کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2525539 | 1119619 | 2008 | 5 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Synthesis, anti-HIV and antitubercular activities of nelfinavir diester derivatives
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کلمات کلیدی
موضوعات مرتبط
علوم پزشکی و سلامت
پزشکی و دندانپزشکی
تومور شناسی
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چکیده انگلیسی
Nelfinavir diesters were prepared by reacting nelfinavir with two molar amount of an appropriate substituted aromatic/aliphatic acid in the presence of dicylohexyl carbodiimide as the carboxyl group activator and 4-dimethylamino pyridine as catalyst. The synthesized compounds were evaluated for their inhibitory effects on the replication of HIV-1 (IIIB) in MT-4 cells by MTT assay method and antimycobacterial activity against Mycobacterium tuberculosis H37Rv by agar dilution method. Compound 3f emerged as the most potent anti-HIV agent with EC50 of 0.043 μM and CC50 more than >10 μM and was more potent than parent nelfinavir (EC50 of 0.060 μM) and also showed antimycobacterial activity (MIC 8.49 μM).
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biomedicine & Pharmacotherapy - Volume 62, Issue 1, January 2008, Pages 1-5
Journal: Biomedicine & Pharmacotherapy - Volume 62, Issue 1, January 2008, Pages 1-5
نویسندگان
Dharmarajan Sriram, Perumal Yogeeswari, Murugesan Dinakaran, Mannila Sowmya,