WO2003097601A1 - Cyanoguanidine prodrugs - Google Patents
Cyanoguanidine prodrugs Download PDFInfo
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- WO2003097601A1 WO2003097601A1 PCT/DK2003/000318 DK0300318W WO03097601A1 WO 2003097601 A1 WO2003097601 A1 WO 2003097601A1 DK 0300318 W DK0300318 W DK 0300318W WO 03097601 A1 WO03097601 A1 WO 03097601A1
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- cyano
- compound
- piperidyl
- tert
- butoxycarbonyl
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- 0 CN(*)C(N(C)c1ccncc1)=NC=NC Chemical compound CN(*)C(N(C)c1ccncc1)=NC=NC 0.000 description 1
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4425—Pyridinium derivatives, e.g. pralidoxime, pyridostigmine
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
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- A—HUMAN NECESSITIES
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
Definitions
- the present invention relates to novel pyridyl cyanoguanidine prodrugs and their inclusion in pharmaceutical compositions, as well as their use in the manufacture of medicaments.
- Pyridyl cyanoguanidines such as pinacidil (N-l,2,2-trimethylpropyl-N'- cyano-N"-(4-pyridyl)guanidine) were originally discovered to be potassium channel openers and were consequently developed as antihypertensive agents. Replacement of the side chain of pinacidil by longer aryl-containing side chains caused a loss of the antihypertensive activity, but such compounds were, on the other hand, found to show antitumour activity on oral administration in a rat model carrying Yoshida ascites tumours.
- pyridyl cyanoguanidines with antiproliferative activity are disclosed in, for instance, EP 660 823, WO 98/54141, WO 98/54143, WO 98/54144, WO 98/54145, WO 00/61559 and WO 00/61561.
- SAR structure- activity relationships
- the compounds were also tested in vivo in nude mice carrying a human lung cancer tumour xenograft. Based on the SAR analysis, a specific compound (N-(6-(4-chlorophenoxy)hexy!)-N'- cyano-N"-(4-pyridyl)guanidine) was selected for its high antiproliferative activity in vitro and potent antitumour activity in the nude mouse model.
- pyridyl cyanoguanidines are promising antitumour agents with an extremely interesting activity profile, they are highly lipophilic and consequently sparingly soluble compounds and are, as such, generally available for oral administration only.
- many cancer patients are in a severely debilitated condition as a result of their illness giving rise to problems with patient compliance with respect to oral administration of drugs.
- the compounds of the present invention exhibit good solubility in water, even at pH values around physiological pH making them ideal candidates for parenteral administration.
- pyridyl cyanoguanidine prodrugs of the invention exhibit an improved gastrointestinal absorption on oral administration. Consequently, it is another object of the invention to provide oral formulations of pyridyl cyanoguanidines as prodrugs with improved bioavailability.
- the present invention relates to a compound of the general formula I
- R 4 R 5 wherein X_ is a straight, branched and/or cyclic hydrocarbon diradical, optionally substituted with one or more hydroxy, halogen, nitro, amino or cyano;
- X 2 is a bond; a straight, branched and/or cyclic hydrocarbon diradical, optionally substituted with one or more hydroxy, halogen, nitro, amino, cyano, aminosulfonyl, alkylsulfonylamino, alkylcarbonyl, formyl, aminocarbonyl or alkylcarbonylamino; a heteroarylene or non-aromatic heterocyclic hydrocarbon diradical, all of which are optionally substituted with one or more straight, branched and/or cyclic non-aromatic hydrocarbon radical, hydroxyl, halogen, amino, nitro, cyano, aminosulfonyl, alkylsulfonylamino, alkylcarbonyl, formyl, aminocarbonyl or alkylcarbonylamino;
- X 3 is a straight, branched and/or cyclic hydrocarbon diradical, optionally substituted with one or more substituents selected from the group consisting of hydroxy, halogen, nitro, amino, cyano, aminosulfonyl, alkylsulfonylamino, alkylcarbonyl, formyl, aminocarbonyl or alkylcarbonylamino; with the proviso that when R 6 is -NH 2 , X 3 comprises five carbon atoms or more; and with the further proviso that when n is 0 and R 6 is a heterocyclic ring or ring system with 3-10 ring atoms, wherein at least 1 ring atom constitutes an aliphatic amine, X 3 may also be a bond;
- Yi is a bond, O, S, S(O), S(0) 2 , C(O), NH-C(O) or C(0)-NH;
- Y 2 is a bond, an ether diradical (R'-O-R"), an amine diradical (R'-N-R"), O, S, S(O), S(0) 2 , C(O), NH-C(O), C(0)-NH, S0 2 -N(R') or N(R')-S0 2 wherein R' and R" are independently straight or branched hydrocarbon diradicals containing up to 4 carbon atoms;
- Y 3 is O
- Ri is hydrogen or straight, branched and/or cyclic alkyl, optionally substituted with phenyl; or an aromatic hydrocarbon radical;
- R 2 is hydrogen, or aryl or heteroaryl, both of which are optionally substituted with one or more substituent selected from the group consisting of halogen, trifluoromethyl, hydroxy, C ⁇ - 4 alkoxy, nitro, cyano, C ⁇ - 4 hydroxyalkyl or C ⁇ - 4 alkyl, optionally substituted with halogen, hydroxy, cyano or nitro; tetrahydropyranyloxy, di-(C 1 . 4 alkoxy)phosphinoyloxy or C ⁇ - alkoxycarbonylamino;
- R 4 and R 5 are independently hydrogen; a straight, branched and/or cyclic hydrocarbon radical, optionally substituted with halogen, hydroxyl, halogen, amino, nitro or cyano;
- R 6 is an amino group or a heterocyclic ring or condensed ring system with 3- 10 ring atoms, wherein at least 1 ring atom constitutes an aliphatic amine;
- A is hydrogen, an optionally substituted, straight, branched and/or cyclic hydrocarbon radical, hydroxy, halogen, nitro, cyano, heteroaryl, heteroaralkyl or thiol;
- n 0 or 1
- Z " is a pharmaceutically acceptable anion, such as chloride, bromide, iodide, sulfate, methanesulfonate, p-toluenesulfonate, nitrate or phosphate.
