WO2009156860A2 - Substituted triazinone derivatives - Google Patents
Substituted triazinone derivatives Download PDFInfo
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- WO2009156860A2 WO2009156860A2 PCT/IB2009/006463 IB2009006463W WO2009156860A2 WO 2009156860 A2 WO2009156860 A2 WO 2009156860A2 IB 2009006463 W IB2009006463 W IB 2009006463W WO 2009156860 A2 WO2009156860 A2 WO 2009156860A2
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- triazin
- pyridin
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- ethylamino
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- C07D487/04—Ortho-condensed systems
Definitions
- the present invention relates to compounds that are useful as an active ingredient of a medicament for preventive and/or therapeutic treatment of neurodegenerative diseases caused by abnormal activity of GSK3 ⁇ .
- GSK3 ⁇ (glycogen synthase kinase 3 ⁇ ) is a proline directed serine, threonine kinase that plays an important role in the control of metabolism, differentiation and survival. It was initially identified as an enzyme able to phosphorylate and hence inhibit glycogen synthase. It was later recognized that GSK3 ⁇ was identical to tau protein kinase 1 (TPK1), an enzyme that phosphorylates tau protein in epitopes that are also found to be hyperphosphorylated in Alzheimer's disease and in several taupathies.
- TPK1 tau protein kinase 1
- protein kinase B (AKT) phosphorylation of GSK3 ⁇ results in a loss of its kinase activity, and it has been hypothesized that this inhibition may mediate some of the effects of neurotrophic factors.
- phosphorylation by GSK3 ⁇ of ⁇ -catenin results in its degradation by an ubiquitinilation dependent proteasome pathway.
- GSK3 ⁇ inhibition may result in neurotrophic activity. Indeed there is evidence that lithium, an uncompetitive inhibitor of GSK3 ⁇ , enhances neuritogenesis in some models and also increases neuronal survival, through the induction of survival factors such as Bcl-2 and the inhibition of the expression of proapoptotic factors such as p53 and Bax.
- GSK3 ⁇ may be the link between the two major pathological processes in Alzheimer's disease: abnormal APP (Amyloid Precursor Protein) processing and tau protein hyperphosphorylation.
- tau hyperphosphorylation results in a destabilization of the neuronal cytoskeleton
- the pathological consequences of abnormal GSK3 ⁇ activity are, most likely, not only due to a pathological phosphorylation of tau protein because, as mentioned above, an excessive activity of this kinase may affect survival through the modulation of the expression of apoptotic and antiapoptotic factors.
- ⁇ -amyloid-induced increase in GSK3 ⁇ activity results in the phosphorylation and, hence the inhibition of pyruvate dehydrogenase, a pivotal enzyme in energy production and acetylcholine synthesis.
- GSK3 ⁇ may find application in the treatment of the neuropathological consequences and the cognitive and attention deficits associated with Alzheimer's disease, as well as other acute and chronic neurodegenerative diseases and other pathologies where GSK3 ⁇ is deregulated (Nature reviews Vol.3, June 2004, p.479-487; Trends in Pharmacological Sciences Vol. 25 No. 9, Sept. 2004, p. 471-480; Journal of neurochemistry 2004, 89, 1313-1317; Medicinal Research Reviews, Vol. 22, No. 4, 373-384, 2002).
- the neurodegenerative diseases include, in a non-limiting manner, Parkinson's disease, tauopathies (e.g. Fronto temporal dementia, corticobasal degeneration, Pick's disease, progressive supranuclear palsy), Wilson's disease, Huntington's disease (The Journal of biological chemistry Vol. 277, No. 37, Issue of September 13, pp. 33791-33798, 2002), Prion disease (Biochem. J. 372, p.129-136, 2003) and other dementia including vascular dementia; acute stroke and other traumatic injuries; cerebrovascular accidents (e.g. age related macular degeneration); brain and spinal cord trauma; amyotrophic lateral sclerosis (European Journal of Neuroscience, Vol. 22, pp.
- tauopathies e.g. Fronto temporal dementia, corticobasal degeneration, Pick's disease, progressive supranuclear palsy
- Wilson's disease Huntington's disease (The Journal of biological chemistry Vol. 277, No. 37, Issue of September 13, pp. 3379
- GSK3 ⁇ peripheral neuropathies; retinopathies and glaucoma.
- ESC embryonic stem cells
- Inhibitors of GSK3 ⁇ may also find application in the treatment of other nervous system disorders, such as bipolar disorders (manic-depressive illness).
