EA200870404A1 - Производные азабицикло[3.1.0.]гексила в качестве модуляторов рецепторов допамина d3 - Google Patents
Производные азабицикло[3.1.0.]гексила в качестве модуляторов рецепторов допамина d3Info
- Publication number
- EA200870404A1 EA200870404A1 EA200870404A EA200870404A EA200870404A1 EA 200870404 A1 EA200870404 A1 EA 200870404A1 EA 200870404 A EA200870404 A EA 200870404A EA 200870404 A EA200870404 A EA 200870404A EA 200870404 A1 EA200870404 A1 EA 200870404A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- group
- halogen
- cyano
- alkoxy
- phenyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- 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
-
- 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
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- 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)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Addiction (AREA)
- Psychology (AREA)
- Gynecology & Obstetrics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Настоящее изобретение относится к новым соединениям формулы (I)'или их солям, где G выбирают из группы, состоящей из фенила, 5- или 6-членной моноциклической гетероарильной группы или 8-11-членной гетероарильной бициклической группы; А представляет собой группу p1или группу p2где р представляет собой целое число в интервале от 0 до 5; Rпредставляет собой галоген, гидрокси, циано, Cалкил, галогенCалкил, Cалкокси, галоген Cалкокси, Cалканоил и SF; или соответствует группе R; и если р представляет собой целое число в интервале от 2 до 5, каждые из Rмогут быть одинаковыми или различными; Rпредставляет собой водород или Cалкил; n представляет собой 3, 4, 5 или 6; Rпредставляет собой фрагмент, выбранный из группы, состоящей из изоксазолила, -CH-N-пирролила, 1,1-диоксидо-2-изотиазолидинила, тиенила, тиазолила, пиридила, 2-пирролидинонила, и такие Rгруппы необязательно замещены одним или двумя заместителями, выбранными из галогена, циано, Cалкила, галоген Cалкила, Cалкокси, Cалканоила; Rвыбирают из группы, состоящей из водорода, галогена, гидрокси, циано, Cалкила, Cциклоалкила, галогенCалкила, Cалкокси, галогенCалкокси, Cалканоила и NR'R"; или Rпредставляет собой фенильную группу, 5-14-членную гетероциклическую группу; причем любая из указанных фенильных или гетероциклических групп необязательно замещена 1, 2, 3 или 4 заместителями, выбранными из группы, состоящей из галогена, циано, Cалкила, галогенCалкила, Cалкокси, Cалканоила, галогенCалкокси и SF; Rвыбирают из группы, состоящей из водорода, галогена, гидрокси, циано, Cалкила, Cциклоалкила, галогенCалкила, Cалкокси, галогенCалкокси, Cалканоила и NR'R"; или Rпредставляет собой фенильную группу, 5-14-членную гетероциклическую группу; и любая из указанных фенильных или гетероциклических групп
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0607892A GB0607892D0 (en) | 2006-04-03 | 2006-04-03 | Novel compounds |
GB0700363A GB0700363D0 (en) | 2007-01-09 | 2007-01-09 | Novel compounds |
GB0703404A GB0703404D0 (en) | 2007-02-21 | 2007-02-21 | Novel compounds |
PCT/EP2007/053074 WO2007113232A1 (en) | 2006-04-03 | 2007-03-30 | Azabicyclo [3. 1. 0] hexyl derivatives as modulators of dopamine d3 receptors |
Publications (1)
Publication Number | Publication Date |
---|---|
EA200870404A1 true EA200870404A1 (ru) | 2009-04-28 |
Family
ID=38283980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200870404A EA200870404A1 (ru) | 2006-04-03 | 2007-03-30 | Производные азабицикло[3.1.0.]гексила в качестве модуляторов рецепторов допамина d3 |