- the invention relates to a compound of formula II, which is the free base form of the compounds of formula I, provided R 4 is hydrogen
- the compounds of the present invention include any tautomeric forms, optical isomers or diastereoisomers thereof, either in pure form or as mixtures thereof. It is further understood that the invention includes pharmaceutically acceptable salts of compounds of formula I or II.
- ester or carbonate group R 6 -X 3 -(Y 3 ) n -C(0)0-CHR 1 - is hydrolysed enzymatically to liberate the active compound of formula III
- the term "prodrug” is intended to indicate a derivative of an active compound which does not, or does not necessarily, exhibit the physiological activity of the active compound, but which may be subjected to enzymatic cleavage such as hydrolysis in vivo so as to release the active compound on administration of the prodrug.
- the prodrug comprises the active compound which in itself is highly lipophilic provided with a side chain with predominantly hydrophilic properties imparting improved solubility characteristics to the prodrug, thereby making it more suitable for parenteral administration in the form of a solution or for oral administration to obtain an improved bioavailability.
- the hydrophilic side chain selected for the compounds of the present invention comprises an ester or carbonate group of formula R 6 -X 3 -(Y 3 ) n -C(0)0-CHRi- (wherein R 6 , Ri, X 3 , Y and n are as indicated above).
- alkyl is intended to indicate a univalent radical derived from straight, branched or cyclic alkane by removing a hydrogen atom from any carbon atom, preferably comprising from 1-8 carbon atoms.
- the term includes the subclasses primary, secondary and tertiary alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, sec. -butyl, isobutyl, tert. -butyl, isopentyl, isohexyl, cyclohexyl, cyclopentyl and cyclopropyl.
- aryl is intended to indicate radicals of carbocyclic aromatic rings, optionally fused bi-, tri- or tetra-cyclic rings wherein at least one ring is aromatic, e.g. phenyl, naphthyl, indanyl, indenyl, 1,4-dihydronaphtyl, flourenyl or tetralinyl.
- heteroaryl is intended to indicate radicals of heterocyclic aromatic rings, in particular 5- or 6-membered rings with 1-3 heteroatoms selected from O, S and N, or optionally fused bicyclic rings, of which at least one is aromatic, with 1-4 heteroatoms, e.g. pyrrolyl, furanyl, thiophenyl, imidazolyl, oxazolyl, thiazolyl, pyrazolyl, pyridyl, pyrimidyl, purinyl, quinolinyl, chromenyl or carbazolyl.
- aralkyl is intended to indicate an aromatic ring with an alkyl side chain as defined above, e.g. benzyl.
- halogen is intended to indicate fluoro, chloro, bromo or iodo.
- aminosulfonyl indicates a radical of the formula -S(0) 2 NR a 2 , wherein each R a independently represents either hydrogen or alkyl as defined above.
- alkylsulfonylamino indicates a radical of the formula -NR a 2 -S(0) 2 -R b , wherein each R a independently represents hydrogen or alkyl as defined above, and R b represents alkyl as defined above.
- alkylcarbonyl indicates a radical of the formula -C(0)R b , wherein R b is as just described.
- amino indicates a radical of the formula -N(R a ) 2 , wherein each R a independently represents hydrogen or alkyl as defined above.
- alkylcarbonylamino indicates a radical of the formula -NR a C(0)R b , wherein R and R b are as just described.
- alkoxy indicates a radical of the formula OR b , wherein R b is as just described.
- alkoxycarbonyl is intended to indicate a radical of the formula -C(0)-OR b , wherein R is as indicated above.
- aminoacylamino is intended to indicate a radical of the formula -NH-C(0)-R c -NH 2 , wherein R c is a diradical known from any natural amino acid, H 2 N-R c -COOH, or its enantiomer.
- aminocarbonyl is intended to indicate a radical of the formula -C(0)-NR a 2 , wherein each R a independently represent hydrogen or alkyl as defined above.
