WO2005012295A1 - Substituierte thiazol-benzoisothiazoldioxidderivative, verfahren zu deren herstellung und deren verwendung - Google Patents
Substituierte thiazol-benzoisothiazoldioxidderivative, verfahren zu deren herstellung und deren verwendung Download PDFInfo
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- WO2005012295A1 WO2005012295A1 PCT/EP2004/007847 EP2004007847W WO2005012295A1 WO 2005012295 A1 WO2005012295 A1 WO 2005012295A1 EP 2004007847 W EP2004007847 W EP 2004007847W WO 2005012295 A1 WO2005012295 A1 WO 2005012295A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Definitions
- the invention relates to substituted thiazole-Benzoisothiazoldioxidderivate and their physiologically acceptable salts and physiologically functional derivatives.
- the object of the invention was to provide compounds with which a prevention and treatment of diabetes mellitus is possible.
- the compounds should develop a therapeutically useful blood sugar lowering effect.
- the compounds should have an improved effect or an improved ADME profile (absorption, distribution, metabolism and excretion) compared with the compounds from WO 02/11722.
- the invention therefore relates to compounds of the formula I,
- Rl, R2 are independently H, Aryb COOH, (C 1 -C 6) -alkylene-COOH, -COO (CC 6) -Alkyb (C ⁇ -C6) -alkylene-COO (C ⁇ -C6) -Alkyb (dC ⁇ -Alkyb (C 2 -C 6 ) -Alkenyb (C 1 -C 6 ) -alkylene-Aryb heterocycle, (C 1 -C 4 -alkylene heterocycle, CF 3 , OCF 3 , CN, (CH 2 ) 1, 6 -OH, O- (C 1 -C 6 ) -alkyl, CO - (-CC 6 ) -A] alkyl, -C (O) O-Alkyb COOH, ' CON (R 9) (R 10) where the aryl radicals and the heterocyclic radicals may be monosubstituted or polysubstituted by F, Cb Br
- R3 H (CC 6 ) -Alkyb (C 1 -C 6 ) -alkylene-Aryb -C (O) -aryb (CC 6 ) -alkylene heterocycle, CO (C 1 -C 6 ) -alkyl where the aryl .
- C -C ⁇ VAlkyl, COOH, COO (C ⁇ -C6) -Alkyb CF 3 or OCF can and heterocyclic radicals mono- or polysubstituted with F, Br Cb, (substituted 3 -;
- R4, R5 independently of one another H, F, Br Cb, (C, -C 6) -Alkyb CF 3, OCF 3, NO 2, N (R9) (R10), CN, O- (C ⁇ -C6) alkyl , CO- (CC 6 ) -alkyl, COOH, (C 1 -C 6 ) -alkylene-COOH, CON (R 9) (R 10), (CC 6 ) -alkylene-CON (R 9) (R 10), COO (dC 6 ) -Alkyb (C 1 -C 6 ) alkylene-COO (C 1 -C 6 ) -Aikyb S (O) o- 2 - (C 1 -C 6 ) -Alkyb S (O) 2 -N (R 9) (R10), CH 2 OH, CH 2 OCH 3;
- R 8 is H, CH 3 , CF 3 , CH 2 OH;
- R 9 H, (C 1 -C 4 ) : Alk 1;
- R 10 is H, (C 1 -C 4 ) -alkyl
- R 9 and RIO together with the N atom to which they are attached form a 3-9 ring-shaped ring system
- Rl Aryb (dC 6) -Alkyb (C 2 -C 6) -Alkenyb (C 1 -C 6) -alkylene-Aryb heterocycle (C_- C 6) -alkylene-heterocycle, CF 3, OCF 3, CN, (CH 2) 1-6 -OH, O- (C 1 -C 6) -Alkyb CO- (dC 6) -Alkyb C (O) O-alkyb COOH, CON (R9) (R10), where the aryl radicals and the heterocyclic radicals may be singly or multiply substituted with F, Cb Br, (CH 2) o- 2 OH, (C ⁇ -C6) alkyl, (C 2 -C 6) -Alkenyb (C 2 -C 6) -Alkinyb CF 3 , OCF 3 , N (R 9) (R 10), piperidinone, piperazine, piperazinone, N- (C 1 -
- R4, R5 independently of one another are H, F, Cb Br, (C 1 -C 6 ) -alkyl, CF 3 , OCF 3 , NO 2 , N (R 9) (R 10), CN, O- (C 1 -C 6 ) - Alkyb CO- (dC 6 ) -Alkyb COOH, (C 1 -C 6 ) -alkylene- 15.
- R6, R7 independently of one another are H, F, Cb Br, (C 1 -C 6 ) -alkyl, cyclopropylb
- R 8 is H, CH 3 , CF 3 , CH 2 OH;
- R 9 and RIO together with the N atom to which they are attached form a 3-9 membered ring system; and their physiologically acceptable salts.
- Particular preference is given to compounds of the formula I in which one or more radicals are the following
- Rl Phenyb Naphthyb Thionaphthyb Pyridyb which may be Phenyb Naphthyb thionaphthyl and pyridyl or multiply substituted with F, Cb Br, (CH 2) o- 2 OH, (dC 6) -Alkyb (C 2 -C 6) -Alkenyb (C 2 -C 6 ) -alkynyl CF 3 , OCF 3 , N (R 9) (R 10), piperidinone, piperazine, piperazinone, N- (C 1 -C 6 -alkylene) -piperazine.
