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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

In Vitro Metabolism of Artepillin C by Rat and Human Liver Microsomes

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Author(s):
Carrao, Daniel Blascke ; Perez de Albuquerque, Nayara Cristina ; Mauriz Marques, Lucas Maciel ; Miller Crotti, Antonio Eduardo ; Pilon, Alan Cesar ; Bolzani, Vanderlan Da Silva ; Berretta, Andresa Aparecida ; Moraes de Oliveira, Anderson Rodrigo
Total Authors: 8
Document type: Journal article
Source: Planta Medica; v. 83, n. 8, p. 737-745, MAY 2017.
Web of Science Citations: 4
Abstract

Artepillin C, a natural product present in the Brazilian green propolis, has several biological properties. Among these properties, the antitumor action of this product is noteworthy and makes it a promising drug candidate for the treatment of several types of cancer. This paper describes the in vitro metabolism of Artcpillin C in rat and human liver microsomcs. Thc rat model suggested a sigrnoidal profile for the metabolism, adapted to the Hill's kinetic model. The enzymatic kinetic parameters were as follows: maximal velocity = 0.757 +/- 0.021 mu mol/mg protein/min, Hill coefficient= 10.90 +/- 2.80, and substrate concentration at which half-maximal velocity of a Hill enzyme is achieved =33.35 +/- 0.55 mu M. Based on these results, the calculated in vitro intrinsic clearance for Artepillin C was 16.63 +/- 1.52 mu L/min/mg protein. The in vitro metabolism assay conducted on the human model did not fit any enzymatic kinetic model. Two novel metabolites were formed in both mammal microsomal models and their chemical structures were elucidated for the first time. The main human cytochromc P450 isoforms involved in Artcpillin C metabolism had been identified, and the results suggest a majority contribution of CYP2E1 and CYP2C9 in the formation of the two metabolites. (AU)

FAPESP's process: 16/07597-0 - Development of chromatographic/electrophoretic methods to be further used in in vitro enzymatic inhibition and drug interaction of chiral pesticides
Grantee:Anderson Rodrigo Moraes de Oliveira
Support type: Regular Research Grants
FAPESP's process: 13/17658-9 - Development and validation of chromatographic and electrophoretic methods for subsequent application in studies of in vitro metabolism and biotransformation - phase 2
Grantee:Anderson Rodrigo Moraes de Oliveira
Support type: Regular Research Grants
FAPESP's process: 13/20094-0 - Evaluation of the anti-parasitary and insecticidal activities of benzofuran derivatives, and study of their gas-phase fragmentation reactions using tandem mass spectrometry
Grantee:Antônio Eduardo Miller Crotti
Support type: Regular Research Grants