- alkoxycarbonylamino is intended to indicate a radical of the formula -NR a -C(0)-OR b , wherein R a and R b are as indicated above.
- hydrocarbon is intended to indicate a compound comprising only hydrogen and carbon atoms, it may contain one or more double or triple carbon-carbon bonds, and it may comprise cyclic moieties in combination with branched or linear moieties.
- Said hydrocarbon preferably comprises 1- 18, e.g. 1-12 carbon atoms.
- non-aromatic heterocyclic which is intended to indicate saturated or partly saturated cyclic compounds with 1-3 heteroatoms selected from O, S or N or optionally fused bicyclic rings with 1-4 heteroatoms, such as pyrrolidinyl, 3-pyrrolinyl, tetrahydrofuranyl, tetrahydrothiophenyl, piperidinyl, piperazinyl.
- a heterocyclic ring or condensed ring system with 3-10 ring atoms, wherein at least 1 ring atom constitutes an aliphatic amine is intended to include radicals, such as pyrrolidinyl, piperidyl, hexahydro-lH- azapinyl, imidazolidinyl, piperazinyl, decahydro-isoquinolinyl, octahydro- isoindolyl, 1,2,3,4-tetrahydro-isoquinolinyl, 2,3-dihydro-lH-isoindolyl and morpholinyl
- pharmaceutically acceptable salt is intended to indicate salts prepared by reacting a compound of formula I or II comprising a basic group with a suitable inorganic or organic acid, e.g. hydrochloric, hydrobromic, hydroiodic, sulfuric, nitric, acetic, phosphoric, lactic, maleic, phthalic, citric, propionic, benzoic, glutaric, gluconic , methanesulfonic, salicylic, succinic, tartaric, toluenesulfonic, sulfamic or fumaric acid.
- a suitable inorganic or organic acid e.g. hydrochloric, hydrobromic, hydroiodic, sulfuric, nitric, acetic, phosphoric, lactic, maleic, phthalic, citric, propionic, benzoic, glutaric, gluconic , methanesulfonic, salicylic, succinic, tartaric, toluenesulfonic,
- X 2 and Yi are both bonds, while Xi is a straight, branched or cyclic, saturated or unsaturated hydrocarbon diradical with 4 to 20 carbon atoms; Y 2 is 0, S, C(O) or a bond;
- R 2 is aryl or heteroaryl, both of which are optionally substituted by one or more substituent selected from the group consisting of halogen, trifluoromethyl, hydroxy, C ⁇ - 4 alkoxy, nitro, cyano, C ⁇ - 4 hydroxyalkyl or C ⁇ - 4 alkyl, optionally substituted with halogen, hydroxy, cyano or nitro; tetrahydropyranyloxy, di-(C ⁇ - alkoxy)phosphinoyloxy or C ⁇ - 4 alkoxycarbonylamino;
- X 3 is a straight hydrocarbon diradical comprising from 1 to 10 carbon atoms.
- R 6 is -NH 2 or piperidyl, attached at the 2, 3 or 4 position to X 3 , and in particular at the 3 or 4 position;
- Ri is hydrogen, straight or branched C ⁇ - 4 alkyl, aralkyl or aryl;
- A, R 4 and R 5 are all hydrogen;
- n is 0 or 1; and
- Z " is a pharmaceutically acceptable anion, such as chloride, bromide, iodide, sulfate, methanesulfonate, p-toluenesulfonate or nitrate.
- R 2 is aryl and in particular phenyl, optionally substituted by one or more substituent selected from the group consisting of halogen, trifluoromethyl, hydroxy, C ⁇ - 4 alkoxy, nitro, cyano, C ⁇ - 4 hydroxyalkyl or C h alky!, optionally substituted with halogen, hydroxy, cyano or nitro.
- a particular preferred substituent is halogen, such as chloro.
- Yi is a bond and Y 2 is O.
- Xi is a C 4 . i2 hydrocarbon diradical and X 2 is a bond.
- an advantage of the prodrug forms of cyanoguanidines of the present invention is an increased solubility compared to the solubility of the cyanoguanidines themselves.
- the cause for said increase lies with at least two factors, i.e. the positive charge at the pyridine nitrogen, and the hydrophilic character of the prodrog moiety, i.e.
- R 5 comprises an aliphatic amine moiety
- aliphatic amines have pK B values in the 3-5 range [Frenna, J. Chem.Soc. Perkin Trans. II, 1865, 1985], which implies that the amine moiety is mainly protonated at physiological pH. The protonation gives rise to a charge which increases solubility.
- R_, R 6 , X 3 , Y 3 , and n are as indicated above, and B is a leaving group, such as CI, Br or I.
- R 6 and X 3 may optionally contain protecting groups.
- reaction of a compound of formula III with a compound of formula IV may be performed in a solvent-free environment or in an inert solvent such as acetonitrile at a temperature between room temperature and 150°C to afford a compound of formula I optionally after removal of protecting groups.
- compounds of formula IV may be prepared by reacting a compound of formula V
- reaction between a compound of formula V and a compound of formula VI may be performed at a temperature between room temperature and - 70°C in an inert organic solvent, such as dichloromethane, in the presence of a suitable base such as pyridine.
