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Synthesis of novel 6-phenyl-2,4-disubstituted pyrimidine-5-carbonitriles as potential antimicrobial agents
被引:44
|作者:
Al-Abdullah, Ebtehal S.
[1
]
Al-Obaid, Abdul-Rahman M.
[1
]
Al-Deeb, Omar A.
[1
]
Habib, Elsayed E.
[2
]
El-Emam, Ali A.
[1
]
机构:
[1] King Saud Univ, Coll Pharm, Dept Pharmaceut Chem, Riyadh 11451, Saudi Arabia
[2] Univ Mansoura, Fac Pharm, Dept Microbiol, Mansoura 35516, Egypt
关键词:
Pyrimidines;
Dihydro-4-oxopyrimidine;
Antimicrobial activity;
REVERSE-TRANSCRIPTASE INHIBITORS;
DIHYDROFOLATE-REDUCTASE INHIBITOR;
ONE-STEP SYNTHESIS;
ETHYL CYANOACETATE;
NUCLEOSIDE ANALOGS;
ANTIVIRAL AGENTS;
IN-VITRO;
DERIVATIVES;
DESIGN;
PYRIMIDINES;
D O I:
10.1016/j.ejmech.2011.08.003
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
New series of 6-phenyl-2,4-disubstituted pyrimidine-5-carbonitriles namely, 2-substitued thio-6-phenyl-3,4-dihydro-4-oxopyrimidine-5-carbonitriles (5a-d, 6, 7a-d, 8), 2-(4-chlorobenzylthio)-4-chloro-6-phenylpyrimidine-5-carbonitrile (9), 2-(4-chlorobenzylthio)-4-arylthio-6-phenylpyrimidine-5-carbonitriles (10a-d) and 2-(4-chlorobenzylthio)-4-arylamino-6-phenylpyrimidine-5-carbonitriles (11a-d) was synthesized and tested for in vitro activities against a panel of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Compounds 5b, 5c, 6, 7a, 7b, 7c, 9 and 11a displayed marked antibacterial activity particularly against the tested Gram-positive bacteria, while compounds 6, 7c, 7d and 9 were moderately or weakly active against C. albicans. (C) 2011 Elsevier Masson SAS. All rights reserved.
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页码:4642 / 4647
页数:6
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