INHIBITORS OF PROTEIN-KINASE-C .3. POTENT AND HIGHLY SELECTIVE BISINDOLYLMALEIMIDES BY CONFORMATIONAL RESTRICTION

被引:167
作者
BIT, RA [1 ]
DAVIS, PD [1 ]
ELLIOTT, LH [1 ]
HARRIS, W [1 ]
HILL, CH [1 ]
KEECH, E [1 ]
KUMAR, H [1 ]
LAWTON, G [1 ]
MAW, A [1 ]
NIXON, JS [1 ]
VESEY, DR [1 ]
WADSWORTH, J [1 ]
WILKINSON, SE [1 ]
机构
[1] ROCHE PROD LTD,RES CTR,BROADWATER RD,WELWYN GARDEN CIT AL7 3AY,HERTS,ENGLAND
关键词
D O I
10.1021/jm00053a003
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The protein kinase inhibitor staurosporine has been used to design a series of selective bisindolylmaleimide inhibitors of protein kinase C (PKC). Guided by molecular graphics, conformational restriction of the cationic side chain has led to ATP competitive inhibitors of improved potency and selectivity. Two compounds have been further evaluated and were shown to inhibit PKC of human origin and prevent T-cell activation in a human allogeneic mixed lymphocyte reaction. One of these compounds was orally absorbed in mice and antagonized a phorbol ester induced paw edema in a dose-dependent manner. This compound also selectively inhibited the secondary T-cell mediated response in a developing adjuvant arthritis model in rats and provides evidence for the potential use of PKC inhibitors as therapeutic immunomodulators.
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页码:21 / 29
页数:9
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共 33 条
  • [1] ADELSTEIN RS, 1981, J BIOL CHEM, V256, P7501
  • [2] PROTEIN KINASE-C AND T-CELL ACTIVATION
    BERRY, N
    NISHIZUKA, Y
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1990, 189 (02): : 205 - 214
  • [3] A DIECKMANN/RING EXPANSION APPROACH TO TETRAHYDROPYRIDO[1,2-A]INDOLES AND TETRAHYDROAZEPINO[1,2-A]INDOLES
    BIT, RA
    DAVIS, PD
    HILL, CH
    KEECH, E
    VESEY, DR
    [J]. TETRAHEDRON, 1991, 47 (26) : 4645 - 4664
  • [4] ACTIVATORS OF PROTEIN KINASE-C DOWN-REGULATE AND PHOSPHORYLATE THE T3/T-CELL ANTIGEN RECEPTOR COMPLEX OF HUMAN LYMPHOCYTES-T
    CANTRELL, DA
    DAVIES, AA
    CRUMPTON, MJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (23) : 8158 - 8162
  • [5] POTENT SELECTIVE INHIBITORS OF PROTEIN KINASE-C
    DAVIS, PD
    HILL, CH
    KEECH, E
    LAWTON, G
    NIXON, JS
    SEDGWICK, AD
    WADSWORTH, J
    WESTMACOTT, D
    WILKINSON, SE
    [J]. FEBS LETTERS, 1989, 259 (01) : 61 - 63
  • [6] INHIBITORS OF PROTEIN-KINASE-C .2. SUBSTITUTED BISINDOLYMALEIMIDES WITH IMPROVED POTENCY AND SELECTIVITY
    DAVIS, PD
    ELLIOTT, LH
    HARRIS, W
    HILL, CH
    HURST, SA
    KEECH, E
    KUMAR, MKH
    LAWTON, G
    NIXON, JS
    WILKINSON, SE
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (06) : 994 - 1001
  • [7] DAVIS PD, 1990, TETRAHEDRON LETT, V31, P2353
  • [8] A MILD CONVERSION OF MALEIC ANHYDRIDES INTO MALEIMIDES
    DAVIS, PD
    BIT, RA
    [J]. TETRAHEDRON LETTERS, 1990, 31 (36) : 5201 - 5204
  • [9] THE DESIGN OF INHIBITORS OF PROTEIN-KINASE-C - THE SOLUTION CONFORMATION OF STAUROSPORINE
    DAVIS, PD
    HILL, CH
    THOMAS, WA
    WHITCOMBE, IWA
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1991, (03) : 182 - 184
  • [10] INHIBITORS OF PROTEIN-KINASE-C .1. 2,3-BISARYLMALEIMIDES
    DAVIS, PD
    HILL, CH
    LAWTON, G
    NIXON, JS
    WILKINSON, SE
    HURST, SA
    KEECH, E
    TURNER, SE
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (01) : 177 - 184