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Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes

Open access
Maksimoska, Jasna, Feng, Li, Harms, Klaus, Yi, Chunling, Kissil, Joseph, Marmorstein, Ronen, Meggers, Eric·2008·Journal of the American Chemical Society

Abstract

A strategy for targeting protein kinases with large ATP-binding sites by using bulky and rigid octahedral ruthenium complexes as structural scaffolds is presented. A highly potent and selective GSK3 and Pim1 half-sandwich complex NP309 was successfully converted into a PAK1 inhibitor by making use of the large octahedral compounds Lambda-FL172 and Lambda-FL411 in which the cyclopentadienyl moiety of NP309 is replaced by a chloride and sterically demanding diimine ligands. A 1.65 A cocrystal structure of PAK1 with Lambda-FL172 reveals how the large coordination sphere of the ruthenium complex matches the size of the active site and serves as a yardstick to discriminate between otherwise closely related binding sites.

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Metadata

Authors
Maksimoska, J., Feng, L., Harms, K., Yi, C., Kissil, J., Marmorstein, R., & Meggers, E.
Venue
Journal of the American Chemical Society
Published
2008-10-31
Volume
130
Issue
47
Pages
15764-15765
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2018431023
Cited by
200
References
0
FWCI
7.55
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes. https://app.cochat.ai/papers/10.1021/ja805555a
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Maksimoska, J., Feng, L., Harms, K., Yi, C., Kissil, J., Marmorstein, R., & Meggers, E. (2008). Targeting Large Kinase Active Site with Rigid, Bulky Octahedral Ruthenium Complexes. Journal of the American Chemical Society. https://doi.org/10.1021/ja805555a

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

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.