Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies
Электронный научный архив УРФУ
Информация об архиве | Просмотр оригинала| Поле | Значение | |
| Заглавие |
Cytotoxic and Infection-Controlled Investigations of Novel Dihydropyridine Hybrids: An Efficient Synthesis and Molecular-Docking Studies
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| Автор |
Guda, M. R.
Zyryanov, G. V. Dubey, A. Munagapati, V. S. Wen, J. -C. |
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| Тематика |
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 MINIMUM BACTERICIDAL CONCENTRATION MINIMUM INHIBITORY CONCENTRATION MOLECULAR DOCKING NONHUMAN PLANT DEFENSE PROTEIN INTERACTION PROTEUS VULGARIS SK-OV-3 CELL LINE STAPHYLOCOCCUS AUREUS SYNTHESIS U-937 CELL LINE ZONE OF INHIBITION |
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| Описание |
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 # 075-15-2022-1118, dated 29 June 2022. The author GMR and GVZ grateful of the Russian Federation’s Ministry of Science and Higher Education (Agreement # 075-15-2022-1118, dated 29 June 2022) and Ural federal university, Russia, for support. They are also thankful to Sri Venkateswara University, Tirupati, India, for collaboration. |
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| Дата |
2024-04-05T16:31:47Z
2024-04-05T16:31:47Z 2023 |
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| Тип |
Article
Journal article (info:eu-repo/semantics/article) |info:eu-repo/semantics/publishedVersion |
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| Идентификатор |
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/ph16081159
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/ph16081159 1424-8247 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=4fbb45027e90947de9de78deaf6c1019 https://www.mdpi.com/1424-8247/16/8/1159/pdf?version=1692086036 http://elar.urfu.ru/handle/10995/130738 10.3390/ph16081159 85168797248 001055660400001 |
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| Язык |
en
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| Права |
Open access (info:eu-repo/semantics/openAccess)
cc-by https://creativecommons.org/licenses/by/4.0/ |
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| Формат |
application/pdf
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| Издатель |
Multidisciplinary Digital Publishing Institute (MDPI)
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| Источник |
Pharmaceuticals
Pharmaceuticals |
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