RU2517693C2 - Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов - Google Patents
Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов Download PDFInfo
- Publication number
- RU2517693C2 RU2517693C2 RU2009138600/04A RU2009138600A RU2517693C2 RU 2517693 C2 RU2517693 C2 RU 2517693C2 RU 2009138600/04 A RU2009138600/04 A RU 2009138600/04A RU 2009138600 A RU2009138600 A RU 2009138600A RU 2517693 C2 RU2517693 C2 RU 2517693C2
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- RU
- Russia
- Prior art keywords
- diazabicyclo
- ylcarbonyl
- nonane
- octane
- compounds
- Prior art date
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- RKMADNHOLDGKEG-UHFFFAOYSA-N Cc([o]c(C(N1CC(CNC2)C2C1)=O)c1)c1Br Chemical compound Cc([o]c(C(N1CC(CNC2)C2C1)=O)c1)c1Br RKMADNHOLDGKEG-UHFFFAOYSA-N 0.000 description 1
- YRXYAPGARVKIAY-UHFFFAOYSA-N Cc([o]cc1)c1C(N1CC(CNC2)C2C1)=O Chemical compound Cc([o]cc1)c1C(N1CC(CNC2)C2C1)=O YRXYAPGARVKIAY-UHFFFAOYSA-N 0.000 description 1
- PSZUWGCXBWLIEH-UHFFFAOYSA-N Cc1c[o]c(C(N2CC(C3)CNCC3C2)=O)c1 Chemical compound Cc1c[o]c(C(N2CC(C3)CNCC3C2)=O)c1 PSZUWGCXBWLIEH-UHFFFAOYSA-N 0.000 description 1
- ZBKNVHICMHEOLA-UHFFFAOYSA-N Cc1cc(F)c(C(N2CC(CNC3)C3C2)=O)[o]1 Chemical compound Cc1cc(F)c(C(N2CC(CNC3)C3C2)=O)[o]1 ZBKNVHICMHEOLA-UHFFFAOYSA-N 0.000 description 1
- FUTCURITYYGPTL-UHFFFAOYSA-N N#Cc1c(C(N2CC(C3)CNCC3C2)=O)[o]cc1 Chemical compound N#Cc1c(C(N2CC(C3)CNCC3C2)=O)[o]cc1 FUTCURITYYGPTL-UHFFFAOYSA-N 0.000 description 1
- 0 NC(N1CC(CNC2)*C2C1)=O Chemical compound NC(N1CC(CNC2)*C2C1)=O 0.000 description 1
- YRJXIUNIRVSCPU-UHFFFAOYSA-N O=C(c([o]1)ccc1F)N1CC(CNC2)C2C1 Chemical compound O=C(c([o]1)ccc1F)N1CC(CNC2)C2C1 YRJXIUNIRVSCPU-UHFFFAOYSA-N 0.000 description 1
- WYTGRFGLIURWGC-UHFFFAOYSA-N O=C(c([o]cc1)c1Cl)N1CC(C2)CNCC2C1 Chemical compound O=C(c([o]cc1)c1Cl)N1CC(C2)CNCC2C1 WYTGRFGLIURWGC-UHFFFAOYSA-N 0.000 description 1
- VQARKUIJPANZHP-UHFFFAOYSA-N O=C(c1cc(-c2cc(F)cc(F)c2)c[o]1)N1CC(CNC2)C2C1 Chemical compound O=C(c1cc(-c2cc(F)cc(F)c2)c[o]1)N1CC(CNC2)C2C1 VQARKUIJPANZHP-UHFFFAOYSA-N 0.000 description 1
- YLTFIHQASWBABS-UHFFFAOYSA-N O=C(c1cc(Br)c[o]1)N1CC(C2)CNCC2C1 Chemical compound O=C(c1cc(Br)c[o]1)N1CC(C2)CNCC2C1 YLTFIHQASWBABS-UHFFFAOYSA-N 0.000 description 1
- ZJOMXSOGGLLQHD-UHFFFAOYSA-N O=C(c1cc(Br)n[o]1)N1CC(C2)CNCC2C1 Chemical compound O=C(c1cc(Br)n[o]1)N1CC(C2)CNCC2C1 ZJOMXSOGGLLQHD-UHFFFAOYSA-N 0.000 description 1
- PVKAPLHLUKVNLF-UHFFFAOYSA-N O=C(c1cc(C(F)(F)F)c[o]1)N1CC(CNC2)C2C1 Chemical compound O=C(c1cc(C(F)(F)F)c[o]1)N1CC(CNC2)C2C1 PVKAPLHLUKVNLF-UHFFFAOYSA-N 0.000 description 1
- DFVICVZMQQSUPU-UHFFFAOYSA-N O=C(c1ccn[o]1)N1CC(CNC2)C2C1 Chemical compound O=C(c1ccn[o]1)N1CC(CNC2)C2C1 DFVICVZMQQSUPU-UHFFFAOYSA-N 0.000 description 1
- TXWHMYDLPZCWIE-UHFFFAOYSA-N O=C(c1n[o]cc1)N1CC(CNC2)C2C1 Chemical compound O=C(c1n[o]cc1)N1CC(CNC2)C2C1 TXWHMYDLPZCWIE-UHFFFAOYSA-N 0.000 description 1
