WO2004037266A1 - Composes pour le traitement de la toux - Google Patents
Composes pour le traitement de la toux Download PDFInfo
- Publication number
- WO2004037266A1 WO2004037266A1 PCT/EP2003/011759 EP0311759W WO2004037266A1 WO 2004037266 A1 WO2004037266 A1 WO 2004037266A1 EP 0311759 W EP0311759 W EP 0311759W WO 2004037266 A1 WO2004037266 A1 WO 2004037266A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phenyl
- methyl
- hydrogen
- alkyl
- cough
- Prior art date
Links
- VYHIUSNJERXVAS-VECJFWGBSA-N CN([C@H](Cc(cc1Cl)ccc1Cl)/C=C/C(NC(C1)C1(CCCCN1)C1=O)=O)C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)=O Chemical compound CN([C@H](Cc(cc1Cl)ccc1Cl)/C=C/C(NC(C1)C1(CCCCN1)C1=O)=O)C(c1cc(C(F)(F)F)cc(C(F)(F)F)c1)=O VYHIUSNJERXVAS-VECJFWGBSA-N 0.000 description 1
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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/14—Antitussive agents
Definitions
- This invention relates to organic compounds and, in particular to their use as pharmaceuticals.
- the invention provides, in one aspect, use of a compound of formula I
- R 1 is phenyl that is unsubstituted or is substituted by 1, 2 or 3 substituents selected from the group halogen, C ⁇ -C -alkyl, trifluoromethyl, hydroxy and C ⁇ -C -alkoxy, R 2 is hydrogen or C ⁇ -C7-alkyl,
- R 3 is hydrogen, C ⁇ -C 7 -alkyl or phenyl that is unsubstituted or is substituted by 1, 2 or 3 substituents selected from the group halogen, C ⁇ -C7-alkyl, trifluoromethyl, hydroxy and C 1 -C7- alkoxy,
- R 4 is phenyl that is unsubstituted or is substituted by 1, 2 or 3 substituents selected from the group halogen, Ci-Cyalkyl, trifluoromethyl, hydroxy and Ci-Cyalkoxy; or is naphthyl, 1H- indol-3-yl or l-C ⁇ -C7-alkyl-indol-3-yl,
- R 5 and R 6 are each independently of the other hydrogen or C ⁇ -C 7 -alkyl, at least one of R 5 and R 6 being hydrogen, and R 7 is C 3 -C8-cycloalkyl, D-azacycloheptan-2-on-3-yl or L-azacycloheptan-2-on-3-yl.
- the invention provides, in another aspect, a method of treating cough, in a subject, particularly a human subject, in need of such treatment, which comprises administering to said subject an effective amount of a compound of formula I as hereinbefore defined.
- Treatment of cough in accordance with the invention may be symptomatic.
- Cough to be treated in accordance with the invention includes conditions associated with an action that occurs as the result of irritation of the throat, larynx and airways. It takes the form of a noisy expulsion of air, and its function is to clear the airways of the substances causing the irritation anything from particles of dust to smoke, chemicals, and virus-laden mucus. Cough may be due to one or more underlying diseases including chronic obstructive pulmonary disease (COPD), upper respiratory tract infections (UR ⁇ ), postnasal drip, acute viral infection, asthma, lung cancer, interstitial lung disease, gastroesophageal reflux disease (GERD), angiotensin converting enzyme-induced cough and heart failure.
- COPD chronic obstructive pulmonary disease
- UR ⁇ upper respiratory tract infections
- postnasal drip postnasal drip
- acute viral infection asthma
- lung cancer interstitial lung disease
- gastroesophageal reflux disease GEF
- angiotensin converting enzyme-induced cough and heart failure angiotensin converting enzyme-
- C ⁇ -C7-alkyl is, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, neopentyl, n-hexyl or n-heptyl, preferably C ⁇ -C 4 alkyl, especially methyl or ethyl, and more especially methyl.
- Halogen is, for example, fluorine, chlorine, bromine or iodine.
- Halophenyl is, for example, (fluoro-, chloro-, bromo- or iodo-)phenyl, preferably fluorophenyl or chlorophenyl, especially 4-fluorophenyl or 4-chlorophenyl, and more especially 4-chlorophenyl.
- Dihalophenyl is, for example, dichlorophenyl, difluorophenyl or chlorofluorophenyl, preferably dichlorophenyl or difluorophenyl, especially 3,4-dichlorophenyl or 3,4- difluorophenyl, and more especially 3,4-dichlorophenyl.