- bipolar disorders manic-depressive illness
- lithium has been used for more than 50 years as a mood stabiliser and the primary treatment for bipolar disorder.
- the therapeutic actions of lithium are observed at doses (1-2 mM) where it is a direct inhibitor of GSK3 ⁇ .
- inhibitors of GSK3 ⁇ could be used to mimic the mood stabilising effects of lithium.
- Alterations in Akt-GSK3 ⁇ signaling have also been implicated in the pathogenesis of schizophrenia.
- GSK3 ⁇ could be useful in treating cancers, such as colorectal, prostate, breast, non-small cell lung carcinoma, thyroid cancer, T or B- cell leukaemia and several virus-induced tumours.
- cancers such as colorectal, prostate, breast, non-small cell lung carcinoma, thyroid cancer, T or B- cell leukaemia and several virus-induced tumours.
- the active form of GSK3 ⁇ has been shown to be elevated in the tumors of colorectal cancer patients and inhibition of GSK3 ⁇ in colorectal cancer cells activates p53-dependent apoptosis and antagonises tumor growth. Inhibition of GSK3 ⁇ also enhances TRAIL-induced apoptosis in prostate cancer cell lines.
- GSK3 ⁇ also plays a role in the dynamics of the mitotic spindle and inhibitors of GSK3 ⁇ prevent chromosome movement and lead to a stabilisation of microtubules and a prometaphase-like arrest that is similar to that observed with low doses of Taxol.
- Other possible applications for GSK3 ⁇ inhibitors include therapy for non-insulin dependent diabetes (such as diabetes type II), obesity and alopecia.
- Inhibitors of human GSK3 ⁇ may also inhibit pfGSK3, an ortholog of this enzyme found in Plasmodium falciparum, as a consequence they could be used for the treatment of malaria (Biochimica et Biophysica Acta 1697, 181- 196, 2004).
- pfGSK3 an ortholog of this enzyme found in Plasmodium falciparum
- Wnt/LPR5 pathway As a major regulator of bone mass accrual.
- Inhibition of GSK3 ⁇ leads to the consequent activation of canonical Wnt signalling.
- GSK3 ⁇ inhibitors may also be used for treating disorders of reduced bone mass, bone-related pathologies, osteoporosis. According to recent data, GSK3 ⁇ inhibitors might be used in the treatment or prevention of Pemphigus vulgaris.
- GSK3beta inhibitor treatment improves neutrophil and megakaryocyte recovery. Therefore, GSK3beta inhibitors will be useful for the treatment of neutropenia induced by cancer chemotherapy.
- Alzheimer's disease Parkinson disease, age-associated memory impairment, mild cognitive impairment, brain trauma, schizophrenia and other conditions in which such deficits are observed.
- Inhibitors of GSK3 ⁇ may also find application in the treatment of parenchymal renal diseases (Nelson PJ, Kidney International Advance online publication 19 dec 2007) and in the prevention or treatment of muscle atrophy (J. Biol. Chem. (283) 2008, 358-366).
- An object of the present invention is to provide compounds useful as an active ingredient of a medicament for preventive and/or therapeutic treatment of a disease caused by abnormal GSK3 ⁇ activity, more particularly of neurodegenerative diseases. More specifically, the object is to provide novel compounds useful as an active ingredient of a medicament that enables prevention and/or treatment of neurodegenerative diseases such as Alzheimer's disease.
- the inventors of the present invention have identified compounds possessing inhibitory activity against GSK3 ⁇ . As a result, they found that compounds represented by the following formula (I) had the desired activity and were useful as an active ingredient of a medicament for preventive and/or therapeutic treatment of the aforementioned diseases.
- the present invention thus provides as an object of the invention the triazinone derivatives represented by formula (I) or salts thereof, solvates thereof or hydrates thereof:
- Z represents a bond, a carbonyl group, a methylene group optionally substituted by one or two groups chosen from a Ci- 6 alkyl group, a hydroxyl group, a C 1 - 6 alkoxy group;
- R1 represents a 4-pyridine ring
- R2 represents a hydrogen atom, a Ci -6 alkyl
- R3 represents a hydrogen atom, a Ci -6 alkyl group
- R2 and R3 may form together a 6 membered cycle with the nitrogens caring R2 and R3 optionally substituted by 1 to 4 substituents selected from a Ci- 6 alkyl group
- R4 represents: - a phenyl ring, this ring being optionally substituted by 1 to 4 substituents selected from a Ci -6 alkyl group, a halogen atom, a Ci_ 2 perhalogenated alkyl group, a Ci_ 3 halogenated alkyl group, a hydroxyl group, a Ci- ⁇ alkoxy group, a Ci- 2 perhalogenated alkoxy group, a Ci- 6 alkylsulfonyl group, a nitro, a cyano, an amino, a Ci -6 monoalkylamino group or a
- a medicament comprising as an active ingredient a substance selected from the group consisting of the triazinone derivatives represented by formula (I) and the physiologically acceptable salts thereof, and the solvates thereof and the hydrates thereof.
