• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

具有CD4阻断和抗1型人类免疫缺陷病毒活性的萘磺酸盐聚合物。

Naphthalene sulfonate polymers with CD4-blocking and anti-human immunodeficiency virus type 1 activities.

作者信息

Rusconi S, Moonis M, Merrill D P, Pallai P V, Neidhardt E A, Singh S K, Willis K J, Osburne M S, Profy A T, Jenson J C, Hirsch M S

机构信息

Infectious Disease Unit, Massachusetts General Hospital, Boston 02114, USA.

出版信息

Antimicrob Agents Chemother. 1996 Jan;40(1):234-6. doi: 10.1128/AAC.40.1.234.

DOI:10.1128/AAC.40.1.234
PMID:8787913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC163090/
Abstract

PIC 024-4 and PRO 2000 are naphthalene sulfonate polymers that bind to CD4 with nanomolar affinity and block binding of gp120. Both have activity against human immunodeficiency virus type 1 in H9 cells, peripheral blood mononuclear cells, and primary monocyte/macrophages, are synergistic with zidovudine, and do not inhibit tetanus toxoid-stimulated T-cell proliferation at anti-human immunodeficiency virus type 1 concentrations.

摘要

PIC 024 - 4和PRO 2000是萘磺酸盐聚合物,它们以纳摩尔亲和力与CD4结合并阻断gp120的结合。二者在H9细胞、外周血单核细胞和原代单核细胞/巨噬细胞中均具有抗1型人类免疫缺陷病毒的活性,与齐多夫定具有协同作用,并且在抗1型人类免疫缺陷病毒浓度下不抑制破伤风类毒素刺激的T细胞增殖。

相似文献

1
Naphthalene sulfonate polymers with CD4-blocking and anti-human immunodeficiency virus type 1 activities.具有CD4阻断和抗1型人类免疫缺陷病毒活性的萘磺酸盐聚合物。
Antimicrob Agents Chemother. 1996 Jan;40(1):234-6. doi: 10.1128/AAC.40.1.234.
2
Assays to detect and characterize human immunodeficiency virus type 1 (HIV-1) receptor antagonists, compounds that inhibit binding of the HIV-1 surface glycoprotein, gp120, to the CD4 receptor on human T lymphocytes.用于检测和鉴定人类免疫缺陷病毒1型(HIV-1)受体拮抗剂的分析方法,这些化合物可抑制HIV-1表面糖蛋白gp120与人T淋巴细胞上CD4受体的结合。
Antimicrob Agents Chemother. 1994 Sep;38(9):2008-13. doi: 10.1128/AAC.38.9.2008.
3
Benzopurpurin and related compounds inhibit the binding of gp120 to galactosyl ceramide/sulfatide and infection of human immunodeficiency virus.
DNA Cell Biol. 1994 Feb;13(2):211-6. doi: 10.1089/dna.1994.13.211.
4
Multiple antiviral activities of cyanovirin-N: blocking of human immunodeficiency virus type 1 gp120 interaction with CD4 and coreceptor and inhibition of diverse enveloped viruses.氰苷菌素-N的多种抗病毒活性:阻断人类免疫缺陷病毒1型gp120与CD4及共受体的相互作用并抑制多种包膜病毒
J Virol. 2000 May;74(10):4562-9. doi: 10.1128/jvi.74.10.4562-4569.2000.
5
Antiviral effects of milk proteins: acylation results in polyanionic compounds with potent activity against human immunodeficiency virus types 1 and 2 in vitro.乳蛋白的抗病毒作用:酰化作用产生在体外对1型和2型人类免疫缺陷病毒具有强效活性的聚阴离子化合物。
AIDS Res Hum Retroviruses. 1996 Jun 10;12(9):769-75. doi: 10.1089/aid.1996.12.769.
6
Multibranched peptide constructs derived from the V3 loop of envelope glycoprotein gp120 inhibit human immunodeficiency virus type 1 infection through interaction with CD4.源自包膜糖蛋白gp120的V3环的多分支肽构建体通过与CD4相互作用抑制1型人类免疫缺陷病毒感染。
Virology. 1995 Jan 10;206(1):457-64. doi: 10.1016/s0042-6822(95)80061-1.
7
Jacalin, a lectin with anti-HIV-1 properties, and HIV-1 gp120 envelope protein interact with distinct regions of the CD4 molecule.具有抗HIV-1特性的凝集素jacalin与HIV-1 gp120包膜蛋白与CD4分子的不同区域相互作用。
Mol Immunol. 1994 Jun;31(8):569-75. doi: 10.1016/0161-5890(94)90164-3.
8
The anti-HIV activity of ADS-J1 targets the HIV-1 gp120.ADS-J1的抗HIV活性作用于HIV-1 gp120。
Virology. 2005 Dec 5;343(1):141-9. doi: 10.1016/j.virol.2005.08.007. Epub 2005 Sep 15.
9
Investigations into the mechanism by which sulfated polysaccharides inhibit HIV infection in vitro.关于硫酸化多糖在体外抑制HIV感染机制的研究。
AIDS Res Hum Retroviruses. 1992 Jan;8(1):19-26. doi: 10.1089/aid.1992.8.19.
10
The differential binding and activity of PRO 2000 against diverse HIV-1 envelopes.PRO 2000对不同HIV-1包膜的差异结合与活性
J Acquir Immune Defic Syndr. 2009 Jun 1;51(2):125-9. doi: 10.1097/QAI.0b013e31819f9e31.

