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Volumn 46, Issue 9, 2003, Pages 1764-1768

Reduction of peptide character of HIV protease inhibitors that exhibit nanomolar potency against multidrug resistant HIV-1 strains

Author keywords

[No Author keywords available]

Indexed keywords

AMPRENAVIR; INDINAVIR; NELFINAVIR; PROTEINASE INHIBITOR; SAQUINAVIR; TYA5; TYB1; TYB5; UNCLASSIFIED DRUG; ZIDOVUDINE;

EID: 0344519605     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm020537i     Document Type: Article
Times cited : (54)

References (21)
  • 1
    • 0025361445 scopus 로고
    • Hydroxyethylamine analogues of the p17/p24 substrate cleavage site are tight-binding inhibitors of HIV protease
    • Rich, D. H.; Green, J.; Toth, M. V.; Marshall, G. R.; Kent, S. B. H. Hydroxyethylamine Analogues of the p17/p24 Substrate Cleavage Site Are Tight-Binding Inhibitors of HIV Protease. J. Med. Chem. 1990, 33, 1285-1288.
    • (1990) J. Med. Chem. , vol.33 , pp. 1285-1288
    • Rich, D.H.1    Green, J.2    Toth, M.V.3    Marshall, G.R.4    Kent, S.B.H.5
  • 6
    • 0028846226 scopus 로고
    • Crystal structure of HIV-1 protease in complex with VX-478, a potent and orally bioavailable inhibitor of the enzyme
    • Kim, E. E.; Baker, C. T.; Dwyer, M. D.; Murko, M. A.; Rao, B. G.; Tung, R. D.; Navia, M. R. Crystal Structure of HIV-1 Protease in Complex with VX-478, a Potent and Orally Bioavailable Inhibitor of the Enzyme. J. Am. Chem. Soc. 1995, 117, 1181-1182.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 1181-1182
    • Kim, E.E.1    Baker, C.T.2    Dwyer, M.D.3    Murko, M.A.4    Rao, B.G.5    Tung, R.D.6    Navia, M.R.7
  • 10
    • 0002052695 scopus 로고    scopus 로고
    • Discovery and development of antiretroviral therapeutics for HIV infection
    • Merigan, T. C., Bartlett, J. G., Bolognesi, D., Eds.; Williams & Wilkins: Baltimore
    • Mitsuya, H.; Erickson, J. Discovery and Development of Antiretroviral Therapeutics for HIV Infection. In Textbook of AIDS Medicine; Merigan, T. C., Bartlett, J. G., Bolognesi, D., Eds.; Williams & Wilkins: Baltimore, 1999; pp 751-780.
    • (1999) Textbook of AIDS Medicine , pp. 751-780
    • Mitsuya, H.1    Erickson, J.2
  • 12
    • 0036006409 scopus 로고    scopus 로고
    • Efficient stereo-selective synthesis of peptidomimetics containing hydroxyethylamine dipeptide isosteres utilizing the Aza-Payne rearrangement and O, N-Acyl transfer reactions
    • Tamamura, H.; Hori, T.; Otaka, A.; Fujii, N. Efficient Stereo-selective Synthesis of Peptidomimetics Containing Hydroxyethylamine Dipeptide Isosteres Utilizing the Aza-Payne Rearrangement and O, N-Acyl Transfer Reactions. J. Chem. Soc., Perkin Trans. 1 2002, 577-580.
    • (2002) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 577-580
    • Tamamura, H.1    Hori, T.2    Otaka, A.3    Fujii, N.4
  • 17
    • 33746385828 scopus 로고    scopus 로고
    • Regiospecific ring-opening reactions of β-aziridinyl α,β-enoates with acids: Application to the stereoselective synthesis of a couple of diastereoisomeric (E)-alkene dipeptide isosteres from a single β-aziridinyl α,β-enoate and to the convenient preparation of amino alcohols bearing α,β-unsaturated ester groups
