Small-Molecule Inhibitors of Protein Geranylgeranyltransferase Type I

Sabrina Castellano, Hannah D. G. Fiji, Sape S. Kinderman, Masaru Watanabe, Pablo de Leon, Fuyuhiko Tamanoi, and Ohyun Kwon*
Department of Chemistry and Biochemistry, Department of Microbiology, Immunology and Molecular Genetics, Jonsson Comprehensive Cancer Center and Molecular Biology Institute, University of California, Los Angeles, California 90095-1569
J. Am. Chem. Soc., 2007, 129 (18), pp 5843–5845
DOI: 10.1021/ja070274n
Publication Date (Web): April 17, 2007
Copyright © 2007 American Chemical Society

 Department of Chemistry and Biochemistry.

,

 Department of Microbiology, Immunology and Molecular Genetics.

, *

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

Abstract

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Small molecules that inhibit the geranylgeranylation of K-Ras4B and RhoA by protein geranylgeranyltransferase type I (GGTase-I) were identified from chemical genetic screens of heterocycles synthesized through phosphine catalysis of allenes. To further improve the efficacy of the GGTase-I inhibitors (GGTIs), 4288 related compounds bearing core dihydropyrrole/pyrrolidine and tetrahydropyridine/piperidine scaffolds were synthesized on SynPhase lanterns in a split-pool manner through phosphine-catalyzed [3 + 2] and [4 + 2] annulations of resin-bound allenoates. Testing of the 4288 analogues resulted in several GGTIs exhibiting submicromolar IC50 values. Because proteins such as Ras and Rho GTPases are implicated in oncogenesis and metastasis, these GGTIs might ultimately lead to the development of novel antitumor therapeutics.

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History

  • Published In Issue May 09, 2007
  • Received January 13, 2007

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