Fluorinated integrin antagonists
AssigneeOcuTerra Therapeutics, Inc.
InventorsBen C. Askew, Richard W. Heidebrecht, Takeru Furuya, Mark E. Duggan, D. Scott Edwards
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Abstract
The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.
Claims25
A method of treating diabetic retinopathy in a subject, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of formula I:
- or a pharmaceutically acceptable salt thereof, wherein:
- Z is
- R and R′ are each independently H or F, or R and R′, together with the carbon atom to which they are attached, form a 3- or 4-membered carbocyclic or heterocyclic ring;
- Q is
- X is CH or N;
- Y is CH or N;
- R1 is C1-C4 alkyl substituted with 1, 2, 3, 4, 5, 6, 7, 8, or 9 fluorine atoms, or C1-C6 alkoxy substituted with 0, 1, 2, 3, 4, 5, 6, or 7 fluorine atoms;
- and
- R2 and R3 are each independently H, F, CH2F, CHF2, or CF3, provided that one of R2 and R3 is not H,
- provided that the compound of formula I contains at least one fluorine atom.
Dependencies are inferred from the claim text.