Lipoxin compounds and their use in treating cell proliferative disorders
Compounds having the active site of natural lipoxins, but a longer tissue half-life are disclosed. In particular, 15-epi-lipoxins and their use in ameliorating undesired cell proliferation, which characterizes diseases such as cancer, are also disclosed.
1. A method of inducing vasodilation to treat or prevent a vasocontractive response or condition, comprising: administering to a subject a pharmaceutical composition that includes a substantially purified 15-epi-lipoxin compound in which the absolute configuration at the 15 carbon is R and a pharmaceutically acceptable carrier.
2. A method of claim 1 , wherein the substantially purified 15-epi-lipoxin compound in which the absolute configuration at the 15 carbon is R is 15R-5,6, 15-trihydroxy-7,9, 13-trans-11-cis-eicsoatetraenoic acid.
3. A method of claim 2 , wherein the 15R-5,6, 15-trihydroxy-7,9, 13-trans-11-cis-eicsoatetraenoic acid has a 5S, 6R configuration.
4. A method of claim 1 , wherein the substantially purified 15-epi-lipoxin compound in which the absolute configuration at the 15 carbon is R is 15R-5,14,15-trihydroxy-6,10,12-trans-8-ciseicosatetraenoic acid.
5. A method of claim 4 , wherein the 15R-5,14,15-trihydroxy-6,10,12-trans-8-ciseicosatetraenoic acid has a 5S, 14R configuration.
6. A method of claim 1 , wherein the vasocontractive response or condition is selected from the group consisting of a renal hemodynamic disease, including glomerular disease, and a cardiovascular disease, including hypertension, myocardial infarction, and myocardial ischemia.
7. A method of claim 6 , wherein the substantially purified 15-epi-lipoxin compound in which the absolute configuration at the 15 carbon is R is 15R-5,6, 15-trihydroxy-7,9, 13-trans-11-cis-eicsoatetraenoic acid.
8. A method of claim 7 , wherein the 15R-5,6, 15-trihydroxy-7,9, 13-trans-11-cis-eicsoatetraenoic acid has a 5S, 6R configuration.
9. A method of claim 6 , wherein the substantially purified 15-epi-lipoxin compound in which the absolute configuration at the 15 carbon is R is 15R-5,14,15-trihydroxy-6,10,12-trans-8-ciseicosatetraenoic acid.
10. A method of claim 9 , wherein the 15R-5,14,15-trihydroxy-6,10,12-trans-8-ciseicosatetraenoic acid has a 5S, 14R configuration.