- the aforementioned medicament which is used for preventive and/or therapeutic treatment of diseases caused by abnormal GSK3 ⁇ activity
- the aforementioned medicament which is used for preventive and/or therapeutic treatment of neurodegenerative diseases and in addition other diseases such as: Non-insulin dependent diabetes (such as diabetes type II) and obesity; malaria, bipolar disorders (manic depressive illness); schizophrenia; alopecia or cancers such as colorectal, prostate, breast cancer, non-small cell lung carcinoma, thyroid cancer, T or B-cell leukaemia, several virus-induced tumours and bone related pathologies; the treatment of parenchymal renal diseases and in the prevention or treatment of muscle atrophy; the treatment of cognitive and memory deficit.
- the medicament could also find an application in regenerative medicine.
- the aforementioned medicament wherein the diseases are neurodegenerative diseases and are selected from the group consisting of Alzheimer's disease, Parkinson's disease, tauopathies (e.g. Fronto temporal dementia, corticobasal degeneration, Pick's disease, progressive supranuclear palsy), Wilson's disease, Huntington's disease, Prion disease and other dementia including vascular dementia; acute stroke and others traumatic injuries; cerebrovascular accidents (e.g. age related macular degeneration); brain and spinal cord trauma; amyotrophic lateral sclerosis; peripheral neuropathies; retinopathies and glaucoma, and the aforementioned medicament in the form of pharmaceutical composition containing the above substance as an active ingredient together with one or more pharmaceutical additives.
- the bones related pathologies are osteoporosis.
- the present invention further provides an inhibitor of GSK3 ⁇ activity comprising as an active ingredient a substance selected from the group consisting of the triazinone derivatives of formula (I) and the salts thereof, and the solvates thereof and the hydrates thereof.
- a method for preventive and/or therapeutic treatment of neurodegenerative diseases caused by abnormal GSK3 ⁇ activity which comprises the step of administering to a patient a preventively and/or therapeutically effective amount of a substance selected from the group consisting of triazinone derivatives of formula (I) and the physiologically acceptable salts thereof, and the solvates thereof and the hydrates thereof; and a use of a substance selected from the group consisting of the triazinone derivatives of formula (I) and the physiologically acceptable salts thereof, and the solvates thereof and the hydrates thereof for the manufacture of the aforementioned medicament.
- the Ci_ 6 alkyl group represents a straight or branched or cyclo alkyl group having 1 to 6 carbon atoms, optionally substituted by a straight, branched or cyclic Ci -6 alkyl group, for example, methyl group, ethyl group, n- propyl group, isopropyl group, n-butyl group, isobutyl group, sec-butyl group, tert- butyl group, n-pentyl group, isopentyl group, neopentyl group, 1 ,1-dimethylpropyl group, n-hexyl group, isohexyl group, cyclopropylmethyl group and the like.
- the Ci- 6 alkoxy group represents an alkyloxy group having 1 to 4 carbon atoms for example, methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, sec-butoxy group, te/f-butoxy group, and the like;
- the halogen atom represents a fluorine, chlorine, bromine or iodine atom
- the Ci- 2 perhalogenated alkyl group represents an alkyl group wherein all the hydrogen atoms have been substituted by a halogeno, for example a CF 3 or
- the Ci- 3 halogenated alkyl group represents an alkyl group wherein at least, one hydrogen has not been substituted by a halogen atom
- the Ci- 6 monoalkylamino group represents an amino group substituted by one C 1-6 alkyl group, for example, methylamino group, ethylamino group, propylamino group, isopropylamino group, butylamino group, isobutylamino group, tert-butylamino group, pentylamino group, isopentylamino group and the like
- the C 2- i 2 dialkylamino group represents an amino group substituted by two Ci -6 alkyl groups, for example, dimethylamino group, ethylmethylamino group, diethylamino group, methylpropylamino group and diisopropylamino group and the like;
- a leaving group L represents a group which could be easily cleaved and substituted; such a group may be for example a tosyl, a mesyl, a bromide and the like.
