Anti-HIV-1 activity of phloroglucinol derivative, 6,6′-bieckol, from Ecklonia cava

被引:155
作者
Artan, Murat [1 ]
Li, Yong [2 ,3 ]
Karadeniz, Fatih [1 ]
Lee, Sang-Hoon [1 ]
Kim, Moon-Moo [4 ]
Kim, Se-Kwon [1 ,2 ]
机构
[1] Pukyong Natl Univ, Dept Chem, Pusan 608737, South Korea
[2] Pukyong Natl Univ, Marine Bioproc Res Ctr, Pusan 608737, South Korea
[3] Acad Sci Tradit Chinese Med Jilin Province, Resource Inst, Changchun 0431, Peoples R China
[4] Dong Eui Univ, Dept Chem, Pusan 614714, South Korea
关键词
anti-HIV-1; 6,6 '-bieckol; phlorotannin; reverse transcriptase;
D O I
10.1016/j.bmc.2008.07.078
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ecklonia cava (EC), which is an edible marine brown alga with a broad range of bioactivities, belongs to the family of Laminariaceae. The bioactive 6,6'-bieckol, one of the main phloroglucinol derivatives naturally occurred from this genus, was isolated and characterized by NMR techniques. For the first time, human immunodeficiency virus type-1 (HIV-1) inhibitory activity of 6,6'-bieckol showed wild inhibition against HIV-1 induced syncytia formation (EC(50) 1.72 mu M), lytic effects (EC(50) 1.23 mu M), and viral p24 antigen production (EC(50) 1.26 mu M), respectively. This result was strongly and clearly supported by the further investigation also, which 6,6'-bieckol selectively inhibited the activity of HIV-1 reverse transcriptase (RT) enzyme with EC(50) of 1.07 mu M, as well as HIV-1 entry. Moreover, unlike most of other tannins, 6,6'-bieckol exhibited no cytotoxicity at concentrations which inhibited HIV-1 replication almost completely. Thus, it can be suggested that the potentially effective 6,6'-bieckol might be employed as a drug candidate for development of new generation therapeutic agents against HIV. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7921 / 7926
页数:6
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