Inhibitors of microsomal triglyceride transfer protein and apo-B secretion
View Patent ↗The present invention relates to compounds which are inhibitors of microsomal triglyceride transfer protein and/or apolipoprotein B (Apo B) secretion. These compounds can be useful for the prevention and treatment of various diseases, particularly atherosclerosis and its clinical sequelae, for lowering serum lipids, and related ailments. The invention further relates to pharmaceutical compositions comprising the compounds and to methods of treating diseases, such as hypertriglyceridemia, hyperchylomicronemia, atherosclerosis, obesity, and related conditions using the compounds. A method for decreasing apolipoprotein B (apo B) secretion is also provided.
1. A compound represented by Formula I:
wherein
R 1 is alkyl, R 4 R 5 NC(O)CH 2 , cycloalkyl, heterocyclyl, or heterocyclylalkyl;
X 1 is O, S, —N(R 6 )—, C(O)NR 6 , or N(R 6 )C(O);
X 2 is O, —N(R 6 )—, or S;
X 3 is a direct bond, O, —N(R 6 )—, —CH 2 —, arylene, or S;
R 3 is H, alkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, heteroalkyl, aralkyl, alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, aryloxycarbonyl, —OH, alkoxy, aryloxy, —SH, thioalkyl, thioaryl, or NR 4 R 5 ;
R 4 and R 5 are, independently for each occurrence, H, alkyl, cycloalkyl, heterocyclyl, aryl, heteroaryl, heteroalkyl, aralkyl, alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, or aryloxycarbonyl;
R 6 is, independently for each occurrence, H or alkyl;
m is 0 or 1; and
n is an integer from 0 to 3;
provided that if m is 0, X 3 is a direct bond or CH 2 ;
wherein each aryl or heteroaryl group is unsubstituted or substituted with one or more substituents selected from the group consisting of alkyl, hydroxy, alkoxy, alkylthio, cyano, halo, amino, and nitro;
wherein each alkyl, cycloalkyl, heterocyclylalkyl, aralkyl, alkylcarbonyl, alkoxycarbonyl, arylcarbonyl, aryloxycarbonyl, alkoxy, aryloxy, thioalkyl, or thioaryl group is unsubstituted or substituted with one or more substituents selected from the group consisting of NH 2 , C 1 -C 6 alkylamino, arylamino, diarylamino, heterocyclylamino, (C 1 -C 6 alkyl)carbonylamino, C 1 -C 6 alkoxy, C 1 -C 6 alkylthio, oxo, ═S, halo, nitro, hydroxyl, cyano, aryl, heteroaryl, aryloxy, arylthio, carbocyclyl, carbocyclyloxy, carbocyclylthio, carbocyclylamino, heterocyclyl, heterocyclyloxy, and heterocyclylthio; and
wherein each heterocyclyl group is unsubstituted or substituted with one or more substituents selected from the group consisting of halo, alkyl, and aryl;
or a pharmaceutically acceptable salt, solvate, ester or hydrate thereof.
2. The compound of claim 1 , wherein X 1 is O.
3. The compound of claim 1 , wherein R 1 is alkyl.
4. The compound of claim 3 , wherein R 1 is methyl.
5. The compound of claim 1 , wherein R 1 and X 1 taken together form a moiety selected from the group consisting of:
H 3 C—O—; CH 3 CH 2 —O—; (CH 3 ) 2 CH—O—;
6. The compound of claim 1 , wherein R 1 and X 1 taken together form CH 3 —O—.
7. The compound of claim 1 , wherein R 3 is unsubstituted or substituted phenyl.
8. The compound of claim 1 , wherein the moiety
represents one of the following groups:
9. A compound of Formula II:
wherein R 11 is selected from the group consisting of:
—OCH 3 ,
and wherein R 12 is selected from the group consisting of:
or a pharmaceutically acceptable salt, solvate, ester, or hydrate thereof.
10. The compound of claim 9 , wherein R 11 is —OCH 3 .
11. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.
12. The pharmaceutical composition of claim 11 further comprising an additional lipid-lowering agent.
13. A pharmaceutical composition comprising a compound of claim 9 and a pharmaceutically acceptable carrier.
14. The pharmaceutical composition of claim 13 further comprising an additional lipid-lowering agent.
15. A compound selected from the group consisting of:
or a pharmaceutically acceptable salt, solvate, ester or hydrate thereof.
16. The compound of claim 15 , wherein the compound is