IP Library Granted Patent US 10,722,601
Granted Patent B2
US 10,722,601 · App. 16/192,185 · Granted Jul 28, 2020

Gadolinium chelate compounds for use in magnetic resonance imaging

Inventors: Markus Berger (Berlin, DE); Jessica Lohrke (Berlin, DE); Christoph-Stephan Hilger (Berlin, DE); Gregor Jost (Berlin, DE); Thomas Frenzel (Berlin, DE); Detlev Suelzle (Berlin, DE); Johannes Platzek (Berlin, DE); Olaf Panknin (Berlin, DE); Hubertus Pietsch (Kleinmachnow, DE)
Assignee: BAYER PHARMA AKTIENGESELLSCHAFT
A61K49/106C07D257/02
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Quick Facts
Patent No.
US 10,722,601
App. No.
16/192,185
Granted
Jul 28, 2020
Kind
B2
Abstract

A compound having the formula of tetragadolinium [4,10-bis(carboxylatomethyl)-7-{-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[{2-[4,7,10-tris(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl} amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclo dodecan-1-yl]acetate wherein the stereochemistry at the chiral carbon of the four alanine substituents is selected from the group consisting of RRRR, SSSS, RSSS, RRSS, and RRRS stereoisomers, and racemic and diastereomeric mixtures of any thereof, or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same is described. The compounds may be used as an MRI contrast imaging agent.

Claims (42)

1. A compound comprising a formula according to formula (I):

wherein a stereochemistry at the chiral carbon of the four alanine substituents is selected from the group consisting of RRRR, SSSS, RSSS, RRSS, and RRRS stereoisomers, and racemic and diastereomeric mixtures of any thereof,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

2. The compound of claim 1 , wherein the compound has the formula:

Tetragadolinium [4,10-bis(carboxylatomethyl)-7-{(2R,16R)-3,6,12,15-tetraoxo-16-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22R)-2-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]-amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

3. The compound of claim 1 , wherein the compound has the formula:

Tetragadolinium [4,10-bis(carboxylatomethyl)-7-{(2S,16S)-3,6,12,15-tetraoxo-16-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22S)-2-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]-amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

4. The compound of claim 1 , wherein the compound has the formula:

Tetragadolinium [4,10-bis(carboxylatomethyl)-7-{(2R,16S)-3,6,12,15-tetraoxo-16-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22S)-2-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]-amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

5. The compound of claim 1 , wherein the compound has the formula:

Tetragadolinium [4,10-bis(carboxylatomethyl)-7-{(2R,16R)-3,6,12,15-tetraoxo-16-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22S)-2-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]-amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

6. The compound of claim 1 , wherein the compound has the formula:

Tetragadolinium [4,10-bis(carboxylatomethyl)-7-{(2S,16R)-3,6,12,15-tetraoxo-16-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22R)-2-[4,7,10-tris-(carboxylatomethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]-amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl]acetate,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

7. The compound of claim 1 , wherein the compound is a racemic mixture of compounds, and wherein the stereochemistry of the racemic mixture is selected from the group consisting of: RRRR and SSSS stereoisomers; and RSSS and SRRR stereoisomers.

8. The compound of claim 1 , wherein the compound is a diastereomeric mixture of two or more of RRRR, SSSS, RSSS, SRRR, and RRSS stereoisomers.

9. A compound comprising a formula according to formula (II):

wherein a stereochemistry at the chiral carbon of the four alanine substituents is selected from the group consisting of RRRR, SSSS, RSSS, RRSS, and RRRS stereoisomers, and racemic and diastereomeric mixtures of any thereof,

or a tautomer, a hydrate, a solvate, or a salt thereof, or a mixture of same.

10. The compound of claim 9 , wherein the compound has the formula:

{4,10-bis(carboxymethyl)-7-[(2R,16R)-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22R)-2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl}-acetic acid,

or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

11. The compound of claim 9 , wherein the compound has the formula:

{4,10-bis(carboxymethyl)-7-[(2S,16S)-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22S)-2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl}-acetic acid,

or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

12. The compound of claim 9 , wherein the compound has the formula:

{4,10-bis(carboxymethyl)-7-[(2S,16S)-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22R)-2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl}-acetic acid,

or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

13. The compound of claim 9 , wherein the compound has the formula:

{4,10-bis(carboxymethyl)-7-[(2S,16R)-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22R)-2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl}-acetic acid,

or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

14. The compound of claim 9 , wherein the compound has the formula:

{4,10-bis(carboxymethyl)-7-[(2R,16S)-3,6,12,15-tetraoxo-16-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]-9,9-bis({[({(22S)-2-[4,7,10-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecan-1-yl]propanoyl}amino)acetyl]amino}methyl)-4,7,11,14-tetraazaheptadecan-2-yl}-1,4,7,10-tetraazacyclododecan-1-yl}-acetic acid,

or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

15. A method of imaging body tissue in a patient, comprising:

administering to the patient an effective amount of one or more compounds having a formula according to Formula (I) according to claim 1 in a pharmaceutically acceptable carrier; and

subjecting the patient to a magnetic resonance imaging procedure.

16. The method of claim 15 , wherein less than 0.5% of the one or more compounds are present in the patient seven days after the administration.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2019
From: BERGER, MARKUS; LOHRKE, JESSICA; HILGER, CHRISTOPH-STEPHAN; JOST, GREGOR; FRENZEL, THOMAS; SUELZLE, DETLEV; PLATZEK, JOHANNES; PANKNIN, OLAF; PIETSCH, HUBERTUS
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 050195/0931 →
Priority Claims (1)
EP 15170658 · Jun 4, 2015 · regional
Continuity (2)
Continuation 15578687
Related Publication 20190083659A1 · Mar 21, 2019
Cited By (1)
US 12,478,696