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Volumn 20, Issue 3, 2010, Pages 1241-1246

Synthesis and biological evaluation of novel allophenylnorstatine-based HIV-1 protease inhibitors incorporating high affinity P2-ligands

Author keywords

Allophenylnorstatine; Darunavir; Design; HIV protease; Inhibitors; Synthesis

Indexed keywords

ALLOPHENYLNORSTATINE; AMPRENAVIR; ANTIVIRUS AGENT; ATAZANAVIR; DARUNAVIR; GRL 02031; GRL 06579; PROTEIN P2; PROTEINASE INHIBITOR; TMC 126; UNCLASSIFIED DRUG; 3-AMINO-2-HYDROXY-4-PHENYLBUTANOIC ACID; ARYLBUTYRIC ACID DERIVATIVE; FURAN DERIVATIVE; HUMAN IMMUNODEFICIENCY VIRUS PROTEINASE; HUMAN IMMUNODEFICIENCY VIRUS PROTEINASE INHIBITOR; LIGAND; P16 PROTEASE, HUMAN IMMUNODEFICIENCY VIRUS 1; PROTEIN BINDING; TETRAHYDROFURAN;

EID: 74049090865     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2009.11.123     Document Type: Article
Times cited : (15)

References (27)
  • 12
    • 84924255825 scopus 로고    scopus 로고
    • note
    • (a) FDA approved Darunavir on June 23, 2006: FDA approved new HIV treatment for patients who do not respond to existing drugs. Please see: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2006/ucm108676.htm (b) On October 21, 2008, FDA granted traditional approval to Prezista (darunavir), co-administered with ritonavir and with other antiretroviral agents, for the treatment of HIV-1 infection in treatment-experienced adult patients. In addition to the traditional approval, a new dosing regimen for treatment-naïve patients was approved.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.