Substituted 2-pyrrolinone inhibitors of HIV-1 integrase

被引:27
作者
Dayam, Raveendra [1 ]
Al-Mawsawi, Laith Q. [1 ]
Neamati, Nouri [1 ]
机构
[1] Univ So Calif, Sch Pharm, Dept Pharmaceut Sci & Pharmacol, Los Angeles, CA 90089 USA
关键词
HIV-1; integrase; beta-diketoacids; pharmacophore; substituted pyrrolin-2-ones; substructure; structure-activity relationship analysis;
D O I
10.1016/j.bmcl.2007.09.061
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The beta-diketoacid class of HIV-1 integrase (IN) inhibitors represent the first potent class of compounds specific for the strand transfer catalytic activity of the viral enzyme. Previously, utilizing a beta-diketoacid pharmacophore as a search query, we identified a substituted 2-pyrrolinone with modest IN inhibitory activity from a database of small-molecules [Dayam, R.; Sanchez, T.; Neamati, N. J. Med. Chem. 2005, 48, 8009]. In efforts to optimize this class of IN inhibitors, we carried out a structure-activity relationship analysis around the 2-pyrrolinone core. Here, we present a new class of 2-pyrrolinone IN inhibitors. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6155 / 6159
页数:5
相关论文
共 50 条
  • [21] Progress in HIV-1 Integrase Inhibitors: A Review of their Chemical Structure Diversity
    Hajimahdi, Zahra
    Zarghi, Afshin
    IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2016, 15 (04): : 595 - 628
  • [22] Structurally diverse HIV-1 integrase inhibitors: Past, present and perspective
    Jiang, XH
    Long, YQ
    CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2004, 24 (11) : 1380 - 1388
  • [23] Oligonucleotide inhibitors of HIV-1 integrase efficiently inhibit HIV-1 reverse transcriptase
    S. P. Korolev
    T. S. Zatsepin
    M. B. Gottikh
    Russian Journal of Bioorganic Chemistry, 2017, 43 : 135 - 139
  • [24] Oligonucleotide Inhibitors of HIV-1 Integrase Efficiently Inhibit HIV-1 Reverse Transcriptase
    Korolev, S. P.
    Zatsepin, T. S.
    Gottikh, M. B.
    RUSSIAN JOURNAL OF BIOORGANIC CHEMISTRY, 2017, 43 (02) : 135 - 139
  • [25] Dipyrimidine-based inhibitors of HIV-1 integrase
    Neamati, N
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2003, 12 (02) : 289 - 292
  • [26] Design and synthesis of novel β-diketo derivatives as HIV-1 integrase inhibitors
    Hu, Liming
    Zhang, Sulei
    He, Xianzhuo
    Luo, Zaigang
    Wang, Xiaoli
    Liu, Wei
    Qin, Xuemei
    BIOORGANIC & MEDICINAL CHEMISTRY, 2012, 20 (01) : 177 - 182
  • [27] Subtype Diversity Associated with the Development of HIV-1 Resistance to Integrase Inhibitors
    Brenner, Bluma G.
    Lowe, Matthew
    Moisi, Daniela
    Hardy, Isabelle
    Gagnon, Simon
    Charest, Hugues
    Baril, Jean Guy
    Wainberg, Mark A.
    Roger, Michel
    JOURNAL OF MEDICAL VIROLOGY, 2011, 83 (05) : 751 - 759
  • [28] QSAR study of substituted 1,3,4-oxadiazole naphthyridines as HIV-1 integrase inhibitors
    Ravichandran, Veerasamy
    Shalini, Sivadasan
    Sundram, Karupiah
    Sokkalingam, Arumugam Dhanaraj
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (07) : 2791 - 2797
  • [29] HIV-1 Integrase Strand Transfer Inhibitors and Neurodevelopment
    Foster, Emma G.
    Gendelman, Howard E.
    Bade, Aditya N.
    PHARMACEUTICALS, 2022, 15 (12)
  • [30] Modeling the HIV-1 Intasome: A Prototype View of the Target of Integrase Inhibitors
    Yin, Zhiqi
    Craigie, Robert
    VIRUSES-BASEL, 2010, 2 (12): : 2777 - 2781