- the compounds represented by the aforementioned formula (I) may form a salt.
- the salt include, when an acidic group exists, salts of alkali metals and alkaline earth metals such as lithium, sodium, potassium, magnesium, and calcium; salts of ammonia and amines such as methylamine, dimethylamine, trimethylamine, dicyclohexylamine, tris(hydroxymethyl)aminomethane, N 1 N- bis(hydroxyethyl)piperazine, 2-amino-2-methyl-1-propanol, ethanolamine, N- methylglucamine, and L-glucamine; or salts with basic amino acids such as lysine, ⁇ -hydroxylysine and arginine.
- the base-addition salts of acidic compounds are prepared by standard procedures well known in the art.
- examples include salts with mineral acids such as hydrochloric acid, hydrobromic acid; salts with organic acids such as acetic acid, propionic acid, tartaric acid, fumaric acid, maleic acid, malic acid, oxalic acid, succinic acid, citric acid, benzoic acid and the like,.
- the acid-addition salts of the basic compounds are prepared by standard procedures well known in the art which include, but are not limited thereto, dissolving the free base in an aqueous alcohol solution containing the appropriate acid and isolating the salt by evaporating the solution, or by reacting the free base and an acid in an organic solvent, in which case the salt separates directly, or is precipitated with a second organic solvent, or can be obtained by concentration of the solution.
- the acids which can be used to prepare the acid-addition salts include preferably those which produce, when combined with the free base, pharmaceutically-acceptable salts, that is, salts whose anions are relatively innocuous to the animal organism in pharmaceutical doses of the salts, so that the beneficial properties inherent in the free base are not compromised by side effects ascribable to the anions.
- pharmaceutically-acceptable salts that is, salts whose anions are relatively innocuous to the animal organism in pharmaceutical doses of the salts, so that the beneficial properties inherent in the free base are not compromised by side effects ascribable to the anions.
- the triazinone derivatives represented by the aforementioned formula (I) may have one or more asymmetric carbon atoms. As for the stereochemistry of such asymmetric carbon atoms, they may independently be either in (R) or (S) configuration, and the derivative may exist as stereoisomers such as optical isomers, or diastereoisomers. Any stereoisomers in pure form, any mixtures of stereoisomers, racemates and the like fall within the scope of the present invention.
- stereoisomers in pure form, any mixtures of stereoisomers, racemates and the like fall within the scope of the present invention.
- Z represents a bond, a carbonyl group, a Ci -6 alkyl group optionally substituted by one or two groups chosen from a Ci -6 alkyl group, a hydroxyl group, a C 1-6 alkoxy group, R1 represents an 4-pyridine ring, R2 is a hydrogen, a Ci -6 alkyl group, R3 represents a hydrogen, a Ci -6 alkyl group;
- R2 and R3 may form together a 6 membered cycle, this cycle being optionally substituted by a a Ci -6 alkyl group;
- R4 represents a phenyl, optionally substituted by 1 to 4 substituents selected from an halogen, Ci -6 alkoxy group and n represents 0, 1 , 2 in the form of a free base or of an addition salt with an acid.
- a further object of the present invention includes the group of compounds of table 1 of formula as defined hereunder:
- the present invention concerns also methods for preparing the triazinone compounds represented by the aforementioned formula (I). These compounds can be prepared, for example, according to methods explained below.
- Triazinone compounds represented by the aforementioned formula (I), may be prepared according to the method described in the scheme 1.
- Compound of formula (III) may be prepared according to the method defined in scheme 2, starting from compound of formula (IV).
- the conditions which may be used are given in the chemical examples.
- the present invention concerns also intermediate (III) for preparing the triazinone compounds represented by the aforementioned formula
- the amidine of formula (IV) 1 wherein R1 is defined for compound of formula (I) is allowed to react with a compound of formula (V).
- the reaction may be carried out in the presence of a base such as sodium hydroxyde, in a mixture of solvent such as toluene/water, at a suitable temperature ranging from 25° to 140 0 C under ordinary air to obtain an intermediate triazinone compound (Ilia).
- the compound of formula (Ilia) is allowed to react with a compound of formula (Vl), wherein L represents a leaving group, such a group may be for example a tosyl, a mesyl, a bromide and the like.
- the reaction may be carried out in the presence of a base such as sodium methoxide, in an alcoholic solvent such as methanol to afford the compound of formula (MIb).