- Trihalophenyl is, for example, trifluorophenyl or trichlorophenyl.
- l-C ⁇ -C7-alkyl-indol-3-yl is, for example, l-methyl-indol-3-yl.
- C 3 -C 8 -Cycloalkyl - and analogously C5-C7-cycloalkyl - is in each case a cycloalkyl radical having the number of ring carbon atoms indicated.
- C.-Cs-Cycloalkyl is therefore, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl, preferably cyclohexyl.
- D-Azacycloheptan-2-on-3-yl corresponds to the following group
- the compounds of formula I may be of formula IA
- Compounds of formula IA are usually preferred for use in accordance with the invention.
- Compounds of formula I having a basic group may, for example, form acid addition salts with suitable mineral acids, such as hydrohalic acids, sulfuric acid or phosphoric acid, for example hydrochlorides, hydrobromides, sulfates, hydrogen sulfates or phosphates.
- suitable mineral acids such as hydrohalic acids, sulfuric acid or phosphoric acid, for example hydrochlorides, hydrobromides, sulfates, hydrogen sulfates or phosphates.
- corresponding salts with bases are also possible, for example corresponding alkali metal or alkaline earth metal salts, for example sodium, potassium or magnesium salts, or salts with ammonia or organic amines, for example ammonium salts.
- the invention relates preferably to the use of compounds of formula I wherein
- R 1 is phenyl, 3,5-bistrifluoromethyl-phenyl or 3,4,5-trimethoxyphenyl,
- R 2 is hydrogen or C ⁇ -C7-alkyl
- R 3 is hydrogen or phenyl
- R 4 is phenyl, halo-phenyl, dihalo-phenyl, trihalo-phenyl, 2-naphthyl, lH-indol-3-yl or 1-C ⁇ -
- R 5 and R 6 are each independently of the other hydrogen or C ⁇ -C7-alkyl, at least one of R 5 and R 6 being hydrogen, and
- R 7 is C5-C7cycloalkyl, D-azacycloheptan-2-on-3-yl or L-azacycloheptan-2-on-3-yl.
- the invention relates especially to the use of compounds of formula I wherein
- R 1 is 3,5-bistrifluoromethyl-phenyl
- R 2 is hydrogen, methyl or ethyl
- R 3 is hydrogen or phenyl
- R 4 is phenyl, 4-chlorophenyl, 4-fluorophenyl, 3,4-dichloro-phenyl, 3,4-difluoro-phenyl, 3- fluoro-4-chloro-phenyl, 3,4,5-trifluoro-phenyl, 2-naphthyl, lH-indol-3-yl or 1 -methyl -indol-
- R 5 and R 6 are each independently of the other hydrogen or methyl, at least one of R s and R 6 being hydrogen, and
- R 7 is cyclohexyl, D-azacycloheptan-2-on-3-yl or L-azacycloheptan-2-on-3-yl.
- the invention relates more especially to the use of compounds of formula I wherein
- R 1 is 3,5-bistrifluoromethyl-phenyl
- R 2 is hydrogen or methyl
- R 3 is hydrogen or phenyl
- R 4 is phenyl, 4-chlorophenyl, 3,4-dichloro-phenyl, 2-naphthyl, lH-indol-3-yl or 1 -methyl - indol-3-yl,
- R 5 and R 6 are hydrogen
- R 7 is cyclohexyl, D-azacycloheptan-2-on-3-yl or L-azacycloheptan-2-on-3-yl. Special mention should be made of each of the following sub-groups of a group of compounds of formula I:
- the invention relates most importantly to the use of (4R)-4-[N'-methyl-N'-(3,5-bistrifluoro- methylbenzoyl)amino]-4-(3,4-dichlorobenzyl)-but-2-enoic acid N-[(R)-epsilon-caprolactam- 3-yl]-amide, i.e. a compound of formula II
- the compounds of formula I in free or pharmaceutically acceptable salt form, may be prepared as described in WO 98/07694 or WO 01/85696. As mentioned therein, they may be in the form of their hydrates and/or may include other solvents, for example solvents which may have been used for the crystallisation of compounds in solid form.
- the compounds of formula I may be obtained in the form of mixtures of stereoisomers, for example mixtures of diastereoisomers or mixtures of enantiomers, such as racemates, or possibly also in the form of pure stereoisomers.
