US20140050786A1 - Combination of triazine derivatives and insulin sensitisers - Google Patents

Combination of triazine derivatives and insulin sensitisers Download PDF

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US20140050786A1
US20140050786A1 US14/063,530 US201314063530A US2014050786A1 US 20140050786 A1 US20140050786 A1 US 20140050786A1 US 201314063530 A US201314063530 A US 201314063530A US 2014050786 A1 US2014050786 A1 US 2014050786A1
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Gerard Moinet
Daniel Cravo
Didier Mesangeau
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Poxel SA
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
    • C07D251/40—Nitrogen atoms
    • C07D251/48—Two nitrogen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42—Oxazoles
    • A61K31/422—Oxazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives

Definitions

  • the present invention relates to a pharmaceutical composition of triazine derivatives or described pharmaceutically acceptable salts thereof with an insulin sensitiser, for the manufacture of a medicament that can be used in the treatment of non-insulin-dependent diabetes and pathologies associated with insulin resistance syndrome.
  • Diabetes mellitus (or diabetes) is one of the most prevalent diseases in the world today. Individuals suffering from diabetes have been divided into two classes, namely type I or insulin-dependent diabetes mellitus and type II or non-insulin-dependent diabetes mellitus (NIDDM).
  • NIDDM non-insulin-dependent diabetes mellitus
  • NIDDM accounts for approximately 90% of all diabetics, and is estimated to affect 12 to 14 million adults in the United States alone (6.6% of the population).
  • NIDDM is characterised both by fasting hyperglycaemia and exaggerated postprandial increases in plasmatic glucose levels.
  • NIDDM is associated with a variety of long-term complications, including microvascular diseases, such as retinopathy, nephropathy and neuropathy, and macrovascular diseases, such as coronary heart disease. Numerous studies in animal models show a causal relationship between long-term complications and hyperglycaemia. Recent results obtained by the Diabetes Control and Complications Trial (DCCT) and the Swedish Prospective Study have for the first time demonstrated this relationship in man by showing that insulin-dependent diabetics have a substantially lower risk of development and progression of these complications if they are subjected to tighter glycaemic control. Tighter control is also expected to benefit NIDDM patients.
  • DCCT Diabetes Control and Complications Trial
  • the Sweden Prospective Study have for the first time demonstrated this relationship in man by showing that insulin-dependent diabetics have a substantially lower risk of development and progression of these complications if they are subjected to tighter glycaemic control. Tighter control is also expected to benefit NIDDM patients.
  • Hyperglycaemia in the case of NIDDM is associated with two biochemical anomalies, namely insulin resistance and insufficiency of insulin secretion.
  • NIDDM neurodegenerative disease 2019
  • the initial treatment of NIDDM is based on a controlled diet and controlled physical exercise, since a considerable number of diabetics are over weight or obese ( ⁇ 67%) and since loss of weight can improve insulin secretion and sensitivity to insulin and lead to normal glycaemia.
  • the monotherapy may show a loss of efficacy over time. This is referred to as “secondary deficiency”. This may represent up to 50% unsatisfactory response after 10 years of treatment.
  • the studies conducted have shown that it is possible to deal with this problem by combining in the same pharmaceutical form metformin with TZDs (EP 869 796 B1 or EP 861 666 B1).
  • metformin-based combinations have adverse effects associated with the use of metformin, in particular intestinal symptoms, such as nausea, diarrhoea and abdominal pain.
  • Triazine derivatives with an antidiabetic effect comparable to metformin have been described in WO 01/55122. However, their combination has never been suggested.
  • the applicant has developed a novel pharmaceutical composition comprising an antidiabetic agent of triazine type, such as those described in WO 01/55122 and an insulin sensitiser.
  • the combinations according to the invention show synergistic activity and significantly reduce the side effects of the known combinations.
  • the present invention relates to a novel pharmaceutical composition to comprising an insulin sensitiser and a compound of the general formula (I):
  • R1, R2, R3 and R4 are independently chosen from the following groups:
  • R1 and R2 on the one hand, and R3 and R4, on the other hand, possibly forming with the nitrogen atom an n-membered ring (n between 3 and 8) optionally containing one or more heteroatoms chosen from N, O and S and possibly being substituted by one or more of the following groups: amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
  • R5 and R6 are independently chosen from the following groups:
  • One particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are compounds of the formula (I) in which R5 is hydrogen.
  • triazine derivatives are to compounds of the formula (I) in which R5 and R6 form with the carbon atom to which they are attached an m-membered ring (m between 3 and 8) optionally containing one or more heteroatoms chosen from N, O and S and possibly being substituted by one or more of the following groups: (C1-C5)alkyl, amino, hydroxyl, (C1-C5)alkylamino, alkoxy(C1-C5), (C1-C5)alkylthio, (C6-C14)aryl, (C6-C14)aryl(C1-C5)alkoxy,
  • C10-C30 polycyclic residue optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl.
  • triazine derivatives are compounds of the formula (I) in which R5 and R6 are independently chosen from the following groups:
  • a more particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are compounds of the formula (I) in which R1 and R2 are a methyl group and R3 and R4 represent a hydrogen.
  • m-membered ring formed by R5 and R6 in particular means a saturated ring, such as a cyclohexyl, piperidyl or tetrahydropyranyl group.
  • polycyclic group formed by R5 and R6 means an optionally substituted carbon-based polycyclic group and in particular a steroid residue.
  • the invention more particularly relates to pharmaceutical compositions chosen from:
  • insulin sensitiser means any compound capable of increasing the sensitivity of tissues to insulin.
  • Insulin sensitisers include, for example, tyrosine phosphatase inhibitors (PTP inhibitors), GSK-3 inhibitors, retinoid X receptor agonists (RXR agonists), glitazones (TZD), non-TZD PPAR ⁇ agonists, PPAR ⁇ /PPAR ⁇ double agonists, agonists based on compounds containing vanadium, and biguanides, for instance metformin.
  • Insulin sensitisers may also be in the form of pharmaceutically acceptable salts, such as, in a non-limiting manner, the hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, phosphate, citrate, methanesulfonate, trifluoroacetate or acetate, the sodium ion, the potassium ion, the calcium ion or the magnesium ion.
  • pharmaceutically acceptable salts such as, in a non-limiting manner, the hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, phosphate, citrate, methanesulfonate, trifluoroacetate or acetate, the sodium ion, the potassium ion, the calcium ion or the magnesium ion.
  • glitazones includes, in a non-limiting manner, englitazone, darglitazone, ciglitazone, DRF2189, BM-13.1246, AY-31637, YM268, AD-5075, DN-108, rosiglitazone, pioglitazone, troglitazone, MCC555, T-174 and KRP297.
  • non-TZD PPAR ⁇ agonist more particularly includes N-(2-benzoylphenyl)-L-tyrosine analogues, such as, in a non-limiting manner, GI-262570 and JTT501.
  • PPAR ⁇ /PPAR ⁇ double agonist includes, in a non-limiting manner, compounds, such as: NNC-61-4655, TZD18, LY-510929, LY-465608, LSN862, GW-409544, Muraglitazar, Ragaglitazar, Tesaglitazar, to and also the compounds described in WO 03/011819 (Example 8) and WO 00/039113 (Example 16b describing oxeglitazar).
  • the compounds of the invention of the formula (I) as defined above, containing a sufficiently basic function, or both, may include the corresponding pharmaceutically acceptable salts of organic or mineral acids.
  • corresponding pharmaceutically acceptable salts of organic or mineral acids means any salt prepared from any non-toxic pharmaceutically acceptable organic or inorganic acid.
  • Such acids include acetic acid, benzenesulfonic acid, benzoic acid, citric acid, carbonic acid, ethanesulfonic acid, fumaric acid, gluconic acid, glutamic acid, hydrobromic acid, hydrochloric acid, lactic acid, mandelic acid, malic acid, maleic acid, methanesulfonic acid, mucic acid, nitric acid, pamoic acid, pantothenic acid, phosphoric acid, succinic acid, tartaric acid and para-toluenesulfonic acid.
  • Hydrochloric acid is advantageously used.
  • the invention also relates to the chiral salts of the compounds of the formula (I) used for the separation of the racemates of the compounds of the formula (I).
