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This conclusion should be helpful when selecting substituents for the synthesis of potential anticancer drugs.
An enormous effort in the design of 5-HT6 receptor ligands has resulted in the synthesis of potential therapeutic agents with activity in CNS and obesity disorders.
The telomerization of 1,3-dienes with functionalized nucleophiles presents an atom efficient and selective synthesis of potential non-ionic surfactants.
In the present study, we aimed towards the synthesis of potential 68Ga labeled monomers and dimers of the EGFR-TKI pharmacophore (3-bromophenyl)quinazoline-4,6-diamine pharmacophore[1,2].
In order to identify novel agents able to block the chaperone activity, following a structure-based approach, we used in silico screening to direct the synthesis of potential inhibitors bearing the triazole scaffold, a widespread motif in drug-like molecules.
For the synthesis of potential cyclization precursors 8a– h (Table 1), a general synthetic approach was developed.
Similar(52)
These findings provide a framework for future research on the regulation and perturbation of FVIII synthesis, and of potential relevance to haemophilia, thromboses, and pulmonary hypertensive states.
In conducting this synthesis, review of potential evidence may not have been exhaustive.
Synthesis of a potential Src family SH2 domain inhibitor incorporating a 1,4-cis-enediol scaffold is reported.
We herein present the synthesis of a potential γ-turn mimetic scaffold, and its incorporation in the 3 5 position of angiotensin II.
This chapter describes how architectural self-construction was uncovered in the course of an efficient, nature-inspired total synthesis of the potential antitumor agent FR182877.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com