| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1378119 | Bioorganic & Medicinal Chemistry Letters | 2005 | 5 Pages |
Three microcolin A and B analogs have been synthesized. Their biological activity profiles were evaluated against several cell lines, revealing the existence of a structural determinant whose role in mediating the antiproliferative effect of the microcolins has heretofore gone unrecognized. While previously described as potent immunosuppressive natural products, we found that these microcolin analogs possessed no selective cytotoxicity when comparing immune cell versus nonimmune cell proliferation. In addition, the amino-terminus of microcolin A has been modified to incorporate a biotinylated polyethylene glycol linker. The biological activity of this biotinylated microcolin A analog was determined. This affinity reagent was shown to retain limited biological activity and thus can serve as a useful probe for elucidating the mechanism of action of microcolin A.
Graphical abstractThe synthesis and biological evaluation of microcolin A and B analogs are reported. Design, synthesis, and biological activity profile of a biotinylated microcolin A analog as a molecular probe are also discussed.Figure optionsDownload full-size imageDownload as PowerPoint slide