引用本文的文献

1
Developing peptide-based fusion inhibitors as an antiviral strategy utilizing coronin 1 as a template.以冠蛋白1为模板开发基于肽的融合抑制剂作为一种抗病毒策略。
RSC Med Chem. 2024 Oct 2;16(1):125-36. doi: 10.1039/d4md00523f.
2
Polymers Inspired by Heparin and Heparan Sulfate for Viral Targeting.受肝素和硫酸乙酰肝素启发用于病毒靶向的聚合物
Macromolecules. 2022 Sep 27;55(18):7957-7973. doi: 10.1021/acs.macromol.2c00675. Epub 2022 Sep 11.
3
Synthesis and Biological Evaluation of 5'--Fatty Acyl Ester Derivatives of 3'-Fluoro-2',3'-dideoxythymidine as Potential Anti-HIV Microbicides.3'-氟-2',3'-二脱氧胸苷 5'-脂肪酸酯衍生物的合成及抗 HIV 活性评价
Molecules. 2022 May 23;27(10):3352. doi: 10.3390/molecules27103352.
4
HIV-1 Entry and Prospects for Protecting against Infection.HIV-1病毒的进入机制及预防感染的前景
Microorganisms. 2021 Jan 22;9(2):228. doi: 10.3390/microorganisms9020228.
5
Polymers in the Medical Antiviral Front-Line.医学抗病毒一线中的聚合物
Polymers (Basel). 2020 Jul 31;12(8):1727. doi: 10.3390/polym12081727.
6
Virtual Screening, Biological Evaluation, and 3D-QSAR Studies of New HIV-1 Entry Inhibitors That Function via the CD4 Primary Receptor.新型 HIV-1 进入抑制剂的虚拟筛选、生物评价及 3D-QSAR 研究:通过 CD4 主要受体发挥作用。
Molecules. 2018 Nov 20;23(11):3036. doi: 10.3390/molecules23113036.
7
Efficacy of HIV antiviral polyanionic carbosilane dendrimer G2-S16 in the presence of semen.HIV抗病毒聚阴离子碳硅烷树枝状大分子G2-S16在精液存在下的疗效。
Int J Nanomedicine. 2016 May 30;11:2443-50. doi: 10.2147/IJN.S104292. eCollection 2016.
8
Design and synthesis of small molecule-sulfotyrosine mimetics that inhibit HIV-1 entry.抑制HIV-1进入的小分子磺基酪氨酸模拟物的设计与合成。
Bioorg Med Chem. 2016 Apr 15;24(8):1718-28. doi: 10.1016/j.bmc.2016.02.044. Epub 2016 Mar 3.
9
A 2,5-Dihydroxybenzoic Acid-Gelatin Conjugate: The Synthesis, Antiviral Activity and Mechanism of Antiviral Action Against Two Alphaherpesviruses.一种2,5-二羟基苯甲酸-明胶缀合物:其合成、抗病毒活性及对两种甲型疱疹病毒的抗病毒作用机制
Viruses. 2015 Oct 15;7(10):5343-60. doi: 10.3390/v7102878.
10
Polymeric drugs: Advances in the development of pharmacologically active polymers.聚合物药物:具有药理活性聚合物开发的进展
J Control Release. 2015 Dec 10;219:369-382. doi: 10.1016/j.jconrel.2015.09.043. Epub 2015 Sep 26.

