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Cited by 213

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Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity

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Davis, Peter D., Elliott, Lucy H., Harris, William, Hill, Christopher H., Hurst, Steven A., Keech, Elizabeth, Kumar, M. K. Hari, Lawton, Geoffrey, Nixon, John S., Wilkinson, Sandra E.·1992·Journal of Medicinal Chemistry

Abstract

A hypothetical mode of inhibition of protein kinase C (PKC) by the natural product staurosporine has been used as a basis for the design of substituted bisindolylmaleimides with improved potency over the parent compound. Structure-activity relationships were consistent with the interaction of a cationic group in the inhibitor with a carboxylate group in the enzyme, and the most potent compound had a Ki of 3 nM. The inhibitors were competitive with ATP but inhibited cAMP-dependent protein kinase (PKA) only at much higher concentrations despite the extensive sequence homology between the ATP-binding regions of PKA and PKC. Three compounds were evaluated further and found to inhibit a human allogeneic mixed lymphocyte reaction pointing to the potential utility of PKC inhibitors in immunosuppressive therapy. One of these compounds was orally absorbed in the rat and represents an attractive lead in the development of PKC inhibitors as drugs.

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Metadata

Authors
Davis, P. D., Elliott, L. H., Harris, W., Hill, C. H., Hurst, S. A., Keech, E., Kumar, M. K. H., Lawton, G., Nixon, J. S., & Wilkinson, S. E.
Venue
Journal of Medicinal Chemistry
Published
1992-03
Volume
35
Issue
6
Pages
994-1001
ISSN
  • 0022-2623 (ISSN-L)
  • 1520-4804
OpenAlex
W2074002103
Cited by
213
References
0
FWCI
4.45
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity. https://app.cochat.ai/papers/10.1021/jm00084a004
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Davis, P. D., Elliott, L. H., Harris, W., Hill, C. H., Hurst, S. A., Keech, E., Kumar, M. K. H., Lawton, G., Nixon, J. S., & Wilkinson, S. E. (1992). Inhibitors of protein kinase C. 2. Substituted bisindolylmaleimides with improved potency and selectivity. Journal of Medicinal Chemistry. https://doi.org/10.1021/jm00084a004

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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