- R2 H (CC 6) -Alkyb COOH, (dC 6) -alkylene-COOH, -COO (dC 6) -Alkyb (dC 6) -alkylene-COO (dC 6) alkyl;
- R3 HH (CC 6 ) -Alkyb (-CC 6 ) -alkylene-Aryb -C (O) -Aryb (dC 6 ) -alkylene- H-heterocycle, CO-CC CeValkyl;
- R 10 is H, (C 1 -C 4 ) -alkyl
- Rl Phenyb wherein phenyl may be mono- or polysubstituted with F, Cb Br, (CH 2 ) o. 2 OH, (dd-alkyb (C 2 -C 6 ) -alkenyl (C 2 -C 6 ) -alkynyl CF 3 , OCF 3 , N (R 9) (R 10), piperidinone, piperazine, piperazinone, N- .
- R3 H (dC 6) -Alkyb (C ⁇ -C6) alkylene-Aryb -C (O) -Aryb (dC 6) -alkylene- heterocycle, CO- (C 1 -C 6) alkyl;
- the invention relates to compounds of the formula I, in the form of their racemates, racemic mixtures and pure enantiomers, and to their diastereomers and mixtures thereof.
- radicals or substituents can occur several times in the compounds of the formula I, they may all independently of one another have the meanings indicated and be identical or different.
- Suitable pharmaceutically acceptable salts are particularly suitable for medical applications because of their higher water solubility compared to the starting or basic compounds. These salts must have a pharmaceutically acceptable anion or cation.
- Suitable pharmaceutically acceptable acid addition salts of the compounds according to the invention are salts of inorganic acids, such as hydrochloric acid, hydrobromic acid, phosphoric acid, metaphosphoric acid, nitric acid and sulfuric acid, and also organic acids, such as, for example, acetic acid, benzenesulfonic, benzoic, citric, ethanesulfonic, fumaric acid.
- Suitable pharmaceutically acceptable basic salts are ammonium salts, alkali metal salts (such as sodium and potassium salts), alkaline earth salts (such as magnesium and calcium salts), salts of trometairiol (2-amino-2-hydroxymethyl-l, 3-propanediol), diethanolamine, lysine or ethylenediamine , Salts with a non-pharmaceutically acceptable anion, such as trifluoroacetate, are also within the scope of the invention as useful intermediates for the preparation or purification of pharmaceutically acceptable salts and / or for use in non-therapeutic, for example, in vitro applications.
- physiologically functional derivative refers to any physiologically acceptable derivative of a compound of formula I, e.g. an ester which, when administered to a mammal, e.g. humans, is able to form (directly or indirectly) a compound of formula I or an active metabolite thereof.
- the physiologically functional derivatives also include prodrugs of the compounds according to the invention, as described, for example, in H. Okada et al., Chem. Pharm. Buh. 1994, 42, 57-61. Such prodrugs can be metabolized in vivo to a compound of the invention. These prodrugs may or may not be effective.
- the compounds of the invention may also be in various polymorphic forms, e.g. as amorphous and crystalline polymorphic forms. All polymo ⁇ hen forms of the compounds of the invention are within the scope of the invention and are a further aspect of the invention.
- alkyl radical is meant a straight or branched hydrocarbon chain having one or more carbons, e.g. Methyl, Ethyb iso-Propyl tert-Butyb Hexyb
- the alkyl radicals may be monosubstituted or polysubstituted by suitable groups, such as, for example: F, Cb Br, I, CF 3 , ⁇ O 2 , N 3 , CN, COOH, COO (dC 6 ) alkybone CONH 2 , CONH (dC 6 ) alkylb CON [(C 1 -C 6 ) alkyl] 2) cycloalkyb (C 2 -C 6 ) alkenyl (C 2 -C 6 ) -alkynoB O- (dC 6 ) -alkyl O-CO- (C 1 -C 6 ) -Alkyb O-CO- (CC 6 ) -Aryb O-CO- (C 1 -C 6 ) heterocycle; PO 3 H 2 , SO 3 H, SO 2 -NH 2 , SO 2 NH (dC 6 ) -Alkyb SO 2 N [(dC 6 ) -alkyl] 2 ,
- alkenyl radical is understood as meaning a straight-chain or branched hydrocarbon chain having two or more carbons and one or more double bonds, such as, for example, Vinyb allyb pentenyl.
- the alkenyl radicals may be monosubstituted or polysubstituted by suitable groups, for example: F, Cb Br, I, CF 3 , NO 2 , N 3 , CN, COOH, COO (CC 6 ) Alkyb CONH 2 , CONH (dC 6 ) Alkyb CON [(d -C 6 ) alkyl] 2 ( Cycloalkyb (dC 10 ) alkyl) (C 2 -C 6 ) -Alkinyb O- (dC 6 ) -alkyl O-CO- (dC 6 ) -Alkyb O-CO- (dC 6 ) -Aryb O-CO- (dC 6 ) -heterocycle 5 ;
- alkyne residue is understood as meaning a straight-chain or branched hydrocarbon chain having two or more carbons and one or more triple bonds, such as, for example, Ethinyb Propinyb Hexinyb
- the alkynyl radicals may be monosubstituted or polysubstituted by suitable groups, such as, for example: F, Cb Br, I, CF 3 , NO 2 , N 3 , CN, COOH, COO (C 1 -C 6 ) alkybone CONH 2 , CONH (dC 6 ) Alkyb CON [(CC 6 ) alkyl] 2j Cycloalkyb (C 2 -C 6 ) alkenyb (dC 10 ) -Acrylic O- (dC 6 ) -alkyl O-CO- (CC 6 ) -Alkyb O-CO- ( dC 6 ) -Aryb O-CO- (dC 6 ) heterocycle; PO 3 H 2 , SO 3 H
- aryl radical is meant a phenyl, naphthyl, biphenyl, tetrahydronaphthyl, alpha- or beta-tetralonic, indanyl or indan-1-onyl radical.
