Withdrawal Notice
This paper was originally published in Oncotarget Advance Online Publications on 01/08/2018.In compliance with Oncotarget's withdrawal policy, the paper was withdrawn in its entirety. It will not appear in Oncotarget internal or any external indexes or archives.
Research Papers:
Coptisine, an alkaloid from Rhizoma Coptidis, inhibits Helicobacter pylori urease activity by targeting its active site and maturation process
Cailan Li1,*, Ping Huang2,*, Kambo Wong3, Yifei Xu2, Lihua Tan1, Hanbin Chen4, Qiang Lu5, Chaodan Luo1, Chunlai Tam3, Lixiang Zhu2, Ziren Su1,6 and Jianhui Xie7
1 Guangdong Provincial Key Laboratory of New Drug Development and Research of Chinese Medicine, Mathematical Engineering Academy of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, China
2 School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, Guangzhou, P. R. China
3 School of Life Sciences, Center for Protein Science and Crystallography, The Chinese University of Hong Kong, Hong Kong, P. R. China
4 The First Affiliated Hospital of Chinese Medicine, Guangzhou University of Chinese Medicine, Guangzhou, P. R. China
5 Key Laboratory of Ministry of Education, Research Center of Chinese Herbal Resources and Engineering, Guangzhou University of Chinese Medicine, Guangzhou, P.R China
6 Dongguan Mathematical Engineering Academy of Chinese Medicine, Guangzhou University of Chinese Medicine, Dongguan, P. R. China
7 Guangdong Provincial Key Laboratory of Clinical Research on Traditional Chinese Medicine Syndrome, The Second Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, P. R. China
* These authors have contributed equally to this work
Correspondence to:
Ziren Su, email: [email protected]
Jianhui Xie, email: [email protected]
Keywords: coptisine; Helicobacter pylori urease; sulfhydryl group; nickel ion; UreG
Received: May 18, 2017 Accepted: January 01, 2018 Epub: January 08, 2018
All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 24002