Synthesis, Reactions, and Biological Activity of Benzo[h][1,6]naphthyridine Derivatives

被引:0
作者
Mostafa, M. A. [1 ]
Bahig, E. E. [1 ]
Hassanin, H. M. [1 ]
机构
[1] Ain Shams Univ, Fac Educ, Dept Chem, Cairo 11711, Egypt
关键词
benzo[h][1,6]naphthyridine; synthetic methods; biological activity; EFFICIENT SYNTHESIS; POTENT; INHIBITORS; QUINOLINE; CYTOTOXICITY; RECEPTORS; LIGANDS;
D O I
10.1134/S1070428024060149
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzo[h][1,6]naphthyridine derivatives are imperative synthetic targets that display a variety of interesting biological activities, including anti-Alzheimer, anticancer, antimalarial, and antiparasitic activities. Despite the interesting findings on these compounds, the literature lacks a comprehensive summary of the synthetic methodologies and pharmacological applications of benzo[h][1,6]naphthyridine derivatives. This review deals with recent advances in the benzonaphthyridine chemistry by discussing various synthetic methods utilized for the preparation of benzo[h][1,6]naphthyridine derivatives which possess promising biological properties. It also gives an updated vision of their most common reactions and the utilization of these derivatives as units for several biologically active compounds.
引用
收藏
页码:1086 / 1106
页数:21
相关论文
共 55 条
  • [1] Regioselective intramolecular electrophilic substitution reactions involving π-deficient pyridine substrates: a new entry to pyridoquinazolines and benzo[h][1,6]naphthyridines
    Agarwal, Piyush K.
    Saifuddin, Mohammad
    Kundu, Bijoy
    [J]. TETRAHEDRON, 2010, 66 (04) : 862 - 870
  • [2] The global pipeline of new medicines for the control and elimination of malaria
    Anthony, Melinda P.
    Burrows, Jeremy N.
    Duparc, Stephan
    JMoehrle, Joerg
    Wells, Timothy N. C.
    [J]. MALARIA JOURNAL, 2012, 11
  • [3] A CONVENIENT ROUTE TO CYANO DERIVATIVES OF BENZONAPHTHYRIDINES
    Bachowska, B.
    [J]. CHEMISTRY OF HETEROCYCLIC COMPOUNDS, 2011, 47 (03) : 332 - 335
  • [4] Antimalarials in Development in 2014
    Barnett, David S.
    Guy, R. Kiplin
    [J]. CHEMICAL REVIEWS, 2014, 114 (22) : 11221 - 11241
  • [5] BARONNET R, 1983, EUR J MED CHEM, V18, P241
  • [6] A new, direct, and efficient synthesis of benzonaphthyridin-5-ones
    Cailly, Thomas
    Fabis, Frederic
    Rault, Sylvain
    [J]. TETRAHEDRON, 2006, 62 (25) : 5862 - 5867
  • [7] Regioselective functionalization of 2-(2′-fluorophenyl)-3-cyanopyridine and its cyclization to benzo[h]1,6-naphthyridines
    Cailly, Thomas
    Begtrup, Mikael
    [J]. TETRAHEDRON, 2010, 66 (06) : 1299 - 1307
  • [8] Synthesis and structure-activity relationship studies in serotonin 5-HT4 receptor ligands based on a benzo[de][2,6]naphthridine scaffold
    Castriconi, Federica
    Paolino, Marco
    Giuliani, Germano
    Anzini, Maurizio
    Campiani, Giuseppe
    Mennuni, Laura
    Sabatini, Chiara
    Lanza, Marco
    Caselli, Gianfranco
    De Rienzo, Francesca
    Menziani, Maria Cristina
    Sbraccia, Maria
    Molinari, Paola
    Costa, Tommaso
    Cappelli, Andrea
    [J]. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2014, 82 : 36 - 46
  • [9] Chemler SR, 2001, ANGEW CHEM INT EDIT, V40, P4544, DOI 10.1002/1521-3773(20011217)40:24<4544::AID-ANIE4544>3.0.CO
  • [10] 2-N