دورية أكاديمية
Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies
| العنوان: | Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies |
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| المؤلفون: | Guda, M. R., Zyryanov, G. V., Dubey, A., Munagapati, V. S., Wen, J. -C. |
| المصدر: | Pharmaceuticals |
| بيانات النشر: | Multidisciplinary Digital Publishing Institute (MDPI) |
| سنة النشر: | 2023 |
| المجموعة: | Ural Federal University (URFU): ELAR / Уральский федеральный университет: электронный архив УрФУ |
| مصطلحات موضوعية: | 1,4-DIHYDROPYRIDINE, COMPUTER STUDIES, CYTOTOXIC ASSAY, GREEN SYNTHESIS, MBC/MFC, MIC, 1,4 DIHYDROPYRIDINE, DIHYDROPYRIDINE, DIHYDROPYRIDINE DERIVATIVE, DIMETHYL 6 AMINO 5 CYANO 4 O TOLYL 1 3 HYDROXY 4 METHOXYPHENYL 1 4 DIHYDROPYRIDINE 2 3 DICARBOXYLATE, DIMETHYL 6 AMINO 5 CYANO 4 P NITROPHENYL 3 HYDROXY 4 METHOXYPHENYL 1 4 DIHYDROPYRIDINE 2 3 DICARBOXYLATE, DIMETHYL 6 AMINO-5 CYANO O NITROPHENYL 1 3 HYDROXY 4 METHOXYPHENYL 1 4 DIHYDROPYRIDINE 2 3 DICARBOXYLATE, DRUG, UNCLASSIFIED DRUG, ALGORITHM, ARTICLE, ASPERGILLUS FLAVUS, ASPERGILLUS NIGER, BACILLUS SUBTILIS, BACTERIAL STRAIN, CYTOTOXICITY, FUNGAL STRAIN, GRAM POSITIVE BACTERIUM, HEP-G2 CELL LINE, HYDROGEN BOND, HYDROPHOBICITY, IC50, IN VITRO STUDY, INFECTION, INFECTIOUS AGENT |
| الوصف: | A sequence of novel 1,4-dihydropyridines (DHP) and their hybrids was developed using a multicomponent strategy under environmentally benign conditions. In addition, computational studies were performed, and the ligand–protein interactions calculated in different bacteria and two fungal strains. Para-hydroxy-linked DHP (5f) showed the best binding energies of 3.591, 3.916, 8.499 and 6.895 kcal/mol against various pathogens used and other substances received a good docking score. The pathogen resistance potential of the synthesized targets against four bacteria and two fungi showed that whole DHP substances exhibit different levels of resistance to each microorganism. Gram-positive bacteria, which are highly sensitive to all molecules, and the MTCC-1884-encoded fungus strongly rejected the studied compounds compared to comparator drugs. In particular, the 5f candidate showed remarkable antimicrobial activity, followed by the substances 5a, 5b, 5j, 5k and 5l. Furthermore, MIC and MBC/MFC properties showed that 5f had a minimum bacterial concentration of 12.5 μg/mL against E. coli and against two fungal pathogens, with its killing activity being effective even at low concentrations. On the other hand, whole motifs were tested for their cytotoxic activity, revealing that the methoxy and hydroxy-linked compounds (5h) showed greater cytotoxic potency, followed by the two hydroxy linked compounds (5d and 5f). Overall, this synthetic approach used represents a prototype for future nature-favored synthesis methods and these biological results serve as a guide for future therapeutic drug research. However, the computer results play an important role in the further development of biological experiments. © 2023 by the authors. ; Ministry of Education and Science of the Russian Federation, Minobrnauka; Ural Federal University, UrFU; Ministry of Science and Higher Education of the Russian Federation: 075-15-2022-1118 ; This research was funded by the Ministry of Science and Higher Education of the Russian Federation, Reference ... |
| نوع الوثيقة: | article in journal/newspaper |
| وصف الملف: | application/pdf |
| اللغة: | English |
| تدمد: | 1424-8247 |
| العلاقة: | Guda, M, Zyryanov, G, Dubey, A, Munagapati, V & Wen, J-C 2023, 'Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies', Pharmaceuticals, Том. 16, № 8, 1159. https://doi.org/10.3390/ph16081159Test; Guda, M., Zyryanov, G., Dubey, A., Munagapati, V., & Wen, J-C. (2023). Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies. Pharmaceuticals, 16(8), [1159]. https://doi.org/10.3390/ph16081159Test; Final; All Open Access, Gold, Green; https://www.scopus.com/inward/record.uri?eid=2-s2.0-85168797248&doi=10.3390%2fph16081159&partnerID=40&md5=4fbb45027e90947de9de78deaf6c1019Test; https://www.mdpi.com/1424-8247/16/8/1159/pdf?version=1692086036Test; http://elar.urfu.ru/handle/10995/130738Test; 85168797248; 001055660400001 |
| DOI: | 10.3390/ph16081159 |
| الإتاحة: | https://doi.org/10.3390/ph16081159Test http://elar.urfu.ru/handle/10995/130738Test https://www.mdpi.com/1424-8247/16/8/1159/pdf?version=1692086036Test |
| حقوق: | info:eu-repo/semantics/openAccess ; cc-by ; https://creativecommons.org/licenses/by/4.0Test/ |
| رقم الانضمام: | edsbas.8D7FB552 |
| قاعدة البيانات: | BASE |
Full Text Finder | تدمد: | 14248247 |
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| DOI: | 10.3390/ph16081159 |