Substituted isoquinolin-1(2H)-one compounds, compositions, and methods thereof
Chemical entities that modulate PI3 kinase activity, pharmaceutical compositions containing the chemical entities, and methods of using these chemical entities for treating diseases and conditions associated with PI3 kinase activity are described herein.
1. A compound of Formula I-1:
or its pharmaceutically acceptable salt thereof, wherein
B is a moiety of Formula II:
wherein W c is aryl, heteroaryl, heterocycloalkyl, or cycloalkyl, and
q is an integer of 0, 1, 2, 3, or 4;
X is absent or —(CH(R 9 )) z —, and z is an integer of 1;
Y is absent or —N(R 9 )—;
W d is
R a′ is hydrogen, halo, phosphate, urea, carbonate, unsubstituted or substituted amino, unsubstituted or substituted alkyl, unsubstituted or substituted alkenyl, unsubstituted or substituted alkynyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted heteroalkyl, or unsubstituted or substituted heterocycloalkyl;
R 1 is hydrogen, alkyl, alkenyl, alkynyl, alkoxy, amido, alkoxycarbonyl, sulfonamido, halo, cyano, or nitro;
R 2 is alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, heteroarylalkyl, alkoxy, amino, halo, cyano, hydroxy, or nitro;
R 3 is hydrogen, alkyl, or halo;
each R 9 is independently hydrogen, alkyl, or heterocycloalkyl; and
R 12 is H, unsubstituted or substituted alkyl, unsubstituted or substituted cyano, unsubstituted or substituted alkynyl, unsubstituted or substituted alkenyl, halo, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted heterocycloalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted amino, carboxylic acid, unsubstituted or substituted alkoxycarbonyl, unsubstituted or substituted amido, unsubstituted or substituted acyl, or unsubstituted or substituted sulfonamido.
2. The compound of claim 1 , wherein the compound of Formula I-1 is selected from:
3. The compound of claim 1 , wherein W d is selected from:
4. The compound of claim 1 , wherein —X—Y—W d is selected from:
5. The compound of claim 1 , wherein R 12 is selected from hydrogen, cyano, halo, unsubstituted or substituted alkyl, unsubstituted or substituted alkynyl, and unsubstituted or substituted alkenyl.
6. The compound of claim 1 , wherein R 12 is selected from unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted heterocycloalkyl, and unsubstituted or substituted cycloalkyl.
7. The compound of claim 1 , wherein R 12 is selected from unsubstituted or substituted amido, carboxylic acid, unsubstituted or substituted alkoxycarbonyl, unsubstituted or substituted acyl, and unsubstituted or substituted sulfonamide.
8. The compound of claim 1 , wherein the compound is selected from:
9. The compound of claim 8 , wherein the compound is selected from:
10. A pharmaceutical composition comprising a compound of any one of claim 1 , 8 , or 9 , or a pharmaceutically acceptable salt thereof, and one or more pharmaceutically acceptable excipients.
11. The compound of claim 1 , wherein R 3 is alkyl.
12. The compound of claim 11 , wherein R 3 is methyl.
13. The compound of claim 1 , wherein R 3 is halo.
14. The compound of claim 13 , wherein R 3 is chloro.