کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1376852 981966 2008 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Synthesis and antimicrobial activity of 3-arylamino-1-chloropropan-2-ols
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Synthesis and antimicrobial activity of 3-arylamino-1-chloropropan-2-ols
چکیده انگلیسی

A series of nine 3-arylamino-1-chloropropan-2-ols 2a–2i were synthesized and their anti-fungal activity against pathogenic strains of Aspergillus fumigatus, Aspergillus flavus, Aspergillus niger and Candida albicans, and antibacterial activity against four pathogenic bacterial strains of Salmonella typhi, Pseudomonas aeruginosa, Streptococcus pneumonae and Staphylococcus aureus were evaluated using different assay systems. 1-Chloro-3-(4′-chlorophenylamino)-propan-2-ol was found to be the most active anti-fungal compound against three pathogenic strains under study, i.e., A. fumigatus, A. flavus and A. niger; the compound showed more than 90% inhibition of growth of A. fumigatus at a concentration of 5.85 μg/ml in disc diffusion assay. Interestingly, 1-chloro-3-(4′-chlorophenylamino)-propan-2-ol did not show any toxicity up to a concentration of 4000 μg/ml. Although 1-chloro-3-(4′-chlorophenylamino)-propan-2-ol was about 8 times less active than the standard compound amphotericin B, its toxicity was many more fold less than the toxicity of amphotericin B. Further, 1-chloro-3-(2′,6′-dichlorophenylamino)-propan-2-ol and 1-chloro-3-(3′,5′-dichlorophenylamino)-propan-2-ol were found to be the most active compounds against C. albicans. In the anti-microbial assay, 1-chloro-3-(2′,4′-dichlorophenylamino)-propan-2-ol and 1-chloro-3-(3′,5′-dichlorophenylamino)-propan-2-ol were found to be the most active compounds against Salmonella typhi and 1-chloro-3-(3′,4′-dichlorophenylamino)-propan-2-ol was found to be the most active compound against P. aeruginosa. Although, the activities of 1-chloro-3-(2′,4′-dichlorophenylamino)-propan-2-ol and 1-chloro-3-(3′,5′-dichlorophenylamino)-propan-2-ol are about half the activity of the standard anti-bacterial compound tetracycline, these compounds also were many fold less toxic than the standard drug.

A series of nine 3-arylamino-1-chloropropan-2-ols have been synthesized and screened for their anti-microbial activity. 1-Chloro-3-(4′-chlorophenylamino)-propan-2-ol exhibited more than 90% inhibition of growth of Aspergillus fumigatus at a concentration of 5.85 μg/ml; interestingly the compound did not show any toxicity up to a concentration of 4000 μg/ml.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 18, Issue 6, 15 March 2008, Pages 2156–2161
نویسندگان
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