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来自白杨树的具有HIV-1潜伏逆转活性的生物活性化合物。

Bioactive Compounds from Pax. with HIV-1 Latency Reversal Activity.

作者信息

Tsai Yu-Chi, Nell Racheal A, Buckendorf Jonathan E, Kúsz Norbert, Mwangi Peter Waweru, Berkecz Róbert, Rédei Dóra, Vasas Andrea, Spivak Adam M, Hohmann Judit

机构信息

Interdisciplinary Excellence Centre, Department of Pharmacognosy, University of Szeged, H-6720 Szeged, Hungary.

Department of Medicine, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.

出版信息

Pharmaceuticals (Basel). 2021 Jul 7;14(7):653. doi: 10.3390/ph14070653.

DOI:10.3390/ph14070653
PMID:34358079
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8308672/
Abstract

is a traditional medicine used for gynecologic, endocrine, and urogenital illnesses in East Africa; however, its constituents and bioactivities have not been investigated. A variety of compounds isolated from species have been shown to have activity against latent HIV-1, the major source of HIV-1 persistence despite antiretroviral therapy. We performed bioactivity-guided isolation to identify 15 new diterpenoids (-, -, , and ) along with 16 known compounds from with HIV-1 latency reversal activity. Euphordraculoate C () exhibits a rare 6/6/3-fused ring system with a 2-methyl-2-cyclopentenone moiety. Usambariphanes A () and B () display an unusual lactone ring constructed between C-17 and C-2 in the jatrophane structure. 4-Crotignoid K () revealed a 250-fold improvement in latency reversal activity compared to crotignoid K (), identifying that configuration at the C-4 of tigliane diterpenoids is critical to HIV-1 latency reversal activity. The primary mechanism of the active diterpenoids - and for the HIV-1 latency reversal activity was activation of PKC, while lignans and that did not increase CD69 expression, suggesting a non-PKC mechanism. Accordingly, natural constituents from have the potential to contribute to the development of HIV-1 eradication strategies.

摘要

在东非,它是一种用于治疗妇科、内分泌和泌尿生殖系统疾病的传统药物;然而,其成分和生物活性尚未得到研究。从该物种中分离出的多种化合物已被证明对潜伏的HIV-1具有活性,尽管进行了抗逆转录病毒治疗,但HIV-1持续存在的主要来源仍是潜伏感染。我们进行了生物活性导向分离,从该物种中鉴定出15种新的二萜类化合物(-、-、-和-)以及16种具有HIV-1潜伏逆转活性的已知化合物。大戟德拉库酯C(-)具有罕见的6/6/3稠环系统和一个2-甲基-2-环戊烯酮部分。乌桑巴里烷A(-)和B(-)在麻风树烷结构的C-17和C-2之间显示出一个不寻常的内酯环。4-克罗替诺伊德K(-)与克罗替诺伊德K(-)相比,潜伏逆转活性提高了250倍,这表明铁海棠二萜类化合物C-4位的构型对HIV-1潜伏逆转活性至关重要。活性二萜类化合物-和-对HIV-1潜伏逆转活性的主要机制是激活蛋白激酶C(PKC),而木脂素-和-并未增加CD69表达,提示其作用机制与PKC无关。因此,该物种的天然成分有可能为HIV-1根除策略的开发做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/10edd6c20f9a/pharmaceuticals-14-00653-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/e06b9aaa8166/pharmaceuticals-14-00653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/154c553710a7/pharmaceuticals-14-00653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/4cd501c3a2bf/pharmaceuticals-14-00653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/1739b8aa6aa6/pharmaceuticals-14-00653-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/6cd1cd0dadb9/pharmaceuticals-14-00653-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/b734344b0b19/pharmaceuticals-14-00653-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/10edd6c20f9a/pharmaceuticals-14-00653-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/e06b9aaa8166/pharmaceuticals-14-00653-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/154c553710a7/pharmaceuticals-14-00653-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/4cd501c3a2bf/pharmaceuticals-14-00653-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/1739b8aa6aa6/pharmaceuticals-14-00653-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/6cd1cd0dadb9/pharmaceuticals-14-00653-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/b734344b0b19/pharmaceuticals-14-00653-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a20/8308672/10edd6c20f9a/pharmaceuticals-14-00653-g007.jpg

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