RU99109596A - APPLICATION OF H +, K + -ATTASE INHIBITOR FOR THE TREATMENT OF NOSE POLYPES - Google Patents
APPLICATION OF H +, K + -ATTASE INHIBITOR FOR THE TREATMENT OF NOSE POLYPESInfo
- Publication number
- RU99109596A RU99109596A RU99109596/14A RU99109596A RU99109596A RU 99109596 A RU99109596 A RU 99109596A RU 99109596/14 A RU99109596/14 A RU 99109596/14A RU 99109596 A RU99109596 A RU 99109596A RU 99109596 A RU99109596 A RU 99109596A
- Authority
- RU
- Russia
- Prior art keywords
- inhibitor
- atpase
- glucocorticoid
- pharmaceutical preparation
- syndrome
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title claims 13
- 239000003862 glucocorticoid Substances 0.000 claims 12
- 239000000825 pharmaceutical preparation Substances 0.000 claims 10
- 125000000217 alkyl group Chemical group 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 238000000034 method Methods 0.000 claims 6
- 208000033309 Analgesic asthma syndrome Diseases 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 4
- 208000006673 asthma Diseases 0.000 claims 3
- 125000004432 carbon atom Chemical group C* 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 208000011580 syndromic disease Diseases 0.000 claims 3
- 208000000592 Nasal Polyps Diseases 0.000 claims 2
- 150000001447 alkali salts Chemical class 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 229940121819 ATPase inhibitor Drugs 0.000 claims 1
- KUVIULQEHSCUHY-XYWKZLDCSA-N Beclometasone Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@]2(Cl)[C@@H]1[C@@H]1C[C@H](C)[C@@](C(=O)COC(=O)CC)(OC(=O)CC)[C@@]1(C)C[C@@H]2O KUVIULQEHSCUHY-XYWKZLDCSA-N 0.000 claims 1
- VOVIALXJUBGFJZ-KWVAZRHASA-N Budesonide Chemical compound C1CC2=CC(=O)C=C[C@]2(C)[C@@H]2[C@@H]1[C@@H]1C[C@H]3OC(CCC)O[C@@]3(C(=O)CO)[C@@]1(C)C[C@@H]2O VOVIALXJUBGFJZ-KWVAZRHASA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 239000000362 adenosine triphosphatase inhibitor Substances 0.000 claims 1
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000004414 alkyl thio group Chemical group 0.000 claims 1
- 125000005466 alkylenyl group Chemical group 0.000 claims 1
- 239000002260 anti-inflammatory agent Substances 0.000 claims 1
- 229950000210 beclometasone dipropionate Drugs 0.000 claims 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 1
- 229960004436 budesonide Drugs 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 229960000289 fluticasone propionate Drugs 0.000 claims 1
- WMWTYOKRWGGJOA-CENSZEJFSA-N fluticasone propionate Chemical compound C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@@H](C)[C@@](C(=O)SCF)(OC(=O)CC)[C@@]2(C)C[C@@H]1O WMWTYOKRWGGJOA-CENSZEJFSA-N 0.000 claims 1
- 159000000011 group IA salts Chemical class 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- -1 or (-) - enantiomer Chemical class 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
Claims (18)
где Het1 является
или
Het2 является
X является
где N в бензимидазольной группировке Het2 означает, что один из кольцевых углеродных атомов, замещенных R6 - R9, возможно может быть заменен на атом азота без каких-либо заместителей;
R1 и R3 каждый независимо представляет собой водород, алкил или алкокси, при условии, что R1 и R3 не представляют собой одновременно алкокси; и R2 представляет собой алкил, алкокси, возможно замещенный фтором, алкилтио или алкоксиалкокси; или один из R1 и R3 является галогеном, а другой водородом, a R2 является 1-морфолино, 1-пиперидино или диалкиламино;
R4 и R5 являются одинаковыми или разными и выбраны из водорода и алкила;
R6 - R9 являются одинаковыми или разными и выбраны из водорода, галогена, алкила, алкокси, галогеноалкокси, алкилкарбонила и алкоксикарбонила;
R10 является водородом, или R10 и R3 вместе образуют кольцо, содержащее от 6 до 8 углеродных атомов; и
