Claims
- 1. A method for inhibiting hyperlipemia or atherosclerosis comprising administering an effective amount of a 2-mercaptobenzimidazole compound represented by formula IV: ##STR13## wherein R.sub.3 and R.sub.4 each represent a hydrogen atom, a halogen atom, or an alkyl, alkoxy, alkoxycarbonyl, carbamoyl, sulfamoyl, acylamino, sulfonylamino, cyano or nitro group;
- R.sub.50 and R.sub.60 each represent a hydrogen atom, alkyl group, or acyl group;
- n.sub.3, n.sub.4, each represent 1 or 2; and
- L.sub.2 represents a connecting group which is an alkylene group or a phenylene group-containing an alkylene group, or
- a pharmaceutically acceptable salt thereof, to a mammal.
- 2. The method of claim 1, wherein the 2-mercaptobenzimidazole compound is a compound represented by formula IV-a: ##STR14## wherein L.sub.2, R.sub.50 and R.sub.60 are as defined in claim 1, R.sub.31 and R.sub.32 are the same as R.sub.3, and R.sub.41 and R.sub.42 are the same as R.sub.4.
- 3. The method of claim 2, wherein R.sub.31, R.sub.32, R.sub.41, R.sub.42, R.sub.50 and R.sub.60 in formula IV-a are hydrogen, and L.sub.2 is an alkylene group having 4 to 10 carbon atoms or an alkylene-phenylene-alkylene group wherein each alkylene moiety of the alkylene-phenylene-alkylene group has 1 to 2 carbon atoms.
- 4. The method of claim 2, wherein one of R.sub.31 and R.sub.32 and one of R.sub.41 and R.sub.42 in formula IV-a are hydrogen, and the other one of R.sub.31 and R.sub.32 and the other one of R.sub.41 and R.sub.42 are lower alkyl, halogen, nitro or lower acylamino, and R.sub.50 and R.sub.60 are hydrogen, lower alkyl or lower alkanoyl.
- 5. The method of claim 2, wherein R.sub.31, R.sub.32, R.sub.41 and R.sub.42 in formula IV-a are halogen, and R.sub.50 and R.sub.60 are hydrogen.
- 6. The method of claim 2, wherein R.sub.31, R.sub.32, R.sub.41 and R.sub.42 in formula IV-a are hydrogen, and R.sub.50 and R.sub.60 are lower alkanoyl or lower alkyl, and L.sub.2 is an alkylene group having 4 to 10 carbon atoms or an alkylene-phenylene-alkylene group, wherein each alkylene moiety of the alkylene-phenylene-alkylene group has 1 to 2 carbon atoms.
- 7. The method of claim 2, wherein R.sub.31, R.sub.32, R.sub.41 and R.sub.42 in formula IV-a are halogen or lower alkyl, and R.sub.50 and R.sub.60 are lower alkanoyl or lower alkyl.
- 8. A method for therapy of hyperlipemia or atherosclerosis in a mammal comprising administering an effective amount of a 2-mercaptobenzimidazole compound represented by formula IV: ##STR15## wherein R.sub.3 and R.sub.4 each represent a hydrogen atom, halogen atom, or alkyl, alkoxy, alkoxycarbonyl, carbamoyl, sulfamoyl, acylamino, sulfonylamino, cyano or nitro group;
- R.sub.50 and R.sub.60 each represent a hydrogen atom, alkyl group, or acyl group;
- n.sub.3, n.sub.4 each represent 1 or 2; and,
- L.sub.2 represents a connecting group which is an alkylene group or phenylene group-containing alkylene group, or
- a pharmaceutically acceptable salt thereof, to a mammal.
- 9. A method for inhibiting foamy macrophages in a mammal comprising contacting a foamy macrophage with an effective amount of a 2-mercaptobenzimidazole compound represented by formula IV: ##STR16## wherein R.sub.3 and R.sub.4 each represent a hydrogen atom, a halogen atom, or an alkyl, alkoxy, alkoxycarbonyl, carbamoyl, sulfamoyl, acylamino, sulfonylamino, cyano or nitro group;
- R.sub.50 and R.sub.60 each represent a hydrogen atom, alkyl group, or acyl group;
- n.sub.3, n.sub.4 each represent 1 or 2; and
- L.sub.2 represents a connecting group which is an alkylene group or a phenylene group-containing an alkylene group, or
- a pharmaceutically acceptable salt.
- 10. A method for reducing the formation of cholesteryl ester in foamy macrophages in a mammal comprising contacting a foamy macrophage with an effective amount of a 2-mercaptobenzimidazole compound represented by formula IV: ##STR17## wherein R.sub.3 and R.sub.4 each represent a hydrogen atom, a halogen atom, or an alkyl, alkoxy, alkoxycarbonyl, carbamoyl, sulfamoyl, acylamino, sulfonylamino, cyano or nitro group;
- R.sub.50 and R.sub.60 each represent a hydrogen atom, alkyl group, or acyl group;
- n.sub.3, n.sub.4 each represent 1 or 2; and
- L.sub.2 represents a connecting group which is an alkylene group or a phenylene group-containing an alkylene group, or
- a pharmaceutically acceptable salt thereof.
Parent Case Info
This is a divisional application of U.S. Ser. No. 08/669,516, filed on Jul. 12, 1996, now abandoned which was a 35 U.S.C. .sctn.371 filing of PCT/JP95/00116, filed on Jan. 30, 1995 which claims priority under 35 U.S.C. .sctn.119 to JP 12876/1994, filed on Feb. 4, 1994, JP 12877/1994, filed on Feb. 4, 1994, JP 77519/1994, filed on Apr. 15, 1994, and JP 176805/1994, filed on Jul. 28, 1994.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
3704130 |
Pollet et al. |
Nov 1972 |
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Foreign Referenced Citations (1)
Number |
Date |
Country |
0520552 A1 |
Dec 1992 |
EPX |
Divisions (1)
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669516 |
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