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. 2013 Jul:88:101-8.
doi: 10.1016/j.fitote.2013.05.001. Epub 2013 May 9.

Pentacyclic triterpenes from Manilkara bidentata resin. Isolation, identification and biological properties

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Pentacyclic triterpenes from Manilkara bidentata resin. Isolation, identification and biological properties

Boutayna Rhourri-Frih et al. Fitoterapia. 2013 Jul.

Abstract

Three pentacyclic triterpenes were isolated for the first time from resinous plant Manilkara bidentata. Ultrasound-assisted extraction with ethanol was chosen after a comparison of various extraction methods. Analysis of the extract was performed by HPLC with evaporative light scattering detection and semi-preparative HPLC has enabled us to isolate two urs-12-enes (3β-O-acetyl-α-amyrin and 3β-O-trans cinnamyl-α-amyrin) and a lupane-type derivative (3β-O-trans cinnamyl lupeol). Structures were elucidated on the basis of HRESIMS, atmospheric pressure photoionization MS, and homo- and heteronuclear correlation NMR experiments. Antioxidant and anti-inflammatory activities were determined on Manilkara extract and isolated fractions. We have also investigated their action on collagen and fibronectin synthesis, two very important proteins of the extracellular matrix. Thus, Manilkara extract was able to decrease IL-1β and IL-8 pro-inflammatory cytokines. These activities exhibit the potential use of Manilkara extract as an anti-inflammatory and anti-aging ingredient for pharmaceutical and cosmetic industries.

Keywords: Anti-inflammatory activity; Extracellular matrix; Manilkara bidentata; Pentacyclic triterpenes; Radical scavenging activity; Sapotaceae.

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