Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases (PTPs)
View Patent ↗The present invention is related to substituted methylene amide derivatives of formula (I) and use thereof for the treatment and/or prevention of metabolic disorders mediated by insulin resistance or pyperglycemia, comprising diabetes type I and/or II, inadequate glucose tolerance, insulin resistance, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, obesity, polycystic ovary syndrome (PCOS). In particular, the present invention is related to the use of substituted methylene amide derivatives of formula (I) to modulate, notably to inhibit the activity of PTPs. Also the present invention relates to a method of treating diabetes type II, obesity and to regulate the appetite of mammals. The present invention is furthermore related to novel substituted methylene amide derivatives and method of preparation thereof. Formula (I).
1. A substituted methylene amide of Formula (I):
as well as its geometrical isomers, its optically active forms as enantiomers,
diastereomers and its racemate forms, as well as pharmaceutically acceptable salts thereof, wherein
(I)
R 1 is CH 2 —CH 2 -phenyl, CH 2 —CH 2 -napthyl, CH 2 -phenyl, or CH 2 -napthyl;
R 2a and R 2b are each independently are H or (C 1 -C 12 )alkyl;
Cy is a phenyl substituted by (1), (2) or (3):
(1) an oxadiazole group;
(2) 1 or 2 moieties selected from the group consisting of —NH—CO—R 3 , —SO 2 —NR 3 R 3′ and —CO—NR 3 R 3′ wherein R 3 and R 3′ are independently selected from H and (C 1 -C 15 )alkyl; or
(3) B-R 4 wherein B is an ethynyl group and R 4 is a (C 1 -C 12 )alkyl phenyl;
(II)
R 2a and R 2b are each H, R 1 is —CH 2 -A with A being phenyl optionally substituted by cyano, halogen, methoxy, hydroxyl, phenoxy, —NO 2 , or trifluoromethyl, and Cy is phenyl or biphenyl substituted by —SO 2 R 3 , or —CO—NR 3 R 3′ where R 3′ is H and R 3 is (C 7 -C 12 )alkyl or (C 7 -C 15 )alkyl; or
(III)
R 2a and R 2b are each H, R 1 is selected from the group consisting of phenyl, benzyl, phenethyl, or 1-methylbenzyl which may be substituted by (C 1 -C 6 )alkyl or cycloalkyl, and Cy is phenyl or biphenyl substituted by —SO 2 R 3 , or —CO—NR 3 R 3 where R 3 is (C 7 -C 1 5 )alkyl.
2. The substituted methylene amide according to claim 1 , wherein R 3′ is H and R 3 is selected from the group consisting of diphenyl-ethyl, dodecyl, octyl, 4-pentyl-benzyl, 4-phenoxy-phenethyl, ethyl-thiophen-2-yl, pentadecyl, tridecyl, hexyloxy-phenyl or (2-ethyl)-hexyl.
3. The substituted methylene amide according to claim 1 wherein:
R 2a and R 2b are each H.
4. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 1 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
5. The pharmaceutical composition according to claim 4 further comprising at least one supplementary drug.
6. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 2 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
7. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 3 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
8. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 2 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
9. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 3 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
10. {{4-[(4-hexylphenyl)ethynyl]benzyl}[4-(trifluoromethyl)benzyl]amino}-(oxo)acetic acid.
11. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 10 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
12. The substituted methylene amide of Formula (I) as well as its geometrical isomers, its optically active forms as enantiomers, diastereomers and its racemate forms, as well as pharmaceutically acceptable salts-thereof according to claim 1 , R 2a and R 2b are each H, R 1 is —CH 2 -A with A being phenyl optionally substituted by cyano, halogen, methoxy, hydroxyl, phenoxy, —NO 2 , or trifluoromethyl, and Cy is phenyl or biphenyl substituted by —SO 2 R 3 , or —CO—NR 3 R 3′ where R 3′ is H and R 3 is (C 7 -C 12 )alkyl or (C 7 -C 15 )alkyl.
13. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 12 and a pharmaceutically acceptable carrier, diluent or excipient thereof.
14. The substituted methylene amide of Formula (I) as well as its geometrical isomers, its optically active forms as enantiomers, diastereomers and its racemate forms, as well as pharmaceutically acceptable salts-thereof according to claim 1 , wherein R 2a and R 2b are each H, R 1 is selected from the group consisting of phenyl, benzyl, phenethyl, or 1-methylbenzyl which may be substituted by (C 1 -C 6 )alkyl or cycloalkyl, and Cy is phenyl or biphenyl substituted by —SO 2 R 3 , or —CO—NR 3 R 3′ where R 3 is (C 7 -C 15 )alkyl.
15. A pharmaceutical composition comprising at least one substituted methylene amide according to claim 14 and a pharmaceutically acceptable carrier, diluent or excipient thereof.