UA74608C2 - Використання сполук 1-феніл-3-диметиламінопропану для лікування нетримання сечі - Google Patents

Використання сполук 1-феніл-3-диметиламінопропану для лікування нетримання сечі Download PDF

Info

Publication number: UA74608C2
Authority: UA; Ukraine
Prior art keywords: unsubstituted; dimethylamino; alkyl; saturated; mono
Prior art date: 2000-11-30

Application number

UA2003066043A

Other languages

English (en)

Russian (ru)

Ukrainian (uk)

Inventor

Томас Крістоф

Ельмар Фрідеріхс

Original Assignee

Грюненталь Гмбх

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2000-11-30

Filing date

2001-11-28

Publication date

2006-01-16

2001-11-28 Application filed by Грюненталь Гмбх filed Critical Грюненталь Гмбх

2006-01-16 Publication of UA74608C2 publication Critical patent/UA74608C2/uk

Links

206010046543 Urinary incontinence Diseases 0.000 title claims abstract description 18
NMXXDRKTOJAAQS-UHFFFAOYSA-N n,n-dimethyl-3-phenylpropan-1-amine Chemical class CN(C)CCCC1=CC=CC=C1 NMXXDRKTOJAAQS-UHFFFAOYSA-N 0.000 title claims abstract description 6
229920006395 saturated elastomer Polymers 0.000 claims description 43
150000001875 compounds Chemical class 0.000 claims description 33
229910052739 hydrogen Inorganic materials 0.000 claims description 17
229940126601 medicinal product Drugs 0.000 claims description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
239000000203 mixture Substances 0.000 claims description 13
-1 CoNB Chemical group 0.000 claims description 12
150000003839 salts Chemical class 0.000 claims description 11
238000011282 treatment Methods 0.000 claims description 11
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 9
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 5
150000007513 acids Chemical class 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
125000004076 pyridyl group Chemical group 0.000 claims description 3
125000000335 thiazolyl group Chemical group 0.000 claims description 3
125000001544 thienyl group Chemical group 0.000 claims description 3
150000003254 radicals Chemical class 0.000 claims 2
239000003814 drug Substances 0.000 abstract description 13
238000000034 method Methods 0.000 abstract description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 5
210000003932 urinary bladder Anatomy 0.000 description 22
239000000126 substance Substances 0.000 description 15
235000002639 sodium chloride Nutrition 0.000 description 11
230000008602 contraction Effects 0.000 description 10
230000000694 effects Effects 0.000 description 10
230000027939 micturition Effects 0.000 description 10
229940079593 drug Drugs 0.000 description 8
238000002360 preparation method Methods 0.000 description 7
241000700159 Rattus Species 0.000 description 6
239000004480 active ingredient Substances 0.000 description 6
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230000037396 body weight Effects 0.000 description 5
239000003826 tablet Substances 0.000 description 5
239000000654 additive Substances 0.000 description 4
239000002552 dosage form Substances 0.000 description 4
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 4
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical compound O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 description 4
210000003205 muscle Anatomy 0.000 description 4
239000000243 solution Substances 0.000 description 4
210000003708 urethra Anatomy 0.000 description 4
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
206010021639 Incontinence Diseases 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
241001465754 Metazoa Species 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
230000000202 analgesic effect Effects 0.000 description 3
239000001506 calcium phosphate Substances 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
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239000000945 filler Substances 0.000 description 3
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229960002920 sorbitol Drugs 0.000 description 3
238000006467 substitution reaction Methods 0.000 description 3
230000001629 suppression Effects 0.000 description 3
KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 2
235000019739 Dicalciumphosphate Nutrition 0.000 description 2
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 2
OZYUPQUCAUTOBP-QXAKKESOSA-N Levallorphan Chemical compound C([C@H]12)CCC[C@@]11CCN(CC=C)[C@@H]2CC2=CC=C(O)C=C21 OZYUPQUCAUTOBP-QXAKKESOSA-N 0.000 description 2
TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
229920001800 Shellac Polymers 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
229930006000 Sucrose Natural products 0.000 description 2
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
208000000921 Urge Urinary Incontinence Diseases 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
YGCFIWIQZPHFLU-UHFFFAOYSA-N acesulfame Chemical compound CC1=CC(=O)NS(=O)(=O)O1 YGCFIWIQZPHFLU-UHFFFAOYSA-N 0.000 description 2
229960005164 acesulfame Drugs 0.000 description 2
229940081735 acetylcellulose Drugs 0.000 description 2
229940035676 analgesics Drugs 0.000 description 2
239000005557 antagonist Substances 0.000 description 2
239000000730 antalgic agent Substances 0.000 description 2
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
229910052796 boron Inorganic materials 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
239000002775 capsule Substances 0.000 description 2
229920002301 cellulose acetate Polymers 0.000 description 2
229960000541 cetyl alcohol Drugs 0.000 description 2
229940125782 compound 2 Drugs 0.000 description 2
229940109275 cyclamate Drugs 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
HCAJEUSONLESMK-UHFFFAOYSA-N cyclohexylsulfamic acid Chemical compound OS(=O)(=O)NC1CCCCC1 HCAJEUSONLESMK-UHFFFAOYSA-N 0.000 description 2
NEFBYIFKOOEVPA-UHFFFAOYSA-K dicalcium phosphate Chemical compound [Ca+2].[Ca+2].[O-]P([O-])([O-])=O NEFBYIFKOOEVPA-UHFFFAOYSA-K 0.000 description 2
229910000390 dicalcium phosphate Inorganic materials 0.000 description 2
229940038472 dicalcium phosphate Drugs 0.000 description 2
201000010099 disease Diseases 0.000 description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
229940093915 gynecological organic acid Drugs 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
239000008101 lactose Substances 0.000 description 2
229960000263 levallorphan Drugs 0.000 description 2
230000007774 longterm Effects 0.000 description 2
235000019359 magnesium stearate Nutrition 0.000 description 2
239000000463 material Substances 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
229960005181 morphine Drugs 0.000 description 2
UZHSEJADLWPNLE-GRGSLBFTSA-N naloxone Chemical compound O=C([C@@H]1O2)CC[C@@]3(O)[C@H]4CC5=CC=C(O)C2=C5[C@@]13CCN4CC=C UZHSEJADLWPNLE-GRGSLBFTSA-N 0.000 description 2
229960004127 naloxone Drugs 0.000 description 2
DQCKKXVULJGBQN-XFWGSAIBSA-N naltrexone Chemical compound N1([C@@H]2CC3=CC=C(C=4O[C@@H]5[C@](C3=4)([C@]2(CCC5=O)O)CC1)O)CC1CC1 DQCKKXVULJGBQN-XFWGSAIBSA-N 0.000 description 2
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CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 2
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125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
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NDVASEGYNIMXJL-UWVGGRQHSA-N (-)-sabinene Chemical compound C=C1CC[C@]2(C(C)C)[C@H]1C2 NDVASEGYNIMXJL-UWVGGRQHSA-N 0.000 description 1
LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
125000006273 (C1-C3) alkyl group Chemical group 0.000 description 1
125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 1
TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
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CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical class C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
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Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/131—Amines acyclic
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/10—Drugs for disorders of the urinary system of the bladder

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Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Urology & Nephrology (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Epidemiology (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

UA2003066043A 2000-11-30 2001-11-28 Використання сполук 1-феніл-3-диметиламінопропану для лікування нетримання сечі UA74608C2 (uk)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10059412A DE10059412A1 (de)	2000-11-30	2000-11-30	Verwendung von 1-Phenyl-3-dimethylamino-propanverbindungen zur Therapie der Harninkontinenz
PCT/EP2001/013918 WO2002043715A2 (de)	2000-11-30	2001-11-28	Verwendung von 1-phenyl-3-dimethylamino-propanverbindungen zur therapie der harninkontinenz

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UA74608C2 true UA74608C2 (uk)	2006-01-16

