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Volumn 39, Issue 21, 1996, Pages 4299-4312

HIV protease inhibitory bis-benzamide cyclic ureas: A quantitative structure-activity relationship analysis

Author keywords

[No Author keywords available]

Indexed keywords

BENZAMIDE DERIVATIVE; PROTEINASE INHIBITOR; UREA DERIVATIVE;

EID: 0029797080     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9602773     Document Type: Article
Times cited : (37)

References (29)
  • 1
    • 0028803422 scopus 로고
    • Current Status of the Development of HIV Protease Inhibitors and Their Clinical Potential
    • Ueno, T.; Mitsuya, H. Current Status of the Development of HIV Protease Inhibitors and Their Clinical Potential. Clin, Immunother. 1995, 4, 451-461.
    • (1995) Clin, Immunother. , vol.4 , pp. 451-461
    • Ueno, T.1    Mitsuya, H.2
  • 5
    • 0000948129 scopus 로고
    • Blatt, A. H., Ed.; John Wiley & Sons: New York
    • Noller, C. M. In Organic Synthesis Collective Volume; Blatt, A. H., Ed.; John Wiley & Sons: New York, 1943; Collect. Vol. II, p 586.
    • (1943) Organic Synthesis Collective Volume , vol.2 COLLECT. VOL , pp. 586
    • Noller, C.M.1
  • 6
    • 0029012283 scopus 로고
    • A Propos de l'Estérification des Acides Carboxyliques par le BOP ou le PyBOP. (Esterification of carboxylic acids by BOP or PyBOP.)
    • Coste, J.; Campagne, J.-M. A Propos de l'Estérification des Acides Carboxyliques par le BOP ou le PyBOP. (Esterification of carboxylic acids by BOP or PyBOP.) Tetrahedron Lett. 1995, 36, 4253-4256.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 4253-4256
    • Coste, J.1    Campagne, J.-M.2
  • 7
    • 49349137641 scopus 로고
    • A Mild, General Method for Conversion of Esters to Amides
    • Basha, A.; Lipton, M.; Weinreb, S. M. A Mild, General Method for Conversion of Esters to Amides. Tetrahedron Lett. 1977, 4171-4174.
    • (1977) Tetrahedron Lett. , pp. 4171-4174
    • Basha, A.1    Lipton, M.2    Weinreb, S.M.3
  • 8
    • 0025641617 scopus 로고
    • Stability and Activity of Human Immunodeficiency Virus Protease: Comparison of the Natural Dimer with a Homologous, Single-chain Tethered Dimer
    • Cheng, Y.-S. E.; Yin, F. H.; Foundling, S.; Blomstrom, D.; Kettner, C. A. Stability and Activity of Human Immunodeficiency Virus Protease: Comparison of the Natural Dimer with a Homologous, Single-chain Tethered Dimer. Proc. Natl. Acad. Sci. U.S.A. 1990, 87, 9660-9664.
    • (1990) Proc. Natl. Acad. Sci. U.S.A. , vol.87 , pp. 9660-9664
    • Cheng, Y.-S.E.1    Yin, F.H.2    Foundling, S.3    Blomstrom, D.4    Kettner, C.A.5
  • 10
    • 0028235440 scopus 로고
    • An Assay for HIV RNA in Infected Cell Lysates, and Its Use for the Rapid Evaluation of Antiviral Efficacy
    • Bacheler, L.; Paul, M.; Otto, M. J.; Jadhav, P. K.; Stone, B. A.; Miller, J. A. An Assay for HIV RNA in Infected Cell Lysates, and Its Use for the Rapid Evaluation of Antiviral Efficacy. Antiviral Chem. Chemother. 1994, 5, 111-121.
    • (1994) Antiviral Chem. Chemother. , vol.5 , pp. 111-121
    • Bacheler, L.1    Paul, M.2    Otto, M.J.3    Jadhav, P.K.4    Stone, B.A.5    Miller, J.A.6
  • 11
    • 0025390935 scopus 로고
    • MOPAC: A Semiemperical Molecular Orbital Program
    • Steward, J. J. P. MOPAC: A Semiemperical Molecular Orbital Program. J. Comput.-Aided Mol. Des. 1990, 4, 1-105.
    • (1990) J. Comput.-Aided Mol. Des. , vol.4 , pp. 1-105
    • Steward, J.J.P.1
  • 12
    • 0027762073 scopus 로고
    • Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules
    • Waller, C. L.; Oprea, T. I.; Giolitti, A.; Marshall, G. R. Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experimentally-Determined Alignment Rules. J. Med. Chem. 1993, 36, 4152-4160.
    • (1993) J. Med. Chem. , vol.36 , pp. 4152-4160