- Mixtures of diastereoisomers obtainable in accordance with the process or by some other method can be separated in customary manner into mixtures of enantiomers, for example racemates, or into individual diastereoisomers, for example on the basis of the physico-chemical differences between the constituents in known manner by fractional crystallisation, distillation and/or chromatography.
- the more active isomer is isolated.
- Mixtures of enantiomers, especially racemates, obtainable in accordance with the process or by some other method can be separated into the individual enantiomers by known methods, for example by recrystallisation from an optically active solvent, with the aid of microorganisms, by chromatography and/or by reaction with an optically active auxiliary compound, for example a base, acid or alcohol, to form mixtures of diastereoisomeric salts or functional derivatives, such as esters, separation thereof and freeing of the desired enantio- mer.
- an optically active auxiliary compound for example a base, acid or alcohol
- compounds of formula I in free form or in pharmaceutically acceptable salt form, may be administered by any appropriate route, for example orally, e.g. in tablet, capsule or liquid form, parenterally, for example in the form of an injectable solution or suspension, or intranasally, for example in the form of an aerosol or other atomisable formulation using an appropriate intranasal delivery device, e.g. a nasal spray such as those known in the art, or by inhalation. Oral administration is however preferred.
- the compound of formula I in free or salt form may be administered in a pharmaceutical composition together with a pharmaceutically acceptable diluent or carrier.
- a pharmaceutical composition may be as described in WO 98/07694, for example dry powders, tablets, capsules, liquids, injection solutions, infusion solutions or inhalation suspensions as described in Examples A to E of WO 98/07694, or may be prepared using other formulating ingredients and techniques known in the art.
- the dosage of the compound of formula I in free or salt form can depend on various factors, such as the activity and duration of action of the active ingredient, the severity of the condition to be treated, the mode of administration, the species, sex, ethnic origin, age and weight of the subject and/or its individual condition.
- the daily dose for administration for example oral administration, to a warm-blooded animal, particularly a human being, weighing about 75 kg is estimated to be from approximately 1 mg to approximately 1000 mg, especially from approximately 5 mg to approximately 200 mg. That dose may be administered, for example, in a single dose or in several part doses of, for example, from 5 to 200 mg.
- the suitability of a compound of formula I for the treatment of cough may be tested by determining the inhibitory effect of a compound of formula I on cough induced by release of endogenous neuropeptides in guinea pigs.
- Unanaesthetised, unrestrained male Dunkin Hartley guinea pigs 250-500 g are placed individually in a transparent plastic whole body plethysmograph (Buxco, USA) and baseline airway function measured for 2 minutes.
- the guinea pigs are exposed to a nebulised (DeVilbiss ultrasonic, USA) aqueous solution of citric acid (0.6 M) for 10 minutes.
- the compound of formula I (0.3, 3.0 or 10.0 mg/kg) or vehicle (2% dimethylsulfoxide (DMSO), 1:5 CREMOPHOR El ⁇ saline) are dosed orally 2 hours prior to the 10 minute citric acid (0.6 M) challenge. Animals are not selected but rather randomly assigned to different groups. Each drug treatment group is further sub-divided into different groups for the different doses. All experiments have appropriate time matched controls. Values are given as means + s.e. mean. For statistical differences the data is analysed using ANONA and post-hoc Tukey's test, with a P value ⁇ 0.05 taken as significant.
- Cough is measured as follows: the plethysmograph chamber is fitted with a microphone and connected to both an external speaker and a computer. The animals are continuously watched by an observer who counts the number of coughs. The criteria for cough are the characteristic high sound with the mouth open, which is readily distinguished from a sneeze. During cough there is a quick large abdominal movement which is detected as a transient increase in airflow over and above the normal flow.
- Cough is measured using this method during the 10 minutes exposure and for a further 5 minutes following exposure.
