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Structure-based drug repositioning explains ibrutinib as VEGFR2 inhibitor

2019-06-21

Abstract excerpt

Many drugs are promiscuous and bind to multiple targets. On the one hand, these targets may be linked to unwanted side effects, but on the other, they may achieve a combined desired effect (polypharmacology) or represent multiple diseases (drug repositioning). With the growth of 3D structures of drug-target complexes, it is today possible to study drug promiscuity at the structural level and to screen vast amounts...

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Literature Corpus work
a3ccdae9-91ac-5a66-a1e7-06da72b9b6e5
DOI
10.1101/678896
Open publication

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Structure-based drug repositioning explains ibrutinib as VEGFR2 inhibitorDOI 10.1101/678896
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