    • Waller, C.L.1    Oprea, T.I.2    Giolitti, A.3    Marshall, G.R.4
  • 13
    • 0028237444 scopus 로고
    • Three-Dimensional Quantitative Structure-Activity Relationship of Human Immunodeficiency Virus (I) Protease Inhibitors. 2. Predictive Power Using Limited Exploration of Alternate Binding Modes
    • Oprea, T. I.; Waller, C. L.; Marshall, G. R. Three-Dimensional Quantitative Structure-Activity Relationship of Human Immunodeficiency Virus (I) Protease Inhibitors. 2. Predictive Power Using Limited Exploration of Alternate Binding Modes. J. Med. Chem. 1994, 37, 2206-2215.
    • (1994) J. Med. Chem. , vol.37 , pp. 2206-2215
    • Oprea, T.I.1    Waller, C.L.2    Marshall, G.R.3
  • 14
    • 5344247073 scopus 로고
    • Field and Resonance Components of Substituent Effects
    • Swain, C. G.; Lupton, E. C., Jr. Field and Resonance Components of Substituent Effects. J. Am. Chem. Soc. 1968, 90, 4328-4337.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 4328-4337
    • Swain, C.G.1    Lupton Jr., E.C.2
  • 18
    • 0015816824 scopus 로고
    • "Aromatic" Substituent Constants for Structure-Activity Correlations
    • Hansch, C.; Leo, A.; Unger, S. H.; Kim, K. H.; Nikaitani, D.; Lien, E. J. "Aromatic" Substituent Constants for Structure-Activity Correlations. J. Med. Chem. 1973, 16, 1207-1216.
    • (1973) J. Med. Chem. , vol.16 , pp. 1207-1216
    • Hansch, C.1    Leo, A.2    Unger, S.H.3    Kim, K.H.4    Nikaitani, D.5    Lien, E.J.6
  • 19
    • 0015417054 scopus 로고
    • Chance Correlations in Structure-Activity Studies Using Multiple Regression Analysis
    • Topliss, J. G.; Costello, R. J. Chance Correlations in Structure-Activity Studies Using Multiple Regression Analysis. J. Med. Chem. 1972, 15, 1066-1068.
    • (1972) J. Med. Chem. , vol.15 , pp. 1066-1068
    • Topliss, J.G.1    Costello, R.J.2
  • 20
    • 0018709674 scopus 로고
    • Chance Factors in Studies of Quantitative Structure-Activity Relationships
    • Topliss, J. G.; Edwards, R. P. Chance Factors in Studies of Quantitative Structure-Activity Relationships. J. Med. Chem. 1979, 22, 1238-1244.
    • (1979) J. Med. Chem. , vol.22 , pp. 1238-1244
    • Topliss, J.G.1    Edwards, R.P.2
  • 22
    • 0001649445 scopus 로고
    • Kubinyi, H., Ed.; ESCOM: Leiden
    • Kim, K. H. In 3D QSAR in Drug Design; Kubinyi, H., Ed.; ESCOM: Leiden, 1993; pp 619-642.
    • (1993) 3D QSAR in Drug Design , pp. 619-642
    • Kim, K.H.1
  • 24
    • 10244250176 scopus 로고    scopus 로고
    • note
    • Test-1- test-8 were synthesized contemporaneously with this study and not used to generate the regression models. They were used to test the predictability of eqs 3 and 4. Test-1 and -2 are characterized in the Experimental Section. Test-3-test-8 are the subject of another publication (manuscript in preparation) by P. K. Jadhav of these laboratories.
  • 25
    • 0028877042 scopus 로고
    • Weak Binding of VX-478 to Human Plasma Proteins and Implications for Anti-Human Immunodeficiency Virus Therapy
    • Livington, D. J.; Pazhanisamy, S,; Porter, D. J.; Partaledis, J A.; Tung, R. D.; Painter, G. R. Weak Binding of VX-478 to Human Plasma Proteins and Implications for Anti-Human Immunodeficiency Virus Therapy. J. Infect. Dis. 1995, 172, 238-245.
    • (1995) J. Infect. Dis. , vol.172 , pp. 238-245
    • Livington, D.J.1    Pazhanisamy, S.2    Porter, D.J.3    Partaledis, J.A.4    Tung, R.D.5    Painter, G.R.6
  • 29
    • 0029011730 scopus 로고
    • Toward Improved Anti-HIV Chemotherapy: Therapeutic Strategies for Intervention with HIV Infections
    • De Clercq, E. Toward Improved Anti-HIV Chemotherapy: Therapeutic Strategies for Intervention with HIV Infections. J. Med. Chem. 1995, 38, 2491-2517.
    • (1995) J. Med. Chem. , vol.38 , pp. 2491-2517
    • De Clercq, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.