DK3053576T3 - Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk - Google Patents

Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk Download PDF

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DK3053576T3
DK3053576T3 DK16161922.6T DK16161922T DK3053576T3 DK 3053576 T3 DK3053576 T3 DK 3053576T3 DK 16161922 T DK16161922 T DK 16161922T DK 3053576 T3 DK3053576 T3 DK 3053576T3
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methyl
ethyl
imidazol
benzyl ester
acid
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Mohammed I Dibas
Ken Chow
John E Donello
Michael E Garst
Daniel W Gil
Liming Wang
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Allergan Inc
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    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4174—Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0014—Skin, i.e. galenical aspects of topical compositions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine

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Claims (3)

1. Sammensætning omfattende en forbindelse med formel I, dens individuelle enantiomerer, dens individuelle diastereoisomerer, dens hydrater, dens solvater, dens krystalformer, dens individuelle tautomerer eller et farmaceutisk acceptabelt salt deraf, til anvendelse i sænkning af intraokulært tryk i et berørt øje af en menneskelig patient med behov for en sådan behandling ved administration af en terapeutisk effektiv mængde af nævnte sammensætning;
Formel i hvor R1 er H eller C1-3 alkyl; R2 er H eller C1-3 alkyl; R3 er H, Ci-10 alkyl, heterocykel eller aryl; og R er Ci-10 alkyl, heterocykel eller aryl, hvor "alkyl" betyder en mættet monovalent alkandel, som har lige eller forgrenede alkandele eller kombinationer deraf, som eventuelt kan substitueres af aminogrupper, arylgrupper, halogener, og et methylen (-CH2-) kan erstattes af carbonyl, -NH-, carboxyl, amid, svovl eller af oxygen, og "heterocykel" betyder en aromatisk eller ikke-aromatisk 5- til 10-leddet monocyklisk eller bicyklisk ring, som indeholder mindst ét heteroatom valgt fra O eller N eller S eller kombinationer deraf, som afbryder den carbocykliske ringstruktur, som eventuelt kan substitueres af C1-6 alkyl, amino, halogen, -O(Ci-e alkyl), -OC(O)(Ci-e alkyl), -C(O)O(Ci-e alkyl), -NHC(O)(Ci-e alkyl), -C(O)NH(Ci-6 alkyl), -S(Ci-e alkyl) grupper, og
"aryl" betyder en organisk del afledt fra et aromatisk carbonhydrid bestående af en monocyklisk eller bicyklisk ring, som indeholder 6-10 kulstofatomer ved fjernelse af et hydrogenatom, såsom phenyl eller naphthyl, som eventuelt kan substitueres af, men ikke begrænset til, Ci-6 alkyl, amino, halogen, -O(Ci-e alkyl), -OC(O)(Ci-e alkyl), - C(O)O(Ci-e alkyl), -NHC(O)(Ci-6 alkyl), -C(O)NH(Ci-6 alkyl), og -S(Ci-e alkyl) grupper.
2-Amino-3-phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methylbenzyl ester.
15. Artikel til fremstilling omfattende indpakningsmateriale og et farmaceutisk middel indeholdt i nævnte indpakningsmateriale, hvor det farmaceutiske middel er terapeutisk effektivt til sænkning af intraokulært tryk og hvor indpakningsmaterialet omfatter et mærke, som indikerer, at det farmaceutiske middel kan anvendes til sænkning af intraokulært tryk og hvor nævnte farmaceutiske middel omfatter en effektiv mængde af en forbindelse valgt fra gruppen bestående af: /'so-smørsyre 3-[(S)-l-(l-/'so-butyryl-lH-imidazol-4-yl)-ethyl]-2-methylbenzyl ester; 2,2-Dimethyl-propionsyre 3-((S)-l-[l-(2,2-dimethyl-propionyl)-lA7-imidazol-4-yl]-ethyl}-2-methyl-benzylester; eddikesyre 3-[(S)-l-(l-acetyl-lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(l-benzoyl-lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
2-Amino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methylbenzyl ester; 2-(2-Amino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og
2-Amino-3-phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eller et farmaceutisk acceptabelt salt deraf.
9. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-8, hvor sammensætningen yderligere omfatter fra 0,001 til 1 vægtprocent af et konserveringsmiddel.
10. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-9, hvor sammensætningen yderligere omfatter fra 0,01 til 0,5 vægtprocent af et konserveringsmiddel.
11. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-10, hvor sammensætningen yderligere omfatter fra 0,001 til 0,01 vægtprocent af et konserveringsmiddel.
12. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-11, hvor sammensætningen yderligere omfatter fra 0,01 til 1 vægtprocent af et cosolvent.
13. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-12, hvor sammensætningen yderligere omfatter fra 0,01 til 2 vægtprocent af et viskositetsfremmende middel.
14. Artikel til fremstilling omfattende indpakningsmateriale og et farmaceutisk middel indeholdt i nævnte indpakningsmateriale, hvor det farmaceutiske middel er terapeutisk effektivt til sænkning af intraokulært tryk og hvor indpakningsmaterialet omfatter et mærke, som indikerer, at det farmaceutiske middel kan anvendes til sænkning af intraokulært tryk og hvor nævnte farmaceutiske middel omfatter en effektiv mængde af en forbindelse valgt fra gruppen bestående af: /'so-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eddikesyre 3-[(S)-l-(l/-/-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
2-Amino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og
2- Amino-3-phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eller et farmaceutisk acceptabelt salt deraf.
8. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-7, hvor sammensætningen omfatter 0,05 til 2 vægtprocent, afen forbindelse valgt fra: /'so-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eddikesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3- Methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
2-Amino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og
2- Amino-3-phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eller et farmaceutisk acceptabelt salt deraf; eller hvor sammensætningen omfatter 0,005 til 2 vægtprocent, afen forbindelse valgt fra: /'so-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eddikesyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3- Methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Phenyl-propionsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
2-Amino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og
2-Amino-3-phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eller hvor forbindelsen er valgt fra: /'so-smørsyre 3-[(S)-l-(l-/so-butyryl-lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-((S)-l-[l-(2,2-dimethyl-propionyl)-lA7-imidazol-4-yl]-ethyl}-2-methyl-benzylester; eddikesyre 3-[(S)-l-(l-acetyl-lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(l-benzoyl-lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3- Methyl-smørsyre 2-methyl-3-{(S)-l-[l-(3-methyl-butyryl)-lH-imidazol- 4- yl]-ethyl}-benzylester; Phenyl-propionsyre 2-methyl-3-{(S)-l-[l-(3-phenyl-propionyl)-lH-imidazol-4-yl]-ethyl}-benzylester; 2-tert-Butoxycarbonylamino-3-methyl-smørsyre 3-{(S)-l-[l-(2-terf·-butoxy carbonylamino-3-methyl-butyryl)-lH-imidazol-4-yl]-ethyl}-2-methyl-benzylester; 2-tert-Butoxycarbonylamino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-{(S)-l-[l-(2-f’erf’-butoxycarbonylamino-3-methyl-butyryl)-lH-imidazol-4-yl]-ethyl}-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og 2-tert-Butoxycarbonylamino-3-phenyl-propionsyre 3-[(S)-l-(lA7-imidazol- 4-yl)-ethyl]-2-methyl-benzylester.
6. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-5, hvor det berørte øje bevarer et intraokulært tryk på mindre end det intraokulære baselinetryk i mindst otte (8) timer; eller hvor det berørte øje bevarer et intraokulært tryk på mindre end det intraokulære baselinetryk i mindst ti (10) timer; eller hvor det berørte øje bevarer et intraokulært tryk på mindre end det intraokulære baselinetryk i mindst tolv (12) timer.
