Synthesis, preliminarily biological evaluation and molecular docking study of new Olaparib analogues as multifunctional PARP-1 and cholinesterase inhibitors-Reference-Cited by-同舟云学术

Synthesis, preliminarily biological evaluation and molecular docking study of new Olaparib analogues as multifunctional PARP-1 and cholinesterase inhibitors

Published:2018-11-14 Issue:1 Volume:34 Page:150-162
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Gao Cheng-Zhi¹,Dong Wei¹,Cui Zhi-Wen¹,Yuan Qiong¹,Hu Xia-Min²,Wu Qing-Ming¹,Han Xianlin³,Xu Yao⁴,Min Zhen-Li¹³

Affiliation:

1. Hubei Province Key Laboratory of Occupational Hazard Identification and Control, Wuhan University of Science and Technology, Wuhan, China;

2. College of Pharmacy, Shanghai University of Medicine & Health Sciences, Shanghai, China;

3. Barshop Institute for Longevity and Aging Studies, University of Texas Health Science Center at San Antonio, San Antonio, TX, USA;

4. College of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/14756366.2018.1530224

Reference39 articles.

1. PARP inhibition: PARP1 and beyond

2. PARP inhibitors stumble in breast cancer

3. Delivering on the promise

4. PARP inhibitors in the management of breast cancer: current data and future prospects

5. Laying a trap to kill cancer cells: PARP inhibitors and their mechanisms of action

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