Design, Synthesis, and Biological Activity of Novel Polycyclic Aza-Amide FKBP12 Ligands

Since the discovery that FK-506 promotes neurite outgrowth, considerable attention has been focused on the development of potent nonimmunosuppressive ligands for FK-506 binding proteins (FKBPs). Such neuroimmunophilin agents have been reported to show neuroregenerative activity in a variety of cell...

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Veröffentlicht in:Journal of medicinal chemistry 2006-02, Vol.49 (3), p.1202-1206
Hauptverfasser: Hudack, Raymond A, Barta, Nancy S, Guo, Chuangxing, Deal, Judith, Dong, Liming, Fay, Lorraine K, Caprathe, Bradley, Chatterjee, Arindam, Vanderpool, Darin, Bigge, Christopher, Showalter, Richard, Bender, Steve, Augelli-Szafran, Corinne E, Lunney, Elizabeth, Hou, Xinjun
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Sprache:eng
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Zusammenfassung:Since the discovery that FK-506 promotes neurite outgrowth, considerable attention has been focused on the development of potent nonimmunosuppressive ligands for FK-506 binding proteins (FKBPs). Such neuroimmunophilin agents have been reported to show neuroregenerative activity in a variety of cell and animal models including neurite outgrowth, age-related cognitive decline, Parkinson's disease, peripheral nerve injury, optic nerve degeneration, and diabetic neuropathy. We have designed and synthesized a unique series of tetracyclic aza-amides that have been shown to be potent FKBP12 rotamase inhibitors. The structure−activity relationships established in this study have demonstrated diverse structural modifications that result in potent rotamase inhibitory activity.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm049161u