  • (+)-D-di-O-benzoyltartaric acid (+)-D-di-O-benzoyltartaric acid, ( ⁇ )-L-di-O-benzoyltartaric acid, ( ⁇ )-L-di-O,O′-p-toluoyl-L-tartaric acid, (+)-D-di-O,O′-p-toluoyl-L-tartaric acid, (R)-(+)-malic acid, (S)-( ⁇ )-malic acid, (+)-camphanic acid, ( ⁇ )-camphanic acid, R-( ⁇ )-1,1′-binaphthalen-2,2′-diylhydrogenophosphonic acid, (+)-camphoric acid, ( ⁇ )-camphoric acid, (S)-(+)-2-phenylpropionic acid, (R)-(+)-2-phenylpropionic acid, D-( ⁇ )-mandelic acid, L-(+)
  • the compounds of the formula (I) above also include the prodrugs of these compounds.
  • prodrugs means compounds which, when administered to the patient, are chemically and/or biologically converted in the live body into compounds of the formula (I).
  • (C6-C14)aryl(C1-C20)alkyl refers to the corresponding -alkylaryl groups. Mention will be made in particular of benzyl and phenethyl groups;
  • (C6-C14)aryl refers to an aromatic group containing from 6 to 14 carbon atoms with at least one of the rings having a system of conjugated pi electrons, and including biaryls, which may be optionally substituted. Mention will be made in particular of biphenyl, phenyl, naphthyl, anthryl and phenanthryl radicals;
  • the compounds that are useful according to the present invention may contain asymmetric centres. These asymmetric centres may be, independently, in R or S configuration. It will be clear to a person skilled in the art that certain compounds that are useful according to the invention may also exhibit geometrical isomerism. It should be understood that the present invention includes individual geometrical isomers and stereoisomers and mixtures thereof, including racemic mixtures, of compounds of the formula (I) above. Isomers of this type can be separated from mixtures thereof by application or adaptation of known processes, for example chromatography techniques or recrystallisation techniques, or they are prepared separately from suitable isomers of their intermediates.
  • the present patent application also concerns the polymorphic forms of the compounds, as obtained according to patent application WO 2004/089917, for instance the A1 polymorphic form of the salt (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride.
  • the present invention also relates to the other polymorphic forms of the compounds, such as the H1 polymorphic form of the salt (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride, which can be prepared as follows:
  • Example 18 Approximately 3 g of the A1 form of Example 18 are dissolved in 50 ml of 1 mol/l HCl at room temperature. The clear solution obtained is left to evaporate at room temperature, in an open beaker, until a solid residue crystallises.
  • compositions according to the present invention are useful in the treatment of pathologies associated with insulin resistance syndrome (syndrome X).
  • Insulin resistance is characterised by a reduction in the action of insulin (cf. Presse Médicale, 1997, 26 (No. 14), 671-677) and is involved in a large number of pathological conditions, such as diabetes and more particularly non-insulin-dependent diabetes (type II diabetes or NIDDM), dyslipidaemia, obesity and arterial hypertension, and also certain microvascular and macrovascular complications, for instance atherosclerosis, retinopathy and neuropathy.
  • NIDDM non-insulin-dependent diabetes
  • the aim of the present invention is to propose a pharmaceutical composition for significantly improving the condition of diabetics.
  • compositions of the invention especially have hypoglycaemiant activity.
  • the compounds of the formula (I) are therefore useful in the treatment of pathologies associated with hyperglycaemia.
  • the pharmaceutical composition comprising the triazine compound of the formula (I) in combination with an insulin sensitiser can be prepared by mixing together the various active principles, either all together or independently with a physiologically acceptable support, an excipient, a binder, a diluent, etc. It is then administered orally or non-orally, for instance via the parenteral, intravenous, cutaneous, nasal or rectal route. If the active principles are formulated independently, the corresponding formulations can be mixed together extemporaneously using a diluent and are then administered or can be administered independently of each other, either successively or sequentially.
  • compositions of the invention include formulations, such as granules, powders, tablets, gel capsules, syrups, emulsions and suspensions, and also forms used for non-oral administration, for instance injections, sprays or suppositories.
  • the pharmaceutical forms can be prepared via the known conventional techniques.
  • an excipient for example lactose, sucrose, starch, mannitol, etc.
  • a disintegrant for example calcium carbonate, calcium carboxymethylcellulose, alginic acid, sodium carboxymethylcellulose, colloidal silicon dioxide, sodium croscarmellose, Crospovidone, guar gum, magnesium aluminium silicate, microcrystalline cellulose, cellulose powder, pregelatinised starch, sodium alginate, starch glycolate, etc.
  • a binder for example alpha-starch, gum arabic, carboxymethylcellulose, polyvinylpyrrolidone, hydroxypropylcellulose, alginic acid, carbomer, dextrin, ethylcellulose, sodium alginate, maltodextrin, liquid glucose, magnesium aluminium silicate, hydroxyethylcellulose, methylcellulose, guar gum, etc.
  • a lubricant for example talc, magnesium stearate
  • the tablet can be coated via the known techniques, in order to mask the taste (for example with cocoa powder, mint, borneol, cinnamon powder, etc.) or to allow enteric dissolution or sustained release of the active principles.
  • the coating products that can be used are, for example, ethylcellulose, hydroxymethylcellulose, polyoxyethylene glycol, cellulose acetophthalate, hydroxypropylmethylcellulose phthalate and Eudragit® (methacrylic acid-acrylic acid copolymer), Opadry® (hydroxypropylmethylcellulose+macrogol+titanium oxide+lactose monohydrate).
  • Pharmaceutically acceptable colorants may be added (for example yellow iron oxide, red iron oxide, quinoline yellow lake, etc.).
  • Pharmaceutical forms, such as tablets, powders, sachets and gel capsules can be used for an oral administration.
  • the liquid pharmaceutical forms for oral administration include solutions, suspensions and emulsions.
  • the aqueous solutions can be obtained by dissolving the active principles in water, followed by addition of flavourings, colorants, stabilisers and thickener, if necessary. In order to improve the solubility, it is possible to add ethanol, propylene glycol or other pharmaceutically acceptable non-aqueous solvents.
  • the aqueous suspensions for oral use can be obtained by dispersing the finely divided active principles in water with a viscous product, such as natural or synthetic gums, resins, methylcellulose or sodium carboxymethylcellulose.
  • the pharmaceutical forms for injection can be obtained, for example, by the following process.
  • the active principle(s) is (are) dissolved, suspended or emulsified either in an aqueous medium (for example distilled water, physiological saline, Ringer's solution, etc.) or in an oily medium (for example a plant oil, such as olive oil, sesameseed oil, cottonseed oil, corn oil, etc., or propylene glycol), with a dispersant (for example Tween 80, HCO 60 (Nikko Chemicals), polyethylene glycol, carboxymethylcellulose, sodium alginate, etc.), a preserving agent (for example methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, benzyl alcohol, chlorobutanol, phenol, etc.), an isotonicity agent (for example sodium chloride, glycerol, sorbitol, glucose, etc.) and also other additives, such as, if desired, a solubilising agent
  • a pharmaceutical form for external use can be obtained from a solid, semi-solid or liquid composition containing the active principle(s).
  • the active principle(s) is (are) treated, alone or as mixtures, with excipients (for example lactose, mannitol, starch, microcrystalline cellulose, sucrose, etc.) and a thickener (for example natural gums, cellulose derivatives, acrylic polymers, etc.) so as to convert them into powder.
  • excipients for example lactose, mannitol, starch, microcrystalline cellulose, sucrose, etc.
  • a thickener for example natural gums, cellulose derivatives, acrylic polymers, etc.
  • compositions may optionally contain a pH regulator (for example carbonic acid, phosphoric acid, citric acid, hydrochloric acid, sodium hydroxide, etc.) and a preserving agent (for example p-hydroxybenzoic acid esters, chlorobutanol, benzalkonium chloride, etc.) and also other additives.
  • a pH regulator for example carbonic acid, phosphoric acid, citric acid, hydrochloric acid, sodium hydroxide, etc.
  • a preserving agent for example p-hydroxybenzoic acid esters, chlorobutanol, benzalkonium chloride, etc.
  • the daily doses of the insulin sensitisers are between 0.5 mg and 50 mg.
  • the daily dose is between 1 mg and 8 mg, more preferably 4 mg. If pioglitazone is used, the daily dose is between 15 mg and 45 mg. If muraglitazar is used, the daily dose is between 0.5 mg and 20 mg, preferably 5 mg.