- OZGDPNGSOUHUSS-UHFFFAOYSA-N [O-][N+](c1ccc(C(N2CC(CNC3)C3C2)=O)[o]1)=O Chemical compound [O-][N+](c1ccc(C(N2CC(CNC3)C3C2)=O)[o]1)=O OZGDPNGSOUHUSS-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
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- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Vascular Medicine (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85607906P | 2006-11-02 | 2006-11-02 | |
| US60/856,079 | 2006-11-02 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2009120674/04A Division RU2448969C2 (ru) | 2006-11-02 | 2007-11-01 | Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов и фармацевтическая композиция и способы лечения с их использованием |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2009138600A RU2009138600A (ru) | 2011-04-27 |
| RU2517693C2 true RU2517693C2 (ru) | 2014-05-27 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2009138600/04A RU2517693C2 (ru) | 2006-11-02 | 2007-11-01 | Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов |
| RU2009120674/04A RU2448969C2 (ru) | 2006-11-02 | 2007-11-01 | Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов и фармацевтическая композиция и способы лечения с их использованием |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2009120674/04A RU2448969C2 (ru) | 2006-11-02 | 2007-11-01 | Амиды диазабициклоалканов, селективные в отношении ацетилхолинового подтипа никотиновых рецепторов и фармацевтическая композиция и способы лечения с их использованием |
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Cited By (15)
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| RU2707751C1 (ru) * | 2017-03-20 | 2019-11-29 | Форма Терапьютикс, Инк. | Пирролопирроловые композиции в качестве активаторов пируваткиназы (pkr) |
| US10640472B2 (en) | 2015-09-04 | 2020-05-05 | Hoffman-La Roche Inc. | Phenoxymethyl derivatives |
| US10647719B2 (en) | 2015-09-24 | 2020-05-12 | Hoffmann-La Roche Inc. | Bicyclic compounds as dual ATX/CA inhibitors |
| US10675274B2 (en) | 2018-09-19 | 2020-06-09 | Forma Therapeutics, Inc. | Activating pyruvate kinase R |
| RU2725138C2 (ru) * | 2015-09-24 | 2020-06-30 | Ф. Хоффманн-Ля Рош Аг | Новые бициклические соединения в качестве двойных ингибиторов аутотаксина (atx)/карбоангидразы (ca) |
| US10787459B2 (en) | 2015-09-24 | 2020-09-29 | Hoffmann-La Roche Inc. | Bicyclic compounds as ATX inhibitors |
| US10800786B2 (en) | 2015-09-24 | 2020-10-13 | Hoffman-La Roche Inc. | Bicyclic compounds as ATX inhibitors |
| US10849881B2 (en) | 2013-11-26 | 2020-12-01 | Hoffmann-La Roche Inc. | Octahydro-cyclobuta[1,2-c;3,4-c′]dipyrrol-2-yl |
| US10882857B2 (en) | 2017-03-16 | 2021-01-05 | Hoffmann-La Roche Inc. | Bicyclic compounds as ATX inhibitors |
| US10913745B2 (en) | 2013-03-12 | 2021-02-09 | Hoffmann-La Roche Inc. | Octahydro-pyrrolo[3,4-c]-pyrrole derivatives and analogs thereof as autotaxin inhibitors |
| US11001588B2 (en) | 2018-09-19 | 2021-05-11 | Forma Therapeutics, Inc. | Activating pyruvate kinase R and mutants thereof |
