WO1998040353A1 - Novel heterocyclic compounds - Google Patents
Novel heterocyclic compounds Download PDFInfo
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- WO1998040353A1 WO1998040353A1 PCT/DK1998/000084 DK9800084W WO9840353A1 WO 1998040353 A1 WO1998040353 A1 WO 1998040353A1 DK 9800084 W DK9800084 W DK 9800084W WO 9840353 A1 WO9840353 A1 WO 9840353A1
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- WIPO (PCT)
- Prior art keywords
- pyrrolidinediol
- compound
- mixture
- hydroxyethyl
- formula
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- 0 CC1C(*)C(C*)NC1 Chemical compound CC1C(*)C(C*)NC1 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/12—Oxygen or sulfur atoms
-
- 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
Definitions
- the present invention relates to novel compounds, the use of these compounds as medicaments, the use of these medicaments in the treatment and/or prevention of diabetes, and especially non-insulin dependent diabetes (NIDDM or type 2 diabetes) including overnight or meal treatment and treatment or prevention of long-term complications, such as retinopathy, neuropathy, nephropathy, and micro- and macroangiopathy; treatment of hyperglycemia, hypercholesterolemia, hypertension, hyperinsulinemia, hyperlipidemia, atherosclerosis, or myocardial ischemia; pharmaceutical compositions containing these compounds, and meth- ods of preparing the compounds.
- NIDDM non-insulin dependent diabetes
- Diabetes is characterized by an impaired glucose metabolism manifesting itself among other things by an elevated blood glucose level in the diabetic patients. Underlying defects lead to a classification of diabetes into two major groups: type 1 diabetes, or insulin demanding dia- betes mellitus (IDDM), which arises when patients lack ⁇ -cells producing insulin in their pancreatic glands, and type 2 diabetes or non-insulin dependent diabetes mellitus (NIDDM), which occurs in patients with an impaired ⁇ -cell function besides a range of other abnormalities.
- IDDM insulin demanding dia- betes mellitus
- NIDDM non-insulin dependent diabetes mellitus
- Type 1 diabetic patients are currently treated with insulin, while the majority of type 2 diabetic patients are treated either with sulfonylureas that stimulate ⁇ -cell function or with agents that enhance the tissue sensitivity of the patients towards insulin or with insulin.
- agents applied to enhance tissue sensitivity towards insulin metformin is a representative example.
- sulfonylureas are widely used in the treatment of NIDDM this therapy is, in most instances, not satisfactory: In a large number of NIDDM patients sulfonylureas do not suffice to normalize blood sugar levels and the patients are, therefore, at high risk for acquiring diabetic complications. Also, many patients gradually lose the ability to respond to treatment with sulfonylureas and are thus gradually forced into insulin treatment. This shift of patients from oral hypoglycaemic agents to insulin therapy is usually ascribed to exhaustion of the ⁇ -cells in NIDDM patients.
- Atherosclerosis a disease of the arteries, is recognized to be the leading cause of death in the United Stated and Western Europe.
- the pathological sequence leading to atherosclero- sis and occlusive heart disease is well known. The earliest stage in this sequence is the formation of "fatty streaks" in the carotid, coronary and cerebral arteries and in the aorta. These lesions are yellow in color due to the presence of lipid deposits found principally within smooth-muscle cells and in macrophages of the intima layer of the arteries and aorta.
- fibrous plaque which consists of accumulated intimal smooth muscle cells laden with lipid and surrounded by extracellular lipid, collagen, elastin and pro- teoglycans.
- the cells plus matrix form a fibrous cap that covers a deeper deposit of cell debris and more extra cellular lipid.
- the lipid is primarily free and esterified cholesterol.
- the fibrous plaque forms slowly, and is likely in time to become calcified and necrotic, advancing to the "complicated lesion” which accounts for the arterial occlusion and tendency toward mural thrombosis and arterial muscle spasm that characterize advanced atherosclerosis.