R11 представляет собой водород, галоген или алкил;
где соединение формулы (I) возможно находится в форме фармацевтически приемлемой щелочной соли или в нейтральной форме, или представляет собой отдельный энантиомер или их рацемическую смесь;
где каждая алкильная или алкиленильная группировка имеет разветвленную или прямую цепь и содержит от 1 до 6 углеродных атомов.7. The use according to any one of claims 1 to 6, where the inhibitor of H + , K + -ATPase is a compound of formula I
where het 1 is
or
Het 2 is
X is
where N in the benzimidazole group Het 2 means that one of the ring carbon atoms substituted by R 6 - R 9 may possibly be replaced by a nitrogen atom without any substituents;
R 1 and R 3 are each independently hydrogen, alkyl or alkoxy, provided that R 1 and R 3 are not alkoxy at the same time; and R 2 is alkyl, alkoxy, possibly substituted by fluorine, alkylthio or alkoxyalkoxy; or one of R 1 and R 3 is halogen and the other is hydrogen, and R 2 is 1-morpholino, 1-piperidino or dialkylamino;
R 4 and R 5 are the same or different and are selected from hydrogen and alkyl;
R 6 - R 9 are the same or different and are selected from hydrogen, halogen, alkyl, alkoxy, haloalkoxy, alkylcarbonyl and alkoxycarbonyl;
R 10 is hydrogen, or R 10 and R 3 together form a ring containing from 6 to 8 carbon atoms; and
R 11 represents hydrogen, halogen or alkyl;
where the compound of formula (I) may be in the form of a pharmaceutically acceptable alkaline salt or in neutral form, or is a separate enantiomer or their racemic mixture;
where each alkyl or alkylenyl moiety has a branched or straight chain and contains from 1 to 6 carbon atoms.
или его щелочной солью, или (-)-энантиомером, или щелочной солью (-)-энантиомера.8. The use according to claim 7, where the compound of formula (I) is a compound of formula Ia
or its alkali salt, or (-) - enantiomer, or alkali salt (-) - enantiomer.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9603725A SE9603725D0 (en) | 1996-10-11 | 1996-10-11 | New teatment |
| SE9603725-4 | 1996-10-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU99109596A true RU99109596A (en) | 2001-02-20 |
| RU2197966C2 RU2197966C2 (en) | 2003-02-10 |
Family
ID=20404214
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU99109596/14A RU2197966C2 (en) | 1996-10-11 | 1997-10-01 | APPLICATION OF H+, K+-ATPase INHIBITOR FOR TREATING NASAL POLYPS |
Country Status (33)
| Country | Link |
|---|---|
| EP (1) | EP0946175B1 (en) |
| JP (1) | JP4100713B2 (en) |
| KR (1) | KR100510812B1 (en) |
| CN (1) | CN1146416C (en) |
| AR (1) | AR008886A1 (en) |
| AT (1) | ATE230597T1 (en) |
| AU (1) | AU738310B2 (en) |
| BR (1) | BR9711896A (en) |
| CA (1) | CA2268305C (en) |
| CZ (1) | CZ298799B6 (en) |
| DE (1) | DE69718347T2 (en) |
| DK (1) | DK0946175T3 (en) |
| EE (1) | EE04043B1 (en) |
| ES (1) | ES2188995T3 (en) |
| HU (1) | HUP0000036A3 (en) |
| ID (1) | ID23692A (en) |
| IL (1) | IL129324A0 (en) |
| IS (1) | IS1930B (en) |
| MY (1) | MY117918A (en) |
| NO (1) | NO321007B1 (en) |
| NZ (1) | NZ334786A (en) |
| PL (1) | PL190902B1 (en) |
| PT (1) | PT946175E (en) |
| RS (1) | RS49599B (en) |
| RU (1) | RU2197966C2 (en) |
| SA (1) | SA97180641B1 (en) |
| SE (1) | SE9603725D0 (en) |
| SK (1) | SK284252B6 (en) |
| TR (1) | TR199900770T2 (en) |
| TW (1) | TW568784B (en) |
| UA (1) | UA59374C2 (en) |
| WO (1) | WO1998016228A1 (en) |
| ZA (1) | ZA978842B (en) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6489346B1 (en) | 1996-01-04 | 2002-12-03 | The Curators Of The University Of Missouri | Substituted benzimidazole dosage forms and method of using same |
| US5840737A (en) | 1996-01-04 | 1998-11-24 | The Curators Of The University Of Missouri | Omeprazole solution and method for using same |
