1n9a
From Proteopedia
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Farnesyltransferase complex with tetrahydropyridine inhibitors
Overview
Inhibitors of farnesyltransferase are effective against a variety of tumors in mouse models of cancer. Clinical trials to evaluate these agents in humans are ongoing. In our effort to develop new farnesyltransferase inhibitors, we have discovered bioavailable aryl tetrahydropyridines that are potent in cell culture. The design, synthesis, SAR and biological properties of these compounds will be discussed.
About this Structure
1N9A is a Protein complex structure of sequences from Rattus norvegicus with , and as ligands. Full crystallographic information is available from OCA.
Reference
Aryl tetrahydropyridine inhibitors of farnesyltransferase: bioavailable analogues with improved cellular potency., Gwaltney SL 2nd, O'Connor SJ, Nelson LT, Sullivan GM, Imade H, Wang W, Hasvold L, Li Q, Cohen J, Gu WZ, Tahir SK, Bauch J, Marsh K, Ng SC, Frost DJ, Zhang H, Muchmore S, Jakob CG, Stoll V, Hutchins C, Rosenberg SH, Sham HL, Bioorg Med Chem Lett. 2003 Apr 7;13(7):1363-6. PMID:12657283
Page seeded by OCA on Thu Feb 21 14:03:35 2008
Categories: Protein complex | Rattus norvegicus | Cohen, J. | Conner, S J.O. | Gu, W Z. | Hasvold, L. | II, S L.Gwaltney. | Imade, H. | Li, Q. | Nelson, L T. | Sullivan, G M. | Wang, W. | FTI | HFP | ZN | Farnesyltransferase | Prenyltransferase | Tetrahydropyridine