- the compound of formula (MIb) can react with a compound of formula (VII) to afford the compound of formula (III).
- the triazinone compounds represented by the aforementioned formula (I) may also be prepared according to the method described in the scheme 3.
- the compounds of the present invention have inhibitory activity against GSK3 ⁇ . Accordingly, the compounds of the present invention are useful as an active ingredient for the preparation of a medicament, which enables preventive and/or therapeutic treatment of a disease caused by abnormal GSK3 ⁇ activity and more particularly of neurodegenerative diseases such as Alzheimer's disease. In addition, the compounds of the present invention are also useful as an active ingredient for the preparation of a medicament for preventive and/or therapeutic treatment of neurodegenerative diseases such as Parkinson's disease, tauopathies (e.g.
- Fronto temporal dementia corticobasal degeneration, Pick's disease, progressive supranuclear palsy), Wilson's disease, Huntington's disease, Prion disease and other dementia including vascular dementia; acute stroke and others traumatic injuries; cerebrovascular accidents (e.g.
- the medicament could also find an application in regenerative medicine.
- the medicament could also find an application in the treatment or prevention of Pemphigus vulgaris.
- the medicament could also find an application in the treatment of neutropenia induced by cancer chemotherapy.
- the medicament could also find an application for therapeutic treatment of a disease characterized by cognitive and memory deficits such as in Alzheimer's disease, Parkinson disease, age associated memory impairment, mild cognitive impairment, brain trauma, schizophrenia and other conditions in which such deficits are observed.
- the present invention further relates to a method for treating neurodegenerative diseases caused by abnormal activity of GSK3 ⁇ and of the aforementioned diseases which comprises administering to a mammalian organism in need thereof an effective amount of a compound of the formula (I).
- a substance may be used which is selected from the group consisting of the compound represented by the aforementioned formula (I) and pharmacologically acceptable salts thereof, and solvates thereof and hydrates thereof.
- the substance, per se, may be administered as the medicament of the present invention; however, it is desirable to administer the medicament in a form of a pharmaceutical composition which comprises the aforementioned substance as an active ingredient and one or more pharmaceutical additives.
- a pharmaceutical composition which comprises the aforementioned substance as an active ingredient and one or more pharmaceutical additives.
- two or more of the aforementioned substances may be used in combination.
- the above pharmaceutical composition may be supplemented with an active ingredient of another medicament for the treatment of the above mentioned diseases.
- the type of pharmaceutical composition is not particularly limited, and the composition may be provided as any formulation for oral or parenteral administration.
- the pharmaceutical composition may be formulated, for example, in the form of pharmaceutical compositions for oral administration such as granules, fine granules, powders, hard capsules, soft capsules, syrups, emulsions, suspensions, solutions and the like, or in the form of pharmaceutical compositions for parenteral administrations such as injections for intravenous, intramuscular, or subcutaneous administration, drip infusions, transdermal preparations, transmucosal preparations, nasal drops, inhalants, suppositories and the like.
- Injections or drip infusions may be prepared as powdery preparations such as in the form of lyophilized preparations, and may be used by dissolving just before use in an appropriate aqueous medium such as physiological saline. Sustained-release preparations such as those coated with a polymer may be directly administered intracerebrally.
- Types of pharmaceutical additives used for the manufacture of the pharmaceutical composition, content ratios of the pharmaceutical additives relative to the active ingredient, and methods for preparing the pharmaceutical composition may be appropriately chosen by those skilled in the art.
- Inorganic or organic substances or solid or liquid substances may be used as pharmaceutical additives.
- the pharmaceutical additives may be incorporated in a ratio ranging from 1% by weight to 90% by weight based on the weight of an active ingredient.
- excipients used for the preparation of solid pharmaceutical compositions include, for example, lactose, sucrose, starch, talc, cellulose, dextrin, kaolin, calcium carbonate and the like.
- a conventional inert diluent such as water or a vegetable oil may be used.
- the liquid composition may contain, in addition to the inert diluent, auxiliaries such as moistening agents, suspension aids, sweeteners, aromatics, colorants, and preservatives.
- the liquid composition may be filled in capsules made of an absorbable material such as gelatin. Examples of solvents or suspension mediums used for the preparation of compositions for parenteral administration, e.g.
- injections, suppositories include water, propylene glycol, polyethylene glycol, benzyl alcohol, ethyl oleate, lecithin and the like.
- base materials used for suppositories include, for example, cacao butter, emulsified cacao butter, lauric lipid, witepsol.
