A MODEL FOR COMPOUNDS ACTIVE AGAINST HUMAN RHINOVIRUS-14 BASED ON X-RAY CRYSTALLOGRAPHY DATA

被引:31
作者
DIANA, GD
TREASURYWALA, AM
BAILEY, TR
OGLESBY, RC
PEVEAR, DC
DUTKO, FJ
机构
[1] Sterling Research Group, Rensselaer
关键词
D O I
10.1021/jm00167a006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A number of (oxazolinylphenyl)isoxazoles have been synthesized and tested against human rhinovirus-14 (HRV-14). Several of the more active compounds have been examined by X-ray crystallography and their orientation in the compound binding site on the capsid protein of HRV-14 has been determined. Based on the minimum inhibitory concentration against HRV-14 and the X-ray conformation of the compounds, a model has been developed which distinguishes between the space-filling properties of the active and inactive compounds in this series. The model was generated by overlaying composite structures and comparing the van der Waals generated volume maps. The results of this study indicate that inactive compounds display areas of excessive bulk particularly around the phenyl ring, while the active compounds occupy space below the pore area of the compound binding site. © 1990, American Chemical Society. All rights reserved.
引用
收藏
页码:1306 / 1311
页数:6
相关论文
共 23 条
  • [1] ALKYNE ISOMERIZATION REAGENTS - MIXED ALKALI-METAL AMIDES
    ABRAMS, SR
    [J]. CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1984, 62 (07): : 1333 - 1334
  • [2] STRUCTURAL-ANALYSIS OF A SERIES OF ANTIVIRAL AGENTS COMPLEXED WITH HUMAN RHINOVIRUS-14
    BADGER, J
    MINOR, I
    KREMER, MJ
    OLIVEIRA, MA
    SMITH, TJ
    GRIFFITH, JP
    GUERIN, DMA
    KRISHNASWAMY, S
    LUO, M
    ROSSMANN, MG
    MCKINLAY, MA
    DIANA, GD
    DUTKO, FJ
    FANCHER, M
    RUECKERT, RR
    HEINZ, BA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (10) : 3304 - 3308
  • [4] BAILEY TR, 1987, 193RD NAT ACS M DENV
  • [5] BILTZ H, 1904, CHEM BER, V37, P4031
  • [6] BRAZIER SA, 1912, J CHEM SOC, V101, P974
  • [7] OXAZOL-SYNTHESEN AUS ALPHA-HALOGEN-KETONEN .4. FORMAMID-REAKTIONEN
    BREDERECK, H
    GOMPPER, R
    [J]. CHEMISCHE BERICHTE-RECUEIL, 1954, 87 (05): : 700 - 707
  • [8] CHARPENT.M, 1968, B SOC CHIM FR, P685
  • [9] STRUCTURE-ACTIVITY STUDIES OF 5-[[4-(4,5-DIHYDRO-2-OXAZOLYL)PHENOXY]ALKYL]-3-METHYLISOXAZOLES - INHIBITORS OF PICORNAVIRUS UNCOATING
    DIANA, GD
    OGLESBY, RC
    AKULLIAN, V
    CARABATEAS, PM
    CUTCLIFFE, D
    MALLAMO, JP
    OTTO, MJ
    MCKINLAY, MA
    MALISKI, EG
    MICHALEC, SJ
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1987, 30 (02) : 383 - 388
  • [10] SYNTHESIS AND STRUCTURE ACTIVITY STUDIES OF SOME DISUBSTITUTED PHENYLISOXAZOLES AGAINST HUMAN PICORNAVIRUS
    DIANA, GD
    CUTCLIFFE, D
    OGLESBY, RC
    OTTO, MJ
    MALLAMO, JP
    AKULLIAN, V
    MCKINLAY, MA
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (02) : 450 - 455