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This compound was shown to be formed by a series of bond-forming steps and bond shifts.
This compound was shown by fluorometric titration to bind to Magmas with a Kd = 33 μM.
This aroma-active compound was shown to be thermally generated by the reaction of cysteine with ribose [25].
While NO release from PYRRO-C3D in the presence of pneumococci was confirmed, the anti-pneumococcal action of the compound was shown to arise exclusively from the β-lactam component and not through NO-mediated effects.
When screened against HRV serotype-14 the best compound was shown to have very good 3CP inhibition (kobs/[I]=270,000 M−1 s−1) and potent in vitro antiviral activity (EC50=7.0 nM).
One compound was shown to have acceptable pharmacokinetic properties and to be a potent inhibitor of AKT signaling and of in vivo xenograft tumor growth in a preclinical model of glioblastoma.
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"The compound was showing a lot of damage – one building was still burning.
TGA/DTG measurement of cinnamic acid and ZCA intercalation compound is shown in Figure 7.
The unit cell structure of the compound is shown in Fig. 1.
The crystal structure of this compound is shown on Fig. 2.
The irreversible formation of a sodiated layered compound is shown from the first electrochemical discharge step.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com