Synthesis and antimicrobial studies of hydroxylated chalcone derivatives with variable chain length.

Abstract:

:A series of (E)-1-(4-alkyloxyphenyl)-3-(hydroxyphenyl)-prop-2-en-1-one have been successfully synthesised via Claisen-Schmidt condensation. The synthesised chalcone derivatives consisted of hydroxyl groups at either ortho, meta or para position and differed in the length of the alkyl groups, C (n) H(2) (n) (+1,) where n = 6, 10, 12 and 14. The structures of all compounds were defined by elemental analysis, IR, (1)H- and (13)C-NMR. The antimicrobial studies were carried out against wild-type Escherichia coli American Type Culture Collection 8739 to evaluate the effect of the hydroxyl and the alkyl groups of the synthesised chalcones. All the synthesised compounds have shown significant antimicrobial activities. The optimum inhibition was dependent on the position of the hydroxyl group as well as the length of the alkyl chains.

journal_name

Nat Prod Res

journal_title

Natural product research

authors

Ngaini Z,Fadzillah SM,Hussain H

doi

10.1080/14786419.2010.502896

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

892-902

issue

10

eissn

1478-6419

issn

1478-6427

pii

938653418

journal_volume

26

pub_type

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