- an inert organic solvent such as dichloromethane
- R 6 and X 3 are as indicated in formula IV and M + is a suitable metal kation, e. g. an alkalimetal kation, or a tertiary ammonium ion, with a compound of formula VIII X-CH(R ⁇ )-CI VIII
- Ri is as indicated above and X is iodo, bromo or chlorosulfonyloxy.
- the reaction between VII and VIII may be performed in a suitable solvent such as dimethylformamide at a suitable temperature, e.g. at room temperature, when X is iodo or bromo.
- a suitable solvent such as dimethylformamide
- X iodo or bromo.
- X chlorosulfonyloxy
- the reaction may be performed under phase transfer conditions as described in Synthetic Communications 14, 857-864 (1984).
- a compound of formula I provided that R 4 is hydrogen may be converted into the corresponding free base of formula II by treating a solution of a compound of formula I in an appropriate inert solvent, e.g. dichloromethane, with a suitable base, e.g. aqueous sodium bicarbonate.
- the free base of formula II may be reconverted into a salt of formula I by treating a solution of a compound of formula II in an appropriate inert solvent, e.g. dichloromethane, with a suitable acid of formula ZH, wherein Z is as indicated above.
- the invention in another aspect, relates to pharmaceutical formulations of a compound of formula I or II intended for the treatment of proliferative diseases.
- the formulations of the present invention both for veterinary and for human medical use, comprise active ingredients in association with a pharmaceutically acceptable carrier(s) and optionally other therapeutic ingredient(s).
- the carrier(s) must be "acceptable” in the sense of being compatible with the other ingredients of the formulations and not deleterious to the recipient thereof.
- the active ingredient comprises from 0.1-100% by weight of the formulation.
- a dosage unit of a formulation contain between 0.07 mg and 1 g of a compound of formula I or II.
- dosage unit a unitary, i.e. a single dose which is capable of being administered to a patient, and which may be readily handled and packed, remaining as a physically and chemically stable unit dose comprising either the active material as such or a mixture of it with solid or liquid pharmaceutical diluents or carriers.
- the formulations include e.g. those in a form suitable for oral (including sustained or timed release), rectal, parenteral (including subcutaneous, intraperitoneal, intramuscular, intraarticular and intravenous), transdermal, ophthalmic, topical, nasal or buccal administration.
- the formulations may conveniently be presented in dosage unit form and may be prepared by any of the methods well known in the art of pharmacy, e.g as disclosed in Remington, The Science and Practice of Pharmacy, 20 th ed., 2000. All methods include the step of bringing the active ingredient into association with the carrier, which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing the active ingredient into association with a liquid carrier or a finely divided solid carrier or both, and then, if necessary, shaping the product into the desired formulation.
- Formulations of the present invention suitable for oral administration may be in the form of discrete units, such as capsules, sachets, tablets or lozenges, each containing a predetermined amount of the active ingredient; in the form of a powder or granules; in the form of a solution or a suspension in an aqueous liquid or non-aqueous liquid, such as ethanol or glycerol; or in the form of an oil-in-water emulsion or a water-in-oil emulsion.
- oils may be edible oils, such as e.g. cottonseed oil, sesame oil, coconut oil or peanut oil.
- Suitable dispersing or suspending agents for aqueous suspensions include synthetic or natural gums such as tragacanth, alginate, acacia, dextran, sodium carboxymethylcellulose, gelatin, methylcellulose, hydroxypropylmethylcellulose, hydroxypropylcellulose, carbomers and polyvinylpyrrolidone.
- the active ingredients may also be administered in the form of a bolus, electuary or paste.
- a tablet may be made by compressing or moulding the active ingredient optionally with one or more accessory ingredients.
- Compressed tablets may be prepared by compressing, in a suitable machine, the active ingredient(s) in a free-flowing form such as a powder or granules, optionally mixed by a binder, such as e.g. lactose, glucose, starch, gelatine, acacia gum, tragacanth gum, sodium alginate, carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, polyethylene glycol, waxes or the like; a lubricant such as e.g.
- Moulded tablets may be made by moulding, in a suitable machine, a mixture of the powdered active ingredient and suitable carrier moistened with an inert liquid diluent.
- Formulations for rectal administration may be may in the form of suppositories in which the compound of the present invention is admixed with low melting water soluble or insoluble solids such as cocoa butter, hydrogenated vegetable oils, polyethylene glycol or fatty acids esters of polyethylene glycols, while elixirs may be prepared using myristyl palmitate.
- low melting water soluble or insoluble solids such as cocoa butter, hydrogenated vegetable oils, polyethylene glycol or fatty acids esters of polyethylene glycols, while elixirs may be prepared using myristyl palmitate.
- Formulations suitable for parenteral administration conveniently comprise a sterile oily or aqueous preparation of the active ingredients, which is preferably isotonic with the blood of the recipient, e.g. isotonic saline, isotonic glucose solution or buffer solution.
