Structural Basis for Potency and Promiscuity in Poly(ADP-ribose) Polymerase (PARP) and Tankyrase Inhibitors-Reference-Cited by-同舟云学术

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Structural Basis for Potency and Promiscuity in Poly(ADP-ribose) Polymerase (PARP) and Tankyrase Inhibitors

Published:2016-12-21 Issue:4 Volume:60 Page:1262-1271
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Thorsell Ann-Gerd,Ekblad Torun,Karlberg Tobias,Löw Mirjam,Pinto Ana Filipa,Trésaugues Lionel,Moche Martin,Cohen Michael S.¹,Schüler Herwig^ORCID

Affiliation:

1. Program in Chemical Biology and Department of Physiology and Pharmacology, Health & Science University, Portland, Oregon 97210, United States

Funder

National Institute of Neurological Disorders and Stroke

Vetenskapsr?det

Svenska S?llskapet f?r Medicinsk Forskning

IngaBritt och Arne Lundbergs Forskningsstiftelse

Stiftelsen f?r?Strategisk Forskning

Cancerfonden

Diamond Light Source Ltd.

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jmedchem.6b00990

Reference70 articles.

1. Therapeutic applications of PARP inhibitors: Anticancer therapy and beyond

2. FDA Approval Summary: Olaparib Monotherapy in Patients with Deleterious Germline BRCA-Mutated Advanced Ovarian Cancer Treated with Three or More Lines of Chemotherapy

3. Chromatin to Clinic: The Molecular Rationale for PARP1 Inhibitor Function

4. PARP inhibitors in ovarian cancer

5. PARP3 affects the relative contribution of homologous recombination and nonhomologous end-joining pathways

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