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Chemo-enzymatic Synthesis and Biological Activity Evaluation of Propenylbenzene Derivatives

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Journal Front Microbiol
Specialty Microbiology
Date 2023 Jul 12
PMID 37434714
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Abstract

Propenylbenzenes, including isosafrole, anethole, isoeugenol, and their derivatives, are natural compounds found in essential oils from various plants. Compounds of this group are important and valuable, and are used in the flavour and fragrance industries as well as the pharmaceutical and cosmetic industries. The aim of this study was to develop an efficient process for synthesising oxygenated derivatives of these compounds and evaluate their potential biological activities. In this paper, we propose a two-step chemo-enzymatic method. The first step involves the synthesis of corresponding diols from propenylbenzenes lipase catalysed epoxidation followed by epoxide hydrolysis. The second step involves the microbial oxidation of a diasteroisomeric mixture of diols to yield the corresponding hydroxy ketones , which in this study was performed on a preparative scale using sp. DSM44016, DSM44534, PCM2150, and PCM2166. Application of scaled-up processes allowed to obtain hydroxy ketones with the following yield range 36-62.5%. The propenylbenzene derivatives thus obtained and the starting compounds were tested for various biological activities, including antimicrobial, antioxidant, haemolytic, and anticancer activities, and their impact on membrane fluidity. Fungistatic activity assay against selected strains of results in MIC value varied from 37 to 124 μg/mL for compounds , , , and . The highest antiradical activity was shown by propenylbenzenes with a double bond in their structure with EC value ranged from 19 to 31 μg/mL. Haemolytic activity assay showed no cytotoxicity of the tested compounds on human RBCs whereas, compounds and affected the fluidity of the RBCs membrane. The tested compounds depending on their concentration showed different antiproliferative activity against HepG2, Caco-2, and MG63. The results indicate the potential utility of these compounds as fungistatics, antioxidants, and proliferation inhibitors of selected cell lines.

References
1.
Lummiss J, Oliveira K, Pranckevicius A, Santos A, Dos Santos E, Fogg D . Chemical plants: high-value molecules from essential oils. J Am Chem Soc. 2012; 134(46):18889-91. DOI: 10.1021/ja310054d. View

2.
Eid A, Hawash M . Biological evaluation of Safrole oil and Safrole oil Nanoemulgel as antioxidant, antidiabetic, antibacterial, antifungal and anticancer. BMC Complement Med Ther. 2021; 21(1):159. PMC: 8164802. DOI: 10.1186/s12906-021-03324-z. View

3.
Cabral P, de Morais Campos R, Fonteles M, Santos C, Leal Cardoso J, Nascimento N . Effects of the essential oil of Croton zehntneri and its major components, anethole and estragole, on the rat corpora cavernosa. Life Sci. 2014; 112(1-2):74-81. DOI: 10.1016/j.lfs.2014.07.022. View

4.
Bhatia R, Shreaz S, Khan N, Muralidhar S, Basir S, Manzoor N . Proton pumping ATPase mediated fungicidal activity of two essential oil components. J Basic Microbiol. 2011; 52(5):504-12. DOI: 10.1002/jobm.201100272. View

5.
Atsumi T, Fujisawa S, Tonosaki K . A comparative study of the antioxidant/prooxidant activities of eugenol and isoeugenol with various concentrations and oxidation conditions. Toxicol In Vitro. 2005; 19(8):1025-33. DOI: 10.1016/j.tiv.2005.04.012. View