- CVD cardiovascular disease
- leaders of the medical profession have placed renewed emphasis on lowering plasma cholesterol levels, and low density lipoprotein cholesterol in particular, as an essential step in prevention of CVD.
- the upper limits of "normal” are now known to be significantly lower than heretofore appreciated.
- independent risk factors include glucose intolerance, left ventricular hypertrophy, hypertension, and being of the male sex.
- Cardiovascular disease is especially prevalent among diabetic subjects, at least in part because of the existence of multiple independent risk factors in this population. Successful treatment of hyperlipidemia in the general population, and in diabetic subjects in particular, is therefore of exceptional medical impor- tance.
- Hypertension is a condition which occurs in the human population as a secondary symptom to various other disorders such as renal artery stenosis, pheo- chromocytoma or endocrine disorders.
- hypertension is also evidenced in many patients in whom the causative agent or disorder is unknown. While such "essential" hypertension is often associated with disorders such as obesity, diabetes and hypertriglyceride- mia, the relationship between these disorders has not been elucidated. Additionally, many patients display the symptoms of high blood pressure in the complete absence of any other signs of disease or disorder.
- hypertension can directly lead to heart failure, renal failure and stroke (brain hemorrhaging). These conditions are capable of causing short-term death in a patient. Hypertension can also contribute to the development of atherosclerosis and coronary disease. These conditions gradually weaken a patient and can lead to long-term death.
- the exact cause of essential hypertension is unknown, though a number of factors are believed to contribute to the onset of the disease. Among such factors are stress, uncontrolled emotions, unregulated hormone release (the renin, angiotensin, aldosterone system), excessive salt and water due to kidney malfunction, wall thickening and hypertrophy of the vasculature resulting in constricted blood vessels and genetic factors.
- stress uncontrolled emotions
- unregulated hormone release the renin, angiotensin, aldosterone system
- excessive salt and water due to kidney malfunction
- wall thickening and hypertrophy of the vasculature resulting in constricted blood vessels and genetic factors.
- Hypertension has been associated with elevated blood insulin levels, a condition known as hyperinsulinemia.
- Insulin a peptide hormone whose primary actions are to promote glucose utilization, protein synthesis and the formation and storage of neutral lipids, also acts to pro- mote vascular cell growth and increase renal sodium retention among other things. These latter functions can be accomplished without affecting glucose levels and are known causes of hypertension.
- Peripheral vasculature growth for example, can cause constriction of peripheral capillaries; while sodium retention increases blood volume.
- the lowering of insulin levels in hyperinsulinemics can prevent abnormal vascular growth and renal sodium retention caused by high insulin levels and thereby alleviate hypertension.
- Cardiac hypertrophy is a significant risk factor in the development of sudden death, myocar- dial infarction, and congestive heart failure. These cardiac events are due, at least in part, to increased susceptibility to myocardial injury after ischemia and reperfusion which can occur in out-patient as well as perioperative settings. There is an unmet medical need to prevent or minimize adverse myocardial perioperative outcomes, particularly perioperative myocardial infarction. Both non-cardiac and cardiac surgery are associated with substantial risks for myocardial infarction or death. Some 7 million patients undergoing non-cardiac surgery are considered to be at risk, with incidences of perioperative death and serious cardiac compli- cations as high as 20-25% in some series.
- perioperative myocardial infarction is estimated to occur in 5% and death in 1-2%.
- drug therapy is anticipated to be life-saving and reduce hospitalizations, enhance quality of life and reduce overall health care costs of high risk patients.
- One object of the present invention is to provide compounds which can be used as medicaments for treating one or more of the above-mentioned diseases and disorders.
- a further object of this invention is to provide compounds which can effectively be used in the treatment of diabetes, preferably type II diabetes, including overnight or meal treatment, and preferably for the treatment of increased plasma glucose levels.
- a still further object of this invention is to provide compounds which can effectively be used as inhibitors of glucose production from the liver.