Country Status (17)
Country | Link |
---|---|
US (1) | US7727988B2 (ru) |
EP (1) | EP2007750B1 (ru) |
JP (1) | JP5189074B2 (ru) |
KR (1) | KR20080109063A (ru) |
AR (1) | AR060237A1 (ru) |
AU (1) | AU2007233715A1 (ru) |
BR (1) | BRPI0709660A2 (ru) |
CA (1) | CA2648087A1 (ru) |
CR (1) | CR10346A (ru) |
EA (1) | EA200870404A1 (ru) |
ES (1) | ES2434337T3 (ru) |
IL (1) | IL194385A0 (ru) |
MA (1) | MA30355B1 (ru) |
MX (1) | MX2008012875A (ru) |
PE (1) | PE20071152A1 (ru) |
TW (1) | TW200815404A (ru) |
WO (1) | WO2007113232A1 (ru) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PT2060570E (pt) * | 2004-02-23 | 2012-05-07 | Glaxo Group Ltd | Derivados de azabiciclo(3.1.0)-hexano úteis como moduladores dos receptores d3 da dopamina |
GB0507602D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
GB0507601D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
ATE484502T1 (de) * | 2005-06-14 | 2010-10-15 | Glaxo Group Ltd | Neue verbindungen |
GB0512099D0 (en) * | 2005-06-14 | 2005-07-20 | Glaxo Group Ltd | Compounds |
EP1919908B1 (en) * | 2005-08-22 | 2010-11-10 | Glaxo Group Limited | Triazole derivatives as modulators of dopamine d3 receptors |
GB0517175D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
GB0517193D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Novel use |
GB0517191D0 (en) | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
GB0517187D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
US8163927B2 (en) * | 2006-04-03 | 2012-04-24 | Glaxo Group Limited | Azabicyclo [3.1.0] hexane derivatives as modulators of dopamine D3 receptors |
WO2007113260A1 (en) * | 2006-04-03 | 2007-10-11 | Glaxo Group Limited | Azabicyclo [3. 1. o] hexyl derivatives as modulators of dopamine d3 receptors |
GB0719235D0 (en) * | 2007-10-02 | 2007-11-14 | Glaxo Group Ltd | Novel compounds |
CN102803224A (zh) | 2009-06-26 | 2012-11-28 | 万能药生物有限公司 | 新的氮杂双环己烷类化合物 |
JP2013526507A (ja) | 2010-05-12 | 2013-06-24 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 新規ccr2受容体アンタゴニスト、その製造方法及び薬物としてのその使用 |
MX2015007921A (es) * | 2012-12-21 | 2016-03-03 | Zenith Epigenetics Corp | Compuestos heterociclicos novedosos como inhibidores de bromodominio. |
WO2015002754A2 (en) | 2013-06-21 | 2015-01-08 | Zenith Epigenetics Corp. | Novel bicyclic bromodomain inhibitors |
WO2015004534A2 (en) | 2013-06-21 | 2015-01-15 | Zenith Epigenetics Corp. | Novel substituted bicyclic compounds as bromodomain inhibitors |
US9855271B2 (en) | 2013-07-31 | 2018-01-02 | Zenith Epigenetics Ltd. | Quinazolinones as bromodomain inhibitors |
EP3227281A4 (en) | 2014-12-01 | 2018-05-30 | Zenith Epigenetics Ltd. | Substituted pyridinones as bromodomain inhibitors |
CA2966303A1 (en) | 2014-12-01 | 2016-06-09 | Zenith Epigenetics Ltd. | Substituted pyridines as bromodomain inhibitors |
JP2017537946A (ja) | 2014-12-11 | 2017-12-21 | ゼニス・エピジェネティクス・リミテッドZenith Epigenetics Ltd. | ブロモドメイン阻害剤としての置換複素環 |
CA2966450A1 (en) | 2014-12-17 | 2016-06-23 | Olesya KHARENKO | Inhibitors of bromodomains |
WO2019146740A1 (ja) | 2018-01-26 | 2019-08-01 | 塩野義製薬株式会社 | ドーパミンd3受容体拮抗作用を有する環式化合物 |
TWI702954B (zh) | 2018-03-01 | 2020-09-01 | 美商美國禮來大藥廠 | Cd73抑制劑 |
WO2022121914A1 (zh) * | 2020-12-10 | 2022-06-16 | 上海翰森生物医药科技有限公司 | 氧代氮环类衍生物调节剂、其制备方法和应用 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6204284B1 (en) | 1991-12-20 | 2001-03-20 | American Cyanamid Company | Use of 1-(substitutedphenyl)-3-azabicyclo[3.1.0]hexanes for the treatment of chemical dependencies |