- the formulation may be conveniently sterilised by for instance filtration through a bacteria retaining filter, addition of sterilising agent to the formulation, irradiation of the formulation or heating of the formulation.
- Liposomal formulations as disclosed in e.g. Encvclopedia of Pharmaceutical Technology, vol.9, 1994, are also suitable for parenteral administration.
- the compound of formula I may be presented as a sterile, solid preparation, e.g. a freeze-dried powder, which is readily dissolved in a sterile solvent immediately prior to use.
- Transdermal formulations may be in the form of a plaster or a patch.
- Formulations suitable ophthalmic administration may be in the form of a sterile aqueous preparation of the active ingredients, which may be in microcrystalline form, for example, in the form of an aqueous microcrystalline suspension.
- Liposomal formulations or biodegradable polymer systems e.g. as disclosed in Encyclopedia of Pharmaceutical Technology, vol.2, 1989, may also be used to present the active ingredient for ophthalmic administration.
- Formulations suitable for topical or ophthalmic administration include liquid or semi-liquid preparations such as liniments, lotions, gels, applicants, oil-in-water or water-in-oil emulsions such as creams, ointments or pastes; or solutions or suspensions such as drops.
- Formulations suitable for nasal or buccal administration include powder, self-propelling and spray formulations, such as aerosols and atomisers.
- the formulations of a compound of formula I or II may include one or more additional ingredients such as diluents, buffers, flavouring agents, colourant, surface active agents, thickeners, preservatives, e.g. methyl hydroxybenzoate (including anti-oxidants), emulsifying agents and the like.
- daily doses of from 0.001-500 mg per kilogram body weight, preferably from 0.002-100 mg/kg of mammal body weight, for example 0.003-20 mg/kg or 0.003 to 5 mg/kg of a compound of formula I or II is administered, typically corresponding to a daily dose for an adult human of from 0.01 to 37000 mg.
- the present invention also provides compounds and compositions intended for administration with longer intervals, e.g. every week, every three weeks or every month.
- ointments, creams or lotions containing from 0.1-750 mg/g, and preferably from 0.1-500 mg/g, for example 0.1-200 mg/g of a compound of formula I or II is administered.
- drops or gels containing from 0.1-750 mg/g, and preferably from 0.1-500 mg/g, for example 0.1-200 mg/g of a compound of formula I or II is administered.
- the oral compositions are formulated, preferably as tablets, capsules, or drops, containing from 0.07-1000 mg, preferably from 0.1-500 mg, of a compound of formula I or II per dosage unit.
- the invention provides pharmaceutical compositions comprising a compound of formula I or II in combination with one or more other pharmacologically active compounds used in the treatment of proliferative diseases.
- compounds used in the treatment of proliferative diseases which may be used together with compounds of the present invention include S-triazine derivatives such as altretamine; enzymes such as asparaginase; antibiotic agents such as bleomycin, dactinomycin, daunorubicin, doxorubicin, idarubicin, mitomycin, epirubicin and plicamycin; alkylating agents such as busulfan, carboplatin, carmustine, chlorambucil, cisplatin, cyclophosphamide, dacarbazine, ifosfamide, lomustine, mechlorethamine, melphalan, procarbazine and thiotepa; antimetabolites such as cladribine, cytarabine, floxuridine
- aromatase inhibitors such as aminoglutethimide, corticosteroids, such as dexamethasone and prednisone, and luteinizing hormone releasing hormone (LH-RH); antiestrogens such as tamoxifen, formestan and letrozol; antiandrogens such as flutamide; biological response modifiers, e.g. lymphokines such as aldesleukin and other interleukines; interferon such as interferon- ⁇ ; growth factors such as erythropoietin, filgrastim and sagramostim; differentiating agents such as vitamin D derivatives, e.g.
- ionising radiation although not readily defined as a compound, is heavily depended on in the treatment of neoplastic diseases, and may be combined with the compounds of the present invention. Due to the severe side effects often experienced by patients receiving anti-neoplastic treatment it is often desirable also to administer therapeutics which are not in themselves anti-neoplastic, but rather help relieving the side effects of anti-neoplastic therapy. Such compounds include amifostin, leucovorin and mesna.
- anti-neoplastic compounds such as paclitaxel, fluorouracil, etoposide, cyclophospamide, cisplatin, carboplatin, vincristine, gemcitabine, vinorelbine, chlorambucil, doxorubicin and melphalan appear beneficial in the combination compositions of the present invention.
- combination composition of the present invention may be provided as mixtures of the compounds or as individual compounds intended for simultaneous or sequential administration. It lies within the capabilities of a skilled physician or veterinarian to decide time intervals in a sequential administration regime.
- the invention relates to a method of treating or ameliorating proliferative diseases or conditions, the method comprising administering, to a patient in need thereof, a pharmaceutical composition comprising a compound of formula I or II, which compound is hydrolysed enzymatically upon administration to provide a compound of formula III, in an amount sufficient to effect treatment or amelioration of said proliferative disease or condition, optionally together with another anti-neoplastic compound and/or ionising radiation.
