Synthesis and cytotoxic activity of non-naturally substituted 4-oxycoumarin derivatives

S. Serra, G. Delogu, L. Casu, S. Vázquez-Rodríguez, L. Santana, E. Uriarte, A. Chicca, J. Gertsch

Résultats de recherche: Contribution à un journal/une revueArticleRevue par des pairs

Résumé

Coumarins are a large family of natural and synthetic compounds exerting different pharmacological effects, including cytotoxic, anti-inflammatory or antimicrobial. In the present communication we report the synthesis of a series of 12 diversely substituted 4-oxycoumarin derivatives including methoxy substituted 4-hydroxycoumarins, methyl, methoxy or unsubstituted 3-aryl-4-hydroxycoumarins and 4-benzyloxycoumarins and their anti-proliferative effects on breast adenocarcinoma cells (MCF-7), human promyelocytic leukemia cells (HL-60), human histiocytic lymphoma cells (U937) and mouse neuroblastoma cells (Neuro2a). The most potent bioactive molecule was the 4-hydroxy-5,7- dimethoxycoumarin (compound 1) which showed similar potency (IC 0.2-2 μM) in all cancer cell lines tested. This non-natural product reveals a simple bioactive scaffold which may be exploited in further studies.
langue originaleAnglais
Pages (de - à)5791-5794
Nombre de pages4
journalBioorganic & Medicinal Chemistry Letters
Volume22
Numéro de publication18
Les DOIs
Etat de la publicationPublié - 15 sept. 2012

Empreinte digitale

Examiner les sujets de recherche de « Synthesis and cytotoxic activity of non-naturally substituted 4-oxycoumarin derivatives ». Ensemble, ils forment une empreinte digitale unique.

Contient cette citation