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The majority of smallmolecule drugs induce their therapeutic effects by seeking out and binding to their intended target while avoiding most other molecules in the dense milieu of the cell interior. Our overall mission at Arrakis is to expand the set of “druggable” targets for small-molecule medicines to include RNA.
Drugs that were developed and commercialised 30+ years ago were relatively simple smallmolecules. Todays smallmolecules are far larger, more complex, and chase highly specific (and difficult to hit) targets, thereby increasing the chances of undesired side effects. This failure is getting more pronounced by the day.
BMC Bioinformatics. Read There’s a news article that breaks down this work. Read Retracted Covid-19 articles: significantly more cited than other articles within their journal of origin. Read Deep learning of genomic contexts predicts protein co-regulation and function. McCafferty C.L. Favate J.S. Debès C.
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