- proliferative diseases or conditions to be treated by the present method include a variety of cancers and neoplastic diseases or conditions including leukaemia, acute myeloid leukaemia, chronic myeloid leukaemia, chronic lymphatic leukaemia, myelodysplasia, multiple myeloma, Hodgkin's disease or non-Hodgkin's lymphoma, small or non-small cell lung carcinoma, gastric, intestinal or colorectal cancer, prostate, ovarian or breast cancer, brain, head or neck cancer, cancer in the urinary tract, kidney or bladder cancer, malignant melanoma, liver cancer, uterine or pancreatic cancer.
- leukaemia acute myeloid leukaemia, chronic myeloid leukaemia, chronic lymphatic leukaemia, myelodysplasia, multiple myeloma
- Hodgkin's disease or non-Hodgkin's lymphoma small or non-small cell lung carcinoma
- Cyanoguanidines are also believed to be useful in the treatment of inflammatory diseases.
- the invention thus provides a method of treating inflammatory diseases, the method comprising administering to a patient an effective amount of a compound of the present invention, either alone or in combination with other therapeutically active compounds.
- the invention also relates to the use of compounds of formula I or II, optionally together with other anti-neoplastic compounds, as indicated above, in the manufacture of medicaments.
- said medicament is intended to be used for the treatment of proliferative diseases, e.g. cancers as mentioned above.
- the compounds of the invention parenterally, such as in a liquid, preferably aqueous, solution intended for intravenous injection or infusion.
- a suitable dosage of the compound of the invention will depend, inter alia, on the age and condition of the patient, the severity of the disease to be treated and other factors well known to the practising physician.
- the compound may be administered either orally or parenterally according to different dosing schedules, e.g. daily or with weekly intervals. In general a single dose will be in the range from 0.1 to 400 mg/kg bodyweight.
- the compound may be administered as a bolus (i.e. the entire dose is administered at once) or in divided doses two or more times a day or preferably as an intravenous infusion.
- Example 1 l-[2-(4-Piperidyl)-ethoxy-carbonyloxymethyl " l-4-rN " -cvano-N " " -C6-(4- chloro-phenoxy)-l-hexy ⁇ -N- ⁇ uanidinol-pyridinium chloride, hydrochloride.
- Example 4 l-[ " 8-Amino-l-octyloxy-carbonyloxymethyl "
- Example 5 l-[4-Piperidyl-carbonyloxymethvn-4-rN " -cvano-N " " -f6-f4-chloro-phenoxy)- 1-hexy ⁇ -N-quanidinol-pyridinium chloride, hydrochloride.
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- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- Urology & Nephrology (AREA)
- Epidemiology (AREA)
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- Diabetes (AREA)
- Neurosurgery (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Abstract
Description
Claims
Priority Applications (15)
Application Number | Priority Date | Filing Date | Title |
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KR1020047018603A KR101010871B1 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
EP03722311A EP1507760B1 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
JP2004505334A JP4625694B2 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrug |
US10/514,500 US7253193B2 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
PL372769A PL228742B1 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
MXPA04011322A MXPA04011322A (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs. |
BR0309996-2A BR0309996A (en) | 2002-05-17 | 2003-05-15 | Compound, pharmaceutical composition, method of treating or ameliorating proliferative diseases or conditions, use of a compound, and method of treating or ameliorating inflammatory diseases |
CA2485351A CA2485351C (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
DE60315288T DE60315288T2 (en) | 2002-05-17 | 2003-05-15 | CYANOGUANIDINE PRODRUGS |
AU2003229534A AU2003229534B2 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
IL165086A IL165086A (en) | 2002-05-17 | 2004-11-08 | Pyridyl cyanoguanidines, pharmaceutical compositions comprising them and uses thereof for the preparation of medicaments |
IS7562A IS7562A (en) | 2002-05-17 | 2004-11-29 | Sýanógúanidínforlyf |
NO20045374A NO330183B1 (en) | 2002-05-17 | 2004-12-08 | Cyanoguanidinprodroger |
HK05108938.3A HK1076812A1 (en) | 2002-05-17 | 2005-10-10 | Cyanoguanidine prodrugs |