| US11059794B2 (en) | 2017-03-16 | 2021-07-13 | Hoffmann-La Roche Inc. | Heterocyclic compounds useful as dual ATX/CA inhibitors |
| US11098048B2 (en) | 2014-03-26 | 2021-08-24 | Hoffmann-La Roche Inc. | Bicyclic compounds as autotaxin (ATX) and lysophosphatidic acid (LPA) production inhibitors |
| US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
| US12161634B2 (en) | 2019-09-19 | 2024-12-10 | Novo Nordisk Health Care Ag | Pyruvate kinase R (PKR) activating compositions |
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| TWI404532B (zh) * | 2006-11-02 | 2013-08-11 | Targacept Inc | 菸鹼乙醯膽鹼受體亞型選擇性之二氮雜雙環烷類醯胺 |
| RU2010140613A (ru) * | 2008-03-05 | 2012-04-10 | Таргасепт, Инк. (Us) | Амиды диазабициклоалканов, селективные в отношении подтипа никотиновых ацетилхолиновых рецепторов |
| WO2009113950A1 (en) * | 2008-03-10 | 2009-09-17 | Astrazeneca Ab | Therapeutic combinations of (a) an antipsychotic and (b) an alpha-4/beta-2 (a4b2)-neuronal nicotinic receptor agonist |
| EP2280959B1 (en) | 2008-06-05 | 2012-04-04 | Glaxo Group Limited | 4-amino-indazoles |
| EP2280705B1 (en) | 2008-06-05 | 2014-10-08 | Glaxo Group Limited | Novel compounds |
| JP5508400B2 (ja) | 2008-06-05 | 2014-05-28 | グラクソ グループ リミテッド | Pi3キナーゼの阻害剤としてのベンズピラゾール誘導体 |
| CN102143963A (zh) * | 2008-09-05 | 2011-08-03 | 塔加西普特公司 | 二氮杂双环辛烷的酰胺及其应用 |
| WO2010028011A1 (en) * | 2008-09-05 | 2010-03-11 | Targacept, Inc. | Amides of diazabicyclononanes and uses thereof |
| WO2010080757A2 (en) | 2009-01-07 | 2010-07-15 | Astrazeneca Ab | Combinations with an alpha-4beta-2 nicotinic agonist |
| US8524751B2 (en) | 2009-03-09 | 2013-09-03 | GlaxoSmithKline Intellecutual Property Development | 4-oxadiazol-2-YL-indazoles as inhibitors of P13 kinases |
| PE20120321A1 (es) | 2009-04-30 | 2012-04-19 | Glaxo Group Ltd | Indazoles sustituidos con oxazol como inhibidores de pi3-quinasa |
| RU2417082C2 (ru) * | 2009-07-14 | 2011-04-27 | Учреждение Российской Академии Наук Институт Физиологически Активных Веществ Ран (Ифав Ран) | Средство для восстановления утраченной памяти в норме и патологии у пациентов всех возрастных групп на основе n, n'-замещенных 3, 7-диазабицикло[3.3.1]нонанов, фармацевтическая композиция на его основе и способ ее применения |
| ES2601905T3 (es) | 2009-11-18 | 2017-02-16 | Suven Life Sciences Limited | Compuestos bicíclicos como ligandos del receptor nicotínico de la acetilcolina alfa4beta2 |
| KR101410903B1 (ko) | 2009-12-29 | 2014-06-23 | 수벤 라이프 사이언시스 리미티드 | α4β2 신경 니코틴성 아세틸콜린 수용체 리간드 |
| GB201018124D0 (en) | 2010-10-27 | 2010-12-08 | Glaxo Group Ltd | Polymorphs and salts |
| ES2986830T3 (es) | 2014-10-20 | 2024-11-12 | Oyster Point Pharma Inc | Métodos de tratamiento de afecciones oculares |
| JP7090551B2 (ja) | 2016-04-07 | 2022-06-24 | オイスター ポイント ファーマ インコーポレイテッド | 眼状態の治療方法 |
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