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Volumn 38, Issue 7, 1995, Pages 1060-1066

Cross-Validated R2-Guided Region Selection for Comparative Molecular Field Analysis: A Simple Method To Achieve Consistent Results

Author keywords

[No Author keywords available]

Indexed keywords

CEPHALOTAXINE; DEOXYHARRINGTONINE; HARRINGTONINE; HARRINGTONINE DERIVATIVE; HOMOHARRINGTONINE; ISOHARRINGTONINE; LIGAND; PROTEINASE INHIBITOR; SEROTONIN 1A RECEPTOR; STEROID; SEROTONIN RECEPTOR;

EID: 0029655006     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm00007a003     Document Type: Article
Times cited : (299)

References (10)
  • 1
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    • Comparative Molecular Field Analysis (CoMFA). 1. Effect of Shape on Binding of Steroids to Carrier Proteins
    • Cramer, R. D., III; Patterson, D. E.; Bunce, J. D. Comparative Molecular Field Analysis (CoMFA). 1. Effect of Shape on Binding of Steroids to Carrier Proteins. J. Am. Chem. Soc. 1988, 110, 5959-5967.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5959-5967
    • Cramer, R.D.1    Patterson, D.E.2    Bunce, J.D.3
  • 3
    • 0002825636 scopus 로고
    • Applications of CoMFA and Related 3D QSAR Approaches
    • Kubinyi, H., Ed.; ESCOM: Leiden
    • Thibaut, U. Applications of CoMFA and Related 3D QSAR Approaches. In 3D QSAR in Drug Design: Theory, Methods, and Applications; Kubinyi, H., Ed.; ESCOM: Leiden, 1993; pp 661-696.
    • (1993) 3D QSAR in Drug Design: Theory, Methods, and Applications , pp. 661-696
    • Thibaut, U.1
  • 4
    • 0027771934 scopus 로고
    • Three-Dimensional Quantitative Structure- Activity Relationships of 5-HT Receptor Binding Data for Tetrahydropyridinylindole Derivatives: A Comparison of the Hansch and CoMFA Methods
    • Agarwal, A.; Pearson, P. P.; Taylor, E. W.; Li, H. B.; Dahlgren, T.; Herslof, M.; Yang, Y.; Lambert, G.; Nelson, D. L.; Regan, J. W.; Martin, A. R. Three-Dimensional Quantitative Structure- Activity Relationships of 5-HT Receptor Binding Data for Tetrahydropyridinylindole Derivatives: A Comparison of the Hansch and CoMFA Methods. J. Med. Chem. 1993, 36, 4006-4014.
    • (1993) J. Med. Chem. , vol.36 , pp. 4006-4014
    • Agarwal, A.1    Pearson, P.P.2    Taylor, E.W.3    Li, H.B.4    Dahlgren, T.5    Herslof, M.6    Yang, Y.7    Lambert, G.8    Nelson, D.L.9    Regan, J.W.10    Martin, A.R.11
  • 5
    • 0016813876 scopus 로고
    • Harringtonine, an Inhibitor of Initiation of Protein Biosynthesis
    • Huang, M. T. Harringtonine, an Inhibitor of Initiation of Protein Biosynthesis. Mol. Pharmacol. 1975, 11, 511-519.
    • (1975) Mol. Pharmacol. , vol.11 , pp. 511-519
    • Huang, M.T.1
  • 6
    • 84912099528 scopus 로고
    • 3-D QSAR for Intrinsic Activity of 5-HTIA Receptor Ligands by the Method of Comparative Molecular Field Analysis
    • Taylor, E. W.; Agarwal, A. 3-D QSAR for Intrinsic Activity of 5-HTIA Receptor Ligands by the Method of Comparative Molecular Field Analysis. J. Comput. Chem. 1993, 14, 237-245.
    • (1993) J. Comput. Chem. , vol.14 , pp. 237-245
    • Taylor, E.W.1    Agarwal, A.2
  • 7
    • 0027762073 scopus 로고
    • Three-Dimensional QSAR of Human Immunodeficiency Virus (I) Protease Inhibitors. 1. A CoMFA Study Employing Experi-mentally-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 Experi-mentally-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
  • 10
    • 0027310371 scopus 로고
    • Generating Optimal Linear PLS Estimations (GOLPE): An Advanced Chemometric Tool for Handling 3D- QSAR Problems
    • Baroni, M.; Costantino, G.; Cruciani, G.; Riganelli, D.; Valigi, R.; Clementi, S. Generating Optimal Linear PLS Estimations (GOLPE): An Advanced Chemometric Tool for Handling 3D- QSAR Problems. Quant. Struct.-Act. Rel. 1993, 12, 9-20.
    • (1993) Quant. Struct.-Act. Rel. , vol.12 , pp. 9-20
    • Baroni, M.1    Costantino, G.2    Cruciani, G.3    Riganelli, D.4    Valigi, R.5    Clementi, S.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.