Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1–P2 scaffold-Reference-Cited by-同舟云学术

Potent inhibitors of the HIV-1 protease incorporating cyclic urea P1–P2 scaffold

Published:2004-11 Issue:22 Volume:14 Page:5685-5687
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Kazmierski Wieslaw M.,Furfine Eric,Gray-Nunez Yolanda,Spaltenstein Andrew,Wright Lois

Publisher

Elsevier BV

Subject

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

Reference10 articles.

1. Novel inhibitors of HIV protease

2. Kazmierski, W.; Andrews, W.; Baker, C.; Bock, B.; Cleary, D.; Furfine, E.; Gray-Nunez, Y.; Hale, M.; Hazen, R.; Salituro, F.; Schairer, W.; Spaltenstein, A.; Tung, R.; Wright, L. Book of Abstracts, 219th ACS National Meeting, San Francisco, CA, March 26–30, 2000; poster MEDI-126

3. Novel spirocyclic pyrrolidones as P2/P1 mimetics in potent inhibitors of HIV-1 protease

4. Novel and Efficient Synthesis of Spirocyclic Morpholinones as Precursors of ψ[CH2O] Dipeptide Isosteres

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