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These multifunctional molecules were prepared by linking lipophilic moiety (LA) to the pentapeptide KTTKS.
Two datasets of same molecules were prepared with two different partial atomic charges; one with Gasteiger–Huckel and another with the ESPFIT charges obtained from the gaussian package.
These hybrid molecules were prepared from 12-vinyl dodecanedioate-23-O-silybin using the enzymatic regioselective acylation procedure with Novozym 435 (lipase B) or with lipase PS.
A series of designed molecules were prepared and screened initially for inhibitions of MMP-2 and MMP-9, respectively, as these are designed followed by other MMPs to observe the broader selectivity.
The new conjugate molecules were prepared via doubly activated amidation modification of Weinreb's amide formation technique, using SmCl3 as an activating agent which produces improved yields for sterically hindered 3-aryl-4-isoxazolecarboxylic esters.
NPs bearing biotin molecules were prepared either for site-specific drug delivery via the targeting of biotin receptors overexpressed on the surface of several cancer cells, or for grafting biotinylated cyclic RGD peptide onto their surface using the strong and highly specific interactions between biotin and the streptavidin protein.
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An effective microspherical zeolite MFI for large molecules was prepared for the first time.
A discovery library of molecules was prepared by attaching different side chains to both sides of the 1,3-diamine motif.
This result is not unprecedented as several reports in recent years have described increased RCY when the molecules are prepared in solutions containing varying percentages of water (Sergeev et al. 2015).
However, aggregation is greatly reduced or eliminated when the conjugated organic molecules are prepared as ligands for binding to the quantum dot surface [5, 40]. Figure 3 shows a structural schematic depicting a CdSe quantum dot with oligo- phenylene vinylene) ligands (CdSe-oligo- phenylenee).
In practice, favorable conditions are identified by screening; a very large batch of the molecules is prepared, and a wide variety of crystallization solutions are tested.
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separatists were prepared
atoms were prepared
cores were prepared
elements were prepared
species were prepared
medications were prepared
models were prepared
suspects were prepared
pathways were prepared
particles were prepared
molecules were compared
molecules were considered
molecules were produced
molecules were chosen
molecules were shown
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