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Exact(6)
The binding mode was proposed from a docking study.
Based on jobs plot and ESI-MS studies, the 1 1 binding mode was proposed.
In addition, the binding mode was proposed based on the job's plot.
The 1 1 binding mode was proposed on the basis of absorption, FTIR and MS studies.
For one class of inhibitors a swapped binding mode was proposed to explain the results.
This two-step binding mode was proposed based on the UV titration, 1H NMR titration and ESI-mass studies.
Similar(54)
Besides, SAR is analyzed and a hypothetical enzymatic binding mode is proposed by molecular docking study, which would be useful for new candidates design.
Based on these findings, a general strategy for the rational design of additional promising p38α isoform selective inhibitors by targeting this novel binding mode is proposed.
The present minor-groove binding mode is proposed to represent the initial surface interactions of binuclear RuII compounds prior to intercalation into AT-rich DNA.
The ability of these systems to bind DNA with different binding modes is proposed to affect their function in vivo.
Preference for binding mode B was proposed based upon the potency of the primary sulphonamide (compound 7, Table 1) in which interaction with the hinge through a bidentate H-bond donor acceptor interaction to Met304 was proposed to place the polar sulphonamide in a more favourable hydrophilic environment.
More suggestions(16)
binding mode was found
binding mode was supported
binding mode was assumed
binding mode was deduced
binding mode was refined
binding mode was performed
binding mode was determined
binding mode was reproduced
binding mode was used
binding mode was proved
binding mode was investigated
binding mode was generated
binding mode was computed
binding mode was analyzed
binding mode was detected
binding mode was validated
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