本文引用的文献

1
Biological cloning of functionally diverse quasispecies of HIV-1.
AIDS Res Hum Retroviruses. 1993 Jun;9(6):541-6. doi: 10.1089/aid.1993.9.541.
2
Influence of host cell type and V3 loop of the surface glycoprotein on susceptibility of human immunodeficiency virus type 1 to polyanion compounds.宿主细胞类型及表面糖蛋白V3环对1型人类免疫缺陷病毒易感性的影响。
Antimicrob Agents Chemother. 1994 Dec;38(12):2910-6. doi: 10.1128/AAC.38.12.2910.
3
A soluble multimeric recombinant CD2 protein identifies CD48 as a low affinity ligand for human CD2: divergence of CD2 ligands during the evolution of humans and mice.一种可溶性多聚体重组CD2蛋白将CD48鉴定为人CD2的低亲和力配体:人类和小鼠进化过程中CD2配体的差异
J Exp Med. 1993 May 1;177(5):1439-50. doi: 10.1084/jem.177.5.1439.
4
Antiviral therapy for human immunodeficiency virus infections.人类免疫缺陷病毒感染的抗病毒治疗。
Clin Microbiol Rev. 1995 Apr;8(2):200-39. doi: 10.1128/CMR.8.2.200.
5
Quantitative analysis of dose-effect relationships: the combined effects of multiple drugs or enzyme inhibitors.剂量-效应关系的定量分析:多种药物或酶抑制剂的联合效应
Adv Enzyme Regul. 1984;22:27-55. doi: 10.1016/0065-2571(84)90007-4.
6
Detection, isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS.从艾滋病患者和艾滋病前期患者中检测、分离并持续生产细胞病变逆转录病毒(HTLV-III)。
Science. 1984 May 4;224(4648):497-500. doi: 10.1126/science.6200935.
7
The CD4 (T4) antigen is an essential component of the receptor for the AIDS retrovirus.CD4(T4)抗原是艾滋病逆转录病毒受体的重要组成部分。
Nature. 1984;312(5996):763-7. doi: 10.1038/312763a0.
8
T-lymphocyte T4 molecule behaves as the receptor for human retrovirus LAV.T淋巴细胞T4分子作为人类逆转录病毒LAV的受体。
Nature. 1984;312(5996):767-8. doi: 10.1038/312767a0.
9
Measurement of ligand binding to proteins by fluorescence spectroscopy.通过荧光光谱法测量配体与蛋白质的结合
Methods Enzymol. 1985;117:400-14. doi: 10.1016/s0076-6879(85)17024-2.
10
The role of mononuclear phagocytes in HTLV-III/LAV infection.单核吞噬细胞在人类嗜T淋巴细胞病毒III型/淋巴腺病相关病毒感染中的作用。
Science. 1986 Jul 11;233(4760):215-9. doi: 10.1126/science.3014648.