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The compound was selected for detailed profiling.
Among the tested oxime library, one imidazolium compound was selected for preliminary in vivo antidotal study in mice.
Ti3SiC2, a ternary compound was selected as one of the most promising candidate material, the most significant aspect of Ti3SiC2 is that it combines some of the most attractive proprieties of ceramics with those of metals.
This compound was selected for further evaluation of cytotoxic activity on several human cancer cells including HT-29 (human colorectal adenocarcinoma), HepG2 (human hepatocellular carcinoma) and HeLa, (human cervical adenocarcinoma cells).
The experimental setup was designed as follows: Given a data set with active compounds, the most active compound was selected as query structure for the experiment.
The parent ion m/z of each analyzed compound was selected by direct injection based on the optimization of MS/MS parameters.
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In Figure 11 the view was zoomed into a cluster, a single compound is selected.
When a cluster and/or a compound is selected, their feature values are indicated in the chart (see Figure 11).
The doses used for each compound were selected accordingly to previous studies in Giardia, some other parasites and mammalian cells.
All published articles outlining an NMDR relationship with a tested compound were selected.
The benefit risk relationship of a drug is largely determined once the target and compound are selected.
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CEO of Professional Science Editing for Scientists @ prosciediting.com