- the dose and frequency of administration of the medicament of the present invention are not particularly limited, and they may be appropriately chosen depending on conditions such as a purpose of preventive and/or therapeutic treatment, a type of a disease, the body weight or age of a patient, severity of a disease and the like.
- a daily dose for oral administration to an adult may be 0.01 to 1 ,000 mg (the weight of an active ingredient), and the dose may be administered once a day or several times a day as divided portions, or once in several days.
- administrations may preferably be performed continuously or intermittently in a daily dose of 0.001 to 100 mg (the weight of an active ingredient) to an adult.
- Example 2 (Compound No. 4 of table 1) Methyl-6-(2-oxo-2-phenyl-ethylamino)-4-pyridin-4-yl-1H-[1 ,3,5]triazin-2-one 2.1 1 -Methyl-6-methylsulfanyl-4-pyridin-4-yl-1 H-[1 ,3,5]triazin-2-one To a suspension of 4g (18.16 mmol) of 6-Methylsulfanyl-4-pyridin-4-yl-1 H- [1 ,3,5]triazin-2-one (synthesis as described in US4406897) in 30 ml_ of anhydrous dimethylformamide was added 2.76g (19.97 mmol) of potassium carbonate. The resulting mixture was allowed to stir at room temperature for 15 mn, cooled at 0 0 C and 1.13mL (18.16 mmol) of methyl iodide were added dropwise.
- Example 3 (Compound No. 9 of table 1) 6-Benzylamino-4-pyridin-4-yl-1 H-[1 ,3,5]triazin-2-one
- benzylamine commercially available
- 6-Methylsulfanyl-4- pyridin-4-yl-1 H-[1 ,3,5]triazin-2-one synthesis as described in US4406897
- 1-Methyl-6-methylsulfanyl-4-pyridin-4-yl-1H-[1 ,3,5]triazin-2-one to afford the product which was transformed into the hyrdochloride salt in the usual manner to give 0.15g (47%) of a white solid.
- Mp 198-200 0 C
- Methoxy-phenyl)-ethylamine (commercially available) in place of phenethylamine and 6-Methylsulfanyl-4-pyridin-4-yl-1 H-[1 ,3,5]triazin-2-one (synthesis as described in US4406897) in place of 1-Methyl-6-methylsulfanyl-4-pyridin-4-yl-1H-
- the compounds have been prepared according to the methods of the examples.
- Me represents a methyl group
- (Rot.) indicates the levorotatory or dextrorotatory properties of the enantiomeric compound
- (dec.) indicates the decomposition of the compound.
- Test Example Inhibitory activity of the medicament of the present invention against GSK3 ⁇ :
- a third protocol 7.5 ⁇ M of prephosphorylated GS1 peptide and 10 ⁇ M ATP (containing 300,000 cpm of 33 P-ATP) were incubated in 50 mM Hepes, pH 7.2, 1 mM DTT, 1 mM MgCI 2 , 1 mM EGTA, 0.01% Tween 20 buffer for one hour at room temperature in the presence of GSK3beta (total reaction volume : 100 microliters).
- a fourth protocol 7.5 ⁇ M of prephosphorylated GS1 peptide and 10 ⁇ M ATP (containing 300,000 cpm of 33 P-ATP) were incubated in 50 mM Hepes, pH 7.2, 1 mM DTT, 1 mM MgCI 2 , 1 mM EGTA, 0.01% Tween 20 buffer for 90 minutes at room temperature in the presence of commercial GSK3beta (Millipore) (total reaction volume : 100 microliters).
- Inhibitors were solubilised in DMSO (final solvent concentration in the reaction medium, 1%).
- the reaction was stopped with 100 microliters of a solution made of 25 g polyphosphoric acid (85% P 2 O 5 ), 126 ml 85% H 3 PO 4 , H 2 O to 500 ml and then diluted to 1 :100 before use. An aliquot of the reaction mixture was then transferred to Whatman P81 cation exchange filters and rinsed with the solution described above. Incorporated 33 P radioactivity was determined by liquid scintillation spectrometry.
- the phosphorylated GS-1 peptide had the following sequence: NH2-YRRAAVPPSPSLSRHSSPHQS(P)EDEE-COOH.(Woodgett, J. R. (1989) Analytical Biochemistry 180, 237-241.
- the GSK3 ⁇ inhibitory activity of the compounds of the present invention are expressed in IC 50 , and as an illustration the range of IC 5 o's of the compounds in table 1 are between 0.1 nanomolar to 3 micromolar concentrations.