  • the daily doses of the compounds of the formula (I) are between 200 mg and 2000 mg.
  • the relative proportion of the constituents of the pharmaceutical compositions of the present invention takes into account the recommended dosages of the respective active principles. These relative proportions of insulin sensitisers, or of pharmaceutically acceptable salts thereof, and of the compounds of the formula (I), or of pharmaceutically acceptable salts thereof, thus vary in consequence.
  • the weight ratio of insulin sensitiser to the compound of the formula (I) ranges between 1/2 and 1/2000, more particularly from 1/4 to 1/2000 and especially from 1/5 to 1/2000.
  • the frequency of administration of the compounds of the invention is between 1 and 2 administrations per day. In the case where the doses of compounds of the formula (I) necessitate more than one daily administration, the amounts of insulin sensitisers and the insulin sensitiser/compound of the formula (I) ratios are adjusted in consequence.
  • the aim of the present invention is also to propose a method of treatment to via co-administration of effective amounts of a compound of the formula (I) and of an insulin sensitiser, and also kits for allowing this co-administration.
  • kits that are suitable for the treatment by the methods described above. These kits comprise a composition containing the compound of the formula (I) in the dosages indicated above and a second composition containing the insulin sensitisers in the dosages indicated above, for a simultaneous, separate or sequential administration, in effective amounts according to the invention.
  • co-administration means the simultaneous, separate or sequential administration of one or more compounds to the same patient, over a period that may be up to 2 hours or even up to 12 hours.
  • co-administration includes (1) a simultaneous administration of the two compounds, (2) an administration of the first, followed 2 hours later by the administration of the second compound, (3) an administration of the first, followed 12 hours later by the administration of the second compound.
  • compositions according to the invention are given as non-limiting illustrations.
  • the amounts are expressed on a weight basis.
  • the capacity of the compounds of the invention in combination with insulin-sensitising antidiabetic compounds to modify the blood glucose levels is evaluated in vivo in diabetic GK rats.
  • the antidiabetic agents are administered twice a day (bid) to the GK rats for 4 days.
  • the oral glucose tolerance test (OGTT) is performed after the last day of treatment.
  • OGTT is performed in the morning after 3 hours of fasting by oral administration of a glucose charge of 2 g/kg of body mass.
  • the blood samples are collected from the tail vein at 0; 10; 20; 30; 45; 60; 90 and 120 minutes to determine the glucose levels.
  • rosiglitazone The combination of rosiglitazone and of the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine was tested as follows. The two compounds were administered alone and in combination. The doses used for the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine were 50 and 100 mg/kg PO twice daily for 4 days. For rosiglitazone, the doses used were 1 and 5 mg/kg PO twice daily for 4 days. The following combination was tested:
  • GK n 8 12.93 +/ ⁇ 0.41 13.10 +/ ⁇ 0.87 3343 + 262 (+)-2-amino-3,6-dihydro-4- 12.95 +/ ⁇ 0.41 11.01 +/ ⁇ 0.37 ⁇ 16% 2688 +/ ⁇ 99 ⁇ 19.6% dimethylamino-6-methyl- 1,3,5-triazine hydrochloride salt 100 mg/kg bid Rosiglitazone 5 mg/kg bid 12.81 +/ ⁇ 0.27 10.52 +/ ⁇ 0.84 ⁇ 19.7% 2954 +/ ⁇ 150 ⁇ 11.6% (+)-2-amino-3,6-dihydro-4- 12.86 +/ ⁇ 0.52 10.03 +/ ⁇ 0.35 ⁇ 23.4% 2311 +/ ⁇ 121 ⁇ 30.9% dimethylamino-6-methyl-
  • rosiglitazone 5 mg/kg and the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine 100 mg/kg showed much better efficacy than each compound individually.
  • an insulin sensitiser such as rosiglitazone
  • a compound such as the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine generates better activity on the glucose tolerance and the plasmatic glucose level of each than that of the compounds.

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Abstract

The present invention relates to combinations of triazine derivatives and of insulin sensitisers.

Description

    FIELD OF THE INVENTION
  • The present invention relates to a pharmaceutical composition of triazine derivatives or described pharmaceutically acceptable salts thereof with an insulin sensitiser, for the manufacture of a medicament that can be used in the treatment of non-insulin-dependent diabetes and pathologies associated with insulin resistance syndrome.
    • TECHNICAL BACKGROUND
  • “Diabetes mellitus” (or diabetes) is one of the most prevalent diseases in the world today. Individuals suffering from diabetes have been divided into two classes, namely type I or insulin-dependent diabetes mellitus and type II or non-insulin-dependent diabetes mellitus (NIDDM). Non-insulin-dependent diabetes mellitus (NIDDM) accounts for approximately 90% of all diabetics, and is estimated to affect 12 to 14 million adults in the United States alone (6.6% of the population). NIDDM is characterised both by fasting hyperglycaemia and exaggerated postprandial increases in plasmatic glucose levels. NIDDM is associated with a variety of long-term complications, including microvascular diseases, such as retinopathy, nephropathy and neuropathy, and macrovascular diseases, such as coronary heart disease. Numerous studies in animal models show a causal relationship between long-term complications and hyperglycaemia. Recent results obtained by the Diabetes Control and Complications Trial (DCCT) and the Stockholm Prospective Study have for the first time demonstrated this relationship in man by showing that insulin-dependent diabetics have a substantially lower risk of development and progression of these complications if they are subjected to tighter glycaemic control. Tighter control is also expected to benefit NIDDM patients.
  • Hyperglycaemia in the case of NIDDM is associated with two biochemical anomalies, namely insulin resistance and insufficiency of insulin secretion.
  • The initial treatment of NIDDM is based on a controlled diet and controlled physical exercise, since a considerable number of diabetics are over weight or obese (˜67%) and since loss of weight can improve insulin secretion and sensitivity to insulin and lead to normal glycaemia.
  • Patients suffering from a hyperglycaemia that cannot be controlled solely by a diet and/or physical exercise are then treated with oral antidiabetics.
  • A number of categories of oral antidiabetics are currently used in monotherapy for the treatment of NIDDM:
      • insulin secretion stimulators. They are represented, firstly, by sulfonylureas (SU) and by “glinides”. As regards SUs, mention will be made in particular of carbutamide (Glucidoral®), glibenclamide/glyburide (Daonil®, Euglucan®), glibomuride (Glutril®), gliclazide (Diamicron®), glimepiride (Amarel®) and glipizide (Glibenese®). As regards the “glinides”, mention will be made in particular of repaglinide (NovoNorm®);
      • agents that reduce glucogenesis, represented by the biguanides. Mention will be made in particular of metformin (Glucophage®, Stagid®);
      • insulin sensitisers, represented mainly by thiazolidinediones (TZD). Mention will be made in particular of pioglitazone (Actos®) and rosiglitazone (Avandia®);
      • alpha-glucosidase inhibitors. Mention will be made in particular of acarbose (Glucor®) and miglitol (Diastabol®).
  • However, the monotherapy may show a loss of efficacy over time. This is referred to as “secondary deficiency”. This may represent up to 50% unsatisfactory response after 10 years of treatment. The studies conducted have shown that it is possible to deal with this problem by combining in the same pharmaceutical form metformin with TZDs (EP 869 796 B1 or EP 861 666 B1).
  • Moreover, the combination metformin+rosiglitazone (Avandamet®) has been marketed.
  • However, these metformin-based combinations have adverse effects associated with the use of metformin, in particular intestinal symptoms, such as nausea, diarrhoea and abdominal pain. Triazine derivatives with an antidiabetic effect comparable to metformin have been described in WO 01/55122. However, their combination has never been suggested.
  • The applicant has developed a novel pharmaceutical composition comprising an antidiabetic agent of triazine type, such as those described in WO 01/55122 and an insulin sensitiser.
  • Unexpectedly, the combinations according to the invention show synergistic activity and significantly reduce the side effects of the known combinations.
