Ghalloo, Bilal Ahmad published the artcilePhytochemical Profiling, In Vitro Biological Activities, and In Silico Molecular Docking Studies of Dracaena reflexa, Quality Control of 627-93-0, the publication is Molecules (2022), 27(3), 913, database is CAplus and MEDLINE.
Dracaena reflexa, a traditionally significant medicinal plant, has not been extensively explored before for its phytochem. and biol. potential. The present study was conducted to evaluate the bioactive phytochems. and in vitro biol. activities of D. reflexa, and perform in silico mol. docking validation of D. reflexa. The bioactive phytochems. were assessed by preliminary phytochem. testing, total bioactive contents, and GC-MS anal. For biol. evaluation, the antioxidant (DPPH, ABTS, CUPRAC, and ABTS), antibacterial, thrombolytic, and enzyme inhibition (tyrosinase and cholinesterase enzymes) potential were determined The highest level of total phenolic contents (92.72 ± 0.79 mg GAE/g extract) was found in the n-butanol fraction while the maximum total flavonoid content (110 ± 0.83 mg QE/g extract) was observed in methanolic extract The results showed that n-butanol fraction exhibited very significant tyrosinase inhibition activity (73.46 ± 0.80) and acetylcholinesterase inhibition activity (64.06 ± 2.65%) as compared to other fractions and comparable to the standard compounds (kojic acid and galantamine). The methanolic extract was considered to have moderate butyrylcholinesterase inhibition activity (50.97 ± 063) as compared to the standard compound galantamine (53.671 ± 0.97%). The GC-MS anal. of the n-hexane fraction resulted in the tentative identification of 120 bioactive phytochems. Furthermore, the major compounds as identified by GC-MS were analyzed using in silico mol. docking studies to determine the binding affinity between the ligands and the enzymes (tyrosinase, acetylcholinesterase, and butyrylcholinesterase enzymes). The results of this study suggest that Dracaena reflexa has unquestionable pharmaceutical importance and it should be further explored for the isolation of secondary metabolites that can be employed for the treatment of different diseases.
Molecules published new progress about 627-93-0. 627-93-0 belongs to esters-buliding-blocks, auxiliary class Ploymers, name is Dimethyl adipate, and the molecular formula is C8H14O4, Quality Control of 627-93-0.
Referemce:
https://en.wikipedia.org/wiki/Ester,
Ester – an overview | ScienceDirect Topics