- the compound No. 1 of table 1 shows an IC 50 of 0.372 ⁇ M and the compound No. 5 of table 1 shows an IC 50 Of 0.050 ⁇ M.
- the compounds of the present invention have GSK3 ⁇ inhibitory activity and are useful as an active ingredient of a medicament for preventive and/or therapeutic treatment of diseases caused by abnormal activity of GSK3 ⁇ and more particularly of neurodegenerative diseases.
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Priority Applications (17)
Application Number | Priority Date | Filing Date | Title |
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CA2729115A CA2729115A1 (en) | 2008-06-26 | 2009-06-25 | Substituted triazinone derivatives |
BRPI0914662A BRPI0914662A2 (en) | 2008-06-26 | 2009-06-25 | substituted triazinone derivatives |
CN2009801334844A CN102137854A (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1H-[1,3,5]triazin-2-one derivatives as GSK3-beta inhibitors for the treatment of neurodegenerative diseases |
ES09769671T ES2379220T3 (en) | 2008-06-26 | 2009-06-25 | Derivatives of 4- (pyridin-4-yl) -1H- [1,3,5] triazin-2-one as GSK3-beta inhibitors for the treatment of neurodegenerative diseases |
PL09769671T PL2321295T3 (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1h-[1,3,5]triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases |
MX2010014235A MX2010014235A (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1h-(1, 3, 5)triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases. |
AT09769671T ATE538114T1 (en) | 2008-06-26 | 2009-06-25 | 4-(PYRIDINE-4-YL)-1H-Ä1,3,5UTRIAZINE-2-ONE DERIVATIVES AS GSK3 BETA INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES |
DK09769671.0T DK2321295T3 (en) | 2008-06-26 | 2009-06-25 | 4- (PYRIDIN-4-YL) -1H- [1,3,5] TRIAZIN-2 OLDER DERIVATIVES AS GSK3-BETA INHIBITORS FOR TREATMENT OF NEURODEGENERATIVE DISEASES |
SI200930201T SI2321295T1 (en) | 2008-06-26 | 2009-06-25 | 4-(PYRIDIN-4-YL)-1H-?á1,3,5?åTRIAZIN-2-ONE DERIVATIVES AS GSK3-BETA INHIBITORS FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES |
EA201170095A EA201170095A1 (en) | 2008-06-26 | 2009-06-25 | DERIVATIVES (4-PYRIDIN-4-IL) -1H- (1,3,5) TRIAZIN-2-SHE AS INHIBITION OF GSK3-BETA FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES |
NZ590116A NZ590116A (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1h-(1, 3, 5)triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases |
EP09769671A EP2321295B1 (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1h-[1,3,5]triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases |
JP2011515667A JP5581318B2 (en) | 2008-06-26 | 2009-06-25 | 4- (Pyridin-4-yl) -1H- (1,3,5) triazin-2-one derivatives as GSK3-beta inhibitors for the treatment of neurodegenerative diseases |
AU2009263846A AU2009263846A1 (en) | 2008-06-26 | 2009-06-25 | 4-(pyridin-4-yl)-1H-(1, 3, 5)triazin-2-one derivatives as GSK3-beta inhibitors for the treatment of neurodegenerative diseases |
US12/968,935 US8592580B2 (en) | 2008-06-26 | 2010-12-15 | Substituted triazinone derivatives |
IL210174A IL210174A0 (en) | 2008-06-26 | 2010-12-22 | 4-(pyridin-4-yl)-1h-(1,3,5)triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases |
ZA2011/00026A ZA201100026B (en) | 2008-06-26 | 2011-01-03 | 4-(pyridin-4-yl)-1h-(1,3,5)triazin-2-one derivatives as gsk3-beta inhibitors for the treatment of neurodegenerative diseases |
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EP08290617A EP2138488A1 (en) | 2008-06-26 | 2008-06-26 | 4-(pyridin-4-yl)-1H-[1,3,5]triazin-2-one derivatives as GSK3-beta inhibitors for the treatment of neurodegenerative diseases |
EP08290617.3 | 2008-06-26 |
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US12/968,935 Continuation US8592580B2 (en) | 2008-06-26 | 2010-12-15 | Substituted triazinone derivatives |