    • DESCRIPTION OF THE INVENTION
  • The present invention relates to a novel pharmaceutical composition to comprising an insulin sensitiser and a compound of the general formula (I):
  • Figure US20140050786A1-20140220-C00001
  • in which:
    R1, R2, R3 and R4 are independently chosen from the following groups:
      • H,
      • (C1-C20)alkyl optionally substituted by halogen, (C1-C5)alkyl, (C1-C5)-alkoxy or (C3-C8)cycloalkyl,
      • (C2-C20)alkenyl optionally substituted by halogen, (C1-C5)alkyl or (C1-C5)alkoxy
      • (C2-C20)alkynyl optionally substituted by halogen, (C1-C5)alkyl or (C1-C5)alkoxy
      • (C3-C8)cycloalkyl optionally substituted by (C1-C5)alkyl or (C1-C5)-alkoxy
      • hetero(C3-C8)cycloalkyl bearing one or more heteroatoms chosen from N, O and S and optionally substituted by (C1-C5)alkyl or (C1-C5)alkoxy
      • (C6-C14)aryl(C1-C20)alkyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C6-C14)aryl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C1-C13)heteroaryl bearing one or more heteroatoms chosen from N, O and S and optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
  • to R1 and R2, on the one hand, and R3 and R4, on the other hand, possibly forming with the nitrogen atom an n-membered ring (n between 3 and 8) optionally containing one or more heteroatoms chosen from N, O and S and possibly being substituted by one or more of the following groups: amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
  • R5 and R6 are independently chosen from the following groups:
      • H,
      • (C1-C20)alkyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C2-C20)alkenyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C2-C20)alkynyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)-aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C3-C8)cycloalkyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • hetero(C3-C8)cycloalkyl bearing one or more heteroatoms chosen from N, O and S and optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C6-C14)aryl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C1-C13)heteroaryl bearing one or more heteroatoms chosen from N, O and S and optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • (C6-C14)aryl(C1-C5)alkyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
      • R5 and R6 possibly forming with the carbon atom to which they are attached an m-membered ring (m between 3 and 8) optionally containing one or more heteroatoms chosen from N, O and S and possibly being substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
        or possibly forming with the carbon atom a C10-C30 polycyclic residue optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl,
        R5 and R6 together also possibly representing the group ═O or ═S, the nitrogen atom of a heterocycloalkyl or heteroaryl group possibly being substituted by a (C1-C5)alkyl, (C3-C8)cycloalkyl, (C6-C14)aryl, (C6-C14)aryl(C1-C5)alkyl or (C1-C6)acyl group,
        and also the racemic forms, tautomers, enantiomers, diastereoisomers, epimers and mixtures thereof, and the pharmaceutically acceptable salts.
  • One particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are compounds of the formula (I) in which R5 is hydrogen.
  • Another particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are to compounds of the formula (I) in which R5 and R6 form with the carbon atom to which they are attached an m-membered ring (m between 3 and 8) optionally containing one or more heteroatoms chosen from N, O and S and possibly being substituted by one or more of the following groups: (C1-C5)alkyl, amino, hydroxyl, (C1-C5)alkylamino, alkoxy(C1-C5), (C1-C5)alkylthio, (C6-C14)aryl, (C6-C14)aryl(C1-C5)alkoxy,
  • or form with the carbon atom a C10-C30 polycyclic residue optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl.
  • Another particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are compounds of the formula (I) in which R5 and R6 are independently chosen from the following groups:
      • (C1-C20)alkyl groups optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl.
  • Preferably, R1, R2, R3 and R4 are independently chosen from H and (C1-C20)alkyl groups optionally substituted by halogen, (C1-C5)alkyl, (C1-C5)alkoxy or (C3-C8)cycloalkyl; more preferably, R1=R2=H and R3=R4=(C1-C20)alkyl optionally substituted by halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C3-C8)cycloalkyl or vice versa.
  • Preferably, R5 and R6 are independently chosen from H and (C1-C20)alkyl groups optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl; more preferably, R5=H and R6=(C1-C20)alkyl optionally substituted by amino, hydroxyl, thio, halogen, (C1-C5)alkyl, (C1-C5)alkoxy, (C1-C5)alkylthio, (C1-C5)alkylamino, (C6-C14)aryloxy, (C6-C14)aryl(C1-C5)alkoxy, cyano, trifluoromethyl, carboxyl, carboxymethyl or carboxyethyl or vice versa.
  • A more particular group of the invention concerns the pharmaceutical compositions according to the invention in which the triazine derivatives are compounds of the formula (I) in which R1 and R2 are a methyl group and R3 and R4 represent a hydrogen.
  • The term “m-membered ring formed by R5 and R6” in particular means a saturated ring, such as a cyclohexyl, piperidyl or tetrahydropyranyl group.
  • The term “polycyclic group formed by R5 and R6” means an optionally substituted carbon-based polycyclic group and in particular a steroid residue.
  • Compounds of the formula (I) that may especially be mentioned include:
  • Formula Salt
     1
    Figure US20140050786A1-20140220-C00002
         		HCl
     2
    Figure US20140050786A1-20140220-C00003
         		HCl
     3
    Figure US20140050786A1-20140220-C00004
     4
    Figure US20140050786A1-20140220-C00005
         		HCl
     5
    Figure US20140050786A1-20140220-C00006
         		Methane- sulfonate
     6
    Figure US20140050786A1-20140220-C00007
     7
    Figure US20140050786A1-20140220-C00008
         		HCl
     8
    Figure US20140050786A1-20140220-C00009
         		HCl
     9
    Figure US20140050786A1-20140220-C00010
         		HCl
    10
    Figure US20140050786A1-20140220-C00011
         		HCl
    11
    Figure US20140050786A1-20140220-C00012
         		HCl
    12
    Figure US20140050786A1-20140220-C00013
         		HCl
    13
    Figure US20140050786A1-20140220-C00014
    14
    Figure US20140050786A1-20140220-C00015
         		Fumarate
    15
    Figure US20140050786A1-20140220-C00016
         		HCl
    16
    Figure US20140050786A1-20140220-C00017
         		HCl
    17
    Figure US20140050786A1-20140220-C00018
         		HCl
    18
    Figure US20140050786A1-20140220-C00019
         		HCl
    19
    Figure US20140050786A1-20140220-C00020
         		HCl
    20
    Figure US20140050786A1-20140220-C00021
         		Carbonate
    21
    Figure US20140050786A1-20140220-C00022
         		Carbonate
    22
    Figure US20140050786A1-20140220-C00023
         		HCl
    23
    Figure US20140050786A1-20140220-C00024
         		HCl
    24
    Figure US20140050786A1-20140220-C00025
         		HCl
    25
    Figure US20140050786A1-20140220-C00026
         		HCl
    26
    Figure US20140050786A1-20140220-C00027
         		HCl
    27
    Figure US20140050786A1-20140220-C00028
         		HCl
    28
    Figure US20140050786A1-20140220-C00029
         		HCl
    29
    Figure US20140050786A1-20140220-C00030
         		Carbonate
    30
    Figure US20140050786A1-20140220-C00031
         		Carbonate
    31
    Figure US20140050786A1-20140220-C00032
         		HCl
    32
    Figure US20140050786A1-20140220-C00033
         		Carbonate
    33
    Figure US20140050786A1-20140220-C00034
         		HCl
    34
    Figure US20140050786A1-20140220-C00035
         		para- Toluene- sulfonate
    35
    Figure US20140050786A1-20140220-C00036
         		HCl
    36
    Figure US20140050786A1-20140220-C00037
         		para- Toluene- sulfonate
    37
    Figure US20140050786A1-20140220-C00038
         		para- Toluene- sulfonate
    38
    Figure US20140050786A1-20140220-C00039
         		HCl
    39
    Figure US20140050786A1-20140220-C00040
         		HCl
    40
    Figure US20140050786A1-20140220-C00041
         		HCl
    41
    Figure US20140050786A1-20140220-C00042
         		para- Toluene- sulfonate
    42
    Figure US20140050786A1-20140220-C00043
         		HCl
    43
    Figure US20140050786A1-20140220-C00044
         		HCl
    44
    Figure US20140050786A1-20140220-C00045
         		HCl
    45
    Figure US20140050786A1-20140220-C00046
         		para- Toluene- sulfonate
  • and more preferably the compound of Example 18.
  • According to yet another preferred embodiment, the invention more particularly relates to pharmaceutical compositions chosen from:
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride, and rosiglitazone;
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride, and troglitazone;
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine to hydrochloride, and pioglitazone;
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride, and muraglitazar.
