| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1364590 | Bioorganic & Medicinal Chemistry Letters | 2008 | 4 Pages |
Lactimidomycin (LTM, 1), iso-migrastatin (iso-MGS, 2) and migrastatin (MGS, 3) are macrolide antitumor antibiotics differing in macrolide ring size but all bearing a glutarimide side chain. To further develop these natural products and related analogs as drug candidates we have produced and evaluated the biological activities of a small library of iso-MGS and LTM-derived agents; congeners evaluated bear either the MGS scaffold or related acyclic (dorrigocin) scaffolds. Scratch wound-healing (SWH) assays with 4T1 mouse and MDA-MB-231 human mammary tumor cell lines, respectively, reveal structural elements crucial to inhibition of cell migration by these compounds. Moreover, two substances, 14 and 17, with activity far superior to that of MGS are unveiled by SWH assays.
Graphical abstractBiological evaluation of new cell migration inhibitors bearing migrastatin (MGS)-derived scaffolds is reported unveiling structural elements crucial to activity and two new MGS analogs with superior activity.Figure optionsDownload full-size imageDownload as PowerPoint slide
