Inhibitors from Natural Products to HIV-1 Reverse Transcriptase, Protease and Integrase

被引:16
作者
Jiang, Y. [1 ,3 ]
Ng, T. B. [2 ]
Wang, C. R. [1 ]
Zhang, D. [1 ]
Cheng, Z. H. [1 ]
Liu, Z. K. [1 ]
Qiao, W. T. [3 ]
Geng, Y. Q. [3 ]
Li, N. [1 ]
Liu, F. [1 ,3 ]
机构
[1] Nankai Univ, Dept Microbiol, Coll Life Sci, Tianjin 300071, Peoples R China
[2] Chinese Univ Hong Kong, Fac Med, Sch Biomed Sci, Hong Kong, Hong Kong, Peoples R China
[3] Nankai Univ, Ctr AIDS Res, Tianjin 300071, Peoples R China
关键词
HIV-1; RT; PR; IN; natural products; HUMAN-IMMUNODEFICIENCY-VIRUS; BIOLOGICAL-PROPERTIES; ANTIFUNGAL PROTEIN; FUNGAL METABOLITE; MEDICINAL-PLANTS; AGASTACHE-RUGOSA; BINDING LECTIN; MUSHROOM; ACID; TRITERPENOIDS;
D O I
10.2174/138955710793564133
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Acquired immunodeficiency syndrome (AIDS), caused by human immunodeficiency virus type 1 (HIV-1) infection, is still one of the most challenging diseases of the early 21st century. Reverse transcriptase (RT), protease (PR) and integrase (IN) are three key enzymes of HIV-1. Despite the shortcomings of chemical drugs such as toxicity, lack of curative and multiple effects, the search for more and better anti-HIV agents has been focused on natural products. Many natural products have been shown to possess promising activities that could assist in the prevention and amelioration of the disease. Most of these natural anti-HIV agents have other medicinal values as well, which afford them further prospective as novel lead compounds for the development of new drugs. These natural products can deal with both the virus and the various disorders that are caused by HIV. In this review, natural inhibitors of RT, PR and IN have been found to be classified and the relationship between structure and inhibitory activity is discussed.
引用
收藏
页码:1331 / 1344
页数:14
相关论文
共 85 条
  • [1] Inhibition of HIV-1 integrase by galloyl glucoses from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis
    Ahn, MJ
    Kim, CY
    Lee, JS
    Kim, TG
    Kim, SH
    Lee, CK
    Lee, BB
    Shin, CG
    Huh, H
    Kim, J
    [J]. PLANTA MEDICA, 2002, 68 (05) : 457 - 459
  • [2] Inhibitory effects of triterpenoids and sterols on human immunodeficiency virus-1 reverse transcriptase
    Akihisa, T
    Ogihara, J
    Kato, J
    Yasukawa, K
    Ukiya, M
    Yamanouchi, S
    Oishi, K
    [J]. LIPIDS, 2001, 36 (05) : 507 - 512
  • [3] Ali NAA, 1996, PHYTOCHEMISTRY, V41, P927, DOI 10.1016/0031-9422(95)00717-2
  • [4] Inhibitory activity on HIV-1 reverse transcriptase and integrase of a carmalol derivative from a brown alga, Ishige okamurae
    Aln, M. -J.
    Yoon, K. -D.
    Kim, C. Y.
    Kim, J. H.
    Shin, C. -G.
    Kim, J.
    [J]. PHYTOTHERAPY RESEARCH, 2006, 20 (08) : 711 - 713
  • [5] Anti-HIV-1 activity of phloroglucinol derivative, 6,6′-bieckol, from Ecklonia cava
    Artan, Murat
    Li, Yong
    Karadeniz, Fatih
    Lee, Sang-Hoon
    Kim, Moon-Moo
    Kim, Se-Kwon
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (17) : 7921 - 7926
  • [6] ARTS EJ, 1994, LEUKEMIA, V8, pS175
  • [7] Chemical modification of glycyrrhizic acid as a route to new bioactive compounds for medicine
    Baltina, LA
    [J]. CURRENT MEDICINAL CHEMISTRY, 2003, 10 (02) : 155 - 171
  • [8] Beatty G. L. J., 2005, 45 C ANT AG CHEM PAN
  • [9] Anti-HIV-1 protease activity of compounds from Boesenbergia pandurata
    Cheenpracha, S
    Karalai, C
    Ponglimanont, C
    Subhadhirasakul, S
    Tewtrakul, S
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (06) : 1710 - 1714
  • [10] Identification of sanguinarine as a novel HIV protease inhibitor from high-throughput screening of 2,000 drugs and natural products with a cell-based assay
    Cheng, TJ
    Goodsell, DS
    Kan, CC
    [J]. LETTERS IN DRUG DESIGN & DISCOVERY, 2005, 2 (05) : 364 - 371