Sentence examples for compound design for from inspiring English sources

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This result can contribute to a compound design for increasing cytotoxicity activity in the future.

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In the study the potential was demonstrated of applying factorial and compound designs for optimization of processes.

The DFOB conjugates with methyl-substituted adamantyl ancillary groups (1 3) were the top and most consistent performers in this class of compound designed for PD.

LASSBio-1755 is a new cycloalkyl-N-acylhydrazone parent compound designed for the development of derivatives with antinociceptive and anti-inflammatory activities.

We evaluated the feasibility, distribution, and effects of intracoronary transfer of the human tPA (htPA) gene in a rabbit heterotopic cardiac transplant model, using a novel cationic liposome compound designed for improved delivery to vascular endothelium.

There is even an ad for a compound designed for cholesterol reduction that puts plant phytosterols in sugary junk food!

In addition, laquinimod, an orally available synthetic compound designed for the treatment of relapsing-remitting MS (RRMS), ameliorates EAE disease course via BDNF-dependent mechanisms and furthermore, glatiramer acetate, a medication used in RRMS, promotes oligodendrogenesis and remyelination through elevation of growth factors including BDNF.

In this review article, the major focus has been paid to the applications of isoxazole compounds in treating multiple diseases, including anticancer, antimicrobial, anti-inflammatory, etc. Strategies for compounds design for preclinical, clinical, and FDA approved drugs were discussed.

The identification of series with alternative core structures but similar SAR trends is highly relevant for lead optimization where SAR information from one series that has been explored historically is ideally used to guide compound design efforts for a new chemotype [6].

Most compounds designed for immobilization in fluorous media feature linear pony tails of the formula (CH2 m(CF2)n−1CF3 [(CH2 mRfn].

Here, we present a fast SFC-MS method for the analysis of medium and high-polarity (−7 ≤ cLogP ≤ 2) compounds, designed for implementation in a high-throughput metabonomics setting.

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