- the aryl radicals may be substituted one or more times by suitable groups, for example: F, Cb Br, I, CF 3, NO 2, N 3, CN, COOH, COO (dC 6) Alkyb CONH 2, CONH (dC 6) Alkyb CON [(CC 6) alkyl] 2> Cycloalkyb (dC 10) -Alkyb (C 2 -C 6) -Alkenyb (C 2 -C 6) -Alkinyb O- (C r C6) -alkyl O-CO- ( CC 6 ) -Alkyb O-CO- (dC 6 ) -Aryb O-CO- (CC 6 ) heterocycle; PO 3 H 2 , SO 3 H, SO 2 -NH 2 , SO 2 NH (dC 6 ) -Alkyb SO 2 N [(dC 6 ) alkyl] 2 , S- (dC 6 ) -Alkyb S- (CH 2 ) n
- a cycloalkyl radical is to be understood as meaning a ring system containing one or more rings which is saturated or partially unsaturated (having one or two double bonds), which is composed exclusively of carbon atoms, e.g. Cyclopropyb cyclopentyb cyclopentenyb cyclohexyl or adamantyb
- the Cycloalkylrestereste may be substituted one or more times by suitable groups, for example: F, Cb Br, I, CF 3, NO 2, N 3, CN, COOH, COO (CC 6) Alkyb CONH 2, CONH (CC 6) Alkyb CON [(dC 6 ) alkyl] 2) Cycloalkyl (dC 10 ) -alkyl (C 2 -C 6 ) -alkenyl (C 2 -C 6 ) -alkynoBy- (CC 6 ) -alkyl O-CO- (dC 6 ) -Alkyb O-CO- (C 1 -C 6 ) -Aryb O-CO- (C 1 -C 6 ) -heterocycle; PO 3 H 2 , SO 3 H, SO 2 -NH 2 , SO 2 NH (dC 6 ) -alkyl SO 2 N [(dC 6 ) -alkyl] 2 , S- (dC 6 ) -
- Heterocycle or heterocyclic radical is understood as meaning rings and ring systems which, in addition to carbon, also contain heteroatoms, such as, for example, nitrogen, oxygen or sulfur. Furthermore, ring systems also belong to this definition, in which the heterocyclic or the heterocyclic radical is condensed with benzene nuclei.
- Suitable "heterocyclic rings” or “heterocyclic radicals” are Acridinyb Azocinyb Benzimidazolyb Benzofuryb Benzothienyb Benzothiophenyb Benzoxazolyb Benzthiazolyb Benztriazolyb Benztetrazolyb Benzisoxazolyb Benzisothiazolyb Benzimidazalinyb Carbazolyb 4aH-Carbazolyb Carbolinyb Chinazolinyb Chinolinyb 4H-Chinolizinyb Chinoxalinyb Chinuclidinyb Chromanyb Chromenyb Cinnolinyb Decahydrochinolinyb 2H, 6H-1,5,2 Dithiazinyl dihydrofuro [2,3-b] tetrahydrofuran, Furyb Furazanyb.
- Pyridyl stands for both 2-, 3- and 4-pyridyl.
- Thienyl stands for both 2- and 3-pyridyl.
- Thienyb furyl stands for both 2 and 3 furyb
- N-oxides of these compounds e.g. l-oxy-2-, 3- or 4-pyridyl.
- heterocyclic rings or heterocyclic radicals may be monosubstituted or polysubstituted by suitable groups, such as, for example: F, Cb Br, I, CF 3 , NO 2 , N 3 , CN, COOH, COO (dC 6 ) alkybone CONH 2 , CONH (CC 6 ) Alkyb CON [(dC 6 ) alkyl] 2, Cycloalkybd (dC 10 ) - Alkyb (C 2 -C 6 ) -Alkenyb (C 2 -C 6 ) -Alkoxyb O- (dC 6 ) -Alkyl- CO- (dC 6) - Alkyb O-CO- (dC 6) -Aryb O-CO- (C 1 -C 6) heterocyclic;
- suitable groups such as, for example: F, Cb Br, I, CF 3 , NO 2 , N 3 , CN, COOH, COO (dC 6 ) alky
- the amount of a compound of Formula I required to achieve the desired biological effect is dependent upon a number of factors, eg, the specific compound chosen, the intended use, the mode of administration, and the clinical condition of the patient.
- the daily dose will be in the range of 0.3 mg to 100 mg (typically 3 mg and 50 mg) per kilogram of body weight per day, eg 3-10 mg / kg / day.
- an intravenous dose may range from 0.3 mg to 1.0 mg / kg, which may conveniently be administered as an infusion of 10 ng to 100 ng per kilogram per minute.
- Suitable infusion solutions for these purposes may contain, for example, from 0.1 ng to 10 mg, typically from 1 ng to 10 mg per milliliter.
- Single doses may contain, for example, from 1 mg to 10 g of the active ingredient.
- injectable ampoules, and orally available single dose formulations such as tablets or capsules, may contain, for example, from 1.0 to 1000 mg, typically from 10 to 600 mg.
- the compounds according to formula I can themselves be used as compound, but they are preferably present with a compatible carrier in the form of a pharmaceutical composition.
- the carrier must of course be compatible in the sense that it is compatible with the other ingredients of the composition and is not harmful to the patient.
- the carrier may be a solid or a liquid, or both, and is preferably formulated with the compound as a single dose, for example, as a tablet, which may contain from 0.05% to 95% by weight of the active ingredient.
- Other pharmaceutically active substances may also be present, including other compounds according to formula I.