US11/823,571 US20070249676A1 (en) | 2002-05-17 | 2007-06-28 | Cyanoguanidine prodrugs |
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US38083602P | 2002-05-17 | 2002-05-17 | |
US60/380,836 | 2002-05-17 |
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US11/823,571 Continuation US20070249676A1 (en) | 2002-05-17 | 2007-06-28 | Cyanoguanidine prodrugs |
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WO2003097601A1 true WO2003097601A1 (en) | 2003-11-27 |
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PCT/DK2003/000318 WO2003097601A1 (en) | 2002-05-17 | 2003-05-15 | Cyanoguanidine prodrugs |
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US (1) | US20070249676A1 (en) |
EP (1) | EP1507760B1 (en) |
JP (1) | JP4625694B2 (en) |
KR (1) | KR101010871B1 (en) |
CN (1) | CN100503570C (en) |
AT (1) | ATE368649T1 (en) |
AU (1) | AU2003229534B2 (en) |
BR (1) | BR0309996A (en) |
CA (1) | CA2485351C (en) |
DE (1) | DE60315288T2 (en) |
ES (1) | ES2290454T3 (en) |
HK (1) | HK1076812A1 (en) |
IL (1) | IL165086A (en) |
IS (1) | IS7562A (en) |
MX (1) | MXPA04011322A (en) |
NO (1) | NO330183B1 (en) |
PL (1) | PL228742B1 (en) |
RU (1) | RU2326867C2 (en) |
WO (1) | WO2003097601A1 (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7253193B2 (en) | 2002-05-17 | 2007-08-07 | Leo Pharma A/S | Cyanoguanidine prodrugs |
EP2197443A2 (en) * | 2007-09-26 | 2010-06-23 | Gemin X Pharmaceuticals Canada Inc. | Compositions and methods for effecting nad+ levels using a nicotinamide phosphoribosyl transferase inhibitor |
WO2010088842A1 (en) | 2009-02-06 | 2010-08-12 | 天津和美生物技术有限公司 | Pharmaceutical compositions containing pyridyl cyanoguanidines, preparation methods and uses thereof |
WO2011006988A1 (en) | 2009-07-17 | 2011-01-20 | Topotarget A/S | Method for predicting the utility of administering nicotinic acid or a precursor or prodrug thereof to reduce the severity of side-effects of cancer treatment with nicotinamide phosphoribosyltransferase inhibitors |
WO2011121055A1 (en) | 2010-03-31 | 2011-10-06 | Topotarget A/S | Pyridinyl derivatives comprising a cyanoguanidine or squaric acid moiety |
US8053446B2 (en) | 2004-12-22 | 2011-11-08 | Leo Pharma A/S | Cyanoguanidine compounds |
EP2693876A1 (en) * | 2011-04-08 | 2014-02-12 | Sphaera Pharma Pte. Ltd | Substituted methylformyl reagents and method of using same to modify physicochemical and/or pharmacokinetic properties of compounds |
US8871747B2 (en) | 2008-08-29 | 2014-10-28 | Topotarget A/S | Urea and thiourea derivatives |
EP2867209A4 (en) * | 2012-06-27 | 2015-11-25 | Sunflower Res Llc | Compounds and therapeutic uses thereof |
US9296697B2 (en) | 2005-08-24 | 2016-03-29 | Abbott Laboratories | Hetaryl-substituted guanidine compounds and use thereof as binding partners for 5-HT5-receptors |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US8912184B1 (en) | 2010-03-01 | 2014-12-16 | Alzheimer's Institute Of America, Inc. | Therapeutic and diagnostic methods |
CN116640238B (en) * | 2023-05-30 | 2024-05-03 | 华侨大学 | Guanidyl pyridine chitosan onium salt and preparation method and application thereof |
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WO1998054144A1 (en) * | 1997-05-29 | 1998-12-03 | Leo Pharmaceutical Products Ltd. A/S (Løvens Kemiske Fabrik Produktionsaktieselskab) | Cyanoguanidines as cell proliferation inhibitors |
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WO2002042265A2 (en) * | 2000-11-21 | 2002-05-30 | Leo Pharma A/S | Cyanoguanidine prodrugs |
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US5919816A (en) * | 1994-11-14 | 1999-07-06 | Bionumerik Pharmaceuticals, Inc. | Formulations and methods of reducing toxicity of antineoplastic agents |
US20030045515A1 (en) * | 2001-05-24 | 2003-03-06 | Lise Binderup | Combination medicament for treatment of neoplastic diseases |
PL372761A1 (en) * | 2002-05-17 | 2005-08-08 | Leo Pharma A/S | Cyanoguanidine prodrugs |
-
2003
- 2003-05-15 ES ES03722311T patent/ES2290454T3/en not_active Expired - Lifetime
- 2003-05-15 DE DE60315288T patent/DE60315288T2/en not_active Expired - Lifetime
- 2003-05-15 CN CNB038140772A patent/CN100503570C/en not_active Expired - Fee Related
- 2003-05-15 MX MXPA04011322A patent/MXPA04011322A/en active IP Right Grant
- 2003-05-15 RU RU2004136991/04A patent/RU2326867C2/en active
- 2003-05-15 EP EP03722311A patent/EP1507760B1/en not_active Expired - Lifetime
- 2003-05-15 JP JP2004505334A patent/JP4625694B2/en not_active Expired - Fee Related