  • The term “insulin sensitiser” means any compound capable of increasing the sensitivity of tissues to insulin. Insulin sensitisers include, for example, tyrosine phosphatase inhibitors (PTP inhibitors), GSK-3 inhibitors, retinoid X receptor agonists (RXR agonists), glitazones (TZD), non-TZD PPARγ agonists, PPARα/PPARγ double agonists, agonists based on compounds containing vanadium, and biguanides, for instance metformin. Insulin sensitisers may also be in the form of pharmaceutically acceptable salts, such as, in a non-limiting manner, the hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, phosphate, citrate, methanesulfonate, trifluoroacetate or acetate, the sodium ion, the potassium ion, the calcium ion or the magnesium ion.
  • The term “glitazones” includes, in a non-limiting manner, englitazone, darglitazone, ciglitazone, DRF2189, BM-13.1246, AY-31637, YM268, AD-5075, DN-108, rosiglitazone, pioglitazone, troglitazone, MCC555, T-174 and KRP297.
  • The term “non-TZD PPARγ agonist” more particularly includes N-(2-benzoylphenyl)-L-tyrosine analogues, such as, in a non-limiting manner, GI-262570 and JTT501.
  • The term “PPARα/PPARγ double agonist” includes, in a non-limiting manner, compounds, such as: NNC-61-4655, TZD18, LY-510929, LY-465608, LSN862, GW-409544, Muraglitazar, Ragaglitazar, Tesaglitazar, to and also the compounds described in WO 03/011819 (Example 8) and WO 00/039113 (Example 16b describing oxeglitazar).
  • The compounds of the invention of the formula (I) as defined above, containing a sufficiently basic function, or both, may include the corresponding pharmaceutically acceptable salts of organic or mineral acids.
  • For the purposes of the present invention, the term “corresponding pharmaceutically acceptable salts of organic or mineral acids” means any salt prepared from any non-toxic pharmaceutically acceptable organic or inorganic acid. Such acids include acetic acid, benzenesulfonic acid, benzoic acid, citric acid, carbonic acid, ethanesulfonic acid, fumaric acid, gluconic acid, glutamic acid, hydrobromic acid, hydrochloric acid, lactic acid, mandelic acid, malic acid, maleic acid, methanesulfonic acid, mucic acid, nitric acid, pamoic acid, pantothenic acid, phosphoric acid, succinic acid, tartaric acid and para-toluenesulfonic acid. Hydrochloric acid is advantageously used.
  • The invention also relates to the chiral salts of the compounds of the formula (I) used for the separation of the racemates of the compounds of the formula (I).
  • By way of example, the following chiral acids are used: (+)-D-di-O-benzoyltartaric acid, (−)-L-di-O-benzoyltartaric acid, (−)-L-di-O,O′-p-toluoyl-L-tartaric acid, (+)-D-di-O,O′-p-toluoyl-L-tartaric acid, (R)-(+)-malic acid, (S)-(−)-malic acid, (+)-camphanic acid, (−)-camphanic acid, R-(−)-1,1′-binaphthalen-2,2′-diylhydrogenophosphonic acid, (+)-camphoric acid, (−)-camphoric acid, (S)-(+)-2-phenylpropionic acid, (R)-(+)-2-phenylpropionic acid, D-(−)-mandelic acid, L-(+)-mandelic acid, D-tartaric acid, L-tartaric acid, or a mixture of two or more thereof.
  • The compounds of the formula (I) above also include the prodrugs of these compounds.
  • The term “prodrugs” means compounds which, when administered to the patient, are chemically and/or biologically converted in the live body into compounds of the formula (I).
  • In the present description, the terms used have, unless otherwise indicated, the following meanings:
      • the term “(C1-C20)alkyl” denotes a linear or branched alkyl radical containing from 1 to 20 carbon atoms. Among the C1-C20 alkyl radicals that may especially be mentioned, in a non-limiting manner, are methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, tert-butyl, pentyl, hexyl, octyl, decyl, dodecyl, hexadecyl and octadecyl radicals;
      • the term “(C1-C20)alkenyl” denotes a linear or branched hydrocarbon-based radical containing one or more unsaturations in double bond form. As alkylene radicals containing from 1 to 20 carbon atoms, mention may be made, in a non-limiting manner, of ethenyl, prop-2-enyl, but-2-enyl, but-3-enyl, pent-2-enyl, pent-3-enyl and pent-4-enyl radicals;
      • the term “(C1-C20)alkynyl” denotes a linear or branched hydrocarbon-based radical containing one or more unsaturations in triple bond form. As alkylene radicals containing from 1 to 20 carbon atoms, mention may be made, in a non-limiting manner, of ethynyl, prop-2-ynyl, but-2-ynyl, but-3-ynyl, pent-2-ynyl, pent-3-ynyl and pent-4-ynyl radicals;
      • the term “alkoxy” refers to the term “alkyl-oxy”;
      • the term “halogen” refers, in a non-limiting manner, to fluorine, chlorine or bromine;
  • the term “(C6-C14)aryl(C1-C20)alkyl” refers to the corresponding -alkylaryl groups. Mention will be made in particular of benzyl and phenethyl groups;
  • the term “(C6-C14)aryl” refers to an aromatic group containing from 6 to 14 carbon atoms with at least one of the rings having a system of conjugated pi electrons, and including biaryls, which may be optionally substituted. Mention will be made in particular of biphenyl, phenyl, naphthyl, anthryl and phenanthryl radicals;
      • the term “hetero(C6-C14)aryl” refers to a 6-14-membered aromatic heterocycle containing 1-4 heteroatoms, the other atoms being carbon atoms. Among the heteroatoms, mention will be made in particular of oxygen, sulfur and nitrogen. Among the heteroaryl radicals, mention will be made more particularly of furyl, thienyl, pyridyl, pyrrolyl, pyrimidyl, pyrazinyl, oxazolyl, oxadiazolyl, isoxazolyl, quinolyl and thiazolyl radicals;
      • the term “(C3-C8)cycloalkyl” refers to a saturated hydrocarbon-based ring and containins monocyclic, bicyclic and polycyclic radicals containing from 3 to 8 carbon atoms. Mention will be made, in a non-limiting manner, of cyclopropyl and cyclobutyl radicals.
  • It will be appreciated that the compounds that are useful according to the present invention may contain asymmetric centres. These asymmetric centres may be, independently, in R or S configuration. It will be clear to a person skilled in the art that certain compounds that are useful according to the invention may also exhibit geometrical isomerism. It should be understood that the present invention includes individual geometrical isomers and stereoisomers and mixtures thereof, including racemic mixtures, of compounds of the formula (I) above. Isomers of this type can be separated from mixtures thereof by application or adaptation of known processes, for example chromatography techniques or recrystallisation techniques, or they are prepared separately from suitable isomers of their intermediates.
  • The enantiomers of the compounds according to the invention and the process for the preparation of them are especially described in patent application WO 2004/089917, the content of which is incorporated herein by reference.
  • The present patent application also concerns the polymorphic forms of the compounds, as obtained according to patent application WO 2004/089917, for instance the A1 polymorphic form of the salt (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride.
  • The present invention also relates to the other polymorphic forms of the compounds, such as the H1 polymorphic form of the salt (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride, which can be prepared as follows:
  • Approximately 3 g of the A1 form of Example 18 are dissolved in 50 ml of 1 mol/l HCl at room temperature. The clear solution obtained is left to evaporate at room temperature, in an open beaker, until a solid residue crystallises.
  • The characterisation is performed by:
  • FT-IR spectroscopy:
      • Brüker Vector 22
      • 2 cm−1 spectral resolution
      • 32 scans
      • KBR discs (analogous to method A AA21505)
      • To evaluate the intensity of the IR bands, the IR spectra were normalised by vectorisation in the spectral range 4000-400 cm−1 as an absorption spectrum.
  • Preadjustment was performed:
      • s: A>0.05
      • m: 0.01<A<0.05
      • w: A<0.01.
  • FT-Raman spectroscopy:
  • Brüker RFS-100
      • excitation: 1064 nm
      • spectral resolution: 1 cm−1
      • 1000 mW
      • 1000 scans
      • focalised
      • aluminium crucible (analogous to method RA AA21505)
      • To evaluate the intensity of the Raman bands, Raman spectra were normalised by vectorisation in the spectral range 3600-200 cm−1. Preadjustment was performed:
        • s: A>0.05
        • m: 0.01<A<0.05
        • w: A<0.01
  • Powder x-ray diffraction (XRD)
      • diffractometer D5000 (Brüker AXS)
      • radiation CuKα1 at 1.5406 Å (U=30 kV, A=40 mA)
      • Transmission mode
      • Detector in sensitive position
      • Primary monochromator
      • Angle range: 3-65 °2θ
      • Stage width: 0.05 °2θ
      • Measuring time/stage: 1.4 s
      • The XRD machine is set at 2θ±0.1°.
