Literature DB >> 25515747

Synthesis and biological evaluation of 1,5-naphthyridines as topoisomerase I inhibitors. A new family of antiproliferative agents.

Concepción Alonso, María Fuertes, María González, Alicia Rodríguez-Gascón, Gloria Rubiales, Francisco Palacios1.   

Abstract

The synthesis of a variety of phenyl- and indeno-1,5-naphthyridine derivatives as new substrates with anticancer activity is described. Several of the prepared products were addressed to in vitro anticancer screening which indicated that some of them exhibited inhibitory effect of Top1 and antiproliferative activity against human colon cancer cells (COLO 205).

Entities:  

Mesh:

Substances:

Year:  2014        PMID: 25515747     DOI: 10.2174/1568026614666141215152441

Source DB:  PubMed          Journal:  Curr Top Med Chem        ISSN: 1568-0266            Impact factor:   3.295


  2 in total

Review 1.  Synthetic Strategies, Reactivity and Applications of 1,5-Naphthyridines.

Authors:  Maria Fuertes; Carme Masdeu; Endika Martin-Encinas; Asier Selas; Gloria Rubiales; Francisco Palacios; Concepcion Alonso
Journal:  Molecules       Date:  2020-07-16       Impact factor: 4.411

2.  Sc(OTf)3-Mediated [4 + 2] Annulations of N-Carbonyl Aryldiazenes with Cyclopentadiene to Construct Cinnoline Derivatives: Azo-Povarov Reaction.

Authors:  Xabier Jiménez-Aberásturi; Francisco Palacios; Jesús M de Los Santos
Journal:  J Org Chem       Date:  2022-08-16       Impact factor: 4.198

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.