@article {62489,
	title = {In Silico Investigation of Some Compounds from the N-Butanol Extract of Centaurea tougourensis Boiss. \&amp; Reut.},
	journal = {Crystals},
	volume = {12},
	number = {3},
	year = {2022},
	month = {2022},
	pages = {355},
	abstract = {
	Bioinformatics as a newly emerging discipline is considered nowadays a reference to characterize the physicochemical and pharmacological properties of the actual biocompounds contained in plants, which has helped the pharmaceutical industry a lot in the drug development process. In this study, a bioinformatics approach known as in silico was performed to predict, for the first time, the physicochemical properties, ADMET profile, pharmacological capacities, cytotoxicity, and nervous system macromolecular targets, as well as the gene expression profiles, of four compounds recently identified from\&nbsp;Centaurea tougourensis\&nbsp;via the gas chromatography{\textendash}mass spectrometry (GC{\textendash}MS) approach. Thus, four compounds were tested from the n-butanol (n-BuOH) extract of this plant, named, respectively, Acridin-9-amine, 1,2,3,4-tetrahydro-5,7-dimethyl- (compound 1), 3-[2,3-Dihydro-2,2-dimethylbenzofuran-7-yl]-5-methoxy-1,3,4-oxadiazol-2(3H)-one (compound 2), 9,9-Dimethoxybicyclo[3.3.1]nona-2,4-dione (compound 3), and 3-[3-Bromophenyl]-7-chloro-3,4-dihydro-10-hydroxy-1,9(2H,10H)-acridinedione (compound 4). The\&nbsp;insilico\&nbsp;investigation revealed that the four tested compounds could be a good candidate to regulate the expression of key genes and may also exert significant cytotoxic effects against several tumor celllines. In addition, these compounds could also be effective in the treatment of some diseases related to diabetes, skin pathologies, cardiovascular, and central nervous system disorders. The bioactive compounds of plant remain the best alternative in the context of the drug discovery and development process.

},
	isbn = {2073-4352},
	url = { https://doi.org/10.3390/cryst12030355},
	author = {Dassamiour, Saliha and Bensaad, Mohamed Sabri and Hambaba, Leila and Melakhessou, Mohamed Akram and Sami, Rokayya and Al-Mushhin, Amina AM and Aljahani, Amani H and Al Masoudi, Luluah M}
}
