Inorganic Chemistry Communications, Год журнала: 2025, Номер unknown, С. 113967 - 113967
Опубликована: Янв. 1, 2025
Язык: Английский
Inorganic Chemistry Communications, Год журнала: 2025, Номер unknown, С. 113967 - 113967
Опубликована: Янв. 1, 2025
Язык: Английский
Scientific Reports, Год журнала: 2023, Номер 13(1)
Опубликована: Сен. 23, 2023
Tuberculosis disease is a serious threat to humans and spreading quickly worldwide, therefore, find potent drug, the synthesis of hydrazone ligands endowed Co(II), Ni(II), Cu(II), Zn(II) metal complexes were carried out well characterized by numerous spectral analytical techniques. The octahedral geometry was confirmed analysis. Further, in vitro antituberculosis efficacy compounds (1-10) revealed that (6), (9), (10) have highest potency control TB malformation with 0.0028 ± 0.0013-0.0063 0.0013 µmol/mL MIC value while complex (0.0028 µmol/mL) has nearly four time suppress comparison streptomycin (0.0107 0.0011 µmol/mL). antimicrobial anti-inflammatory evaluations more active lowest (0.0057-0.0114 IC50 (7.14 0.05 µM) values, correspondingly which are comparable their respective standard drugs. Furthermore, theoretical studies such as molecular docking, DFT, MESP ADMET employed authenticate HL2 ligand (2) its (7-10) zinc(II) might be utilized novel drug candidate for tuberculosis dysfunctions. So, present research gives new insight vivo investigation compounds.
Язык: Английский
Процитировано
61Inorganic Chemistry Communications, Год журнала: 2023, Номер 158, С. 111486 - 111486
Опубликована: Сен. 24, 2023
Язык: Английский
Процитировано
61Journal of Coordination Chemistry, Год журнала: 2023, Номер 76(5-6), С. 546 - 580
Опубликована: Март 19, 2023
The discovery of new chemical entities having enhanced bioactivities and improved functionalities to overcome the prevailing antibiotic resistance emerging diseases has evolved as one most needed research areas in pharmaceutical field. Intensive been done on metal-based drugs a result, metal complexes various Schiff bases are acknowledged potential area bioinorganic chemistry account their promising applicable uses several fields science. base sulfonamides versatile pharmacophores forming stable compounds by coordinating with metals oxidation states. As therapeutic candidates, they have actively used many applications including antifungal, analgesic, anti-inflammatory, antiviral, antitumor, antibacterial more. There worldwide risk drug medical field pathogenic microbes capable deactivating substances. This review summarizes developments that taken place from 2008 2022 activities derived compounds.
Язык: Английский
Процитировано
51Journal of Molecular Structure, Год журнала: 2023, Номер 1288, С. 135744 - 135744
Опубликована: Май 9, 2023
Язык: Английский
Процитировано
46Inorganic Chemistry Communications, Год журнала: 2024, Номер 162, С. 112248 - 112248
Опубликована: Фев. 28, 2024
Язык: Английский
Процитировано
33Coordination Chemistry Reviews, Год журнала: 2023, Номер 501, С. 215568 - 215568
Опубликована: Ноя. 24, 2023
Язык: Английский
Процитировано
36Inorganic Chemistry Communications, Год журнала: 2023, Номер 158, С. 111587 - 111587
Опубликована: Окт. 14, 2023
Язык: Английский
Процитировано
26Results in Chemistry, Год журнала: 2024, Номер 7, С. 101503 - 101503
Опубликована: Янв. 1, 2024
Alzheimer's dementia (AD), the most prevalent neurodegenerative disorder adversely affecting elderly citizens worldwide, is an incurable with no effective medication found till date. Taking into account seriousness of this issue, imidazopyridine-based benzothiazole-oxadiazole hybrid derivatives were synthesized as anti-Alzheimer's agents. The efficacy these scaffolds was compared standard Donepezil (IC50 = 14.47 ± 1.20 μM for AChE and 19.90 2.40 BuChE). All novel exhibited biological activity covering a range IC50 6.70 1.65 41.65 7.20 6.40 1.80 44.65 7.40 BuChE. Analog 6p having BuChE lead candidate series maximum inhibition due to presence small sized highly electronegative fluoro moieties, inhibiting enzymes through hydrogen bonds. These interactions also studied in molecular docking investigations compounds. Furthermore, ADME analysis conducted study assisted drug likeness potent analogs. Synthetic structural confirmation achieved 13C NMR, 1H NMR HREI-MS.
Язык: Английский
Процитировано
17Inorganic Chemistry Communications, Год журнала: 2024, Номер 166, С. 112585 - 112585
Опубликована: Май 25, 2024
Язык: Английский
Процитировано
16BioMetals, Год журнала: 2024, Номер unknown
Опубликована: Март 28, 2024
Язык: Английский
Процитировано
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