- the pharmaceutical compositions according to the invention can be prepared by one of the known pharmaceutical methods, which consist essentially in that the ingredients with pharmacologically acceptable carrier and / or Adjuvants are mixed.
- compositions according to the invention are those which are suitable for oral, rectal, topical, peroral (eg sublingual) and parenteral (eg subcutaneous, intramuscular, intradermal or intravenous) administration, although the most suitable mode of administration in each individual case is the nature and severity of the disease condition to be treated and on the nature of the particular compound used in accordance with formula I is dependent.
- coated formulations and coated slow release formulations are within the scope of the invention. Preference is given to acid and enteric formulations. Suitable enteric coatings include cellulose acetate phthalate, polyvinyl acetate phthalate,
- Hydroxypropylmethylcellulosephthalat and anionic polymers of methacrylic acid and methyl methacrylate are examples of hydroxypropylmethylcellulosephthalat and anionic polymers of methacrylic acid and methyl methacrylate.
- Suitable pharmaceutical compounds for oral administration may be in separate units, such as capsules, cachets, lozenges or tablets, each containing a certain amount of the compound of formula I; as a powder or granules; as a solution or suspension in an aqueous or non-aqueous liquid; or as an oil-in-water or water-in-oil emulsion.
- these compositions may be prepared by any suitable pharmaceutical method comprising a step of contacting the active ingredient and the carrier (which may consist of one or more additional ingredients).
- the compositions are prepared by uniformly and homogeneously mixing the active ingredient with a liquid and / or finely divided solid carrier, after which the product is molded, if necessary.
- a tablet can be prepared by resuspending or molding a powder or granules of the compound, optionally with one or more additional ingredients.
- Compressed tablets can be prepared by tableting the compound in free-flowing form, such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent and / or surfactant / dispersant in a suitable machine.
- Molded tablets may be prepared by shaping the powdered compound moistened with an inert liquid diluent in a suitable machine.
- compositions suitable for peroral (sublingual) administration include lozenges containing a compound of formula I with a flavor, usually sucrose and gum arabic or tragacanth, and lozenges containing the compound in an inert base such as gelatin and glycerol or sucrose and gum arabic.
- Suitable pharmaceutical compositions for parenteral administration preferably comprise sterile aqueous preparations of a compound according to formula I which are preferably isotonic with the blood of the intended recipient. These preparations are preferably administered intravenously, although the administration may also be subcutaneous, intramuscular or intradermal as an injection. These preparations may preferably be prepared by mixing the compound with water and rendering the resulting solution sterile and isotonic with the blood. Injectable compositions of the invention generally contain from 0.1% to 5% by weight of the active compound.
- Suitable pharmaceutical compositions for rectal administration are preferably as single dose suppositories. These can be prepared by mixing a compound according to formula I with one or more conventional solid carriers, for example cocoa butter, and shaping the resulting mixture.
- Suitable pharmaceutical compositions for topical application to the skin are preferably as an ointment, cream, lotion, paste, spray, aerosol or oil.
- Vaseline, lanolin, polyethylene glycols, alcohols and combinations of two or more of these substances can be used as the carrier.
- the active ingredient is generally in one. Concentration of 0.1 to 15 wt .-% of. Composition present, for example, from 0.5 to 2%.
- Suitable pharmaceutical compositions for transdermal applications may be as single patches suitable for long-term close contact with the epidermis of the patient. Such patches suitably contain the active ingredient in an optionally buffered aqueous solution, dissolved and / or dispersed in an adhesive or dispersed in a polymer.
- a suitable Whkstoff concentration is about 1% to 35%, preferably about 3% to 15%.
- the active ingredient can be released by electrotransport or iontophoresis as described, for example, in Pharmaceutical Research, 2 (6): 318 (1986).
- the compound (s) of the formula (I) can also be administered in combination with other active substances.
- active ingredients for the combination preparations are suitable: All Antidiabetika, which are mentioned in the red list 2003, chapter 12. They can be combined with the compounds of the formula I according to the invention in particular for the synergistic effect improvement.
- the administration of the active ingredient combination can be carried out either by separate administration of the active ingredients to the patient or in the form of combination preparations in which several active ingredients are present in a pharmaceutical preparation.
- Most of the drugs listed below are disclosed in the USP Dictionary of US AN and International Drag Names, US Pharmacopeia, Rockville 2001.
- Antidiabetics include insulin and insulin derivatives, such as Lantus ® (see www.lantus.com) or HMR 1964 fast-acting insulins (see US No. 6,221,633), GLP-1 derivatives such as those described in WO 97/26265, WO 99 / 03861, WO 01/04156, WO 00/34331, WO00 / 34332, WO91 / 11457 and US 6,380,357, as well as orally active hypoglycemic agents.
- insulin and insulin derivatives such as Lantus ® (see www.lantus.com) or HMR 1964 fast-acting insulins (see US No. 6,221,633)
- GLP-1 derivatives such as those described in WO 97/26265, WO 99 / 03861, WO 01/04156, WO 00/34331, WO00 / 34332, WO91 / 11457 and US 6,380,357, as well as orally active hypoglycemic agents.
- the orally active hypoglycemic agents preferably include sulphonylureas, biguanidines, meglitinides, oxadiazolidinediones, thiazolidinediones, glucosidase inhibitors, glucagon antagonists, GLP-1 agonists, potassium channel openers, such as those described in WO 97/26265 and WO 99/03861 of Novo Nordisk A / S, insulin sensitizers, inhibitors of liver enzymes involved in the stimulation of gluconeogenesis and / or glycogenolysis, modulators of glucose uptake, lipid metabolism altering compounds such as antihyperlipidemic agents and antilipidemic agents, compounds that reduce food intake, PPAR and PXR agonists and drugs acting on the ATP-dependent potassium channel of the beta cells.
