4.7 Article

Synthesis and potent antimicrobial activity of some novel 2-phenyl or methyl-4H-1-benzopyran-4-ones carrying amidinobenzimidazoles

Journal

BIOORGANIC & MEDICINAL CHEMISTRY
Volume 13, Issue 5, Pages 1707-1714

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmc.2004.12.006

Keywords

methicillin-resistant S. aureus; methicillin-resistant S. epidermidis; 4H-1-benzopyran-4-one; amidinobenzimidazoles

Funding

  1. NIAID NIH HHS [AI-46365] Funding Source: Medline

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Series of flavones and methyl-4H-1-benzopyran-4-ones carrying mono or diamidinobenzimidazoles at different positions were synthesized and evaluated for antibacterial and antifungal activities against E coli, S. aureus, MRSA (methicillin-resistant S. aureus), MRSE (methicillin-resistant S. epidermidis), S. faecalis and C albicans, C. krusei. The results showed that while all diamidines are inactive, the compounds having monoamidinobenzimidazoles at the C-6 position of the 2-phenyl-4H-1-benzopyran-4-one have potent antibacterial activities, particularly, against Gram-positive bacteria. Compounds 23 and 22 exhibited the best inhibitory activity with MIC values of 1.56 mug/mL against S. aureus, MRSA, MRSE and 3.12 mug/mL against C. albicans, respectively. (C) 2004 Elsevier Ltd. All rights reserved.

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