Chemokine receptor binding heterocyclic compounds
AssigneeAnorMED, Inc.
InventorsGary James Bridger, Eva Maria Boehringer, Zhongren Wang, Dominique Schols, Renato Tony Skerlj, David Earl Bogucki
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Abstract
The present invention is drawn to novel antiviral compounds, pharmaceutical compositions and their use. More specifically this invention is drawn to derivatives of monocyclic polyamines which have activity in standard tests against HIV- or FIV-infected cells as well as other biological activity related to binding of ligands to chemokine receptors that mediate a number of mammalian embryonic developmental processes.
Claims11
A method to treat atherosclerosis comprises comprising administering to a subject in need of such treatment a compound of the formula
- V—CR2—Ar1—CR2NR—(CR2)x—Ar2
- wherein V is a heterocycle of 9–24 members containing 2–4 optionally substituted amine nitrogen atoms spaced from each other by 2 or more optionally substituted carbon atoms, and which heterocycle may optionally comprise a fused aromatic or heteroaromatic ring, and wherein
- (a) said heterocycle contains at least one O or S, said O or S spaced from any adjacent heteroatom by at least 2 carbon atoms, and wherein said S is optionally oxidized, or
- (b) the heterocycle contains 3 N and at least one carbon atom in said heterocycle is substituted by at least one fluoro substituent, or
- (c) both (a) and (b);
- and wherein each R is independently H or a straight chain, branched or cyclic alkyl containing 1–6C;
- x is 0–4;
- Ar1 is an unsubstituted or substituted aromatic or heteroaromatic moiety;
- and
- Ar2 is an unsubstituted or substituted aromatic or heterocyclic group;
- or
- the pharmaceutically acceptable salts and protected forms thereof.
Dependencies are inferred from the claim text.