Design and Synthesis of N-phosphoryl Peptide Modified Podophyllotoxin Derivatives as Potent Anticancer Agents-Reference-Cited by-同舟云学术

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Design and Synthesis of N-phosphoryl Peptide Modified Podophyllotoxin Derivatives as Potent Anticancer Agents

Published:2011-12-01 Issue:12 Volume:18 Page:1258-1264
ISSN:0929-8665
Container-title:Protein & Peptide Letters
language:en
Short-container-title:PPL

Author:

Hu Xiangming,Gao Chunmei,Tan Chunyan,Zhang Cunlong,Zhang Hualin,Li Shangfu,Liu Hongxia,Jiang Yuyang

Publisher

Bentham Science Publishers Ltd.

Subject

Biochemistry,General Medicine,Structural Biology

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. Application of Amino Acids in the Structural Modification of Natural Products: A Review;Frontiers in Chemistry;2021-04-29

2. Design, synthesis and evaluation of azaacridine derivatives as dual-target EGFR and Src kinase inhibitors for antitumor treatment;European Journal of Medicinal Chemistry;2017-08

3. Recent Advances in the Chemistry and Biology of Podophyllotoxins;Chemistry - A European Journal;2017-01-09

4. Design, synthesis and evaluation of acridine derivatives as multi-target Src and MEK kinase inhibitors for anti-tumor treatment;Bioorganic & Medicinal Chemistry;2016-01

5. pH-responsive polymer–drug conjugates as multifunctional micelles for cancer-drug delivery;Nanotechnology;2014-07-30

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