Antiproliferative Flavanoid Dimers Isolated from Brazilian Red Propolis

Thais Petrochelli Banzato, Juliana R. Gubiani, Darlon I. Bernardi, Cláudio Rodrigo Nogueira, A. F. M. Monteiro, Fernanda Francetto Juliano, Severino Matias de Alencar, Ronaldo A. Pilli, Carolina A. de Lima, Giovanna Barbarini Longato,

Journal of Natural Products · 2020 · 29 citations · 26 references

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Abstract

Herein reported are results of the chemical and biological investigation of red propolis collected at the Brazilian Northeast coastline. New propolones A–D (1–4), with a 3-{3-[(2-phenylbenzofuran-3-yl)methyl]phenyl}chromane skeleton; propolonones A–C (5–7), with a 3-[3-(3-benzylbenzofuran-2-yl)phenyl]chromane skeleton; and propolol A (8), with a 6-(3-benzylbenzofuran-2-yl)-3-phenylchromane skeleton, were isolated as constituents of Brazilian red propolis by cytotoxicity-guided assays and structurally identified by analysis of their spectroscopic data. Propolone B (2) and propolonone A (5) display significant cytotoxic activities against an ovarian cancer cell line expressing a multiple drug resistance phenotype when compared with doxorubicin.

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