- a still further object of this invention is to provide further compounds which can be effectively used as phosphorylase inhibitors, preferably as glycogen phosphorylase inhibitors.
- the compounds of this invention can be used in the treatment of diabetes.
- the compounds of this invention are active as inhibitors of glucose production from the liver. Consequently, the compounds of this invention can be used for the treatment of the increased plasma glucose levels in diabetics.
- the compounds of the invention are compounds of the general formula I
- R 1 is straight or branched C 1-14 -alkyl optionally substituted with C 3-7 -cycloalkyl, C 1-6 alkoxy, phenoxy, perhalomethyl, halogen, optionally substituted phenyl;
- .2 c — R is optionally c R or c R
- R 2 is oxygen, hydroxy, halogen, amino or mercapto
- R 3 and R 4 independently are hydroxy, halogen, amino or mercapto.
- the compounds of formula I may be presented as a mixture of enantiomers which, if desired, may be resolved into the individual pure enantiomers. This resolution may conveniently be performed by fractional crystallization from various solvents, of the salts of compounds of the formula I with optical active acids or by other methods known ger se, for ex- ample, chiral column chromatography. This invention includes all isomers, whether resolved or mixtures thereof.
- Examples of pharmaceutically acceptable salts are acid addition salts with non-toxic acids, either inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulphuric acid and phosphoric acid, or organic acids such as formic acid, acetic acid, trifluoroacetic acid, trichloroacetic acid, propinoic acid, succinic acid, gluconic acid, lactic acid, citric acid, ascorbic acid, benzoic acid, embonic acid, methanesulphonic and ethanesulfonic acid, ma- Ionic acid, oxalic acid, maleic acid, pyruvic acid, tartaric acid, fumaric acid, mandelic acid, cinnamic acid, picric acid and the like acids, and include the pharmaceutically acceptable salts listed in Journal of Pharmaceutical Science, 66, 2 (1977) and incorporated herein by reference; pharmaceutically acceptable metal salts, such as lithium, sodium, potassium, or magnesium salts and the like.
- inorganic acids
- acid addition salts are the hydrates which the present compounds are able to form.
- the acid addition salts may be obtained as the direct products of compound synthesis.
- the free base may be dissolved in a suitable solvent containing the appropriate acid, and the salt isolated by evaporating the solvent or otherwise separating the salt and solvent.
- the compounds of this invention may form solvates with standard low molecular weight solvents using methods known to the skilled artisan.
- the following terms have the indicated meaning:
- C 1-6 -alkoxy as used herein, alone or in combination, is intended to include those C 1-6 alkyl groups of the designated length in either a linear or branched or cyclic configuration linked through an ether oxygen having its free valence bond from the ether oxygen.
- linear alkoxy groups are methoxy, ethoxy, propoxy, butoxy, pentoxy, and hexoxy.
- branched alkoxy groups are isopropoxy, sec-butoxy, tert-butoxy, isopentoxy, and isohexoxy.
- cyclic alkoxy groups are cyclopropyloxy, cyclobutyloxy, cyclopenty- loxy, and cyclohexyloxy.
- C 3 _ 7 -cycloalkyl refers to a radical of a saturated cyclic hydrocarbon with the indicated number of carbons such as cyclopropyl, cyclobutyl, cyclopentyl, cyclo- hexyl or cycloheptyl.
- halogen means fluorine, chlorine, bromine or iodine.
- perhalomethyl means trifluoromethyl, trichloromethyl, tribromomethyl or triio- domethyl.
- C 1-14 -alkyl refers to a straight or branched, saturated hydrocarbon chain having the indicated number of carbon atoms.
- Typical C 1-14 alkyl groups include, but are not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, 2-methylbutyl, 3-methylbutyl, 4-methylpentyl, neopentyl, n-hexyl, 1 ,2-dimethylpropyI, 2,2-dimethylpropyl, 1,2,2-trimethylpropyl, tridecyl and the like.
