Journal of Molecular Structure, Год журнала: 2024, Номер unknown, С. 140720 - 140720
Опубликована: Ноя. 1, 2024
Язык: Английский
Journal of Molecular Structure, Год журнала: 2024, Номер unknown, С. 140720 - 140720
Опубликована: Ноя. 1, 2024
Язык: Английский
Bioorganic Chemistry, Год журнала: 2024, Номер 145, С. 107234 - 107234
Опубликована: Фев. 22, 2024
Язык: Английский
Процитировано
3Tissue and Cell, Год журнала: 2024, Номер 90, С. 102529 - 102529
Опубликована: Авг. 22, 2024
Язык: Английский
Процитировано
2ACS Omega, Год журнала: 2023, Номер 8(46), С. 44312 - 44327
Опубликована: Ноя. 10, 2023
The resistance of microorganisms to antimicrobials has endangered the health many people across world. Overcoming problem will require invention molecules with a new mechanism action so that no cross-resistance existing therapies occurs. Because their powerful antibacterial activity against wide spectrum Gram-positive and Gram-negative bacterial strains, heterocyclic compounds are appealing candidates for medicinal chemists. In this regard, as unique hybrid compounds, we synthesized novel family bis-thiazoles linked quinoxaline or thienothiophene via 2-phenoxy-N-arylacetamide moiety. target were by reacting relevant bis(α-haloketones) corresponding thiosemicarbazones in EtOH at reflux few drops TEA. Under comparable reaction conditions, isomeric bis(thiazoles) appropriate bis(thiosemicarbazone) respective α-haloketones. structures confirmed using elements spectral data. All tested vitro. With an inhibitory zone width 12 mm, compound 12a had same reference medication tobramycin Staphylococcus aureus. Compound 12b showed 20 mg/mL minimum concentration (MIC) Bacillus subtilis. Some molecular docking two proteins (dihydrofolate reductase tyrosyl-tRNA synthetase).
Язык: Английский
Процитировано
6Journal of Molecular Structure, Год журнала: 2023, Номер 1295, С. 136708 - 136708
Опубликована: Сен. 29, 2023
Язык: Английский
Процитировано
4Clinical Cancer Investigation Journal, Год журнала: 2024, Номер 13(2), С. 40 - 44
Опубликована: Янв. 1, 2024
Язык: Английский
Процитировано
1Journal of Enzyme Inhibition and Medicinal Chemistry, Год журнала: 2023, Номер 38(1)
Опубликована: Авг. 7, 2023
Hexahydroquinoline (HHQ) scaffold was constructed and recruited for development of new series anticancer agents. Thirty-two compounds were synthesised where x-ray crystallography performed to confirm enantiomerism. Thirteen showed moderate good activity against NCI 60 cancer cell lines, with GI % mean up 74%
Язык: Английский
Процитировано
3Arabian Journal of Chemistry, Год журнала: 2023, Номер 16(12), С. 105291 - 105291
Опубликована: Сен. 26, 2023
Ferula ferulaeoides (Steud.) Korovin is a traditional ethnopharmacological plant used for lump elimination and as spice, especially in places like India. It has also been employed the livestock food industries. This investigation aimed to explore anti-tumor mechanisms of ethyl acetate extract fractions dried roots (FF-EtOAc) on esophageal cancer (EC) cells. Furthermore, it was hypothesized that FF-EtOAc could inhibit EC cells growths by inducing apoptosis. In time- dose-dependent manner, considerably reduced number migrating And inhibited growth vivo, less toxic nude mice. terms anticancer mechanism, findings revealed activating mitochondrial signaling pathways PI3K/Akt/Bad pathways. Through both vitro vivo experiments, significantly exhibited anti-esophageal activity. The anti-EC activity may be due activation apoptotic
Язык: Английский
Процитировано
2Journal of Molecular Structure, Год журнала: 2024, Номер unknown, С. 140720 - 140720
Опубликована: Ноя. 1, 2024
Язык: Английский
Процитировано
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