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来自褐藻的间苯三酚衍生物6,6'-二 Eckol对HIV-1的抑制活性。

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

作者信息

Artan Murat, Li Yong, Karadeniz Fatih, Lee Sang-Hoon, Kim Moon-Moo, Kim Se-Kwon

机构信息

Department of Chemistry, Pukyong National University, Busan 608-737, Republic of Korea.

出版信息

Bioorg Med Chem. 2008 Sep 1;16(17):7921-6. doi: 10.1016/j.bmc.2008.07.078. Epub 2008 Jul 29.

Abstract

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 microM), lytic effects (EC(50) 1.23 microM), and viral p24 antigen production (EC(50) 1.26 microM), 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 microM, 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.

摘要

海蕴是一种可食用的褐藻,具有广泛的生物活性,属于海带科。具有生物活性的6,6'-联二没食子酰基间苯三酚是该属天然存在的主要间苯三酚衍生物之一,通过核磁共振技术进行了分离和表征。6,6'-联二没食子酰基间苯三酚首次表现出对1型人类免疫缺陷病毒(HIV-1)的抑制活性,分别对HIV-1诱导的合胞体形成(半数有效浓度[EC50]为1.72微摩尔)、裂解作用(EC50为1.23微摩尔)和病毒p24抗原产生(EC50为1.26微摩尔)具有显著抑制作用。进一步的研究也有力且明确地支持了这一结果,即6,6'-联二没食子酰基间苯三酚以1.07微摩尔的EC50选择性抑制HIV-1逆转录酶(RT)的活性,以及HIV-1的进入。此外,与大多数其他单宁不同,6,6'-联二没食子酰基间苯三酚在几乎完全抑制HIV-1复制的浓度下没有细胞毒性。因此,可以认为具有潜在效力的6,6'-联二没食子酰基间苯三酚可能被用作开发新一代抗HIV治疗药物的候选药物。

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