    • Tamamura, H.; Yamashita, M.; Nakajima, Y.; Sakano, K.; Otaka, A.; Ohno, H.; Ibuka, T.; Fujii, N. Regiospecific Ring-opening Reactions of β-Aziridinyl α,β-Enoates with Acids: Application to the Stereoselective Synthesis of a Couple of Diastereoisomeric (E)-Alkene Dipeptide Isosteres from a Single β-Aziridinyl α,β-Enoate and to the Convenient Preparation of Amino Alcohols Bearing α,β-Unsaturated Ester Groups. J. Chem. Soc., Perkin Trans. 1 1999, 2983-2996.
    • (1999) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 2983-2996
    • Tamamura, H.1    Yamashita, M.2    Nakajima, Y.3    Sakano, K.4    Otaka, A.5    Ohno, H.6    Ibuka, T.7    Fujii, N.8
  • 18
    • 0036145503 scopus 로고    scopus 로고
    • A potent human immunodeficiency virus type 1 protease inhibitor, UIC-94003 (TMC-126), and selection of a novel (A28S) mutation in the protease active site
    • Yoshimura, K.; Kato, R.; Kavlick, M. F.; Nguyen, A.; Maroun, V.; Maeda, K.; Hussain, K. A.; Ghosh, A. K.; Gulnik, S. V.; Erickson, J. W.; Mitsuya, H. A Potent Human Immunodeficiency Virus Type 1 Protease Inhibitor, UIC-94003 (TMC-126), and Selection of a Novel (A28S) Mutation in the Protease Active Site. J. Virol. 2002, 76, 1349-1358.
    • (2002) J. Virol. , vol.76 , pp. 1349-1358
    • Yoshimura, K.1    Kato, R.2    Kavlick, M.F.3    Nguyen, A.4    Maroun, V.5    Maeda, K.6    Hussain, K.A.7    Ghosh, A.K.8    Gulnik, S.V.9    Erickson, J.W.10    Mitsuya, H.11
  • 19
    • 0032576977 scopus 로고    scopus 로고
    • Bactericidal domain of lactoferrin: Detection, quantitation and characterization of lactoferricin in serum by SELDI affinity mass spectrometry
    • Kuwata, H.; Yip, T.-T.; Yip, C. L.; Tomita, M.; Hutchens, T. W. Bactericidal Domain of Lactoferrin: Detection, Quantitation and Characterization of Lactoferricin in Serum by SELDI Affinity Mass Spectrometry. Biochem. Biophys. Res. Commun. 1998, 245, 764-773.
    • (1998) Biochem. Biophys. Res. Commun. , vol.245 , pp. 764-773
    • Kuwata, H.1    Yip, T.-T.2    Yip, C.L.3    Tomita, M.4    Hutchens, T.W.5
  • 20
    • 0035964269 scopus 로고    scopus 로고
    • Subsite specificity of memapsin 2 (β-secretase): Implications for inhibitor design
    • Turner, R. T., III.; Koelsch, G.; Hong, L.; Castanheira, P.; Ghosh, A.; Tang, J. Subsite Specificity of Memapsin 2 (β-Secretase): Implications for Inhibitor Design. Biochemistry 2001, 40, 10001-10006.
    • (2001) Biochemistry , vol.40 , pp. 10001-10006
    • Turner R.T. III1    Koelsch, G.2    Hong, L.3    Castanheira, P.4    Ghosh, A.5    Tang, J.6
  • 21
    • 0036393768 scopus 로고    scopus 로고
    • Discovery of nonpeptide, peptidomimetic peptidase inhibitors that target alternate enzyme active site conformations
    • Rich, D. H.; Bursavich, M. G.; Estiarte, M. A. Discovery of Nonpeptide, Peptidomimetic Peptidase Inhibitors that Target Alternate Enzyme Active Site Conformations. Biopolymers 2002, 66, 115-125.
    • (2002) Biopolymers , vol.66 , pp. 115-125
    • Rich, D.H.1    Bursavich, M.G.2    Estiarte, M.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.