- sulphonylureas biguanidines, meglitinides, oxadiazolidinediones, thiazolidinediones, glu
- the compounds of formula I are administered in combination with an HMGCoA reductase inhibitor such as simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin, rosuvastatin.
- an HMGCoA reductase inhibitor such as simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin, rosuvastatin.
- the compounds of formula I are administered in combination with a cholesterol reso ⁇ tion inhibitor, e.g. Ezetimibe,. Tiqueside, Pamaqueside.
- a cholesterol reso ⁇ tion inhibitor e.g. Ezetimibe,. Tiqueside, Pamaqueside.
- the compounds of formula I are administered in combination with a PPAR gamma agonist, e.g. Rosiglitazone, pioglitazone, JTT-501, Gl 262570.
- a PPAR gamma agonist e.g. Rosiglitazone, pioglitazone, JTT-501, Gl 262570.
- the compounds of formula I in combination with PPAR alpha agonist e.g. GW 9578, GW 7647.
- the compounds of formula I in combination with a mixed PPAR alpha / gamma agonist e.g. GW 1536, AVE 8042, AVE 8134, AVE 0847, or as described in PCT / US00 / 11833, PCT / US 11490, DE10142734.4.
- a mixed PPAR alpha / gamma agonist e.g. GW 1536, AVE 8042, AVE 8134, AVE 0847, or as described in PCT / US00 / 11833, PCT / US 11490, DE10142734.4.
- the compounds of formula I are used in combination with a fibrate, e.g. Fenofibrate, clofibrate, bezafibrate.
- a fibrate e.g. Fenofibrate, clofibrate, bezafibrate.
- the compounds of formula I are administered in combination with an MTP inhibitor, e.g. Implitapide, BMS-201038, R-103757.
- an MTP inhibitor e.g. Implitapide, BMS-201038, R-103757.
- the compounds of the formula I are administered in combination with bile acid resorption inhibitor (see, for example, US Pat. No. 6,245,744 or US Pat. No. 6,221,897), for example HMR 1741.
- the compounds of the formula I are administered in combination with a CETP inhibitor, such as JTT-705.
- the compounds of formula I are used in combination with a polymeric bile acid adsorber, e.g. Cholestyramine, colesevelam.
- a polymeric bile acid adsorber e.g. Cholestyramine, colesevelam.
- the compounds of formula I are used in combination with an LDL receptor inducer (see US 6,342,512), e.g. HMR1171, HMR1586.
- the compounds of formula I are administered in combination with an ACAT inhibitor, e.g. Avasimibe, administered.
- an ACAT inhibitor e.g. Avasimibe
- the compounds of formula I in combination with an antioxidant, e.g. OPC-14117 administered.
- the compounds of formula I are used in combination with a lipoprotein lipase inhibitor, e.g. NO-1886, administered.
- a lipoprotein lipase inhibitor e.g. NO-1886
- the compounds of formula I are used in combination with an ATP citrate lyase inhibitor, e.g. SB-204990 administered.
- the compounds of formula I in combination with a squalene synthetase inhibitor, e.g. BMS-188494.
- the compounds of formula I in combination with a lipoprotein (a) antagonist, e.g. CI-1027 or nicotinic acid.
- a lipoprotein (a) antagonist e.g. CI-1027 or nicotinic acid.
- the compounds of formula I are administered in combination with a lipase inhibitor, such as orlistat. In one embodiment of the invention, the compounds of the formula I are administered in combination with insulin.
- the compounds of formula I in combination with a sulphonylurea such as e.g. Tolbutamide, ghostclamide, glipizide or glimepiride.
- a sulphonylurea such as e.g. Tolbutamide, ghostclamide, glipizide or glimepiride.
- the compounds of formula I are used in combination with a biguanide, e.g. Metformin, administered.
- the compounds of formula I in combination with a meglitinide, e.g. Repaglinide, administered.
- a meglitinide e.g. Repaglinide
- the compounds of formula I are used in combination with a thiazolidinedione, e.g. Troglitazone, ciglitazone, pioglitazone, rosiglitazone or those described in WO 97/41097 by Dr. med. Reddy's Research Foundation disclosed compounds, particularly 5 - [[4- [(3,4-dihydro-3-methyl-4-oxo-2-quinazolinylmethoxy) phenyl] methyl] -2,4-thiazolidinedione.
- a thiazolidinedione e.g. Troglitazone, ciglitazone, pioglitazone, rosiglitazone or those described in WO 97/41097 by Dr. med. Reddy's Research Foundation disclosed compounds, particularly 5 - [[4- [(3,4-dihydro-3-methyl-4-oxo-2-quinazolinylmethoxy) phenyl]
- the compounds of formula I are administered in combination with an ⁇ -glucosidase inhibitor, e.g. Miglitol or acarbose, administered.
- the compounds of formula I are administered in combination with an agent which acts on the ATP-dependent potassium channel of the beta cells, e.g. Tolbutamide, Ghbenclamide, Glipizide, Glimepiride or Repaglinide.
- the compounds of formula I are used in combination with more than one of the aforementioned compounds, e.g. in combination with a sulphonylurea and metformin, a sulphonylurea and acarbose, repaglinide and metformin, insulin and a sulphonylurea, insulin and metformin, insulin and troglitazone, insulin and lovastatin, etc.
