Preparation of S14161 and its analogues and the discovery of 6-bromo-8-ethoxy-3-nitro-2H-chromene as a more potent antitumor agent in vitro-Reference-Cited by-同舟云学术

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Preparation of S14161 and its analogues and the discovery of 6-bromo-8-ethoxy-3-nitro-2H-chromene as a more potent antitumor agent in vitro

Published:2013-06 Issue:11 Volume:23 Page:3314-3319
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Yin Shu-Qiang,Shi Min,Kong Ting-Ting,Zhang Cheng-Mei,Han Kunkun,Cao Biyin,Zhang Zubin,Du Xiaolin,Tang Long-Qian,Mao Xinliang,Liu Zhao-Peng

Funder

Shandong Provincial Natural Science Foundation

National Natural Science Foundation of China

Natural Science Foundation of Jiangsu Province

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference23 articles.

1. The phosphoinositide (PI) 3-kinase family

2. Targeting PI3K signalling in cancer: opportunities, challenges and limitations

3. Present and Future of PI3K Pathway Inhibition in Cancer: Perspectives and Limitations

4. Targeting the Phosphatidylinositol 3-Kinase Pathway in Multiple Myeloma: Fig. 1.

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