دورية أكاديمية

Synthesis, antitumor activity, antimicrobial evaluation and molecular docking studies of some hydrazone, 1,3,4-oxadiazole, 1,2,4-triazole and pyrazole derivatives bearing nicotinoyl moiety

التفاصيل البيبلوغرافية
العنوان: Synthesis, antitumor activity, antimicrobial evaluation and molecular docking studies of some hydrazone, 1,3,4-oxadiazole, 1,2,4-triazole and pyrazole derivatives bearing nicotinoyl moiety
المؤلفون: Abdel-Rahman Farghaly, Saleh A. Ahmed, Khatib S. Ismail, Diaa Ibrahim, Nasser Amri, Sameh Elgogary
المصدر: Results in Chemistry, Vol 7, Iss , Pp 101474- (2024)
بيانات النشر: Elsevier, 2024.
سنة النشر: 2024
المجموعة: LCC:Chemistry
مصطلحات موضوعية: Nicotine hydrazide, Hydrazones, 1,3,4-Oxadiazoles, 1,2,4-Triazoles, Pyrazoles, Antitumor Activity, Chemistry, QD1-999
الوصف: In this study, we synthesized a number of new intriguing azoles bearing nicotinoyl moiety, their antimicrobial and antitumor activities were investigated as well. We succeeded to prepare sequence of hydrazones 2,4, 1,3,4-oxadiazoles 5, 6, 11, 12, 1,2,4-triazole 8, pyrazoles 9, 10, 13, 14, 16, 18, 20, 22, 25 and pyrazolo[3,4-d]pyrimidines 15, 23, and 24. Most of the synthesized compounds were tested against strains of fungus and bacteria. Some compounds that demonstrated significant biological activity were selected to test for their activity against cancer cells. It is interesting to note that, some of the tested compounds showed moderate to potent antibacterial activity. Strong antibacterial activity was demonstrated by compounds 16 and 23 (MIC = 2.5–5 µg/mL) against most of the microorganisms. Compounds 24 and 4a demonstrated a reasonable response to the microorganisms. Compound 2 explained a weak activity towards one of the tested microorganisms. Also, it was found that at a given concentration (3.16 µg/mL) the amino nitrile 9 exhibited strong cell-growth inhibiting action (>50 %). Based on these findings, compound 9 and 23 seems like good lead candidates to investigate further as potential anticancer and antibacterial agent respectively.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2211-7156
Relation: http://www.sciencedirect.com/science/article/pii/S221171562400170X; https://doaj.org/toc/2211-7156
DOI: 10.1016/j.rechem.2024.101474
URL الوصول: https://doaj.org/article/16334099c3164ae2951c66c14c694a96
رقم الأكسشن: edsdoj.16334099c3164ae2951c66c14c694a96
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:22117156
DOI:10.1016/j.rechem.2024.101474