7. Sammensætningen til anvendelse ifølge et hvilket som helst af kravene 1-6, hvor sammensætningen omfatter 0,0005 til 5 vægtprocent, afen forbindelse valgt fra: /'so-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eddikesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
2-Amino-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-Amino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og
2. Sammensætningen til anvendelse ifølge krav 1, hvor forbindelsen er af formel II, dens individuelle diastereoisomerer, dens hydrater, dens solvater, dens krystalformer, dens individuelle tautomerer eller et farmaceutisk acceptabelt salt deraf,
Formel II hvor R1, R2, R3 og R er som defineret i krav 1.
3. Sammensætningen til anvendelse ifølge krav 1, hvor forbindelsen er af formel III, dens individuelle diastereoisomerer, dens hydrater, dens solvater, dens krystalformer, dens individuelle tautomerer eller et farmaceutisk acceptabelt salt deraf,
Formel III hvor R1, R2, R3 og R er som defineret i krav 1.
4. Sammensætningen til anvendelse ifølge krav 2, hvor R1 er C1-3 alkyl, R2 er C1-3 alkyl, R3 er H og R er C1-10 alkyl; eller hvor R1 er methyl, R2 er methyl, R3 er H og R er C1-4 alkyl.
5. Sammensætningen til anvendelse ifølge krav 2, hvor forbindelsen er valgt fra: /'so-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2,2-Dimethyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; eddikesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; benzoesyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3-Phenyl-propionsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester;
3- Methyl-smørsyre 2-methyl-3-{(S)-l-[l-(3-methyl-butyryl)-lH-imidazol- 4- yl]-ethyl}-benzylester; Phenyl-propionsyre 2-methyl-3-{(S)-l-[l-(3-phenyl-propionyl)-lH-imidazol-4-yl]-ethyl}-benzylester; 2-terf’-Butoxycarbonylamino-3-methyl-smørsyre 3-{(S)-l-[l-(2-terf·-butoxy carbonylamino-3-methyl-butyryl)-lH-imidazol-4-yl]-ethyl}-2-methyl-benzylester; 2-ίβΓί·-ΒυίοχγεθΓ0οηγΙθΓηϊηο-3-Γη6ίήγΙ-5Γη0Γ5γΓ6 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-{(S)-l-[l-(2-f’erf’-butoxycarbonylamino-3-methyl-butyryl)-lH-imidazol-4-yl]-ethyl}-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-3-methyl-butyrylamino)-3-methyl-smørsyre 3-[(S)-l-(lH-imidazol-4-yl)-ethyl]-2-methyl-benzylester; 2-(2-terf’-Butoxycarbonylamino-acetylamino)-3-methyl-smørsyre 3-[(S)-l-(lA7-imidazol-4-yl)-ethyl]-2-methyl-benzylester; og 2-tert-Butoxycarbonylamino-3-phenyl-propionsyre 3-[(S)-l-(lA7-imidazol- 4-yl)-ethyl]-2-methyl-benzylester.
DK16161922.6T 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk DK3053576T3 (da)

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US38337010P 2010-09-16 2010-09-16
EP11760962.8A EP2616068B1 (en) 2010-09-16 2011-09-16 Ester pro-drugs of [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl]methanol for lowering intraocular pressure

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DK19194325.7T DK3636263T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl]-methanol
DK16161922.6T DK3053576T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk
DK16161920.0T DK3050563T3 (da) 2010-09-16 2011-09-16 Ester-pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til behandling af hudsygdomme og -tilstande
DK16161921.8T DK3078376T3 (da) 2010-09-16 2011-09-16 Ester-pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til behandling af nethindesygdomme
DK18157147.2T DK3338777T3 (da) 2010-09-16 2011-09-16 Ester-pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til behandling af nethindesygdomme
DK18160174.1T DK3348264T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk
DK11760962.8T DK2616068T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol til sænkning af intraokulært tryk
DK16161923T DK3050564T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl]-methanol
DK11760963.6T DK2616069T3 (da) 2010-09-16 2011-09-16 Ester pro-drugs af [3-(1-(1h-imidazol-4-yl)ethyl)-2-methylphenyl] methanol

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