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This molecule would be an exact copy of the genome of a small bacterium.
On this scale a DNA molecule would be a thin string 2 mm thick, and the average chromosome would contain 40 km (25 miles) of DNA.
The same conclusion about the shape of the molecule would be drawn from another possible Lewis structure, in which each bond is single: The actual molecule is a resonance hybrid of these and related structures; but, as each one corresponds to the same geometry, no particular Lewis structure need be selected before one can make a prediction based on VSEPR theory.
Lower path length 3 rich in atomic mass and lesser degree of unsaturation in the molecule would be favorable for COX-1 inhibition.
This is relevant to future protein biochips where dilute arrays of protein binding sites, each designed to immobilize no more than one protein molecule, would be ideal.
An accurate prediction algorithm would ensure that the highest similarity values lay on the diagonal of such matrix, i.e. the experimental spectrum of any given molecule would be more similar to its simulation than to simulated spectra of other molecules.
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Even molecules would be rare; galaxies, stars and planets would be impossible.
Those molecules would be pumped into a giant steel tank, where bacteria would eat them and excrete ethanol.
Such molecules would be useful for treating overdoses.
Mainly, aniline molecules would be bounded through weak π interactions onto the mesostructures.
The proportion of participating molecules would be the factor deciding the gelling capacity of the sample.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com