2016
DOI: 10.1007/s00044-016-1677-9
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Chemical profiling of Phlomis thapsoides (Lamiaceae) and in vitro testing of its biological activities

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Cited by 35 publications
(24 citation statements)
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“…This was briefly done by the addition of hydrogen atoms to the enzymes and cleansing of all undesirable interactions. Consequently, the binding site was defined through the determination of the binding manner of the bioactive conformation for the lead compounds cocrystallized with HPA, MGAM and AR Then, the identified compounds were docked within the active site in which CHARMm force field was allocated and the binding energies for the best docking poses were computed as described before …”
Section: Methodsmentioning
confidence: 99%
“…This was briefly done by the addition of hydrogen atoms to the enzymes and cleansing of all undesirable interactions. Consequently, the binding site was defined through the determination of the binding manner of the bioactive conformation for the lead compounds cocrystallized with HPA, MGAM and AR Then, the identified compounds were docked within the active site in which CHARMm force field was allocated and the binding energies for the best docking poses were computed as described before …”
Section: Methodsmentioning
confidence: 99%
“…In vitro antioxidant activities of the bark extract were determined using two commonly assays DPPH (2,2-diphenyl-1-picrylhydrazyl radical) and FRAP [ 43 ] following the protocol described by [ 44 ]. In brief, DPPH scavenging capacity assay was done following the standard assay reported by Blois [ 45 ] with some modifications adapted to a 96-well microplate.…”
Section: Methodsmentioning
confidence: 99%
“…Then the cells were maintained as a monolayer culture adopting serial subculturing. Cells growing in the logarithmic phase were employed in all experiments [ 41 ].…”
Section: Methodsmentioning
confidence: 99%