    Results
  • A1 form:
    • XRD:
  • No. d[Å] 2θ l/lo
    1 5.98 14.8 85
    2 5.26 16.8 83
    3 4.35 20.4 30
    4 3.57 24.9 100
    5 3.50 25.4 53
    6 3.36 26.5 96
    7 3.31 26.9 52
    8 3.04 29.3 57
    9 2.90 30.8 30
    10 2.74 32.7 35

    FT-IR bands (in cm−1):
    3384+/−1.5 (m), 3199+/−1.5 (m), 3163+/−1.5 (m), 3107+/−1.5 (m), 2993+/−1.5 (m), 2983+/−1.5 (m), 1652+/−1.5 (s), 1606+/−1.5 (s), 1576+/−1.5 (s), 1557+/−1.5 (s), 1505+/−1.5 (s), 1449+/−1.5 (m), 1427+/−1.5 (m), 1405+/−1.5 (m), 1383+/−1.5 (m), 1348+/−1.5 (m), 1306+/−1.5 (m), 1263+/−1.5 (w), 1235+/−1.5 (w), 1185+/−1.5 (w), 1096+/−1.5 (w), 1068+/−1.5 (w), 980+/−1.5 (w), 946+/−1.5 (w), 868+/−1.5 (w), 761+/−1.5 (w), 687+/−1.5 (m), 655+/−1.5 (m), 558+/−1.5 (w), 521+/−1.5 (w), 478+/−1.5 (w)
    FT-Raman bands (in cm−1):
    3217+/−1.5 (w), 2994+/−1.5 (m), 2983+/−1.5 (m), 2936+/−1.5 (s), 2883+/−1.5 (m), 1645+/−1.5 (w), 1602+/−1.5 (m), 1554+/−1.5 (m), 1453+/−1.5 (m), 1428+/−1.5 (m), 1349+/−1.5 (w), 1308+/−1.5 (w), 979+/−1.5 (m), 866+/−1.5 (w), 761+/−1.5 (w), 686+/−1.5 (s), 583+/−1.5 (m), 555+/−1.5 (s), 525+/−1.5 (m), 479+/−1.5 (m), 410+/−1.5 (m), 401+/−1.5 (m), 307+/−1.5 (m)
    H1 form
    • XRD:
  • No. d[Å] 2θ l/lo
    1 8.03 11.0 69
    2 7.27 12.2 25
    3 6.11 14.5 24
    4 4.01 22.1 86
    5 3.64 24.5 100
    6 3.26 27.3 51
    7 3.08 29.0 29
    8 3.04 29.4 34
    9 2.82 31.7 61
    10 2.66 33.6 26

    FT-IR bands (in cm−1):
    3386+/−1.5 (m), 3080+/−3 (m), 1706+/−1.5 (s), 1691+/−1.5 (s), 1634+/−1.5 (m), 1513+/−1.5 (m), 1445+/−1.5 (w), 1241+/−1.5 (w), 1079+/−1.5 (w), 989+/−1.5 (w), 940+/−1.5 (w), 861+/−1.5 (w), 823+/−1.5 (w), 675+/−1.5 (w), 603+/−1.5 (w), 573+/−1.5 (w), 549+/−1.5 (w), 527+/−1.5 (w)
  • For the purposes of this text, it is understood that the tautomeric forms are included in the mention of a given group, for example thio/mercapto or oxo/hydroxy.
  • The pharmaceutical compositions according to the present invention are useful in the treatment of pathologies associated with insulin resistance syndrome (syndrome X).
  • Insulin resistance is characterised by a reduction in the action of insulin (cf. Presse Médicale, 1997, 26 (No. 14), 671-677) and is involved in a large number of pathological conditions, such as diabetes and more particularly non-insulin-dependent diabetes (type II diabetes or NIDDM), dyslipidaemia, obesity and arterial hypertension, and also certain microvascular and macrovascular complications, for instance atherosclerosis, retinopathy and neuropathy.
  • In this respect, reference will be made, for example, to Diabetes, vol. 37, 1988, 1595-1607; Journal of Diabetes and its Complications, 1998, 12, 110-119 or Horm. Res., 1992, 38, 28-32.
  • The aim of the present invention is to propose a pharmaceutical composition for significantly improving the condition of diabetics.
  • The pharmaceutical compositions of the invention especially have hypoglycaemiant activity.
  • The compounds of the formula (I) are therefore useful in the treatment of pathologies associated with hyperglycaemia.
  • The pharmaceutical composition comprising the triazine compound of the formula (I) in combination with an insulin sensitiser can be prepared by mixing together the various active principles, either all together or independently with a physiologically acceptable support, an excipient, a binder, a diluent, etc. It is then administered orally or non-orally, for instance via the parenteral, intravenous, cutaneous, nasal or rectal route. If the active principles are formulated independently, the corresponding formulations can be mixed together extemporaneously using a diluent and are then administered or can be administered independently of each other, either successively or sequentially.
  • The pharmaceutical compositions of the invention include formulations, such as granules, powders, tablets, gel capsules, syrups, emulsions and suspensions, and also forms used for non-oral administration, for instance injections, sprays or suppositories.
  • The pharmaceutical forms can be prepared via the known conventional techniques.
  • The preparation of an orally administered solid pharmaceutical form will be performed by the following process: an excipient (for example lactose, sucrose, starch, mannitol, etc.), a disintegrant (for example calcium carbonate, calcium carboxymethylcellulose, alginic acid, sodium carboxymethylcellulose, colloidal silicon dioxide, sodium croscarmellose, Crospovidone, guar gum, magnesium aluminium silicate, microcrystalline cellulose, cellulose powder, pregelatinised starch, sodium alginate, starch glycolate, etc.), a binder (for example alpha-starch, gum arabic, carboxymethylcellulose, polyvinylpyrrolidone, hydroxypropylcellulose, alginic acid, carbomer, dextrin, ethylcellulose, sodium alginate, maltodextrin, liquid glucose, magnesium aluminium silicate, hydroxyethylcellulose, methylcellulose, guar gum, etc.) and a lubricant (for example talc, magnesium stearate, polyethylene 6000, etc.) are, for example, added to to the active principle(s) and the mixture obtained is then tabletted. If necessary, the tablet can be coated via the known techniques, in order to mask the taste (for example with cocoa powder, mint, borneol, cinnamon powder, etc.) or to allow enteric dissolution or sustained release of the active principles. The coating products that can be used are, for example, ethylcellulose, hydroxymethylcellulose, polyoxyethylene glycol, cellulose acetophthalate, hydroxypropylmethylcellulose phthalate and Eudragit® (methacrylic acid-acrylic acid copolymer), Opadry® (hydroxypropylmethylcellulose+macrogol+titanium oxide+lactose monohydrate). Pharmaceutically acceptable colorants may be added (for example yellow iron oxide, red iron oxide, quinoline yellow lake, etc.). Pharmaceutical forms, such as tablets, powders, sachets and gel capsules can be used for an oral administration.
  • The liquid pharmaceutical forms for oral administration include solutions, suspensions and emulsions. The aqueous solutions can be obtained by dissolving the active principles in water, followed by addition of flavourings, colorants, stabilisers and thickener, if necessary. In order to improve the solubility, it is possible to add ethanol, propylene glycol or other pharmaceutically acceptable non-aqueous solvents. The aqueous suspensions for oral use can be obtained by dispersing the finely divided active principles in water with a viscous product, such as natural or synthetic gums, resins, methylcellulose or sodium carboxymethylcellulose.
  • The pharmaceutical forms for injection can be obtained, for example, by the following process. The active principle(s) is (are) dissolved, suspended or emulsified either in an aqueous medium (for example distilled water, physiological saline, Ringer's solution, etc.) or in an oily medium (for example a plant oil, such as olive oil, sesameseed oil, cottonseed oil, corn oil, etc., or propylene glycol), with a dispersant (for example Tween 80, HCO 60 (Nikko Chemicals), polyethylene glycol, carboxymethylcellulose, sodium alginate, etc.), a preserving agent (for example methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, benzyl alcohol, chlorobutanol, phenol, etc.), an isotonicity agent (for example sodium chloride, glycerol, sorbitol, glucose, etc.) and also other additives, such as, if desired, a solubilising agent (for example sodium salicylate, sodium acetate, etc.) or a stabiliser (for example human serum albumin).