- the compounds of the formula I are administered in combination with CART modulators (see “Cocaine-amphetamine-regulated transcript-influenced transient-influencing energy metabolism, anxiety and gastric emptying in mice" Asakawa, A, et., M.: Hormones and Metaboly Research (2001), 33 (9), 554-558), NPY antagonists eg naphthalene-1-sulfonic acid ⁇ 4 - [(4-amino-quinazolin-2-ylamino) -methyl] -cyclohexylmethyl ⁇ -amide; hydrochloride (CGP 71683A)), MC4 agonists (eg, l-amino-l, 2,3,4-tetrahydronaphthalene-2 carboxylic acid [2- (3a-benzyl-2-methyl-3-oxo-2,3,3a, 4,6,7-hexahydro-pyrazolo [4,3-c] pyridin-5-yl) -l-
- CRF BP antagonists eg, urocortin
- urocortin agonists eg, urocortin
- 33 agonists eg, 1- (4-chloro-3-methanesulfonylmethylphenyl) -2- [2- (2,3-dimethyl) lH-indol-6-yloxy) - ethylaminojethanol; hydrochloride (WO 01/83451)
- MSH melanocyte stimulating hormone
- CCK-A agonists eg, ⁇ 2- [4- (4-chloro-2 , 5-dimethoxy-phenyl) -5- (2-cyclohexyl-ethyl) -thiazol-2-ylcarbamoyl] -5,7-dimethylindol-1-yl ⁇ -acetic acid
- Trifluoroacetic acid salt (WO 99/15525)); Serotonin reuptake inhibitors (e.g., dexfenfluramines), mixed serotonin and noradrenergic compounds (e.g., WO 00/71549), 5HT agonists, e.g.
- DA agonists bromocriptine, doprexin
- lipase / amylase inhibitors e.g., WO 00/40569
- PPAR modulators e.g., WO 00/78312
- RXR modulators or TR- ⁇ agonists.
- the further active ingredient is leptin; see, e.g. "Perspectives in the therapeutic use of leptin", Salvador, Javier; Gomez-Ambrosi, Javier; Fruhbeck, Gema, Expert Opinion on Pharmacotherapy (2001), 2 (10), 1615-1622.
- the further active ingredient is dexamphetamine or amphetamine.
- the other active ingredient is a blood pressure reducer, such as an ACE inhibitor.
- the other active ingredient is fenfluramine or dexfenfluramine.
- the other active ingredient is sibutramine.
- the other active ingredient is orlistat.
- the other active ingredient is mazindol or phentermine.
- the compounds of formula I in combination with bulking agents preferably insoluble bulking agents
- bulking agents preferably insoluble bulking agents
- Caromax is a carob-containing product of the company Nutrinova, Nutrition Specialties & Food Ingredients GmbH, Industriepark availability, 65926 Frankfurt / Main)) administered.
- Combination with Caromax ® is possible in one preparation or by separate administration of compounds of the formula I and Caromax ®.
- Caromax ® can also be administered in the form of food, such as in baked goods or muesli bars.
- JTT-501 The following examples serve to illustrate the invention, but without limiting it.
- the compounds of the formula I were tested for their phosphatase-inhibiting activity in an in vitro assay.
- the enzyme preparation and the performance of the assay was carried out as follows.
- cDNA encoding the regulatory and catalytic domains of the human PTPIB but without the carboxy-terminal hydrophobic region (corresponding to 1-299 aa) was purified via polymerase chain reaction via primers with attached cloning sites and appropriate cDNA templates (available, for example, from invitrogen ) and then cloned into baculovirus expression vectors (Amersham Pharmacia Biotech.).
- the recombinant baculoviruses were prepared by the Bac-to-Bac baculoviral expression system (available from Gibco-BRL). The gene was cloned into the pFASTBAC donor plasmid (available from Life Technologies).
- the resulting plasmid was transformed into competent DH10BAC Escherichia coli cells (available from Life Technologies). After transposition and antibiotic selection, the recombinant plasmid DNA was isolated from selected E. coli colonies and then used for the transfection of Sf9 insect cells. The viral particle in the supernatant medium was amplified three times, except for a viral stock volume of 500 ml.
- B) Production of Recombinant Protein Baculovirus infection of a 500 ml spinner culture of Sf9 cells was performed essentially as described by Summers and Smith (supra).
- Sf9 cells at a density of 1-3 x 10 6 cells ml were pelleted by centrifugation at 300 g for 5 min, the supernatant was removed and the cells were collected at a density of 1 x 10 7 cells ml in a suitable recombinant viral stock (MOI 10). resuspended. After gentle shaking for 1.5 h at room temperature, fresh medium was added to achieve a cell density of 1 ⁇ 10 6 cells ml. The cells were then cultured in suspension at 28 ° C for appropriate periods after post infection.
- MOI 10 recombinant viral stock
- A) Dephosphorylation of a Phosphopeptide This assay is based on the release of phosphate from a consensus substrate peptide which has been measured in the nanomolar concentration range by the MalacMtgreen-ammonium molybdate method (Lanzetta, PA, Alvarez, LJ, Reinach, PS, Candia, OA Anal Biochem., 100: 95-97, 1979) adapted for the microtitre plate format.
- the dodecatrisphosphopeptide, TRDIYETDYYRK (Biotrend, Cologne) corresponds to the amino acids 1142-1153 of the catalytic domain of the insulin receptor and is (auto) phosphorylated at the Tyrosine residues 1146, 1150, and 1151.
- the recombinant hPTPIB was diluted with assay buffer (40 mM Tris / HCl, pH 7.4, 1 mM EDTA, 20 mM DTT) corresponding to an activity of 1000-1500 nmol / min / mg protein and (a 20 ⁇ l portion) then pre-incubated (15 min, 30 ° C) in absence or presence of the test substance (5 ⁇ l) in the desired concentration (final conc. DMSO 2% max.) In a total volume of
- the peptide substrate (10 ⁇ B preheated to 30 ° C.) was added to the preincubated enzyme preparation with or without test substance (final concentration 0.2-200 ⁇ M) and the incubation continued for 1 h.