- C 1-14 -alkyl as used herein also includes secondary C 3-6 -alkyl and tertiary C 4-6 -alkyl.
- prodrug refers to e.g. to compounds of formula I in which an ester group has been introduced. Certain of the above defined terms may occur more than once in the above formula I, and upon such occurrence each term shall be defined independently of the other.
- the compounds of the invention may have one or more asymmetric centres and it is intended that stereoisomers (optical isomers) , as separated, pure, or partially purified stereoisomers or racemic mixtures thereof are included in the scope of the invention.
- R2 has the meaning defined above, and preferably is hydroxy.
- R3 and R4 are both hydroxy.
- Preferred compounds of the invention are:
- the present invention also relates to an optical isomer or mixture of optical isomers, including a racemic mixture of compounds of formula I selected from the group consisting of:
- the present invention also relates to the use of the novel compounds of the formula I as disclosed in the examples herein, and as defined in the compound claims herein, for the prepa- ration of a medicament, especially for the preparation of a medicament for the treatment and/or prevention of hyperglycaemia or diabetes mellitus, preferably NIDDM.
- the compounds of the present invention reduce elevated plasma glucose levels, and hence make them useful in the treatment and prevention of various diseases of the endocrinological system, especially ailments related to carbohydrate metabolism and especially the glucose me- tabolism, e.g.
- NIDDM non-insulin dependent diabetes mellitus
- the present compounds are useful in the prophylactic treatment of hyperlipidaemia, hypertension, liver and bile diseases, and atherosclerosis associated with diabetes.
- the present compounds are especially useful in the treatment of diseases associated with the activity of the liver enzyme glycogen phosphorylase, due to their capability of inhibiting said enzymatic activity.
- the invention relates to a compound of the general formula I, or a pharmaceutically acceptable acid addition salts or hydrates or prodrugs thereof for use as a therapeutically active substance, preferably for use as a therapeutically active substance in the treatment or prevention of diseases of the endocrinological system, preferably hyperglycaemia or diabetes.
- the invention also relates to the use of the inventive compounds of formula I for the preparation of medicaments useful for treating or preventing hyperglycaemia or diabetes.
- the invention relates to a method of treating or preventing diseases of the endocrinological system, preferably diabetes, in a subject in need thereof comprising administer- ing an effective amount of a compound according to the invention.
- the invention also relates to methods of preparing the above mentioned compounds. These methods comprise:
- R 5 is R 3 optionally substituted with a protection group, preferably benzyl
- R 6 is R 4 optionally substituted with a protection group, preferably benzyl
- R 3 and R 4 are as defined above with R 1 MgX wherein R 1 is as defined above and X is halogen, preferably bromine or chlorine, to form a compound of formula III
- R 2 is oxygen and R 1 , R 5 and R 6 have the meanings set forth above, followed by de- benzylation and optionally deprotection of a compound of formula (III) by catalytic reduction to form a compound of the general formula (I), or
- a reducing agent preferably LiAIH 4 in THF to form a compound of formula IV
- R 2 is hydroxy and R 1 , R 5 and R 6 have the meanings set forth above, followed by debenzylation and optionally deprotection of a compound of formula (IV) by catalytic reduction to form a compound of the general formula (I).
- the starting materials employed in the synthesis of the compounds of formula II are either known or may be prepared in conventional manner from commercially available materials, e.g according to the methods described in the examples.
- Other compounds of the general formula I can be prepared by the above strategy.
- a variety of functional groups can be introduced in the compounds prepared as outlined above by methods well known to those skilled in the art.
- compositions comprising, as an active ingredient, at least one compound of formula I or a pharmaceutically acceptable salt thereof in connection with a pharmaceutically acceptable carrier or diluent.
- Such compositions may be in the form of powders, solutions, suspensions, or aerosols, or which may or may not be divided in unit dosage form or in the form of capsules or tablets.
- Liquid compositions include sterile solutions, suspensions and emulsions suitable for parenteral injection.
