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US 8,299,090 B2Granted
Thiazolyl-and oxazolyl-isoquinolinones and methods for using them
AssigneesRoberto Pellicciari, Flavio Moroni
InventorsRoberto Pellicciari, Flavio Moroni, Adam Matthew Gilbert
Life of this patent
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Abstract
The present invention relates to substituted thiazolyl- and oxazoyl-isoquinolinones that act, for example, as modulators of poly(ADP-ribose) polymerase (PARP). The present invention also relates to processes for the preparation of substituted thiazolyl- and oxazolyl-isoquinolinones and to their use in treating various diseases and disorders.
Claims16
A compound of Formula I:
- wherein:
- X is C1-C9 alkylene, C2-C9 alkenylene, or C2-C9 alkynylene;
- Y is O or S;
- R1 is hydrogen, hydroxy, or OR7;
- R2, R3, and R4 are independently hydrogen;
- R5 and R6 are each, independently, C1 C6 alkyl, wherein the alkyl is optionally substituted with one or more groups selected from hydroxy, C1-C4 alkoxy, —CO2H, C1-C6 alkoxycarbonyl, NH2, C1-C6 mono- or dialkylamino, and halogen;
- or
- R5 and R6 together with the nitrogen to which they are attached form a saturated, partially unsaturated, or unsaturated 3 to 12 membered monocyclic or bicyclic heterocyclic ring optionally comprising from one to three additional ring heteroatoms selected from N, O, and S, and the remainder of the ring atoms are carbon atoms;
- R7 is C1-C6 alkyl, C2-C6 alkenyl, or C3-C7 cycloalkyl wherein the alkyl, alkenyl, and rings of the cycloalkyl are optionally substituted with one or more groups selected from hydroxy, C1-C4 alkoxy, —CO2H, C1-C6 alkoxycarbonyl, NH2, C1-C6 mono- or dialkylamino, and halogen;
- or a pharmaceutically acceptable salt form thereof.
7 more elements
Dependencies are inferred from the claim text.