| US7354894B2 (en) | 1998-08-18 | 2008-04-08 | The Regents Of The University Of California | Preventing airway mucus production by administration of EGF-R antagonists |
| HRP20010119B1 (en) | 1998-08-18 | 2008-05-31 | The Regents Of The University Of California | PREVENTION OF SLAUGHTERS IN THE AIRWAYS USED BY EGF-R ANTAGONISTS |
| US6846799B1 (en) * | 1998-08-18 | 2005-01-25 | The Regents Of The University Of California | Preventing airway mucus production by administration of EGF-R antagonists |
| JP4543553B2 (en) * | 1999-03-03 | 2010-09-15 | オプティノーズ アズ | Nasal infeed device |
| CA2467652A1 (en) * | 2001-11-19 | 2003-05-30 | Altana Pharma Ag | Reversible proton pump inhibitors for the treatment of airway disorders |
| AU2003218726A1 (en) * | 2002-03-14 | 2003-09-22 | Altana Pharma Ag | Use of proton pump inhibitors for the treatment of airway disorders |
| NZ536918A (en) * | 2002-05-07 | 2006-09-29 | Altana Pharma Ag | Combination of pantoprazole and a respiratory agent for the treatment of respiratory diseases |
| JP2005528418A (en) * | 2002-05-07 | 2005-09-22 | アルタナ ファルマ アクチエンゲゼルシャフト | Novel combinations for treating airway diseases |
| FR2845915B1 (en) * | 2002-10-21 | 2006-06-23 | Negma Gild | USE OF TENATOPRAZOLE FOR THE TREATMENT OF GASTRO-OESOPHAGEAL REFLUX |
| AU2003293833B2 (en) | 2002-12-12 | 2009-10-01 | Covis Pharma B.V. | Combination medicament |
| US8993599B2 (en) | 2003-07-18 | 2015-03-31 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| US8371292B2 (en) | 2003-09-16 | 2013-02-12 | Nycomed Gmbh | Use of ciclesonide for the treatment of respiratory diseases |
| RU2252025C1 (en) * | 2003-11-28 | 2005-05-20 | Дальневосточный государственный медицинский университет | Method for treating excessive granulation tissue of larynx and trachea |
| US8906940B2 (en) | 2004-05-25 | 2014-12-09 | Santarus, Inc. | Pharmaceutical formulations useful for inhibiting acid secretion and methods for making and using them |
| CN104408249B (en) * | 2014-11-24 | 2017-09-26 | 广州供电局有限公司 | The hot determination method for parameter of single-core cable conductor and system |
| KR101974504B1 (en) * | 2017-04-10 | 2019-05-03 | 재단법인 아산사회복지재단 | An Animal Model with Eosinophilic Nasal Polyps |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1429184A (en) * | 1972-04-20 | 1976-03-24 | Allen & Hanburys Ltd | Physically anti-inflammatory steroids for use in aerosols |
| GB1571629A (en) * | 1977-11-30 | 1980-07-16 | Fisons Ltd | Pharmaceutical compositions containing beclomethasone dipropionate |
-
1996
- 1996-10-11 SE SE9603725A patent/SE9603725D0/en unknown
-
1997
- 1997-01-10 UA UA99042004A patent/UA59374C2/en unknown
- 1997-10-01 DE DE69718347T patent/DE69718347T2/en not_active Expired - Fee Related
- 1997-10-01 ES ES97945135T patent/ES2188995T3/en not_active Expired - Lifetime
- 1997-10-01 KR KR10-1999-7003115A patent/KR100510812B1/en not_active Expired - Fee Related
- 1997-10-01 IL IL12932497A patent/IL129324A0/en not_active IP Right Cessation
- 1997-10-01 TR TR1999/00770T patent/TR199900770T2/en unknown
- 1997-10-01 ID IDW990139D patent/ID23692A/en unknown
- 1997-10-01 JP JP51824698A patent/JP4100713B2/en not_active Expired - Fee Related
- 1997-10-01 NZ NZ334786A patent/NZ334786A/en unknown
- 1997-10-01 CZ CZ0122999A patent/CZ298799B6/en not_active IP Right Cessation
- 1997-10-01 RU RU99109596/14A patent/RU2197966C2/en not_active IP Right Cessation
- 1997-10-01 DK DK97945135T patent/DK0946175T3/en active
- 1997-10-01 CN CNB971985847A patent/CN1146416C/en not_active Expired - Fee Related
- 1997-10-01 CA CA002268305A patent/CA2268305C/en not_active Expired - Fee Related
- 1997-10-01 EP EP97945135A patent/EP0946175B1/en not_active Expired - Lifetime