- compositions of this invention may comprise carriers, diluents, absorption enhancers, tablet disintegrating agents and other ingredients which are conventionally used in the art.
- the powders and tablets preferably contain from 5 to 99%, more preferred from 10 to 90% of the active ingredient.
- solid carriers are magnesium carbonate, magnesium stearate, dextrin, lactose, sugar, talc, gelatine, pectin, tragacanth, methyl cellulose, sodium carboxymethyl cellulose, low melting waxes and cocoa butter.
- the route of administration of the compositions containing a compound of formula I may be any route which effectively transports the active compound to its site of action, such as oral, pulmonary, transdermal or parenteral e.g. rectal, depot, subcutaneous, intravenous, in- traurethral or intramuscular, the oral route being preferred.
- a solid carrier is used for oral administration the preparation may be tabletted, placed in a hard gelatin capsule in powder or pellet form, or it can be in the form of a troche or lozenge.
- a liquid carrier is used the preparation may be in the form of a syrup, emulsion, soft gelatin capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution. Tablets, dragees, or capsules having talc and/or a carbohydrate carrier or binder or the like are particularly suitable for oral application.
- Preferable carriers for tablets, dragees, and capsules include lactose, corn starch, and/or potato starch.
- injectable solutions or suspensions pref- erably aqueous solutons with the active compound dissolved in polyhydroxylated castor oil.
- a typical tablet which may be prepared by conventional tabletting techniques may contain:
- Active compound (as free compound or salt thereof) 50 mg
- the compounds of the invention may be administered to a mammal, especially a human in need of such treatment, prevention, elimination, alleviation or amelioration of the various diseases as mentioned above and especially diabetes.
- mammals include also animals, both domestic animals, e.g. household pets, and non-domestic animals such as wildlife.
- compositions according to the present invention should be determined by those skilled in the art.
- the daily dose to be administered in therapy can be determined by a physician and will depend on the particular compound em- ployed, on the route of administration and on the age and the condition of the patient.
- the compounds of the invention are effective over a wide dosage range. For example, in the treatment of adult humans, dosages from about 2 to about 500 mg per day may be used. The exact dosage will depend upon the mode of administration, on the therapy desired, form in which administered, the subject to be treated and the body weight of the subject to be treated, and the preference and experience of the physician or veterinarian in charge.
- the present invention relates to a method of treating and/or preventing diabetes.
- the present invention relates to the use of one or more compounds of the general formula I or pharmaceutically acceptable salts thereof for the preparation of a medicament for the treatment and/or prevention of diabetes.
- mice Female ob/OB mice (20 g) fasted for 3 hours were used. Test compounds or NaCI (0.9%; controls) were administered intraveneously (hereinafter designated i.v.). Glu- cagon were administered subcutaneously (herein-after designated s.c.) in order to increase hepatic glucose output derived from glycogen. Blood samples were drawn from the orbital vain and analyzed for glucose using a glucose oxidase method.
- Rat hepatocytes were isolated using a standard two step collagenase technique, and cul- tured onto collagen coated culture dishes for 72 hours in medium 199 with the addition of dexamethazone (0.1 mM); penicillin/Streptomycin ((100 u/100 mg)/ml) and insulin (1 nM). During the last 24 hours, the hepatocytes were cultured in the presence of high levels of insulin (5 nM) and glucose (15 mM), which result in the incorporation of glucose into glycogen. Therefore, at the time of the experiment, the cells mimic livers from fed animals. Experiments were initiated after 48 hours of culture by 2 times wash of cells and addition of a 20 mM HEPES experimental buffer including balanced salts, but without glucose.
- test compound was added simultaneously with the experimental buffer.
- gluca- gon 0.5 nM was added after 10 minutes in order to stimulate glucose production from liver cells.