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- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2003274067A AU2003274067A1 (en) | 2002-10-24 | 2003-10-23 | Compounds for the treatment of cough |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0224788.0 | 2002-10-24 | ||
GBGB0224788.0A GB0224788D0 (en) | 2002-10-24 | 2002-10-24 | Organic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004037266A1 true WO2004037266A1 (fr) | 2004-05-06 |
Family
ID=9946528
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2003/011759 WO2004037266A1 (fr) | 2002-10-24 | 2003-10-23 | Composes pour le traitement de la toux |
Country Status (4)
Country | Link |
---|---|
AU (1) | AU2003274067A1 (fr) |
GB (1) | GB0224788D0 (fr) |
TW (1) | TW200418488A (fr) |
WO (1) | WO2004037266A1 (fr) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006045820A1 (fr) * | 2004-10-27 | 2006-05-04 | Laboratori Guidotti S.P.A. | Compositions pharmaceutiques a base d'antagonistes de nk2 pour usage pediatrique |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996026183A1 (fr) * | 1995-02-22 | 1996-08-29 | Novartis Ag | Composes 1-aryl-2-acylamino-ethane et leur utilisation en tant qu'antagonistes des neurokinines et notamment des neurokinines 1 |
WO1998007694A1 (fr) * | 1996-08-22 | 1998-02-26 | Novartis Ag | Derives d'acylaminoalkenylene comme antagonistes de nk1 et nk2 |
WO2002051440A1 (fr) * | 2000-12-22 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Medicaments de combinaison |
-
2002
- 2002-10-24 GB GBGB0224788.0A patent/GB0224788D0/en not_active Ceased
-
2003
- 2003-10-23 WO PCT/EP2003/011759 patent/WO2004037266A1/fr not_active Application Discontinuation
- 2003-10-23 AU AU2003274067A patent/AU2003274067A1/en not_active Abandoned
- 2003-10-23 TW TW092129433A patent/TW200418488A/zh unknown
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996026183A1 (fr) * | 1995-02-22 | 1996-08-29 | Novartis Ag | Composes 1-aryl-2-acylamino-ethane et leur utilisation en tant qu'antagonistes des neurokinines et notamment des neurokinines 1 |
WO1998007694A1 (fr) * | 1996-08-22 | 1998-02-26 | Novartis Ag | Derives d'acylaminoalkenylene comme antagonistes de nk1 et nk2 |
WO2002051440A1 (fr) * | 2000-12-22 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Medicaments de combinaison |
EP1352659A1 (fr) * | 2000-12-22 | 2003-10-15 | Takeda Chemical Industries, Ltd. | Medicaments de combinaison |
Non-Patent Citations (3)
Title |
---|
GAO Z ET AL: "Recent advances in neurokinin receptor antagonists", CURRENT MEDICINAL CHEMISTRY 1999 NETHERLANDS, vol. 6, no. 5, 1999, pages 375 - 388, XP009024134, ISSN: 0929-8673 * |
GERSPACHER M ET AL: "Dual neurokinin NK1/NK2 antagonists: N-[(R,R)-(E)-1-arylmethyl-3-(2- oxo-azepan-3-yl)carbamoyl]allyl-N-methyl-3,5- bis(trifluoromethyl)benzamides and 3-[N'-3,5- bis(trifluoromethyl)benzoyl-N-arylmethyl-N'-methylhydrazino]-N-[(R)- 2-oxo-azepan-3-yl]propionamides", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, OXFORD, GB, vol. 11, no. 23, 2001, pages 3081 - 3084, XP002240091, ISSN: 0960-894X * |
YASUMITSU R ET AL: "Effects of specific tachykinin receptor antagonists on citric acid-induced cough and bronchoconstriction in unanesthetized guinea pigs.", EUROPEAN JOURNAL OF PHARMACOLOGY. NETHERLANDS 11 APR 1996, vol. 300, no. 3, 11 April 1996 (1996-04-11), pages 215 - 219, XP002267169, ISSN: 0014-2999 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006045820A1 (fr) * | 2004-10-27 | 2006-05-04 | Laboratori Guidotti S.P.A. | Compositions pharmaceutiques a base d'antagonistes de nk2 pour usage pediatrique |
EA012264B1 (ru) * | 2004-10-27 | 2009-08-28 | Лаборатори Гуидотти С.П.А. | Фармацевтические композиции, основанные на антагонистах nk2, для применения в педиатрической практике |
US7727955B2 (en) | 2004-10-27 | 2010-06-01 | Laboratori Guidotti S.P.A. | Pharmaceutical compositions based on NK2 antagonists for pediatric use |
NO338586B1 (no) * | 2004-10-27 | 2016-09-12 | Laboratori Guidotti Spa | Anvendelse av tachykininantagonist for fremstilling av farmasøytiske formuleringer, oral farmasøytisk sammensetning for pediatrisk anvendelse, og matprodukt omfattende nevnte farmasøytiske sammensetning |
Also Published As
Publication number | Publication date |
---|---|
AU2003274067A1 (en) | 2004-05-13 |
GB0224788D0 (en) | 2002-12-04 |
TW200418488A (en) | 2004-10-01 |
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