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Among the various vanadium-based catalysts studied, vanadyl tetraphenoxyphthalocyanine (VOPc) was found to be best from conversion as well as selectivity for hydroxy compounds points of view.
Spectroelectrochemical monitoring of the gradual oxidation of the compounds points to a first oxidation centred on the indenofluorenyl core for both molecules.
The inability of Vch_cass2+ gene to directly confer resistance to cationic compounds points to the need for protein factors in addition to the effector domain to be present for effective regulation of their cellular metabolism.
The cyano group of both compounds points towards the same region of space as the C17 carbonyl group of androstenedione, where it may interact with the backbone NH of Met374 as a hydrogen bond acceptor.
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The sorting of the compounds pointed here is implemented in the software system ChemProp [50, 51].
Its superior biological profiles compared with known compounds point to its potential use as therapeutic agents for neurological disorders.
Sensory data correlated well with selected volatile compounds pointing to dimethyl disulphide, pentanal, hexanal and heptanal as potential markers of fresh milk quality.
Nevertheless, these compounds point to the critical role that InhA and mycolic acid biosynthesis has on mycobacterial physiology and as a drug target.
In these genotypes, the heterologous configuration is for both compounds to biorient toward opposite poles at metaphase I arrest, with the nonheterologous configuration having both compounds pointed to the same pole.
Chelerythrine binds flat in the PrgI binding site, while the compound points into the corresponding Bcl-xL binding site partially overlaying helix α4.
All these factors indicate that the decision to pursue development of an oral compound points to the need for multiple, well designed trials and population pharmacokinetic studies.
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