- 2003-05-15 KR KR1020047018603A patent/KR101010871B1/en active IP Right Grant
- 2003-05-15 BR BR0309996-2A patent/BR0309996A/en not_active Application Discontinuation
- 2003-05-15 AU AU2003229534A patent/AU2003229534B2/en not_active Ceased
- 2003-05-15 CA CA2485351A patent/CA2485351C/en not_active Expired - Lifetime
- 2003-05-15 PL PL372769A patent/PL228742B1/en unknown
- 2003-05-15 AT AT03722311T patent/ATE368649T1/en not_active IP Right Cessation
- 2003-05-15 WO PCT/DK2003/000318 patent/WO2003097601A1/en active IP Right Grant
-
2004
- 2004-11-08 IL IL165086A patent/IL165086A/en active IP Right Grant
- 2004-11-29 IS IS7562A patent/IS7562A/en unknown
- 2004-12-08 NO NO20045374A patent/NO330183B1/en not_active IP Right Cessation
-
2005
- 2005-10-10 HK HK05108938.3A patent/HK1076812A1/en not_active IP Right Cessation
-
2007
- 2007-06-28 US US11/823,571 patent/US20070249676A1/en not_active Abandoned
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WO1998054144A1 (en) * | 1997-05-29 | 1998-12-03 | Leo Pharmaceutical Products Ltd. A/S (Løvens Kemiske Fabrik Produktionsaktieselskab) | Cyanoguanidines as cell proliferation inhibitors |
WO2000061559A1 (en) * | 1999-04-09 | 2000-10-19 | Shionogi Bioresearch Corp. | N-substituted cyanoguanidine compounds |
WO2002042265A2 (en) * | 2000-11-21 | 2002-05-30 | Leo Pharma A/S | Cyanoguanidine prodrugs |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
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US7253193B2 (en) | 2002-05-17 | 2007-08-07 | Leo Pharma A/S | Cyanoguanidine prodrugs |
US8053446B2 (en) | 2004-12-22 | 2011-11-08 | Leo Pharma A/S | Cyanoguanidine compounds |
US9296697B2 (en) | 2005-08-24 | 2016-03-29 | Abbott Laboratories | Hetaryl-substituted guanidine compounds and use thereof as binding partners for 5-HT5-receptors |
EP2197443A2 (en) * | 2007-09-26 | 2010-06-23 | Gemin X Pharmaceuticals Canada Inc. | Compositions and methods for effecting nad+ levels using a nicotinamide phosphoribosyl transferase inhibitor |
EP2197443A4 (en) * | 2007-09-26 | 2014-01-01 | Gemin X Pharmaceuticals Canada Inc | Compositions and methods for effecting nad+ levels using a nicotinamide phosphoribosyl transferase inhibitor |
US8871747B2 (en) | 2008-08-29 | 2014-10-28 | Topotarget A/S | Urea and thiourea derivatives |
WO2010088842A1 (en) | 2009-02-06 | 2010-08-12 | 天津和美生物技术有限公司 | Pharmaceutical compositions containing pyridyl cyanoguanidines, preparation methods and uses thereof |
WO2011006988A1 (en) | 2009-07-17 | 2011-01-20 | Topotarget A/S | Method for predicting the utility of administering nicotinic acid or a precursor or prodrug thereof to reduce the severity of side-effects of cancer treatment with nicotinamide phosphoribosyltransferase inhibitors |
WO2011121055A1 (en) | 2010-03-31 | 2011-10-06 | Topotarget A/S | Pyridinyl derivatives comprising a cyanoguanidine or squaric acid moiety |
EP2693876A1 (en) * | 2011-04-08 | 2014-02-12 | Sphaera Pharma Pte. Ltd | Substituted methylformyl reagents and method of using same to modify physicochemical and/or pharmacokinetic properties of compounds |
EP2693876A4 (en) * | 2011-04-08 | 2014-09-17 | Sphaera Pharma Pte Ltd | Substituted methylformyl reagents and method of using same to modify physicochemical and/or pharmacokinetic properties of compounds |
EP2867209A4 (en) * | 2012-06-27 | 2015-11-25 | Sunflower Res Llc | Compounds and therapeutic uses thereof |
Also Published As
Publication number | Publication date |
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US20070249676A1 (en) | 2007-10-25 |
CN100503570C (en) | 2009-06-24 |
JP4625694B2 (en) | 2011-02-02 |
RU2326867C2 (en) | 2008-06-20 |
HK1076812A1 (en) | 2006-01-27 |
JP2005538949A (en) | 2005-12-22 |
DE60315288D1 (en) | 2007-09-13 |
ES2290454T3 (en) | 2008-02-16 |
KR20050016412A (en) | 2005-02-21 |
BR0309996A (en) | 2005-02-22 |
NO330183B1 (en) | 2011-02-28 |
CN1662501A (en) | 2005-08-31 |
CA2485351A1 (en) | 2003-11-27 |
IL165086A (en) | 2011-11-30 |
IL165086A0 (en) | 2005-12-18 |
IS7562A (en) | 2004-11-29 |
NO20045374L (en) | 2004-12-08 |
PL372769A1 (en) | 2005-08-08 |
AU2003229534B2 (en) | 2009-08-27 |
DE60315288T2 (en) | 2008-04-10 |
KR101010871B1 (en) | 2011-01-26 |
AU2003229534A1 (en) | 2003-12-02 |
EP1507760A1 (en) | 2005-02-23 |
PL228742B1 (en) | 2018-05-30 |
ATE368649T1 (en) | 2007-08-15 |
EP1507760B1 (en) | 2007-08-01 |
CA2485351C (en) | 2011-12-06 |
RU2004136991A (en) | 2005-06-10 |
MXPA04011322A (en) | 2005-02-17 |
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