4 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Evaluation and Structural Basis for the Inhibition of Tankyrases by PARP Inhibitors.
University of Oulu
One-pot tandem Hurtley-retro-Claisen-cyclisation reactions in the synthesis of 3-substituted analogues of 5-aminoisoquinolin-1-one (5-AIQ), a water-soluble inhibitor of PARPs.
University of Bath
Design, synthesis, and evaluation in vitro of quinoline-8-carboxamides, a new class of poly(adenosine-diphosphate-ribose)polymerase-1 (PARP-1) inhibitor.
University of Bath