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US (1)	US6841575B2 (da)
EP (1)	EP1438034B1 (da)
JP (1)	JP4284066B2 (da)
KR (1)	KR100853364B1 (da)
CN (1)	CN100421654C (da)
AT (1)	ATE402694T1 (da)
AU (2)	AU3321002A (da)
BR (1)	BR0115882A (da)
CA (1)	CA2430332C (da)
CY (1)	CY1108377T1 (da)
CZ (1)	CZ20031508A3 (da)
DE (2)	DE10059412A1 (da)
DK (1)	DK1438034T3 (da)
EC (1)	ECSP034635A (da)
ES (1)	ES2311030T3 (da)
HU (1)	HU228827B1 (da)
IL (2)	IL156170A0 (da)
MX (1)	MXPA03004712A (da)
NO (1)	NO334109B1 (da)
NZ (1)	NZ526603A (da)
PL (1)	PL205081B1 (da)
PT (1)	PT1438034E (da)
RU (1)	RU2286768C2 (da)
SI (1)	SI1438034T1 (da)
SK (1)	SK287420B6 (da)
UA (1)	UA74608C2 (da)
WO (1)	WO2002043715A2 (da)
ZA (1)	ZA200305006B (da)

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Publication number	Priority date	Publication date	Assignee	Title
DE10109763A1 (de) *	2001-02-28	2002-09-05	Gruenenthal Gmbh	Pharmazeutische Salze
US20050176790A1 (en)	2001-02-28	2005-08-11	Johannes Bartholomaus	Pharmaceutical salts
DE10146275A1 (de) *	2001-09-18	2003-04-24	Gruenenthal Gmbh	Kombination ausgewählter Opioide mit Muscarin-Antagonisten zur Therapie der Harninkontinenz
US7410965B2 (en)	2002-05-29	2008-08-12	Gruenenthal Gmbh	Delayed release pharmaceutical composition containing 1-dimethyl-amino-3-(3-methoxyphenyl)-2-methyl-pentan-3-ol
DE10224108A1 (de) *	2002-05-29	2004-01-29	Grünenthal GmbH	1-Dimethylamino-3-(3-methoxy-phenyl)-2-methyl-pentan-3-ol enthaltendes Arzneimiitel mit verzögerter Wirkstofffreisetzung
DE10224624A1 (de) *	2002-05-30	2003-12-11	Gruenenthal Gmbh	Metabolite und Prodrugs von 1-Dimethylamino-3-(3-methoxy-phenyl)-2-methyl-pentan-3-ol
DE10224556A1 (de) *	2002-05-31	2004-01-08	Grünenthal GmbH	1-Dimethylamino- 3-(3-methoxy-phenyl)2-methyl-pentan-3-ol entaltendes Arzneimittel in verschiedenen Formulierungen
DE10225315A1 (de) *	2002-06-06	2003-12-24	Gruenenthal Gmbh	Wirkstoffsalze und Ester von 1-Dimethylamino-3-(3-methoxy-phenyl)-2-methyl- pentan-3-ol und 3-(3-Dimethylamino-1-ethyl-1-hydroxy-2-methyl- propyl)-phenol
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2000
- 2000-11-30 DE DE10059412A patent/DE10059412A1/de not_active Withdrawn
2001
- 2001-11-28 DE DE50114181T patent/DE50114181D1/de not_active Expired - Lifetime
- 2001-11-28 IL IL15617001A patent/IL156170A0/xx active IP Right Grant
- 2001-11-28 SK SK663-2003A patent/SK287420B6/sk not_active IP Right Cessation
- 2001-11-28 WO PCT/EP2001/013918 patent/WO2002043715A2/de not_active Ceased
- 2001-11-28 AU AU3321002A patent/AU3321002A/xx active Pending
- 2001-11-28 DK DK01984781T patent/DK1438034T3/da active
- 2001-11-28 NZ NZ526603A patent/NZ526603A/en not_active IP Right Cessation
- 2001-11-28 CZ CZ20031508A patent/CZ20031508A3/cs unknown
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- 2001-11-28 MX MXPA03004712A patent/MXPA03004712A/es active IP Right Grant
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- 2001-11-28 EP EP01984781A patent/EP1438034B1/de not_active Expired - Lifetime
- 2001-11-28 AT AT01984781T patent/ATE402694T1/de active
- 2001-11-28 JP JP2002545686A patent/JP4284066B2/ja not_active Expired - Fee Related
- 2001-11-28 PT PT01984781T patent/PT1438034E/pt unknown
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- 2001-11-28 KR KR1020037007270A patent/KR100853364B1/ko not_active Expired - Fee Related
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- 2001-11-28 RU RU2003117707/15A patent/RU2286768C2/ru not_active IP Right Cessation
- 2001-11-28 HU HU0302430A patent/HU228827B1/hu not_active IP Right Cessation
- 2001-11-28 CN CNB018223478A patent/CN100421654C/zh not_active Expired - Fee Related
- 2001-11-28 CA CA2430332A patent/CA2430332C/en not_active Expired - Fee Related
2003
- 2003-05-27 NO NO20032406A patent/NO334109B1/no not_active IP Right Cessation
- 2003-05-28 IL IL156170A patent/IL156170A/en not_active IP Right Cessation
- 2003-05-30 EC EC2003004635A patent/ECSP034635A/es unknown
- 2003-05-30 US US10/448,454 patent/US6841575B2/en not_active Expired - Fee Related
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Also Published As

