Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/10495/41216
Título : Synthesis and biological evaluation of combretastatin A-4 and three combretastatin-based hybrids
Autor : Agudelo Goméz, Lee Solbay
Tangarife Castaño, Verónica
Betancur Galvis, Liliana Amparo
Zapata Londoño, María Bibiana
Pérez Guaita, David
González, Miguel
metadata.dc.subject.*: Antifúngicos
Antifungal Agents
Antivirales
Antiviral Agents
Biología Molecular
Molecular Biology
Estilbenos
Stilbenes
https://id.nlm.nih.gov/mesh/D000935
https://id.nlm.nih.gov/mesh/D000998
https://id.nlm.nih.gov/mesh/D008967
https://id.nlm.nih.gov/mesh/D013267
Fecha de publicación : 2012
Editorial : SAGE Publications
Citación : González MA, Pérez-Guaita D, Agudelo-Goméz LS, Tangarife-Castaño V, Zapata B, Betancur-Galvis L. Synthesis and Biological Evaluation of Combretastatin A-4 and Three Combretastatin-Based Hybrids. Natural Product Communications. 2012;7(8). doi:10.1177/1934578X1200700822
Resumen : ABSTRACT: The syntheses of combretastatin A-4 from gallic acid and of three combretastatin-based hybrids are described. Starting from commercial gallic acid, thephosphonium salt (3,4,5-trimethoxybenzylphosphonium bromide) is synthesized and coupled, through a Wittig reaction, with several aldehydes, includingmethoxymethyl-protected isovanillin, the aldehyde γ-bicyclohomofarnesal having a labdane skeleton, 3-(3-pyridyl) propanal, and furfural. The biologicalproperties of the cis-coupled compounds as cytotoxic, antiviral and antifungal agents are also reported. In addition, pyrogallol, gallic and 3,4,5-trimethoxybenzoic acids have been studied biologically.
metadata.dc.identifier.eissn: 1555-9475
ISSN : 1934-578X
metadata.dc.identifier.doi: 10.1177/1934578X1200700822
Aparece en las colecciones: Artículos de Revista en Ciencias Médicas

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