Design, synthesis and antiviral activity of novel pyridazines-Reference-Cited by-同舟云学术

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Design, synthesis and antiviral activity of novel pyridazines

Published:2012-08 Issue: Volume:54 Page:33-41
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Wang Ziwen,Wang Mingxiao,Yao Xue,Li Yue,Tan Juan,Wang Lizhong,Qiao Wentao,Geng Yunqi,Liu Yuxiu,Wang Qingmin

Funder

Chinese Ministry of Health

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference27 articles.

1. HIV-1 integrase inhibitors: update and perspectives;Pommier;Nat. Rev. Drug Discov.,2005

2. Structure-based HIV-1 integrase inhibitor design: a future perspective;Neamati;Expert Opin. Invest. Drugs,2001

3. HIV integrase inhibitors as therapeutic agents in AIDS;Nair;Rev. Med. Virol.,2007

4. Discovery of raltegravir, a potent, selective orally bioavailable HIV-integrase inhibitor for the treatment of HIV-AIDS infection;Summa;J. Med. Chem.,2008

5. Quinolone carboxylic acids as a novel monoketo acid class of human immunodeficiency virus type 1 integrase inhibitors;Sato;J. Med. Chem.,2009

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