Salts of thrombin inhibitors

Details Salts of thrombin inhibitors Salts of thrombin inhibitors

2000-04-27

2002-06-18

Russel, Jeffrey E. (Department: 1653)

Drug, bio-affecting and body treating compositions

Designated organic active ingredient containing

Peptide containing doai

C210S500240, C210S646000, C422S045000, C514S970000, C514S973000, C623S001430, C623S001460, C623S002420

Reexamination Certificate

active

06407067

ABSTRACT:

The invention relates to novel salts of thrombin inhibitors, their preparation and use for producing drugs with antithrombotic effect.
The invention specifically relates to novel compounds of the general formula I or II
where
n is 0.5, 1, 2 and
HX is
 and HX is optionally substituted once or twice by methyl, ethyl or hydroxyl, and the tautomers and stereoisomers thereof, and m is from 0 to 4.
The preferred meanings of HX are as follows:
The particularly preferred active substance of the formula I has the R configuration of cyclohexylalanine and the S configuration of dehydroproline.
The preparation of the thrombin inhibitor I with HX=HOAc is described in WO 96/25426, and that of the thrombin inhibitor II with n=0 is described in WO 94/29336. The salts are usually amorphous. Storage of these products, especially at elevated temperature, leads to the formation of a number of byproducts.
It is an object of the present invention to find storage-stable forms of the active substances.
The betaines of the active substances are obtained by titrating the acidic salts to the isoelectric point, precipitation or crystallization, filtration or centrifugation and drying. The salts of the general formula I and II are obtained by reacting the betaines with HX, or else the alkali metal salt of HX is reacted with the mineral acid salts or C
1
-C
4
-carboxylic acid salts of I or II. Suitable solvents are water, C
1
-C
6
-alcohols, C
1
-C
6
-ethers, C
1
-C
6
-esters, toluene, xylenes, DMF, DMSO, THF. Water is the very preferred solvent. The product is isolated by filtration or centrifugation and drying or from a solution by freeze drying or spray drying.
All conventional methods are suitable for producing crystals, as described, for example, in Houben-Weyl, volume I/1, Georg Thieme Verlag, Stuttgart, 1958, 341; Römpps Chemie-Lexikon, 8th edition, Franckh'sche Verlagshandlung, Stuttgart, 1983, 2244, and the literature quoted therein.
The usual physiologically tolerated salts of I and II are normally amorphous solids. We have now found, surprisingly, that, in particular, the salts with acesulfame-K and saccharin are compounds which crystallize well. They precipitate spontaneously from water. However, addition of minimal amounts of water in the range from 5 to 500% by weight to a solid, stoichiometric mixture of I or II with HX also suffices to obtain crystalline substances.
The salt formation is normally carried out batchwise in reaction vessels. However, continuous production, for example in a cascade of stirred vessels or in an extruder, is also possible. The process is so robust that it can also be carried out by mixing solids in an apparatus suitable for this purpose, preferably in one used for formulating pharmaceutical active substances.
The crystallization temperature is generally in the range from −80 to 200° C., preferably in the range from −20 to 150° C.
The pressure is in the range from 1 bar to 2000 bar.
The crystallinity of the samples has been assessed on the basis of Debye-Scherrer photographs.
The thermal decomposition of the compounds of the general formula I and II has been investigated in a stability test. This was done by storing the compounds I or II in an atmospheric pressure at 70° C. for 10 days and determining the relative decrease in the content by HPLC analysis at an interval of 7 days in each case.
We have now found, surprisingly, that the salts of the general formula I and II are considerably more stable than the betaine and salts of mineral acids and C
1
-C
4
-carboxylic acids. The crystallinity of the salts is particularly advantageous for the stability of the active substance.
The novel salts of the general formula I or II can be employed for the following indications:
diseases whose pathomechanism is based directly or indirectly on the proteolytic effect of thrombin,
diseases whose pathomechanism is based on thrombin-dependent activation of receptors and signal transduction,
diseases associated with stimulation (for example by PAI-1, PDGF (plated derived growth factor), P-selectin, ICAM-1, tissue factor or inhibition (for example NO synthesis in smooth muscle cells) of the expression of genes in body cells,
diseases based on the mitogenic effect of thrombin,
diseases based on a thrombin-dependent change in contractility and permeability of epithelial cells (for example vascular endothelial cells),
thrombin-dependent thromboembolic events such as deep vein thrombosis, pulmonary embolism, myocardial or cerebral infarct, atrial fibrillation, bypass occlusion,
disseminated intravascular coagulation (DIC),
reocclusion and for reducing the reperfusion time on comedication with thrombolytics such as streptokinase, urokinase, prourokinase, t-PA, APSAC, plasminogen activators from the salivary glands of animals, and the recombinant and mutated forms of all these substances,
the occurrence of early reocclusion and late restenosis after PTCA,
thrombin-dependent proliferation of smooth muscle cells,
accumulation of active thrombin in the CNS (for example in Alzheimer's disease),
tumor growth, and to prevent adhesion and metastasis of tumor cells.
The novel compounds can be employed in particular for the therapy and prophylaxis of thrombin-dependent thromboembolic events such as deep vein thromboses, pulmonary embolisms, myocardial or cerebral infarcts and unstable angina, also for the therapy of disseminated intravascular coagulation (DIC). They are also suitable for combination therapy with thrombolytics such as streptokinase, urokinase, prourokinase, t-PA, APSAC and other plasminogen activators to reduce the reperfusion time and extend the reocclusion time.
Further preferred areas of use are the prevention of thrombin-dependent early reocclusion and late restenosis after percutaneous transluminal coronary angioplasty, the prevention of thrombin-induced proliferation of smooth muscle cells, the prevention of the accumulation of active thrombin in the CNS (for example in Alzheimer's disease), the control of tumors and the prevention of mechanisms which lead to the adhesion and metastasis of tumor cells.
The novel compounds can also be used for coating artificial surfaces such as hemodialysis membranes and the tubing systems and lines necessary therefor, and oxygenators of an extravascular circulation, stents and heart valves.
The novel compounds can also be employed for diseases whose pathomechanism is based directly or indirectly on the proteolytic effect of kininogenases, in particular kallikrein, for example for inflammatory diseases such as asthma, pancreatitis, rhinitis, arthritis, urticaria and other internal inflammatory diseases.
The compounds according to the invention can be administered orally or parenterally (subcutaneously, intravenously, intramuscularly, intraperitoneally, rectally) in a conventional way. Administration can also take place with vapors or sprays through the nasopharyngeal space. The compounds can, in particular, be given orally.
The dosage depends on the age, condition and weight of the patient and on the mode of administration. The daily dose of active substance per person is usually between about 10 and 2000 mg on oral administration and between about 1 and 200 mg on parenteral administration. This dose can be given in 2 to 4 single doses or once a day as depot form.
The novel compounds can be used in conventional solid or liquid pharmaceutical forms, for example as uncoated or (film-)coated tablets, capsules, powders, granules, suppositories, solutions, ointments, creams or sprays. These are produced in a conventional way. The active substances can for this purpose be processed with conventional pharmaceutical excipients such as tablet binders, bulking agents, preservatives, tablet disintegrants, flow regulators, plasticizers, wetting agents, dispersants, emulsifiers, solvents, release-slowing agents, antioxidants and/or propellant gases (cf. H. Sucker et al.: Pharmazeutische Technologie, Thieme-Verlag, Stuttgart, 1978). The administration forms obtained in this way normally contain the active su

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