Portuguese
desenho de fármacos Spanish
diseño de fármaco 
Inventive process of finding new medications based on the knowledge of a biological target.
Synonyms
Examples for "rational drug design"
Examples for "rational drug design"
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I'm a believer in this what you call rational drug design.
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A recent trend toward more rational drug design was observed.
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The discovery of these agents has not always been the result of rational drug design.
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This advanced in silico approach is valuable to achieve rational drug design of selective G4 binders.
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Gene silencing by double-stranded RNA, denoted RNA interference, represents a new paradigm for rational drug design.
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These findings have implications for the rational design of new electrosurgical instruments.
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This calls for rational design of enzymes capable of catalyzing their biotransformation.
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These findings will aid in the rational design of future immunotherapy clinical trials.
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For rational design of new vaccine candidates, correlates of protection are highly desirable.
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This inhibitor-binding-induced pocket presents an opportunity for the rational design of PfHT1-specific inhibitors.
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This study also demonstrates the capabilities of MicroED for structure-based drug design.
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These results provide a mechanistic foundation for future aGPCR-targeted drug design.
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It is likely to prove useful for protein and drug design.
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More generally, these findings provide a basis for a novel drug design platform.
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XtalPi uses AI, cloud computing and quantum physics to improve drug design processes.
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I'm a believer in this what you call rational drug design.
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Thanks to improvements in drug design, research techniques and experimental methods, alternatives do exist.
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These results bring new insights for studies with venom compounds, PIs, and drug design.
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Using a structure-based drug design approach, a series of 5-substituted triclosan derivatives was developed.
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A recent trend toward more rational drug design was observed.
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These findings provide the basis for new targets for drug design or cancer therapy.
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Our findings thus far provide evidence in support of this new approach to drug design.
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Accordingly, computational prediction of protein-carbohydrate binding free energies is of enormous interest for drug design.
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The discovery of these agents has not always been the result of rational drug design.
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Its essential character in bacterial cells makes it an attractive target for antibacterial drug design.
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Conclusion: A novel perspective is presented, suggesting new molecular properties to be included in drug design.