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Since a drug usually has multiple side effects (see Figure 1), the prediction should provide a series of candidate side effects ranging from the most likely one to the least likely one, rather than only giving the most likely one.
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Besides screening for novel ligands capable of activating GR signaling in vivo, an additional application of the larvae may be the rescreening of drug candidates for side effects on GC signaling that can be determined only in an intact organism.
The potent in vitro antiproliferative activity of these derivatives and their selectivity for L02 are quite important points for an anticancer drug candidate with fewer side effects.
In a patient study by Béhé et al. Y-DTPA- D Glu-(Glu)5-Ala-TY-DTPA- D Glu--Asp-Phe-NH2 (Y-DTPA- D Glu-iniGlu 5-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2erapy candidate, caused serious side effects, includinGlu 5-Ala-Tyr-Gly-Trp-Met-Asp-Phe-NH2 toxicity [ 5].
This combination may only be suitable to test drug candidates for side effect profiles at partially efficacious levels but not the maximum efficacious levels.
In drug discovery, this approach can identify potential alternate uses for drug candidates or predict side effects of pharmaceuticals that might arise from unintended interactions with other targets (i.e., off-target effects), thus producing adverse outcomes.
Ethoxylated adjuvants found in glyphosate-based herbicides were up to 10.000 times more toxic than the so-called active AP glyphosate [ 1] and are better candidates for secondary side effects.
This has had a big impact on Merck's drug-discovery and development pipeline: microarrays have helped to identify drug candidates with potentially nasty side effects, which can then be refined or eliminated.
Legislators might tweak the disclosures so that the lobby filings link to the campaign reports or list the candidates someone worked for (side effects might include — surprise! — increased political profiling, by partisan identification, of lobbyists).
Since CA I and II are off-targets of antitumor carbonic anhydrase inhibitors (CAIs), the obtained results represent an encouraging achievement for the development of new anticancer candidates without the common side effects of non-selective CAIs.
Moreover, through data integration, our method could mine some meaningful information for drug research, such as potential drug candidates, possible drug repositioning, side effects and information about pharmacology.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com