Quinolines and isoquinolines as HIV-1 inhibitors: Chemical structures, action targets, and biological activities

S Hu, J Chen, JX Cao, SS Zhang, SX Gu, FE Chen - Bioorganic Chemistry, 2023 - Elsevier
Human immunodeficiency virus type 1 (HIV-1), a lentivirus that causes acquired
immunodeficiency syndrome (AIDS), poses a serious threat to global public health. Since …

[HTML][HTML] Progress in HIV-1 integrase inhibitors: A review of their chemical structure diversity

Z Hajimahdi, A Zarghi - Iranian journal of pharmaceutical research …, 2016 - ncbi.nlm.nih.gov
Abstract HIV-1 integrase (IN) enzyme, one of the three main enzymes of HIV-1, catalyzed the
insertion of the viral DNA into the genome of host cells. Because of the lack of its homologue …

[HTML][HTML] Synthesis, crystal structure analysis, spectral IR, UV–Vis, NMR assessments, electronic and nonlinear optical properties of potent quinoline based derivatives …

M Khalid, MA Ullah, M Adeel, MU Khan… - Journal of Saudi …, 2019 - Elsevier
Quinoline and its derivatives are widely studied by both synthetic and computational
chemists due to their exciting perspectives in biological and nonlinear optical (NLO) …

Design, synthesis and antiviral activity of novel quinazolinones

Z Wang, M Wang, X Yao, Y Li, J Tan, L Wang… - European journal of …, 2012 - Elsevier
HIV-1 integrase (IN) is a validated therapeutic target for antiviral drug design. However, the
emergence of viral strains resistant to clinically studied IN inhibitors demands the discovery …

Investigation of antifungal properties of synthetic dimethyl-4-bromo-1-(substituted benzoyl) pyrrolo [1, 2-a] quinoline-2, 3-dicarboxylates analogues: Molecular docking …

V Uppar, S Chandrashekharappa, C Shivamallu, SP… - Molecules, 2021 - mdpi.com
Candida albicans, an opportunistic fungal pathogen, frequently colonizes immune-
compromised patients and causes mild to severe systemic reactions. Only few antifungal …

Cytotoxicity and Antimycobacterial Properties of Pyrrolo[1,2-a]quinoline Derivatives: Molecular Target Identification and Molecular Docking Studies

KN Venugopala, V Uppar, S Chandrashekharappa… - Antibiotics, 2020 - mdpi.com
A series of ethyl 1-(substituted benzoyl)-5-methylpyrrolo [1, 2-a] quinoline-3-carboxylates 4a–
f and dimethyl 1-(substituted benzoyl)-5-methylpyrrolo [1, 2-a] quinoline-2, 3-dicarboxylates …

Design, synthesis and anti-HIV activity of novel quinoxaline derivatives

SB Patel, BD Patel, C Pannecouque… - European journal of …, 2016 - Elsevier
In order to design novel anti-HIV agents, pharmacophore modelling, virtual screening, 3D-
QSAR and molecular docking studies were performed. Pharmacophore model was …

Quinolones as prospective drugs: Their syntheses and biological applications

AA Aly, M Ramadan, GEDA Abuo-Rahma… - Advances in heterocyclic …, 2021 - Elsevier
Quinolones continue to receive significant attention owing to their diverse range of biological
activities. They provide an important scaffold in anticancer, antibacterial and antiviral drug …

Recent developed nitrogen/sulfur heterocyclic compounds with marked and selective antiviral activities (microreview)

F Mutalabisin, M Ghafarikhaligh… - Current Organic …, 2023 - benthamdirect.com
Millions of deaths have been reported due to viral infections in medical history, and various
viral infections are mentioned as the main cause of death. Although different types of …

Synthesis, biopharmaceutical characterization, antimicrobial and antioxidant activities of 1-(4′-O-β-d-glucopyranosyloxy-2′-hydroxyphenyl)-3-aryl-propane-1, 3 …

J Sheikh, A Parvez, H Juneja, V Ingle, Z Chohan… - European journal of …, 2011 - Elsevier
This research communication is toward the investigation of the antibacterial, antifungal and
antioxidant activities of the synthesized compounds 1-(4′-O-β-d-glucopyranosyloxy-2 …