IP Library Granted Patent US 7,608,623
Granted Patent B2
US 7,608,623 · App. 11/287,480 · Granted Oct 27, 2009

Hydroxyamidine and hydroxyguanidine compounds as urokinase inhibitors

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Quick Facts
Patent No.
US 7,608,623
App. No.
11/287,480
Granted
Oct 27, 2009
Kind
B2
Abstract

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.

Claims (26)

1. A pharmaceutical composition, which comprises, as an active compound, one or more compounds of the formula

in which E is a group

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 radical selected from the group consisting of a cycloalkyl-, aryl-, and bicyclic-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 ,

R 6 is —H, —C 1 -C 6 -alkyl, —C 2 -C 6 -alkenyl or —C 2 -C 6 -alkynyl, or a radical selected from the group consisting of a cycloalkyl-, aryl-, and bicyclic-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 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 radical selected from the group consisting of a cycloalkyl-, aryl-, and bicyclic-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 a salt of said compound

and a pharmaceutically customary carrier, diluent or/and adjuvant.

2. The pharmaceutical composition of claim 1 , wherein said active compound is selected from the group consisting of

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyamidino-(L)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyamidino-(D)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyamidino-(D,L)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(L)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(D)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(D,L)-phenylalanine-4-ethoxycarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(L)-phenylalanine-4-ethylaminocarbonylpiperazide,

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(D)-phenylalanine-4-ethylaminocarbonylpiperazide, and

N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyguanidino-(D,L)-phenylalanine-4-ethylaminocarbonylpiperazide,

or a physiologically compatible salt thereof;

and a pharmaceutically acceptable carrier, diluent or/and adjuvant.

3. The pharmaceutical composition as claimed in claim 1 , wherein the composition is in an orally administrable form.

4. The pharmaceutical composition as claimed in claim 1 , wherein the compound is present as a sulfate or hydrogen sulfate salt.

5. The pharmaceutical composition as claimed in claim 2 , in which the compound is N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyamidino-(L)-phenylalanine-4-ethoxycarbonylpiperazinium hydrogen sulfate or N-α-(2,4,6-triisopropylphenylsulfonyl)-3-hydroxyamidino-(L)-phenylalanine-4-ethoxycarbonylpiperazinium sulfate.

6. A salt of a compound of the formula I,

in which E is

and R5 is ethoxy and wherein the salt is in the form of a hydrogen sulfate or sulfate.

Assignments (3)
RE-RECORD TO CORRECT PROPERTY NUMBER ON A DOCUMENT PREVIOUSLY RECORDED AT REEL 022127, FRAME 0451. (ASSIGNMENT OF ASSIGNOR'S INTEREST) Recorded Apr 20, 2009
From: WILEX AG
To: WILEX AG
Reel/Frame 022575/0312 →
CHANGE OF ADDRESS WITH TRANSLATION Recorded Jan 16, 2009
From: WILEX AG
To: WILEX AG
Reel/Frame 022127/0451 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 1, 2006
From: SPERL, STEFAN; BUERGLE, MARCUS; SCHMALIX, WOLFGANG; WOSIKOWSKI, KATJA; CLEMENT, BERND
To: WILEX AG
Reel/Frame 017300/0595 →