Hydroxyamidine and hydroxyguanidine compounds as urokinase inhibitors
View Patent ↗The present invention relates to novel compounds for inhibiting the urokinase plasminogen activator (uPA), which have high bioavailability and oral administerability, and also to the use thereof as therapeutic active compounds for the treatment of urokinase- or/and urokinase receptor-associated disorders such as, for example, tumors and metastasizing. The invention relates in particular to compounds containing hydroxyamidine or hydroxyguanidine groups.
1. A method for treating diseases associated with pathological overexpression of urokinase and/or urokinase receptor comprising administering to a subject in need of such treatment a pharmaceutically effective amount of at least one compound of the formula
in which E is
R 3 is —H,
R 5 is —OR 6 , —N(R 6 ) 2 , —C 1 -C 6 -alkyl, —C 2 -C 6 -alkenyl or —C 2 -C 6 -alkynyl, said alkyl, alkenyl and alkynyl moieties being straight-chained or branched and being unsubstituted or substituted by at least one substituent selected from the group consisting of halogen, —OR 6 , —OCOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 , COOR 6 , and a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C 1 -C 3 -alkyl, —C 1 -C 3 -alkoxy,
halogen, —OR 6 , ═O, —N0 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 ,
R 6 is —H, —C 1 -C 6 -alkyl, —C 2 -C 6 -alkenyl or —C 2 -C 6 -alkynyl, or a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C 1 -C 3 -alkyl, —C 1 -C 3 -alkoxy, halogen, —OR 6 , ═O, —NO 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 ,
said alkyl, alkenyl or alkynyl moieties being straight-chained or branched and being unsubstituted or substituted by at least one substituent selected from the group consisting of halogen, —OR 6 , —OCOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 , COOR 6 , and a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C 1 -C 3 -alkyl, —C 1 -C 3 -alkoxy, halogen, —OR 6 , ═O, —NO 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 ,
or salts of said compound, wherein the disease treated is a tumor susceptible to urokinase inhibition, wherein said tumor is selected from the group consisting of breast, colon, and pancreatic tumors.
2. A method for treating diseases associated with pathological overexpression of urokinase and/or urokinase receptor comprising administering to a subject in need of such treatment a pharmaceutically effective amount of at least one compound of the formula
in which E is
R 3 is —H,
R 5 is —OR 6 , —N(R 6 ) 2 , —C 1 -C 6 -alkyl, —C 2 -C 6 -alkenyl or —C 2 -C 6 -alkynyl, said alkyl, alkenyl and alkynyl moieties being straight-chained or branched and being unsubstituted or substituted by at least one substituent selected from the group consisting of halogen, —OR 6 , —OCOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 , COOR 6 , and a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C l -C 3 -alkyl, —C 1 -C 3 -alkoxy,
halogen, —OR 6 , ═O, —N 0 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 ,
R 6 is —H, —C 1 -C 6 -alkyl, —C 2 -C 6 -alkenyl or —C 2 -C 6 -alkynyl, or a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C 1 -C 3 -alkyl, —C 1 -C 3 -alkoxy, halogen, —OR 6 , ═O, —NO 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 ,
said alkyl, alkenyl or alkynyl moieties being straight-chained or branched and being unsubstituted or substituted by at least one substituent selected from the group consisting of halogen, —OR 6 , —OCOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 , COOR 6 , and a cyclic radical which is unsubstituted or substituted by at least one substituent selected from the group consisting of —C 1 -C 3 -alkyl, —C 1 -C 3 -alkoxy, halogen, —OR 6 , ═O, —NO 2 , —CN, —COOR 6 , —N(R 6 ) 2 , —NR 6 COR 6 , —NR 6 CON(R 6 ) 2 and —OCOR 6 , or salts of said compound, wherein the disease treated is characterized by the formation of metastases from breast, colon, or pancreatic tumors.
3. The method of claim 1 , wherein the tumor is a primary tumor susceptible to urokinase inhibition.
4. The method of claim 1 , wherein the compound is administered orally.
5. The method of claim 1 , wherein the compound is administered in the form of tablets, coated tablets, capsules, pellets, a solution, an emulsion or/and suspension.
6. The method of claim 1 , wherein the subject is a human.
7. A method for treating a breast, colon, or pancreatic tumor or metastases thereof susceptible to urokinase inhibition comprising administering to a subject in need of such treatment a pharmaceutically effective amount of at least one compound of the formula
in which E is
R 3 is —H, and R5 is ethoxy, wherein the compound is in the form of a hydrogen sulfate or sulfate salt.
8. A method for treating a breast, colon, or pancreatic tumor or metastases thereof susceptible to urokinase inhibition comprising administering to a subject in need of such treatment a pharmaceutically effective amount of at least one compound of the formula
in which E is
and R5 is ethoxy, wherein the compound is in the form of a hydrogen sulfate or sulfate salt.