DE4338396A1 (de) | 1993-11-10 | 1995-05-11 | Basf Ag | N-Substituierte Azabicycloalkan-Derivate, ihre Herstellung und Verwendung |
DE4425143A1 (de) * | 1994-07-15 | 1996-01-18 | Basf Ag | Substituierte Pyrimidinverbindungen und deren Verwendung |
DE10311065A1 (de) | 2003-03-13 | 2004-09-23 | Abbott Gmbh & Co. Kg | Pyrimidin-2-on-Verbindungen und ihre therapeutische Verwendung |
PT2060570E (pt) * | 2004-02-23 | 2012-05-07 | Glaxo Group Ltd | Derivados de azabiciclo(3.1.0)-hexano úteis como moduladores dos receptores d3 da dopamina |
DE102004027359A1 (de) * | 2004-06-04 | 2005-12-29 | Abbott Gmbh & Co. Kg | Pyridin-2-onverbindungen und deren Verwendung |
DE102004061593A1 (de) * | 2004-12-21 | 2006-06-22 | Abbott Gmbh & Co. Kg | Substituierte N-heterocyclische Verbindungen und ihre therapeutische Verwendung |
GB0507602D0 (en) * | 2005-04-14 | 2005-05-18 | Glaxo Group Ltd | Compounds |
GB0512099D0 (en) | 2005-06-14 | 2005-07-20 | Glaxo Group Ltd | Compounds |
GB0517191D0 (en) * | 2005-08-22 | 2005-09-28 | Glaxo Group Ltd | Compounds |
WO2007113260A1 (en) | 2006-04-03 | 2007-10-11 | Glaxo Group Limited | Azabicyclo [3. 1. o] hexyl derivatives as modulators of dopamine d3 receptors |
US8163927B2 (en) | 2006-04-03 | 2012-04-24 | Glaxo Group Limited | Azabicyclo [3.1.0] hexane derivatives as modulators of dopamine D3 receptors |
-
2007
- 2007-03-30 BR BRPI0709660-7A patent/BRPI0709660A2/pt not_active Application Discontinuation
- 2007-03-30 JP JP2009503547A patent/JP5189074B2/ja not_active Expired - Fee Related
- 2007-03-30 EP EP07727546.9A patent/EP2007750B1/en active Active
- 2007-03-30 EA EA200870404A patent/EA200870404A1/ru unknown
- 2007-03-30 MX MX2008012875A patent/MX2008012875A/es unknown
- 2007-03-30 AU AU2007233715A patent/AU2007233715A1/en not_active Abandoned
- 2007-03-30 KR KR1020087026817A patent/KR20080109063A/ko not_active Application Discontinuation
- 2007-03-30 AR ARP070101352A patent/AR060237A1/es unknown
- 2007-03-30 PE PE2007000392A patent/PE20071152A1/es not_active Application Discontinuation
- 2007-03-30 WO PCT/EP2007/053074 patent/WO2007113232A1/en active Application Filing
- 2007-03-30 CA CA002648087A patent/CA2648087A1/en not_active Abandoned
- 2007-03-30 ES ES07727546T patent/ES2434337T3/es active Active
- 2007-03-30 US US11/693,756 patent/US7727988B2/en not_active Expired - Fee Related
- 2007-04-02 TW TW096111521A patent/TW200815404A/zh unknown
-
2008
- 2008-09-25 IL IL194385A patent/IL194385A0/en unknown
- 2008-10-07 CR CR10346A patent/CR10346A/es not_active Application Discontinuation
- 2008-10-23 MA MA31328A patent/MA30355B1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
TW200815404A (en) | 2008-04-01 |
MA30355B1 (fr) | 2009-04-01 |
AU2007233715A1 (en) | 2007-10-11 |
WO2007113232A1 (en) | 2007-10-11 |
JP2009532424A (ja) | 2009-09-10 |
JP5189074B2 (ja) | 2013-04-24 |
CA2648087A1 (en) | 2007-10-11 |
KR20080109063A (ko) | 2008-12-16 |
MX2008012875A (es) | 2008-10-13 |
EP2007750B1 (en) | 2013-08-21 |
IL194385A0 (en) | 2009-08-03 |
AR060237A1 (es) | 2008-06-04 |
US7727988B2 (en) | 2010-06-01 |
CR10346A (es) | 2008-10-29 |
EP2007750A1 (en) | 2008-12-31 |
US20070249642A1 (en) | 2007-10-25 |
ES2434337T3 (es) | 2013-12-16 |
BRPI0709660A2 (pt) | 2011-07-19 |
PE20071152A1 (es) | 2007-12-16 |
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