Sentence examples for bioactive compounds were identified from inspiring English sources

Phytochemical screening was condcuted on the oleoresin extracts and a total number of 26 bioactive compounds were identified.

A wide variety of potentially bioactive compounds were identified in Sargassum species including sulphated polysaccharides fucoxanthin, steroids, terpenoids, and flavonoids (Milledge et al. 2016; Yende et al. 2014).

Based on functional conservation of MYBs in a subgroup, SmMYBs potentially involved in the biosynthesis of bioactive compounds were identified.

Disk agar diffusion method was employed to determine the QSI and bioactive compounds were identified by GC-MS analysis.

Based on the results of MIC determination experiments, the sublethal concentrations of both bioactive compounds were identified and used during the assay of conjugative effect.

Gene clusters encoding bioactive compounds were identified using BLASTp analysis of reference gene clusters, using E-value cut-off of 10−5 and a identity >60 % and a identity of >70%% in case of NRPS/PKS biosysnthesis clusters.

Four major bioactives compounds were identified: α-Linoleic acid, Campesterol, β- sitosterol and stigmasterol.

In recent years many sorbicillin related bioactive compounds were re-identified in P. notatum [ 14], Trichoderma [ 15], and other fungal species isolated from different environments [ 16].

The two additional bioactive compounds were the main conversion products, being identified as the quinoneimine (m/ z 413.1985, C25H25N4O2+, Δ 115.0990 u) and the hydroquinone (m/ z 415.2134, C25H27N4O2+, Δ 113.0841 u), both being present in all conversion samples.

By coupling LC to on-line biochemical detection (BCD) and mass spectrometry (MS), bioactive mixtures can be screened more rapidly and comprehensively as bioactive compounds are simultaneously identified and unknowns may be structurally elucidated [ 1– 6].

These bioactive compounds were subsequently tested in a tertiary polyglutamine aggregation assay, which identified five inhibitors.