Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1366094 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
Soluble guanylate cyclase (sGC) is activated by the known benzylindazole derivative YC-1 [1-benzyl-3-(5′-hydroxymethyl-2′-furyl)-indazole]. YC-1 also acts synergistically with CO, activating sGC to a level comparable to that achieved upon binding of nitric oxide, the endogenous activator of sGC. We here describe the synthesis of a YC-1 phosphonate analogue with improved aqueous solubility as well as its effects on sGC.
Graphical abstractThe synthesis and testing of a phosphonate analogue of the soluble guanylate cyclase (sGC) activator YC-1 is described. With enhanced aqueous solubility, the effects of this analogue on sGC are reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
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Organic Chemistry
Authors
Nathaniel I. Martin, Emily R. Derbyshire, Michael A. Marletta,