메뉴 건너뛰기




Volumn 2, Issue 11, 2003, Pages 857-858

Atazanavir sulphate. Market analysis

Author keywords

[No Author keywords available]

Indexed keywords

AMPRENAVIR; ANTIRETROVIRUS AGENT; ATAZANAVIR; DIDANOSINE; EFAVIRENZ; EMTRICITABINE; FORTAVASE; LAMIVUDINE; LOPINAVIR PLUS RITONAVIR; NELFINAVIR; PROTEINASE INHIBITOR; RITONAVIR; RNA DIRECTED DNA POLYMERASE INHIBITOR; SAQUINAVIR; STAVUDINE; TENOFOVIR DISOPROXIL; UNCLASSIFIED DRUG; VIDEX EC; ZIDOVUDINE;

EID: 0242521455     PISSN: 14741776     EISSN: None     Source Type: Journal    
DOI: 10.1038/nrd1232     Document Type: Note
Times cited : (45)

References (8)
  • 1
    • 0037624182 scopus 로고    scopus 로고
    • Twenty years of therapy for HIV-1 infection
    • Pomerantz, R. J. & Horn, D. L. Twenty years of therapy for HIV-1 infection. Nature Med. 9, 867-873 (2003).
    • (2003) Nature Med. , vol.9 , pp. 867-873
    • Pomerantz, R.J.1    Horn, D.L.2
  • 2
    • 0043069555 scopus 로고    scopus 로고
    • Toxicity of antiretroviral therapy and implications for drug development
    • Carr, A. Toxicity of antiretroviral therapy and implications for drug development. Nature Rev. Drug Discov. 2, 624-634 (2003).
    • (2003) Nature Rev. Drug Discov. , vol.2 , pp. 624-634
    • Carr, A.1
  • 3
    • 0029746483 scopus 로고    scopus 로고
    • Aza-peptide analogues as potent human immunodeficiency virus type-1 protease inhibitors with oral bioavailability
    • Fässler, A. et al. Aza-peptide analogues as potent human immunodeficiency virus type-1 protease inhibitors with oral bioavailability J. Med. Chem. 39, 3203-3216 (1996).
    • (1996) J. Med. Chem. , vol.39 , pp. 3203-3216
    • Fässler, A.1
  • 4
    • 0029644476 scopus 로고
    • Comparative analysis of the X-ray structures of HIV-1 and HIV-2 proteases in complex with CGP 53820, a novel pseudosymmetric inhibitor
    • Priestle, J. P. et al. Comparative analysis of the X-ray structures of HIV-1 and HIV-2 proteases in complex with CGP 53820, a novel pseudosymmetric inhibitor. Structure 3, 381-389 (1995).
    • (1995) Structure , vol.3 , pp. 381-389
    • Priestle, J.P.1
  • 5
    • 15144353143 scopus 로고    scopus 로고
    • New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: Candidates for clinical development
    • Bold, G. et al. New aza-dipeptide analogues as potent and orally absorbed HIV-1 protease inhibitors: candidates for clinical development. J. Med. Chem. 41, 3387-3401 (1998).
    • (1998) J. Med. Chem. , vol.41 , pp. 3387-3401
    • Bold, G.1
  • 6
    • 0033931167 scopus 로고    scopus 로고
    • BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents
    • Robinson, B. S. et al. BMS-232632, a highly potent human immunodeficiency virus protease inhibitor that can be used in combination with other available antiretroviral agents. Antimicrob. Agents Chemother. 44, 2093-2099 (2000).
    • (2000) Antimicrob. Agents Chemother. , vol.44 , pp. 2093-2099
    • Robinson, B.S.1
  • 7
    • 0242567884 scopus 로고    scopus 로고
    • FDA Drug Approvals List [online]
    • (cited 9 September 2003)
    • FDA Drug Approvals List [online] (cited 9 September 2003). http://www.fda.gov/cder/foi/label/2003/21567_reyataz_lbl.pdf (2003).
    • (2003)
  • 8
    • 0035833452 scopus 로고    scopus 로고
    • Nelfinavir, efavirenz, or both after the failure of nucleoside treatment of HIV infection
    • Albrecht, M. A. et al. Nelfinavir, efavirenz, or both after the failure of nucleoside treatment of HIV infection. N. Eng. J Med. 345, 398-407 (2001).
    • (2001) N. Eng. J. Med. , vol.345 , pp. 398-407
    • Albrecht, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.