- 1997-10-01 PL PL332692A patent/PL190902B1/en not_active IP Right Cessation
- 1997-10-01 RS YUP-163/99A patent/RS49599B/en unknown
- 1997-10-01 AT AT97945135T patent/ATE230597T1/en not_active IP Right Cessation
- 1997-10-01 PT PT97945135T patent/PT946175E/en unknown
- 1997-10-01 EE EEP199900118A patent/EE04043B1/en not_active IP Right Cessation
- 1997-10-01 SK SK384-99A patent/SK284252B6/en unknown
- 1997-10-01 BR BR9711896A patent/BR9711896A/en not_active Application Discontinuation
- 1997-10-01 HU HU0000036A patent/HUP0000036A3/en unknown
- 1997-10-01 WO PCT/SE1997/001651 patent/WO1998016228A1/en not_active Ceased
- 1997-10-01 AU AU46409/97A patent/AU738310B2/en not_active Ceased
- 1997-10-02 ZA ZA9708842A patent/ZA978842B/en unknown
- 1997-10-07 MY MYPI97004697A patent/MY117918A/en unknown
- 1997-10-07 TW TW086114622A patent/TW568784B/en not_active IP Right Cessation
- 1997-10-08 AR ARP970104655A patent/AR008886A1/en unknown
- 1997-11-23 SA SA97180641A patent/SA97180641B1/en unknown
-
1999
- 1999-04-06 NO NO19991619A patent/NO321007B1/en unknown
- 1999-04-08 IS IS5021A patent/IS1930B/en unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU99109596A (en) | APPLICATION OF H +, K + -ATTASE INHIBITOR FOR THE TREATMENT OF NOSE POLYPES | |
| RU2004120781A (en) | ACETYLENE DERIVATIVES WITH ANTAGONISTIC ACTIVITY AGAINST METABOTROPIC GLUTAMATE RECEPTORS (MGIUR5) | |
| ATE361077T1 (en) | INDANYL DERIVATIVES FOR THE TREATMENT OF RESPIRATORY DISEASES | |
| BR0015193A (en) | Compound, pharmaceutical composition, use of a compound, and, method for treating a condition associated with reduced nicotine transmission, for treatment or prophylaxis of psychotic disorders or disorders of intellectual impairment and for treatment or prophylaxis of human diseases or conditions | |
| EA200600892A1 (en) | NEW QUINOLINE DERIVATIVES | |
| RU2005135016A (en) | Quinoline derivatives as phosphodiesterase inhibitors | |
| HUP0300544A2 (en) | Pharmaceutical compositions containing integrin expression inhibitors | |
| RU2005106846A (en) | DERIVATIVES OF BENZOTIAZOLE, CHARACTERIZED BY AN AGONISTIC ACTIVITY TO BETA-2-ADRENORECEPTORS | |
| RU2197966C2 (en) | APPLICATION OF H+, K+-ATPase INHIBITOR FOR TREATING NASAL POLYPS | |
| JPH0656698A (en) | Composition for preventing or curing of esthiomenous gastrointestinal sympton | |
| AR047962A1 (en) | COMBINATION OF BETA-2 ADRENOCEPTOR AGONISTS AND CORTICOSTEROIDS FOR THE TREATMENT OF RESPIRATORY DISEASES | |
| RU2002110328A (en) | Substituted benzimidazole preparation | |
| JP2005511724A (en) | Use of H1 antagonists and safe steroids to treat rhinitis | |
| DK1109560T3 (en) | Compounds useful as AICARFT inhibitors | |
| JPH1036365A5 (en) | ||
| AR023111A1 (en) | USEFUL SULFONAMIDE DERIVATIVES AS ANTAGONISTS OF THE 5-HT7 RECEPTOR, A PROCEDURE FOR THE PREPARATION AND PHARMACEUTICAL COMPOSITION THAT UNDERSTAND | |
| RU2004111787A (en) | RETINOID AGONISTS (1), ALKYL UREA DERIVATIVES | |
| RU2008127260A (en) | Quinazoline derivatives as vanilloid antagonists | |
| ATE214064T1 (en) | INDANE-1-OL DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| KR950016753A (en) | New method of use of benzo [mouse (G)] quinoline | |
| RU2006121328A (en) | New piperidine-substituted indoles or hetero derivatives | |
| DE69831416T2 (en) | CHINOLIN UREA DERIVATIVES FOR THE TREATMENT OF DENTAL SYNDROME AND BRAIN DAMAGE CAUSED BY DENTAL SYNDROME | |
| RU2005126459A (en) | DIAZEPANE DERIVATIVES USED AS LFA INHIBITORS | |
| JP2005511544A5 (en) | ||
| RU93058393A (en) | ETHANOLAMINE DERIVATIVES THAT DISTRIBUTE SYMPATHOMOMETIC AND ANTIPOLAKIURIAL ACTIVITY, METHOD OF THEIR PRODUCTION, PHARMACEUTICAL COMPOSITION, METHOD OF TREATMENT |