- Phosphorylase was either purchased from Sigma or extracted from rat livers according to Stalmans et. al. (Eur.J. Biochem. 49 (1974), 415). The activity of phosphorylase was deter- mined as described by Bergmeyer (1983; in: Meth. of Enzymatic Analysis, 2, 293-295, We- inheim, (ed.) Verlag Chemie).
- Compounds of the invention shows their effect in lowering the glucagon mediated increase in plasma glucose.
- N-Chlorosuccinimide (7.05 g, 52.6 mmol) was added to a solution of (3R,4R)-3,4- dibenzyloxypyrrolidine (15 g, 52.8 mmol) in diethyl ether (300 ml). The resulting mixture was stirred at room temperature for 3 hours under a nitrogen atmosphere. Addition of toluene (250 ml) and water (200 ml), washing of the organic phase with 2 M sodium thiosufate (200 ml) and water (200 ml), drying with magnesium sulphate gave a solution of (3R,4R)-3,4- dibenzyloxy-1-chloropyrrolidine in toluene. The compound is unstable and was used without further purification.
- the toluene solution was added to a solution of 1 ,8-diazabicyclo[5.4.0]undec-7-ene (16 g, 105 mmol) in toluene (200 ml). The mixture was stirred at room temperature for 20 hours under a nitrogen atmosphere. Water (250 ml) was added, the organic phase was isolated and the water phase was extracted with toluene (100 ml). The combined organic phases were washed with water (200 ml), dried with magnesium sulphate giving a toluene solution of (3R,4R)-3,4-dibenzyloxy-1-pyrroline. The compound is unstable and was used without further purification.
- the oil of 1-benzyl-3,4-dibenzyloxy-pyrrolidine-2-carbonitrile contains a mixture of two stereoisomers. A small amount of the two isomers were isolated on a reverse phase C18 column (Eluent: Acetonitrile:water (7:1 ) + 0.1 % trifluoroacetic acid) giving 540 mg of (2R,3R,4R)-1-benzyl-3,4-dibenzyloxypyrrolidine-2-carbonitrile as an light yellow oil H-NMR (CDCI 3 ) in ppm: ⁇ 7.3 (m,15 H), 4.55 (d,2H), 4.5 (s,2H), 4.23 (t,1H), 4.1 (m,1H), 3.8 (d.d,2H), 3.5 (s,1H), 3.2-2.6 (m,2H);
- (2R,3R,4R)-1-Benzyl-3,4-dibenzyloxy-2-(1-hydroxyethyl)pyrrolidine can be separated on an optically active column into (2R,3R,4R)-1-benzyl-3,4-dibenzyloxy-2-((1R)-1- hydroxyethyl)pyrrolidine and (2R,3R,4R)-1-benzyl-3,4-dibenzyloxy-2-((1S)-1- hydroxyethyl)pyrrolidine;
- (2S,3R,4R)-1-Benzyl-3,4-dibenzyloxy-2-(1-hydroxyethyl)pyrrolidine can be separated on an optically active column into (2S,3R,4R)-1-benzyl-3,4-dibenzyloxy-2-((1R)-1- hydroxyethyl)pyrrolidine and (2S,3R,4R)-1-benzyl-3,4-dibenzyloxy-2-((1S)-1- hydroxyethyl)pyrrolidine.
