Abstract: The present invention relates to quinobenzoxazines analogs having the general formula: and pharmaceutically acceptable salts, esters and prodrugs thereof; wherein A, U, V, W, X and Z are substituents. The present invention also relates to methods for using such compounds.
Type:
Grant
Filed:
July 30, 2004
Date of Patent:
April 8, 2008
Assignee:
Cylene Pharmaceuticals
Inventors:
Jeffrey P. Whitten, Michael Schwaebe, Adam Siddiqui-Jain, Terence Moran
Abstract: Expanded porphyrin comprising substitutions for at least two NH groups by S, Se or Te are non-photoactive and are selective for binding G-quadruplexes characteristic of the c-MYC control region. Accordingly, these expanded porphyrins are useful to modulate the expression of genes controlled by the formation of c-MYC type G-quadruplexes, such as c-MYC itself.