دورية أكاديمية

Antimicrobial and anticancer activity of some novel fluorinated thiourea derivatives carrying sulfonamide moieties: synthesis, biological evaluation and molecular docking

التفاصيل البيبلوغرافية
العنوان: Antimicrobial and anticancer activity of some novel fluorinated thiourea derivatives carrying sulfonamide moieties: synthesis, biological evaluation and molecular docking
المؤلفون: Mostafa M. Ghorab, Mansour S. Alsaid, Mohamed S. A. El-Gaby, Mahmoud M. Elaasser, Yassin M. Nissan
المصدر: Chemistry Central Journal, Vol 11, Iss 1, Pp 1-14 (2017)
بيانات النشر: BMC, 2017.
سنة النشر: 2017
المجموعة: LCC:Chemistry
مصطلحات موضوعية: Isothiocyanate, Sulfonamide, Fluorinated thiourea, Antimicrobial and anticancer activity, Chemistry, QD1-999
الوصف: Abstract Background Various thiourea derivatives have been used as starting materials for compounds with better biological activities. Molecular modeling tools are used to explore their mechanism of action. Results A new series of thioureas were synthesized. Fluorinated pyridine derivative 4a showed the highest antimicrobial activity (with MIC values ranged from 1.95 to 15.63 µg/mL). Interestingly, thiadiazole derivative 4c and coumarin derivative 4d exhibited selective antibacterial activities against Gram positive bacteria. Fluorinated pyridine derivative 4a was the most active against HepG2 with IC50 value of 4.8 μg/mL. Molecular docking was performed on the active site of MK-2 with good results. Conclusion Novel compounds were obtained with good anticancer and antibacterial activity especially fluorinated pyridine derivative 4a and molecular docking study suggest good activity as mitogen activated protein kinase-2 inhibitor. Graphical abstract Compound 4a in the active site of MK-2
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1752-153X
Relation: http://link.springer.com/article/10.1186/s13065-017-0258-4; https://doaj.org/toc/1752-153X
DOI: 10.1186/s13065-017-0258-4
URL الوصول: https://doaj.org/article/1937e12809ab459fa143cd227757e66d
رقم الأكسشن: edsdoj.1937e12809ab459fa143cd227757e66d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1752153X
DOI:10.1186/s13065-017-0258-4