A new structural alternative in benzo[b]furans for antimicrobial activity.

Abstract:

:Two series of 2-substituted and three new diacetyl benzofurans were synthesized through palladium-catalyzed reactions and their in vitro antimicrobial spectra were assessed. The compounds demonstrated mild to significant growth inhibition against antibiotic-susceptible standard and clinically isolated strains of Gram-positive and Gram-negative bacteria as well as human fungal pathogens. Ampicillin and kanamycin were used as references for antibacterial screening; nystatin and amphotericin B were used for antifungal screening. Varying substitution at the benzofuran moiety and subsequent antimicrobial screening identified the C-3-acetyl functionality as a new structural alternative for optimal antimicrobial property in the benzofuran class of compounds.

journal_name

Bioorg Med Chem

authors

Wahab Khan M,Jahangir Alam M,Rashid MA,Chowdhury R

doi

10.1016/j.bmc.2005.05.009

subject

Has Abstract

pub_date

2005-08-15 00:00:00

pages

4796-805

issue

16

eissn

0968-0896

issn

1464-3391

pii

S0968-0896(05)00419-0

journal_volume

13

pub_type

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