Improvement of antibacterial activity of some sulfa drugs through linkage to certain phthalazin-1(2H)-one scaffolds

被引:84
作者
Ibrahim, Hany S. [1 ]
Eldehna, Wagdy M. [1 ]
Abdel-Aziz, Hatem A. [2 ,3 ]
Elaasser, Mahmoud M. [4 ]
Abdel-Aziz, Marwa M. [4 ]
机构
[1] Egyptian Russian Univ, Fac Pharm, Dept Pharmaceut Chem, Badr City 11829, Helwan, Egypt
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
[3] Natl Res Ctr, Dept Appl Organ Chem, Cairo 12622, Egypt
[4] Al Azhar Univ, Reg Ctr Mycol & Biotechnol, Cairo, Egypt
关键词
Sulfa drugs; Phthalazin-1(2H)-4-one; Antibacterial agents; RAB1; DIHYDROFOLATE-REDUCTASE; SULFONAMIDE RESISTANCE; ANTIMICROBIAL ACTIVITY; DIHYDROPTEROATE SYNTHASE; BACILLUS-ANTHRACIS; CRYSTAL-STRUCTURE; ESCHERICHIA-COLI; ACID; TRIMETHOPRIM; DERIVATIVES;
D O I
10.1016/j.ejmech.2014.08.016
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
RAB1 5 is a lead antibacterial agent in which trimethoprim is linked to phthalazine moiety. Similarly, our strategy in this research depends on the interconnection between some sulfa drugs and certain phthalazin-1(2H)-one scaffolds in an attempt to enhance their antibacterial activity. This approach was achieved through the combination of 4-substituted phthalazin-1(2H)-ones 9a, b or 14a, b with sulfanilamide 1a, sulfathiazole 1b or sulfadiazine 1c through amide linkers 6a, b to produce the target compounds 10a-d and 15a-e, respectively. The antibacterial activity of the newly synthesized compounds showed that all tested compounds have antibacterial activity higher than that of their reference sulfa drugs 1a-c. Compound 10c represented the highest antibacterial activity against Gram-positive bacteria Streptococcus pneumonia and Staphylococcus aureus with MIC = 0.39 mu mol/mL. Moreover, compound 10d displayed excellent antibacterial activity against Gram-negative bacteria Escherichia coli and Salmonella Lyphimurium with MIC = 0.39 and 0.78 mu mol/mL, respectively. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:480 / 486
页数:7
相关论文
共 40 条
[1]   Synthesis and reactions of some novel 4-biphenyl-4-(2H)-phthalazin-1-one derivatives with an expected antimicrobial activity [J].
Abubshait, Samar A. ;
Kassab, Rafika R. ;
Al-Shehri, Aisha H. ;
Abubshait, Haya A. .
JOURNAL OF SAUDI CHEMICAL SOCIETY, 2011, 15 (01) :59-65
[2]  
Arif Jamal M, 2006, Asian Pac J Cancer Prev, V7, P249
[3]   Crystal structure of 7,8-dihydropteroate synthase from Bacillus anthracis:: Mechanism and novel inhibitor design [J].
Babaoglu, K ;
Qi, JJ ;
Lee, RE ;
White, SW .
STRUCTURE, 2004, 12 (09) :1705-1717
[4]   In vitro efficacy of new antifolates against trimethoprim-resistant Bacillus anthracis [J].
Barrow, Esther W. ;
Dreier, Jurg ;
Reinelt, Stefan ;
Bourne, Philip C. ;
Barrow, William W. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (12) :4447-4452
[5]   EFFECTS OF PONALRESTAT, AN ALDOSE REDUCTASE INHIBITOR, ON NEUTROPHIL KILLING OF ESCHERICHIA-COLI AND AUTONOMIC FUNCTION IN PATIENTS WITH DIABETES-MELLITUS [J].
BOLAND, OM ;
BLACKWELL, CC ;
CLARKE, BF ;
EWING, DJ .
DIABETES, 1993, 42 (02) :336-340
[6]   Inhibition of Antibiotic-Resistant Staphylococcus aureus by the Broad-Spectrum Dihydrofolate Reductase Inhibitor RAB1 [J].
Bourne, C. R. ;
Barrow, E. W. ;
Bunce, R. A. ;
Bourne, P. C. ;
Berlin, K. D. ;
Barrow, W. W. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (09) :3825-3833
[7]   Structure-activity relationship for enantiomers of potent inhibitors of B. anthracis dihydrofolate reductase [J].
Bourne, Christina R. ;
Wakeham, Nancy ;
Nammalwar, Baskar ;
Tseitin, Vladimir ;
Bourne, Philip C. ;
Barrow, Esther W. ;
Mylvaganam, Shankari ;
Ramnarayan, Kal ;
Bunce, Richard A. ;
Berlin, K. Darrell ;
Barrow, William W. .
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS, 2013, 1834 (01) :46-52
[8]   Crystal Structure of Bacillus anthracis Dihydrofolate Reductase with the Dihydrophthalazine-Based Trimethoprim Derivative RAB1 Provides a Structural Explanation of Potency and Selectivity [J].
Bourne, Christina R. ;
Bunce, Richard A. ;
Bourne, Philip C. ;
Berlin, K. Darrell ;
Barrow, Esther W. ;
Barrow, William W. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2009, 53 (07) :3065-3073
[9]   Synthesis and in vitro antimicrobial studies of medicinally important novel N-alkyl and N-sulfonyl derivatives of 1-[bis(4-fluorophenyl)-methyl]piperazine [J].
Chandra, J. N. Narendra Sharath ;
Sadashiva, C. T. ;
Kavitha, C. V. ;
Rangappa, K. S. .
BIOORGANIC & MEDICINAL CHEMISTRY, 2006, 14 (19) :6621-6627
[10]   Structure-activity relationships in a series of bisquaternary bisphthalimidine derivatives modulating the muscarinic M2-receptor allosterically [J].
Cid, HMB ;
Tränkle, C ;
Baumann, K ;
Pick, R ;
Mies-Klomfass, E ;
Kostenis, E ;
Mohr, K ;
Holzgrabe, U .
JOURNAL OF MEDICINAL CHEMISTRY, 2000, 43 (11) :2155-2164