  • A pharmaceutical form for external use can be obtained from a solid, semi-solid or liquid composition containing the active principle(s). For example, to obtain a solid form, the active principle(s) is (are) treated, alone or as mixtures, with excipients (for example lactose, mannitol, starch, microcrystalline cellulose, sucrose, etc.) and a thickener (for example natural gums, cellulose derivatives, acrylic polymers, etc.) so as to convert them into powder. The liquid pharmaceutical compositions are prepared in substantially the same way as the forms for injection, as indicated previously. The semi-solid pharmaceutical forms are preferably in the form of aqueous or oily gels or in the form of a pomade. These compositions may optionally contain a pH regulator (for example carbonic acid, phosphoric acid, citric acid, hydrochloric acid, sodium hydroxide, etc.) and a preserving agent (for example p-hydroxybenzoic acid esters, chlorobutanol, benzalkonium chloride, etc.) and also other additives.
  • The daily doses of the insulin sensitisers are between 0.5 mg and 50 mg.
  • More particularly, if, in the present invention, rosiglitazone is used, the daily dose is between 1 mg and 8 mg, more preferably 4 mg. If pioglitazone is used, the daily dose is between 15 mg and 45 mg. If muraglitazar is used, the daily dose is between 0.5 mg and 20 mg, preferably 5 mg.
  • The daily doses of the compounds of the formula (I) are between 200 mg and 2000 mg.
  • The relative proportion of the constituents of the pharmaceutical compositions of the present invention takes into account the recommended dosages of the respective active principles. These relative proportions of insulin sensitisers, or of pharmaceutically acceptable salts thereof, and of the compounds of the formula (I), or of pharmaceutically acceptable salts thereof, thus vary in consequence. Preferably, the weight ratio of insulin sensitiser to the compound of the formula (I) ranges between 1/2 and 1/2000, more particularly from 1/4 to 1/2000 and especially from 1/5 to 1/2000. The frequency of administration of the compounds of the invention is between 1 and 2 administrations per day. In the case where the doses of compounds of the formula (I) necessitate more than one daily administration, the amounts of insulin sensitisers and the insulin sensitiser/compound of the formula (I) ratios are adjusted in consequence.
  • The aim of the present invention is also to propose a method of treatment to via co-administration of effective amounts of a compound of the formula (I) and of an insulin sensitiser, and also kits for allowing this co-administration.
  • The present invention also relates to kits that are suitable for the treatment by the methods described above. These kits comprise a composition containing the compound of the formula (I) in the dosages indicated above and a second composition containing the insulin sensitisers in the dosages indicated above, for a simultaneous, separate or sequential administration, in effective amounts according to the invention.
  • The term “co-administration” means the simultaneous, separate or sequential administration of one or more compounds to the same patient, over a period that may be up to 2 hours or even up to 12 hours. For example, the term co-administration includes (1) a simultaneous administration of the two compounds, (2) an administration of the first, followed 2 hours later by the administration of the second compound, (3) an administration of the first, followed 12 hours later by the administration of the second compound.
  • The examples below of compositions according to the invention are given as non-limiting illustrations.
    • EXAMPLES
  • The amounts are expressed on a weight basis.
    • Formulation Example 1
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride: 1000 mg
      • rosiglitazone: 4 mg
      • microcrystalline cellulose: 114 mg
      • croscarmellose: 28 mg
      • polyvinylpyrrolidone: 40 mg
      • magnesium stearate: 14 mg
      • Opadry: 24 mg
    Formulation Example 2
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride: 1000 mg
      • pioglitazone: 25 mg
      • microcrystalline cellulose: 115.5 mg
      • croscarmellose: 28 mg
      • polyvinylpyrrolidone: 40 mg
      • magnesium stearate: 9 mg
      • Opadry®: 24 mg
    Formulation Example 3
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride: 750 mg
      • rosiglitazone: 2 mg
      • microcrystalline cellulose: 110 mg
      • croscarmellose: 21 mg
      • polyvinylpyrrolidone: 30 mg
      • magnesium stearate: 10.5 mg
      • Opadry®: 18 mg
    Formulation Example 4
      • (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine hydrochloride: 1000 mg
      • muraglitazar: 5 mg
      • microcrystalline cellulose: 150 mg
      • croscarmellose: 24 mg
      • polyvinylpyrrolidone: 44 mg
      • magnesium stearate: 8 mg
      • Eudragit®: 24 mg
  • Biological Test: Modulation of Glucose Levels with the Combinations Of the Invention with Insulin Sensitisers
  • The capacity of the compounds of the invention in combination with insulin-sensitising antidiabetic compounds to modify the blood glucose levels is evaluated in vivo in diabetic GK rats.
  • Alone or in combination, the antidiabetic agents are administered twice a day (bid) to the GK rats for 4 days. The oral glucose tolerance test (OGTT) is performed after the last day of treatment.
  • OGTT is performed in the morning after 3 hours of fasting by oral administration of a glucose charge of 2 g/kg of body mass. The blood samples are collected from the tail vein at 0; 10; 20; 30; 45; 60; 90 and 120 minutes to determine the glucose levels.
  • Results for the Combinations According to the Invention
  • The combination of rosiglitazone and of the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine was tested as follows. The two compounds were administered alone and in combination. The doses used for the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine were 50 and 100 mg/kg PO twice daily for 4 days. For rosiglitazone, the doses used were 1 and 5 mg/kg PO twice daily for 4 days. The following combination was tested:
      • the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine: 100 mg/kg and rosiglitazone: 5 mg/kg PO twice daily for 4 days.
  • Glycaemia
    Glycaemia after 4 days Glycaemia % de-
    before of R under the crease in
    treatment treatment % variation curve AUC vs
    Treatment mmol/l mmol/l vs control (AUC) control
    Control GK n=8 12.93 +/− 0.41 13.10 +/− 0.87 3343 + 262
    (+)-2-amino-3,6-dihydro-4- 12.95 +/− 0.41 11.01 +/− 0.37   −16% 2688 +/− 99 −19.6%
    dimethylamino-6-methyl-
    1,3,5-triazine hydrochloride
    salt 100 mg/kg bid
    Rosiglitazone 5 mg/kg bid 12.81 +/− 0.27 10.52 +/− 0.84 −19.7% 2954 +/− 150 −11.6%
    (+)-2-amino-3,6-dihydro-4- 12.86 +/− 0.52 10.03 +/− 0.35 −23.4% 2311 +/− 121 −30.9%
    dimethylamino-6-methyl-
    1,3,5-triazine hydrochloride
    salt 100 mg/kg bid +
    Rosiglitazone 5 mg/kg bid
  • After four days of treatment (placebo), the glycaemia of the control GK diabetic rats was not modified or increased significantly. At doses of 5 mg/kg of rosiglitazone and 100 mg/kg of the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine, these agents induced a decrease in the fasted plasmatic glucose level. However, better glucose tolerance was observed with the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine than with rosiglitazone.
  • In combination, rosiglitazone 5 mg/kg and the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine 100 mg/kg showed much better efficacy than each compound individually. The combination of an insulin sensitiser, such as rosiglitazone and of a compound, such as the hydrochloride salt of (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine generates better activity on the glucose tolerance and the plasmatic glucose level of each than that of the compounds.