Publication number	Publication date
KR20030059294A (ko)	2003-07-07
JP2004538246A (ja)	2004-12-24
NZ526603A (en)	2005-10-28
DK1438034T3 (da)	2008-12-01
NO334109B1 (no)	2013-12-09
HUP0302430A3 (en)	2009-08-28
PL205081B1 (pl)	2010-03-31
CA2430332A1 (en)	2002-06-06
DE10059412A1 (de)	2002-06-13
US20040034105A1 (en)	2004-02-19
WO2002043715A3 (de)	2004-04-15
CN1622803A (zh)	2005-06-01
JP4284066B2 (ja)	2009-06-24
MXPA03004712A (es)	2003-08-19
PL366051A1 (en)	2005-01-24
CA2430332C (en)	2011-03-15
KR100853364B1 (ko)	2008-08-22
HUP0302430A2 (hu)	2003-10-28
ES2311030T3 (es)	2009-02-01
CY1108377T1 (el)	2014-02-12
NO20032406D0 (no)	2003-05-27
ZA200305006B (en)	2007-11-28
AU3321002A (en)	2002-06-11
AU2002233210B2 (en)	2006-05-11
NO20032406L (no)	2003-05-27
PT1438034E (pt)	2008-08-22
US6841575B2 (en)	2005-01-11
EP1438034A2 (de)	2004-07-21
ATE402694T1 (de)	2008-08-15
IL156170A0 (en)	2003-12-23
EP1438034B1 (de)	2008-07-30
CZ20031508A3 (cs)	2003-10-15
DE50114181D1 (de)	2008-09-11
HK1068274A1 (zh)	2005-04-29
ECSP034635A (es)	2003-07-25
WO2002043715A2 (de)	2002-06-06
BR0115882A (pt)	2003-12-02
CN100421654C (zh)	2008-10-01
IL156170A (en)	2007-02-11
SK287420B6 (sk)	2010-09-07
SK6632003A3 (en)	2004-08-03
RU2286768C2 (ru)	2006-11-10
SI1438034T1 (sl)	2008-12-31
HU228827B1 (hu)	2013-05-28

Publication	Publication Date	Title
UA74608C2 (uk)	2006-01-16	Використання сполук 1-феніл-3-диметиламінопропану для лікування нетримання сечі
AU2002223688B2 (en)	2006-06-01	Use of substituted 6-dimethylaminomethyl-1-phenyl-cyclohexane compounds for treating urinary incontinence
US6908944B2 (en)	2005-06-21	Use of 6-dimethylaminomethyl-1-phenyl-cyclohexane compounds for treatment of urinary incontinence