Dihydropyridophthalazinone inhibitors of poly(ADP-ribose)polymerase (PARP) for use in treatment of diseases associated with a PTEN deficiency
A compound having the structure set forth in Formula (I) and Formula (II): wherein the substituents Y, Z, A, B, R 1 , R 2 , R 3 , R 4 and R 5 are as defined herein. Provided herein are inhibitors of poly(ADP-ribose)polymerase activity. Also described herein are pharmaceutical compositions that include at least one compound described herein and the use of a compound or pharmaceutical composition described herein to treat diseases, disorders and conditions associated with a PTEN deficiency that are ameliorated by the inhibition of PARP activity.
1. A method of treating small cell lung cancer associated with a PTEN deficiency in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of the compound:
5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)-8,9-dihydro-2H-pyrido[4,3,2-de]phthalazin-3(7H)-one, or a pharmaceutically acceptable salt or solvate thereof.
2. The method of claim 1 , wherein said administration is in combination with ionizing radiation, one or more chemotherapeutic agents, or a combination thereof.
3. A method of treating small cell lung cancer associated with a PTEN deficiency in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of the compound:
(8S,9R)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1H-1,2,4-triazol-5-yl)-8,9-dihydro-2H-pyrido [4,3,2-de]phthalazin-3(7H)-one, or a pharmaceutically acceptable salt thereof.
4. The method of claim 3 , wherein said administration is in combination with ionizing radiation, one or more chemotherapeutic agents, or a combination thereof.
5. The method of claim 1 , wherein the patient is a human.
6. The method of claim 2 , wherein the patient is a human.
7. The method of claim 3 , wherein the patient is a human.
8. The method of claim 4 , wherein the patient is a human.