STRUCTURE-BASED DRUG DESIGN

被引:62
作者
COLMAN, PM
机构
[1] Biomolecular Research Institute, Parkville, 3052
关键词
D O I
10.1016/0959-440X(94)90268-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There are now many successful examples of the design of new ligands based on knowledge of target protein structures. In most cases those ligands are unsuitable as drugs because of problems of toxicity, stability or bioavailability. The past twelve months have also seen the description of the structures of many proteins which are either known to be targets for existing drugs or have clear potential to be utilized in therapy.
引用
收藏
页码:868 / 874
页数:7
相关论文
共 66 条
  • [1] STRUCTURE-BASED DESIGN OF A CYCLOPHILIN-CALCINEURIN BRIDGING LIGAND
    ALBERG, DG
    SCHREIBER, SL
    [J]. SCIENCE, 1993, 262 (5131) : 248 - 250
  • [2] PICORNAVIRAL 3C CYSTEINE PROTEINASES HAVE A FOLD SIMILAR TO CHYMOTRYPSIN-LIKE SERINE PROTEINASES
    ALLAIRE, M
    CHERNAIA, MM
    MALCOLM, BA
    JAMES, MNG
    [J]. NATURE, 1994, 369 (6475) : 72 - 76
  • [3] SYNTHESIS OF SOME NOVEL POTENT AND SELECTIVE CATECHOL O-METHYLTRANSFERASE INHIBITORS
    BACKSTROM, R
    HONKANEN, E
    PIPPURI, A
    KAIRISALO, P
    PYSTYNEN, J
    HEINOLA, K
    NISSINEN, E
    LINDEN, IB
    MANNISTO, PT
    KAAKKOLA, S
    POHTO, P
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (04) : 841 - 846
  • [4] ENDOTHELIAL-LEUKOCYTE ADHESION MOLECULES
    BEVILACQUA, MP
    [J]. ANNUAL REVIEW OF IMMUNOLOGY, 1993, 11 : 767 - 804
  • [5] METALLOPROTEINASE SUPER-FAMILIES AND DRUG DESIGN
    BLUNDELL, TL
    [J]. NATURE STRUCTURAL BIOLOGY, 1994, 1 (02): : 73 - 75
  • [6] THE X-RAY CRYSTAL-STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN NEUTROPHIL COLLAGENASE INHIBITED BY A SUBSTRATE-ANALOG REVEALS THE ESSENTIALS FOR CATALYSIS AND SPECIFICITY
    BODE, W
    REINEMER, P
    HUBER, R
    KLEINE, T
    SCHNIERER, S
    TSCHESCHE, H
    [J]. EMBO JOURNAL, 1994, 13 (06) : 1263 - 1269
  • [7] INHIBITION OF THE FUSION-INDUCING CONFORMATIONAL CHANGE OF INFLUENZA HEMAGGLUTININ BY BENZOQUINONES AND HYDROQUINONES
    BODIAN, DL
    YAMASAKI, RB
    BUSWELL, RL
    STEARNS, JF
    WHITE, JM
    KUNTZ, ID
    [J]. BIOCHEMISTRY, 1993, 32 (12) : 2967 - 2978
  • [8] STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN FIBROBLAST COLLAGENASE COMPLEXED WITH AN INHIBITOR
    BORKAKOTI, N
    WINKLER, FK
    WILLIAMS, DH
    DARCY, A
    BROADHURST, MJ
    BROWN, PA
    JOHNSON, WH
    MURRAY, EJ
    [J]. NATURE STRUCTURAL BIOLOGY, 1994, 1 (02): : 106 - 110
  • [9] DESIGN OF ORALLY-ACTIVE, NONPEPTIDIC INHIBITORS OF HUMAN-LEUKOCYTE ELASTASE
    BROWN, FJ
    ANDISIK, DW
    BERNSTEIN, PR
    BRYANT, CB
    CECCARELLI, C
    DAMEWOOD, JR
    WOOLSON, SA
    EDWARDS, PD
    EARLEY, RA
    FEENEY, S
    GREEN, RC
    GOMES, B
    KOSMIDER, BJ
    KRELL, RD
    SHAW, A
    STEELMAN, GB
    THOMAS, RN
    VACEK, EP
    VEALE, CA
    TUTHILL, PA
    WARNER, P
    WILLIAMS, JC
    WOLANIN, DJ
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (09) : 1259 - 1261
  • [10] DRUGS BY DESIGN
    BUGG, CE
    CARSON, WM
    MONTGOMERY, JA
    [J]. SCIENTIFIC AMERICAN, 1993, 269 (06) : 92 - 98