Discovery of a Potent Allosteric Kinase Modulator by Combining Computational and Synthetic Methods-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Discovery of a Potent Allosteric Kinase Modulator by Combining Computational and Synthetic Methods

Published:2015-09-04 Issue:47 Volume:127 Page:14139-14142
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Kroon Edwin¹,Schulze Jörg O.²,Süß Evelyn²,Camacho Carlos J.³,Biondi Ricardo M.²,Dömling Alexander¹

Affiliation:

1. University of Groningen, Department of Drug Design, A. Deusinglaan 1, 9713 AV Groningen (The Netherlands) http://www.drugdesign.nl

2. Universitätsklinikum Frankfurt, Theodor‐Stern‐Kai 7, 60590 Frankfurt (Germany)

3. University of Pittsburgh, 200 Lothrop Street, Pittsburgh, PA 15261 (USA)

Funder

NIH

DFG

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ange.201506310

Reference45 articles.

1.

2. 2013 Philip S. Portoghese Medicinal Chemistry Lectureship: Drug Discovery Targeting Allosteric Sites

3. Emerging paradigms in GPCR allostery: implications for drug discovery

4.

5. AGC protein kinases: From structural mechanism of regulation to allosteric drug development for the treatment of human diseases

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Dibenzothiazepine Based MCR Chemistry;European Journal of Organic Chemistry;2022-05-24

2. Experimental and Computational Studies on N-alkylation Reaction of N-Benzoyl 5-(Aminomethyl)Tetrazole;Chemistry;2021-07-05

3. Enantiomeric Resolution and Absolute Configuration of a Chiral δ-Lactam, Useful Intermediate for the Synthesis of Bioactive Compounds;Molecules;2020-12-19

4. TEAD–YAP Interaction Inhibitors and MDM2 Binders from DNA‐Encoded Indole‐Focused Ugi Peptidomimetics;Angewandte Chemie International Edition;2020-07-15

5. TEAD–YAP Interaction Inhibitors and MDM2 Binders from DNA‐Encoded Indole‐Focused Ugi Peptidomimetics;Angewandte Chemie;2020-07-15

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3