- the reaction was terminated by adding 100 ⁇ l of malactate green hydrochloride (0.45%, 3 parts), ammonium bromide tetrahydrate (4.2% in
- This assay is based on the change in absorbance of the non-physiological substrate p-nitrophenyl phosphate during cleavage to nitrophenol under standard conditions (Tonks, NK, Diltz, CD: Fischer, EHJ Biol. Chem. 263: 6731-6737, 1988, Burke TR, Ye , B., Yan, XJ, Wang, SM, Jia, ZC, Chen, L., Zhang,
- the inhibitors are pipetted in appropriate dilution to the reaction mixtures containing 0.5-5 mM p-nitrophenyl phosphate.
- the following buffers were used (total volume 100 ⁇ l): (a) 100 mM sodium acetate (pH 5.5), 50 mM Nad, 0.1% (w / v) bovine serum albumin, 5 mM glutathione, 5 mM DTT, 0.4 mM EGTA and 1 mM EDTA ;
- results were expressed as percent of control in which the amount of p-nitrophenol produced in the test substance-treated samples (nmol / min / mg protein) was compared to the amount in the untreated samples. Mean and standard deviation were calculated, IC50 values were determined by regression analysis of the linear portion of the inhibition curves.
- the compounds of the formula I inhibit the activity of phosphotyrosine phosphatase 1B (PTPIB) and thereby reduce the Blood sugar levels are well suited. They are particularly suitable for the treatment of diabetes type I and II, insulin resistance, dyslipidaemias, metabolic syndrome / syndrome X, morbid obesity and weight loss in mammals.
- PTPIB phosphotyrosine phosphatase 1B
- compounds of the formula I because of their inhibition of PTPIB, for the treatment of hyperglyceridemia, hypertension, AtherosMerose, Immune system malfunctions, autoimmunity, allergic diseases such as asthma, arthritis, osteoarthritis, osteoporosis, proliferative disorders such as cancer and psoriasis, diseases with reduced or increased production of growth factors, hormones or cytoMnen that trigger the release of growth hormones.
- the compounds are also useful for treating nervous system disorders, such as Alzheimer's or multiple sclerosis.
- the compounds are also useful in treating disorders of sensation and other psychiatric indications, such as depression, anxiety, anxiety disorders, schizophrenia, treating disorders associated with the circadian rhythm, and treating drug abuse.
- Diazabicycloundecene (34.1 g, 33.42 mL, 0.22 mol) is added to a solution of compound 1 (25 g, 0.107 mol) in DMF (1 L) at RT and the reaction mixture is stirred at 130 ° C. for 2 h , Then the solvent is distilled off in vacuo, the residue with water (400 mL), treated with HCl (2n, 400 mL) and the product extracted several times with dichloromethane. The combined organic phases are dried (Na SO 4 ) and the solvent is distilled off under reduced pressure. The remaining residue is stirred with a little cold isopropanol and the reaction product is then filtered off.
- the solvent is removed under reduced pressure, the oily residue is stirred with diethyl ether and the reaction product is filtered off.
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Abstract
Description
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Priority Applications (16)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002533673A CA2533673A1 (en) | 2003-07-28 | 2004-07-15 | Substituted thiazole-benzoisothiazole dioxide derivatives, method for the production thereof and use of the same |
SI200430126T SI1651644T1 (sl) | 2003-07-28 | 2004-07-15 | Substituirani tiazol-benzoizotiazol dioksidni derivati, postopek za njihovo pripravo in njihova uporaba |
DK04741034T DK1651644T3 (da) | 2003-07-28 | 2004-07-15 | Substituerede derivater af thiazol-benzoisothiazoldioxid, fremgangsmåde deraf og deres anvendelse |
AU2004261370A AU2004261370B2 (en) | 2003-07-28 | 2004-07-15 | Substituted thiazole-benzoisothiazole dioxide derivatives, method for the production thereof and use of the same |
YUP-2006/0015A RS20060015A (en) | 2003-07-28 | 2004-07-15 | Substituted thiazole- benzoisothiazole dioxide derivatives, method for the production thereof and use of the same |
BRPI0412997-0A BRPI0412997A (pt) | 2003-07-28 | 2004-07-15 | derivados de dióxido de tiazol-benzoisotiazol substituìdos, método para produzir os mesmos e seu uso |
EP04741034A EP1651644B1 (de) | 2003-07-28 | 2004-07-15 | Substituierte thiazol-benzoisothiazoldioxidderivative, verfahren zu deren herstellung und deren verwendung |
JP2006521446A JP2007500145A (ja) | 2003-07-28 | 2004-07-15 | 置換チアゾール−ベンゾイソチアゾールジオキシド誘導体、それらの製造方法、およびそれらの使用 |
PL04741034T PL1651644T3 (pl) | 2003-07-28 | 2004-07-15 | Podstawione pochodne tiazolo-ditlenku benzoizotiazolu, sposób ich wytwarzania i zastosowanie |
NZ544975A NZ544975A (en) | 2003-07-28 | 2004-07-15 | Substituted thiazole-benzoisothiazole dioxide derivatives, method for the production thereof and use of the same |
DE502004002117T DE502004002117D1 (de) | 2003-07-28 | 2004-07-15 | Substituierte thiazol-benzoisothiazoldioxidderivative, verfahren zu deren herstellung und deren verwendung |
IL173289A IL173289A0 (en) | 2003-07-28 | 2006-01-22 | Substituted thiazole-benzoisothiazole dioxide derivatives, method for the production thereof and use of the same |
