Synthesis and preliminary biological evaluation of truncated zoanthenol analogues
Graphic Zoanthamines are a family of marine alkaloids that have complex heptacyclic structures and are reported to be interleukin-6 modulators. While the structure of zoanthamines, especially the ABC-ring portion, is similar to that of steroids, the CDEFG-ring portion, composed of aminoacetal and la...
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Veröffentlicht in: | Bioorganic & medicinal chemistry letters 2004-05, Vol.14 (10), p.2647-2651 |
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Format: | Artikel |
Sprache: | eng |
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Zoanthamines are a family of marine alkaloids that have complex heptacyclic structures and are reported to be interleukin-6 modulators. While the structure of zoanthamines, especially the ABC-ring portion, is similar to that of steroids, the CDEFG-ring portion, composed of aminoacetal and lactone core, is a unique structural element. In this report, we designed and synthesized ABC-ring
6 and CDEFG-ring
7, which are truncated analogues of the northern and southern hemispheres of zoanthenol
5, respectively, and which incorporate all of the functionality of each hemisphere. A preliminary SAR study suggested that the hydrochloride of the CEFG-ring portion is an active pharmacophore for suppressing the growth of interleukin-6-dependent MH60 cells. |
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ISSN: | 0960-894X 1464-3405 |
DOI: | 10.1016/j.bmcl.2004.02.064 |