Synthesis and Biological Activity Studies of Methyl-5-(Hydroxymethyl)-2-Furan Carboxylate and Derivatives

Author:

Phutdhawong Weerachai1,Inpang Siwaporn2,Taechowisan Thongchai3,Phutdhawong Waya S.2ORCID

Affiliation:

1. Department of Science, Faculty of Liberal Arts and Science, Kasetsart University, Kamphaeng Sean campus,Nakhon Pathom, 73140,

2. Department of Chemistry, Faculty of Science, Silpakorn University, Nakhon Pathom 73000, Thailand.

3. Department of Microbiology, Faculty of Science, Silpakorn University, Nakhon Pathom 73000, Thailand.

Abstract

Methyl-5-(hydroxymethyl)-2-furan carboxylate and derivatives were prepared from furfuryl alcohol and their biological activities were studied for cytotoxicity against cancer cell lines HeLa, HepG2 and Vero, and Gram (+) and Gram (-) bacteria. The amine derivative, (5-(((2-(1H-indol-3-yl)ethyl)amino)methyl) furan-2-yl)methyl acetate, was found to have the most potent biological activity with IC50 62.37 µg/mL against the HeLa cell line and MIC 250 µg/mL against the photogenic bacteria.

Publisher

Oriental Scientific Publishing Company

Subject

Drug Discovery,Environmental Chemistry,Biochemistry,General Chemistry

Reference21 articles.

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2. Nii-Trebi, N.I. Biomed. Res. Int. 2017, 2017, 1-15.

3. Shekhar, C. Cell Chem. Biol. 2010,17, 413–414.

4. Mansouri, M.; Movahedian, A.; Rostami, M.; Fassihi, A. Res. Pharm. Sci. 2012, 7, 257-264.

5. Dasagrandhi, C.; Ellamar, J. B.; Kim, Y. S.; Kim, H. R. Food Sci. Biotechnol. 2016, 25, 1671-1675.

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