Modification and biological evaluation of novel 4-hydroxy-pyrone derivatives as non-peptidic HIV-1 protease inhibitors-Reference-Cited by-同舟云学术

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Modification and biological evaluation of novel 4-hydroxy-pyrone derivatives as non-peptidic HIV-1 protease inhibitors

Published:2010-02-02 Issue:2 Volume:20 Page:200-209
ISSN:1054-2523
Container-title:Medicinal Chemistry Research
language:en
Short-container-title:Med Chem Res

Author:

He Meizi,Yang Ning,Sun Chunlai,Yao Xiaojian,Yang Ming

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Link

http://link.springer.com/content/pdf/10.1007/s00044-010-9307-4.pdf

Reference23 articles.

1. Chien AI, Liao WH, Yang DM, Wang CT (2006) A domain directly C-terminal to the major homology region of human immunodeficiency type 1 capsid protein plays a crucial role in directing both virus assembly and incorporation of Gag-Pol. Virology 348:84–95

2. Huang XQ, Xu LS, Luo XM, Fan KN, Ji RY, Pei G, Chen KX, Jiang HL (2002) Elucidating the inhibiting mode of AHPBA derivatives against HIV-1 protease and building predictive 3D-QSAR models. J Med Chem 45:333–343

3. Huff JR (1991) HIV protease: a novel chemotherapeutic target for AIDS. J Med Chem 34:2305–2314

4. Lebon F, Ledecq M (2000) Approaches to the design of effective HIV-1 protease inhibitors. Curr Med Chem 7:455–477

5. Leung D, Abbenante G, Fairlie DP (2000) Protease inhibitors: current status and future prospects. J Med Chem 43:305–341

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