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Diverse heterocyclic scaffolds as dCTP pyrophosphatase 1 inhibitors. Part 1: Triazoles, triazolopyrimidines, triazinoindoles, quinoline hydrazones and arylpiperazines
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).
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Number of Authors: 92017 (English)In: Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, E-ISSN 1464-3405, Vol. 27, no 16, p. 3897-3904Article in journal (Refereed) Published
Abstract [en]

A high-throughput screening campaign using a commercial compound library (ChemBridge DiverSET) revealed diverse chemotypes as inhibitors of the human dCTP pyrophosphatase 1 (dCTPase). Triazole, triazolopyrimidine, triazinoindole, quinoline hydrazone and arylpiperazine hits were clustered, confirmed by IC50 determinations, and their preliminary structure-activity-relationships (SAR) and ligand efficiency scores are discussed in this letter.
Place, publisher, year, edition, pages
2017. Vol. 27, no 16, p. 3897-3904
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Chemical Sciences
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URN: urn:nbn:se:su:diva-146994DOI: 10.1016/j.bmcl.2017.06.038ISI: 000407532900051PubMedID: 28687206OAI: oai:DiVA.org:su-146994DiVA, id: diva2:1142082
Available from: 2017-09-18 Created: 2017-09-18 Last updated: 2022-02-28Bibliographically approved

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Häggblad, MariaMartens, UlfLundgren, Bo

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