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Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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AU62910/98A AU6291098A (en) | 1997-03-07 | 1998-03-06 | Novel heterocyclic compounds |
JP53910098A JP2001514632A (en) | 1997-03-07 | 1998-03-06 | New heterocyclic compounds |
EP98906859A EP0973738A1 (en) | 1997-03-07 | 1998-03-06 | Novel heterocyclic compounds |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DK0248/97 | 1997-03-04 | ||
DK24897 | 1997-03-07 |
Publications (1)
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WO1998040353A1 true WO1998040353A1 (en) | 1998-09-17 |
Family
ID=8091404
Family Applications (1)
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PCT/DK1998/000084 WO1998040353A1 (en) | 1997-03-07 | 1998-03-06 | Novel heterocyclic compounds |
Country Status (5)
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EP (1) | EP0973738A1 (en) |
JP (1) | JP2001514632A (en) |
AU (1) | AU6291098A (en) |
WO (1) | WO1998040353A1 (en) |
ZA (1) | ZA981920B (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6239163B1 (en) | 1999-03-15 | 2001-05-29 | Novo Nordisk A/S | Salt of (2R,3R,4R)-3,4-dihydroxy-2-hydroxymethylpyrrolidine |
US6316489B1 (en) * | 1999-03-15 | 2001-11-13 | Novo Nordisk A/S | Salt of (2R,3R,4R)-3,4-dihydroxy-2-hydroxymethylpyrrolidine |
US6867184B2 (en) | 2000-01-24 | 2005-03-15 | Pfizer, Inc. | Methods of treating diabetic cardiomyopathy using glycogen phosphorylase inhibitors |
US7115648B2 (en) | 2002-03-06 | 2006-10-03 | Astrazeneca Ab | Indole-amide derivatives and their use as glycogen phosphorylase inhibitors |
US7122567B2 (en) | 2002-03-06 | 2006-10-17 | Astrazeneca Ab | Heterocyclic amide derivatives having glycogen phosphorylase inhibitory activity |
US7129249B2 (en) | 2002-03-06 | 2006-10-31 | Astrazeneca Ab | Heterocyclic amide derivatives as inhibitors of glycogen phoshorylase |
US7138415B2 (en) | 2002-03-06 | 2006-11-21 | Astrazeneca Ab | Indolamid derivatives which possess glycogenphosphorylase inhibitory activity |
US7166636B2 (en) | 2002-03-06 | 2007-01-23 | Astrazeneca Ab | Indole-amid derivatives which possess glycogen phosphorylase inhibitory activity |
US7169927B2 (en) | 2002-03-06 | 2007-01-30 | Astrazeneca Ab | Indole-amide derivatives and their use as glycogen phosphorylase inhibitors |
WO2008012555A3 (en) * | 2006-07-27 | 2008-09-25 | Isis Innovation | Epitope reduction therapy |
WO2013133685A1 (en) | 2012-03-09 | 2013-09-12 | Biotropics Malaysia Berhad | Extract formulations of rhodamnia cinerea and uses thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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JP2005239647A (en) * | 2004-02-27 | 2005-09-08 | Ukima Kagaku Kenkyusho:Kk | 2-substituted-3,4-dihydroxypyrrolidine enzyme inhibitor |
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US4996329A (en) * | 1989-10-20 | 1991-02-26 | Monsanto Company | Derivatives of 1,4-dideoxy-1,4-imino-D-mannitol and a process for their preparation |
WO1997009040A1 (en) * | 1995-09-08 | 1997-03-13 | Novo Nordisk A/S | 2-alkylpyrrolidines |
-
1998
- 1998-03-06 JP JP53910098A patent/JP2001514632A/en active Pending
- 1998-03-06 EP EP98906859A patent/EP0973738A1/en not_active Withdrawn
- 1998-03-06 WO PCT/DK1998/000084 patent/WO1998040353A1/en not_active Application Discontinuation
- 1998-03-06 AU AU62910/98A patent/AU6291098A/en not_active Abandoned
- 1998-03-06 ZA ZA981920A patent/ZA981920B/en unknown
Patent Citations (2)
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US4996329A (en) * | 1989-10-20 | 1991-02-26 | Monsanto Company | Derivatives of 1,4-dideoxy-1,4-imino-D-mannitol and a process for their preparation |
WO1997009040A1 (en) * | 1995-09-08 | 1997-03-13 | Novo Nordisk A/S | 2-alkylpyrrolidines |
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Also Published As
Publication number | Publication date |
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ZA981920B (en) | 1998-09-07 |
EP0973738A1 (en) | 2000-01-26 |
JP2001514632A (en) | 2001-09-11 |
AU6291098A (en) | 1998-09-29 |
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