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WO2009156860A3 WO2009156860A3 (en) | 2010-03-04 |
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US (1) | US8592580B2 (en) |
EP (2) | EP2138488A1 (en) |
JP (1) | JP5581318B2 (en) |
KR (1) | KR20110025219A (en) |
CN (1) | CN102137854A (en) |
AR (1) | AR072227A1 (en) |
AT (1) | ATE538114T1 (en) |
AU (1) | AU2009263846A1 (en) |
BR (1) | BRPI0914662A2 (en) |
CA (1) | CA2729115A1 (en) |
CY (1) | CY1112642T1 (en) |
DK (1) | DK2321295T3 (en) |
EA (1) | EA201170095A1 (en) |
ES (1) | ES2379220T3 (en) |
IL (1) | IL210174A0 (en) |
MX (1) | MX2010014235A (en) |
NZ (1) | NZ590116A (en) |
PL (1) | PL2321295T3 (en) |
PT (1) | PT2321295E (en) |
SI (1) | SI2321295T1 (en) |
TW (1) | TW201004935A (en) |
WO (1) | WO2009156860A2 (en) |
ZA (1) | ZA201100026B (en) |
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WO2012004269A1 (en) | 2010-07-05 | 2012-01-12 | Sanofi | (2-aryloxy-acetylamino)-phenyl-propionic acid derivatives, method for producing same and use thereof as pharmaceuticals |
WO2012004270A1 (en) | 2010-07-05 | 2012-01-12 | Sanofi | Spirocyclically substituted 1,3-propane dioxide derivatives, methods for the production thereof and use of the same as medicament |
WO2012010413A1 (en) | 2010-07-05 | 2012-01-26 | Sanofi | Aryloxy-alkylene substituted hydroxyphenyl hexynoic acids, methods for the production thereof and use of the same as medicament |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2011161030A1 (en) | 2010-06-21 | 2011-12-29 | Sanofi | Heterocyclic substituted methoxyphenyl derivatives having an oxo group, method for producing same, and use thereof as gpr40 receptor modulators |
WO2012004269A1 (en) | 2010-07-05 | 2012-01-12 | Sanofi | (2-aryloxy-acetylamino)-phenyl-propionic acid derivatives, method for producing same and use thereof as pharmaceuticals |
WO2012004270A1 (en) | 2010-07-05 | 2012-01-12 | Sanofi | Spirocyclically substituted 1,3-propane dioxide derivatives, methods for the production thereof and use of the same as medicament |
WO2012010413A1 (en) | 2010-07-05 | 2012-01-26 | Sanofi | Aryloxy-alkylene substituted hydroxyphenyl hexynoic acids, methods for the production thereof and use of the same as medicament |
WO2013037390A1 (en) | 2011-09-12 | 2013-03-21 | Sanofi | 6-(4-hydroxy-phenyl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
WO2013045413A1 (en) | 2011-09-27 | 2013-04-04 | Sanofi | 6-(4-hydroxy-phenyl)-3-alkyl-1h-pyrazolo[3,4-b]pyridine-4-carboxylic acid amide derivatives as kinase inhibitors |
RU2772907C2 (en) * | 2015-08-17 | 2022-05-27 | Джапан Тобакко Инк. | Hydroxytriazine compound and its application for medical purposes |
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TW201004935A (en) | 2010-02-01 |
BRPI0914662A2 (en) | 2015-10-20 |
MX2010014235A (en) | 2011-06-24 |
ES2379220T3 (en) | 2012-04-23 |
ATE538114T1 (en) | 2012-01-15 |
CY1112642T1 (en) | 2016-02-10 |
ZA201100026B (en) | 2012-04-25 |
EP2321295B1 (en) | 2011-12-21 |
IL210174A0 (en) | 2011-03-31 |
CA2729115A1 (en) | 2009-12-30 |
JP2011525905A (en) | 2011-09-29 |
JP5581318B2 (en) | 2014-08-27 |
CN102137854A (en) | 2011-07-27 |
EP2138488A1 (en) | 2009-12-30 |
US20110144114A1 (en) | 2011-06-16 |
WO2009156860A3 (en) | 2010-03-04 |
PL2321295T3 (en) | 2012-06-29 |
PT2321295E (en) | 2012-03-23 |
KR20110025219A (en) | 2011-03-09 |
AU2009263846A1 (en) | 2009-12-30 |
AR072227A1 (en) | 2010-08-11 |
EP2321295A2 (en) | 2011-05-18 |
NZ590116A (en) | 2011-10-28 |
DK2321295T3 (en) | 2012-04-10 |
US8592580B2 (en) | 2013-11-26 |
EA201170095A1 (en) | 2011-08-30 |
SI2321295T1 (en) | 2012-04-30 |
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