Claims (28)

1. Pharmaceutical composition comprising, as active principle:
i) an insulin sensitiser, wherein the insulin sensitiser is a glitazone (TZD), and
ii) a compound of the formula (I)
in combination with one or more pharmaceutically acceptable excipients
Figure US20140050786A1-20140220-C00047
in which:
R1, R2, R3 and R4 are independently chosen from the following groups:
H,
(C1-C20)alkyl optionally substituted by (C1-C5)alkyl,
(C2-C20)alkenyl, or
(C6-C14)aryl(C1-C20)alkyl,
or R1 and R2, on the one hand, and R3 and R4, on the other hand, possibly forming with the nitrogen atom an n-membered ring with n being between 3 and 8,
R5 and R6 are independently chosen from the following groups:
H,
(C1-C20)alkyl optionally substituted by hydroxyl, halogen, (C1-C5)alkyl or trifluoromethyl,
(C3-C8)cycloalkyl,
(C6-C14)aryl optionally substituted by hydroxyl or (C1-C5)alkoxy,
(C1-C13)heteroaryl bearing one or more heteroatoms chosen from N, O and S, or
(C6-C14)aryl(C1-C5)alkyl,
or R5 and R6 possibly forming with the carbon atom to which they are attached an m-membered ring with m being between 3 and 8, optionally containing one or more heteroatoms chosen from N, O and S and optionally being substituted by hydroxyl, (C1-C5)alkyl, or (C6-C14)aryl(C1-C5)alkoxy,
or R5 and R6 forming with the carbon atom a C10-C30 polycyclic residue optionally substituted by hydroxyl, (C1-C5)alkyl, carboxyl, carboxymethyl or carboxyethyl,
or a racemic form, tautomer, enantiomer, diastereoisomer, epimer or polymorph thereof, or a mixture thereof, or a pharmaceutically acceptable salt thereof.
2. The pharmaceutical composition according to claim 1, comprising a compound of the formula (I) in which R5 is hydrogen.
3. The pharmaceutical composition according to claim 1, comprising a compound of the formula (I) in which R5 and R6 are independently chosen from H and (C1-C20)alkyl groups optionally substituted by hydroxyl, halogen, (C1-C5)alkyl, (C6-C14)aryloxy or trifluoromethyl.
4. The pharmaceutical composition according to claim 1, wherein R1, R2, R3 and R4 are independently chosen from H and (C1-C20)alkyl groups optionally substituted by (C1-C5)alkyl.
5. (canceled)
6. The pharmaceutical composition according to claim 1, comprising a compound of the formula (I) in which R1 and R2 are a methyl group and R3 and R4 represent a hydrogen.
7. The pharmaceutical composition according to claim 1, wherein the compound of formula (I) is 2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine, or a pharmaceutically acceptable salt thereof.
8. The pharmaceutical composition according to claim 1, wherein the compound of formula (I) is (−)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine, or a pharmaceutically acceptable salt thereof.
9. The pharmaceutical composition according to claim 1, wherein the compound of formula (I) is (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine, or a pharmaceutically acceptable salt thereof.
10. The pharmaceutical composition according to claim 1, wherein the compound of the formula (I) is in the form of a hydrochloride salt.
11-12. (canceled)
13. The pharmaceutical composition according to claim 1, wherein the insulin sensitiser is selected from the group consisting of rosiglitazone and pioglitazone.
14. (canceled)
15. The pharmaceutical composition according to claim 1, wherein the insulin sensitiser is in the form of a pharmaceutically acceptable salt.
16. The pharmaceutical composition according to claim 1, wherein the composition contains between 0.5 mg and 50 mg of insulin sensitiser.
17. The pharmaceutical composition according to claim 1, wherein the composition contains between 200 mg and 2000 mg of compound of the formula (I).
18. The pharmaceutical composition according to claim 1, wherein the weight ratio of insulin sensitiser to the compound of the formula (I) is between 1/2 and 1/2000.
19. The pharmaceutical composition according to claim 1, wherein the insulin sensitiser is rosiglitazone and the compound of the formula (I) is (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine, or its hydrochloride salt.
20. The pharmaceutical composition according to claim 1, wherein the insulin sensitiser is pioglitazone and the compound of the formula (I) is (+)-2-amino-3,6-dihydro-4-dimethylamino-6-methyl-1,3,5-triazine or its hydrochloride salt.
21-22. (canceled)
23. The pharmaceutical composition according to claim 1, which is suitable for oral administration, in which the pharmaceutical composition is a powder, a coated tablet, a gel capsule, a sachet, a solution, a suspension or an emulsion.
24. A method for the treatment of diabetes comprising administering an insulin sensitiser, wherein the insulin sensitiser is a glitazone (TZD) in combination with a compound of the formula (I) according to claim 1.
25. The method according to claim 24, for the treatment of non-insulin-dependent diabetes.
26. A method for the treatment of at least one of the pathologies associated with insulin resistance syndrome, selected from the group consisting of dyslipidaemia, obesity, arterial hypertension, and microvascular and macrovascular complications, comprising administering an insulin sensitiser, wherein the insulin sensitiser is a glitazone (TZD), in combination with a compound of formula (I) according to claim 1.
27. The method according to claim 24, wherein the insulin sensitiser is selected from the group consisting of rosiglitazone and pioglitazone.
28. (canceled)
29. The method according to claim 24, wherein the administration of the compound of formula (I) and that of the insulin sensitiser are simultaneous, separate or sequential.
30. A kit comprising a compound of the formula (I) and an insulin sensitiser, for simultaneous, separate or sequential administration wherein the insulin sensitiser is a glitazone and formula (I) is as follows:
Figure US20140050786A1-20140220-C00048
in which:
R1, R2. R3 and R4 are independently chosen from the following groups:
H,
C1-C20)alkyl optionally substituted by (C1-C5)alkyl,
(C2-C20)alkenyl,
(C6-C14)aryl(C1-C20)alkyl,
or R1 and R2, on the one hand, and R3 and R4, on the other hand, possibly forming with the nitrogen atom an n-membered ring with n being between 3 and 8,
R5 and R6 are independently chosen from the following groups:
H,
(C1-C20)alkyl optionally substituted by hydroxyl, halogen, (C1-C5)alkyl or trifluoromethyl,
(C3-C8)cycloalkyl,
(C6-C14)aryl optionally substituted by hydroxyl or (C1-C5)alkoxy,
(C1-C13)heteroaryl bearing one or more heteroatoms chosen from N, O and S or
(C6-C14)aryl(C1-C5)alkyl,
or R5 and R6 possibly forming with the carbon atom to which they are attached an m-membered ring with m being between 3 and 8, optionally containing one or more heteroatoms chosen from N, O and S and optionally being substituted by hydroxyl, (C1-C5)alkyl, or (C6-C14)aryl(C1-C5)alkoxy,
or R5 and R6 forming with the carbon atom a C10-C30 polycyclic residue optionally substituted by hydroxyl, (C1-C5)alkyl, carboxyl, carboxymethyl or carboxyethyl,
or a racemic form, tautomer, enantiomer, diastereoisomer, epimer or polymorph thereof or a mixture thereof, or a pharmaceutically acceptable salt thereof.
US14/063,530 2006-01-13 2013-10-25 Combination of triazine derivatives and insulin sensitisers Abandoned US20140050786A1 (en)

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FR0600344A FR2896159B1 (en) 2006-01-13 2006-01-13 COMBINATION OF TRIAZINE DERIVATIVES AND INSULIN SENSITIZING AGENTS.
PCT/EP2006/012185 WO2007079917A2 (en) 2006-01-13 2006-12-18 Combination of triazine derivatives and insulin sensitisers
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CA2640897C (en) 2015-10-20
KR101482685B1 (en) 2015-01-14
PT1971330E (en) 2010-09-09
KR20140033498A (en) 2014-03-18
US20100285117A1 (en) 2010-11-11
EP1971330B1 (en) 2010-08-04
FR2896159A1 (en) 2007-07-20
BRPI0620985A2 (en) 2011-11-29
SI1971330T1 (en) 2010-11-30
JP2009523142A (en) 2009-06-18
KR20080088630A (en) 2008-10-02
ES2347177T3 (en) 2010-10-26
ATE476179T1 (en) 2010-08-15
CA2640897A1 (en) 2007-07-19
EP1971330A2 (en) 2008-09-24
CY1110789T1 (en) 2015-06-10
PL1971330T3 (en) 2011-01-31
AR059032A1 (en) 2008-03-12
AU2006334734B2 (en) 2012-07-19
WO2007079917A3 (en) 2007-08-30
BRPI0620985B1 (en) 2020-04-28
IL192558A (en) 2013-04-30
US8791115B2 (en) 2014-07-29
DE602006016014D1 (en) 2010-09-16
ZA200806947B (en) 2009-11-25
AU2006334734A1 (en) 2007-07-19
EA200801676A1 (en) 2008-12-30
WO2007079917A2 (en) 2007-07-19
BRPI0620985B8 (en) 2021-05-25
CN101355933A (en) 2009-01-28
FR2896159B1 (en) 2008-09-12
DK1971330T3 (en) 2010-10-25
JP5249782B2 (en) 2013-07-31

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