TNP2006000030A TNSN06030A1 (en) | 2003-07-28 | 2006-01-27 | Substituted thiazole-benzoisothiazole dioxide derivavites, method for the production thereof and use of the same |
NO20060908A NO20060908L (no) | 2003-07-28 | 2006-02-24 | Substituerte tazol-benzoisotiazoldioksidderivater, deres fremstilling og anvendelse |
HK06112382A HK1091825A1 (en) | 2003-07-28 | 2006-11-10 | Substituted thiazole-benzoisothiazole dioxide derivatives, method for the production thereof and useof the same |
CY20071100112T CY1105962T1 (el) | 2003-07-28 | 2007-01-29 | Υποκατεστημενα παραγωγα διοξειδιου θειαζολο-βενζοϊσοθειαζολιου, μεθοδος για την παραγωγη αυτων και η χρηση αυτων |
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DE10334309.1 | 2003-07-28 | ||
DE10334309A DE10334309A1 (de) | 2003-07-28 | 2003-07-28 | Substituierte Thiazol-Benzoisothiazoldioxidderivate, Verfahren zu deren Herstellung und deren Verwendung |
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WO2005012295A1 true WO2005012295A1 (de) | 2005-02-10 |
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PCT/EP2004/007847 WO2005012295A1 (de) | 2003-07-28 | 2004-07-15 | Substituierte thiazol-benzoisothiazoldioxidderivative, verfahren zu deren herstellung und deren verwendung |
Country Status (38)
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EP (1) | EP1651644B1 (de) |
JP (1) | JP2007500145A (de) |
KR (1) | KR20060052886A (de) |
CN (1) | CN100413862C (de) |
AR (1) | AR045113A1 (de) |
AT (1) | ATE346065T1 (de) |
AU (1) | AU2004261370B2 (de) |
BR (1) | BRPI0412997A (de) |
CA (1) | CA2533673A1 (de) |
CR (1) | CR8202A (de) |
CY (1) | CY1105962T1 (de) |
DE (2) | DE10334309A1 (de) |
DK (1) | DK1651644T3 (de) |
EC (1) | ECSP066326A (de) |
ES (1) | ES2276319T3 (de) |
GT (1) | GT200400146A (de) |
HK (1) | HK1091825A1 (de) |
IL (1) | IL173289A0 (de) |
JO (1) | JO2449B1 (de) |
MA (1) | MA27932A1 (de) |
MY (1) | MY141197A (de) |
NO (1) | NO20060908L (de) |
NZ (1) | NZ544975A (de) |
OA (1) | OA13198A (de) |
PA (1) | PA8607201A1 (de) |
PE (1) | PE20050326A1 (de) |
PL (1) | PL1651644T3 (de) |
PT (1) | PT1651644E (de) |
RS (1) | RS20060015A (de) |
RU (1) | RU2350613C2 (de) |
SA (1) | SA04250332B1 (de) |
SI (1) | SI1651644T1 (de) |
TN (1) | TNSN06030A1 (de) |
TW (1) | TW200524923A (de) |
UA (1) | UA83057C2 (de) |
UY (1) | UY28443A1 (de) |
WO (1) | WO2005012295A1 (de) |
ZA (1) | ZA200510378B (de) |
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US7453000B2 (en) * | 2004-05-29 | 2008-11-18 | Sanofi-Aventis Deutschland Gmbh | Substituted oxazolobenzoisothiazole dioxide derivatives method for production and use thereof |
WO2009021740A2 (de) | 2007-08-15 | 2009-02-19 | Sanofis-Aventis | Substituierte tetrahydronaphthaline, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
WO2010003624A2 (en) | 2008-07-09 | 2010-01-14 | Sanofi-Aventis | Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof |
WO2010068601A1 (en) | 2008-12-08 | 2010-06-17 | Sanofi-Aventis | A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof |
WO2011023754A1 (en) | 2009-08-26 | 2011-03-03 | Sanofi-Aventis | Novel crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use |
WO2011107494A1 (de) | 2010-03-03 | 2011-09-09 | Sanofi | Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
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WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
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WO2012120050A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2012120057A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2012120054A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Di- und trisubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
WO2012120051A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
EP2567959A1 (de) | 2011-09-12 | 2013-03-13 | Sanofi | 6-(4-Hydroxy-phenyl)-3-styryl-1H-pyrazolo[3,4-b]pyridin-4-Carbonsäureamid-Derivate als Kinaseinhibitoren |
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 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3539584A (en) * | 1967-11-14 | 1970-11-10 | Colgate Palmolive Co | 5-substituted-2,1-benzisothiazolines |
WO1992005164A1 (en) * | 1990-09-19 | 1992-04-02 | Pfizer Inc. | Novel aminobenzosultam derivatives as lipoxygenase inhibitors |
WO2000076501A1 (en) * | 1999-06-16 | 2000-12-21 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
US20020055523A1 (en) * | 2000-08-09 | 2002-05-09 | Stefan Petry | Substituted and unsubstituted benzooxathiazoles and compounds derived therefrom |
-
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3539584A (en) * | 1967-11-14 | 1970-11-10 | Colgate Palmolive Co | 5-substituted-2,1-benzisothiazolines |
WO1992005164A1 (en) * | 1990-09-19 | 1992-04-02 | Pfizer Inc. | Novel aminobenzosultam derivatives as lipoxygenase inhibitors |
WO2000076501A1 (en) * | 1999-06-16 | 2000-12-21 | Smithkline Beecham Corporation | Il-8 receptor antagonists |
US20020055523A1 (en) * | 2000-08-09 | 2002-05-09 | Stefan Petry | Substituted and unsubstituted benzooxathiazoles and compounds derived therefrom |
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