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

被引:81
作者
Göker, H [1 ]
Boykin, DW
Yildiz, S
机构
[1] Georgia State Univ, Dept Chem, Atlanta, GA 30303 USA
[2] Ankara Univ, Fac Pharm, Dept Pharmaceut Chem, TR-06100 Ankara, Turkey
[3] Ankara Univ, Fac Pharm, Dept Microbiol, TR-06100 Ankara, Turkey
关键词
methicillin-resistant S. aureus; methicillin-resistant S. epidermidis; 4H-1-benzopyran-4-one; amidinobenzimidazoles;
D O I
10.1016/j.bmc.2004.12.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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.
引用
收藏
页码:1707 / 1714
页数:8
相关论文
共 24 条
[1]
THE SOMMELET REACTION .3. THE CHOICE OF SOLVENT AND THE EFFECT OF SUBSTITUENTS [J].
ANGYAL, SJ ;
MORRIS, PJ ;
TETAZ, JR ;
WILSON, JG .
JOURNAL OF THE CHEMICAL SOCIETY, 1950, (AUG) :2141-2145
[2]
Molecular rearrangement of some o-acyloxyacetophenones and the mechanism of the production of 3-acylchromones [J].
Baker, W .
JOURNAL OF THE CHEMICAL SOCIETY, 1933, :1381-1389
[3]
Briet P., 1978, 6',2-(2'arylchromonyl) propionic acids, and analgesic and anti-inflammatory derivatives there of patent, Patent No. [US 4122200, 4122200]
[4]
Detection of inhibition of bovine viral diarrhea virus by aromatic cationic molecules [J].
Givens, MD ;
Dykstra, CC ;
Brock, KV ;
Stringfellow, DA ;
Kumar, A ;
Stephens, CE ;
Goker, H ;
Boykin, DW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (07) :2223-2230
[5]
Göker H, 2000, HETEROCYCL COMMUN, V6, P385
[6]
Flavonolignan and flavone inhibitors of a Staphylococcus aureus multidrug resistance pump:: Structure-activity relationships [J].
Guz, NR ;
Stermitz, FR ;
Johnson, JB ;
Beeson, TD ;
Willen, S ;
Hsiang, JF ;
Lewis, K .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (02) :261-268
[7]
Advances in flavonoid research since 1992 [J].
Harborne, JB ;
Williams, CA .
PHYTOCHEMISTRY, 2000, 55 (06) :481-504
[8]
The biochemistry and medical significance of the flavonoids [J].
Havsteen, BH .
PHARMACOLOGY & THERAPEUTICS, 2002, 96 (2-3) :67-202
[9]
Synthesis and antiprotozoal activity of aza-analogues of furamidine [J].
Ismail, MA ;
Brun, R ;
Easterbrook, JD ;
Tanious, FA ;
Wilson, WD ;
Boykin, DW .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (22) :4761-4769
[10]
LINUMA M, 1994, J PHARM PHARMACOL, V46, P892