Inhibiting ataxia telangiectasia and Rad3-related protein (ATR)
Novel compounds inhibiting ATR protein kinase include compounds of formula (I) disclosed herein, as well as liposome formulations comprising ATR protein kinase inhibitor compounds. The compositions are useful for the treatment of cancer.
1. An ATR protein kinase inhibitor compound of formula (Ia), or a pharmaceutically acceptable salt thereof:
wherein R′ is an alkyl-amino moiety comprising a tertiary alkyl-substituted amine having a pKa of 9.5 or greater.
2. A compound of the formula of Compound 5, or a pharmaceutically acceptable salt thereof:
3. A compound of the formula of Compound 6, or a pharmaceutically acceptable salt thereof:
4. A liposome composition comprising an ATR protein kinase inhibitor compound, or a pharmaceutically acceptable salt thereof, encapsulated in a liposome and having a plasma half-life of at least about 5 hours in mice, wherein the ATR protein kinase inhibitor compound is Compound A
wherein the liposome comprises hydrogenated soy phosphatidylcholine (HSPC) and cholesterol.
5. A liposome composition comprising an ATR protein kinase inhibitor compound, or a pharmaceutically acceptable salt thereof, encapsulated in a liposome and having a plasma half-life of at least about 5 hours in mice, wherein the ATR protein kinase inhibitor compound is a compound of formula (I), or a pharmaceutically acceptable salt thereof:
wherein R is a moiety comprising an amine with a pK a of greater than 7.0.
6. The liposome composition of claim 5 , wherein the ATR protein kinase inhibitor compound is a compound selected from the group consisting of:
7. The liposome composition of claim 5 , wherein the ATR protein kinase inhibitor compound is a compound selected from the group consisting of:
8. The composition of claim 4 , wherein the liposome further comprises PEG(2000)-distearoylglycerol (PEG-DSG).
9. The composition of claim 8 , wherein the liposome comprises HSPC, cholesterol and PEG-DSG in a molar ratio of about 3:2:0.15.
10. The composition of claim 5 obtained by a process comprising the steps of
forming a liposome encapsulating sucrose octasulfate encapsulated in a vesicle comprising a phospholipid and cholesterol; and
contacting the liposome from step (a) with the ATR protein kinase inhibitor under conditions effective to load the ATR protein kinase inhibitor into the lipsosome.
11. The composition of claim 10 , wherein ammonium sulfate has a concentration of about 1.1 M prior to contacting the liposome with the ATR protein kinase inhibitor compound.
12. The liposome composition of claim 5 , wherein the ATR protein kinase inhibitor compound is Compound 1:
13. The composition of claim 5 , wherein the liposome comprises hydrogenated soy phosphatidylcholine (HSPC) and cholesterol.
14. The composition of claim 13 , wherein the liposome further comprises PEG(2000)-distearoylglycerol (PEG-DSG).
15. The composition of claim 14 , wherein the liposome comprises HSPC, cholesterol and PEG-DSG in a molar ratio of about 3:2:0.15.