV integrase, a brief overview from chemistry to therapeutics [J].
Craigie, R .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (26) :23213-23216
[2]   HIV integrase structure and function [J].
Esposito, D ;
Craigie, R .
ADVANCES IN VIRUS RESEARCH, VOL 52, 1999, 52 :319-333
[3]   Isolation and characterization of novel human immunodeficiency virus integrase inhibitors from fungal metabolites [J].
Hazuda, D ;
Blau, CU ;
Felock, P ;
Hastings, J ;
Pramanik, B ;
Wolfe, A ;
Bushman, F ;
Farnet, C ;
Goetz, M ;
Williams, M ;
Silverman, K ;
Lingham, R ;
Singh, S .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1999, 10 (02) :63-70
[4]   Inhibitors of strand transfer that prevent integration and inhibit HIV-1 replication in cells [J].
Hazuda, DJ ;
Felock, P ;
Witmer, M ;
Wolfe, A ;
Stillmock, K ;
Grobler, JA ;
Espeseth, A ;
Gabryelski, L ;
Schleif, W ;
Blau, C ;
Miller, MD .
SCIENCE, 2000, 287 (5453) :646-650
[5]  
HEDGE VR, 1993, J ANTIBIOT, V46, P207
[6]  
KOYAMA K, 1989, CHEM PHARM BULL, V37, P2022
[7]  
KOYAMA K, 1987, CHEM PHARM BULL, V35, P4049
[8]  
KOYAMA K, 1987, CHEM PHARM BULL, V35, P578
[9]  
KOYAMA K, 1988, CHEM PHARM BULL, V36, P146
[10]   CEPHALOCHROMIN, DIHYDROISO-USTILAGINOIDIN-A, AND ISO-USTILAGINOIDIN-A FROM VERTICILLIUM SP K-113 [J].
MATSUMOTO, M ;
MINATO, H ;
KONDO, E ;
MITSUGI, T ;
KATAGIRI, K .
JOURNAL OF ANTIBIOTICS, 1975, 28 (08) :602-604