JP4685861B2 - ドーパミンアゴニストとしての3−ピペリジニルイソクロマン−5−オール - Google Patents
ドーパミンアゴニストとしての3−ピペリジニルイソクロマン−5−オール Download PDFInfo
- Publication number
- JP4685861B2 JP4685861B2 JP2007510941A JP2007510941A JP4685861B2 JP 4685861 B2 JP4685861 B2 JP 4685861B2 JP 2007510941 A JP2007510941 A JP 2007510941A JP 2007510941 A JP2007510941 A JP 2007510941A JP 4685861 B2 JP4685861 B2 JP 4685861B2
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- isochroman
- piperidin
- aminomethyl
- hydroxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- YTPSNVCCUHTPNY-PMACEKPBSA-N CC(C)CCN(CC1)CCC1[C@H]1O[C@@H](CN)c2ccc(C)c(O)c2C1 Chemical compound CC(C)CCN(CC1)CCC1[C@H]1O[C@@H](CN)c2ccc(C)c(O)c2C1 YTPSNVCCUHTPNY-PMACEKPBSA-N 0.000 description 1
- VJOHTYSVUHBOJW-GSIQFNFPSA-N CC(CCN(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)NC(c(ccc(Cl)c1)c1Cl)=O Chemical compound CC(CCN(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)NC(c(ccc(Cl)c1)c1Cl)=O VJOHTYSVUHBOJW-GSIQFNFPSA-N 0.000 description 1
- ZAYXGXUNAAGLML-MQTLACETSA-N CC(CCN(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)NC(c1ccc(C(F)(F)F)cc1)=O Chemical compound CC(CCN(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)NC(c1ccc(C(F)(F)F)cc1)=O ZAYXGXUNAAGLML-MQTLACETSA-N 0.000 description 1
- CTOKPZPVKRHVEP-ROUUACIJSA-N CCCC(N(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)=O Chemical compound CCCC(N(CC1)CCC1[C@H](C1)O[C@@H](CN)c2c1c(O)c(C)cc2)=O CTOKPZPVKRHVEP-ROUUACIJSA-N 0.000 description 1
- IJYVHWNEVCDUIM-NSOVKSMOSA-N CCCN(CCC)C[C@@H](c1ccc(C)c(O)c1C1)O[C@@H]1C1CCN(Cc2ccccc2)CC1 Chemical compound CCCN(CCC)C[C@@H](c1ccc(C)c(O)c1C1)O[C@@H]1C1CCN(Cc2ccccc2)CC1 IJYVHWNEVCDUIM-NSOVKSMOSA-N 0.000 description 1
- PVKYISGSUZAXQS-FDJRJZQMSA-N CCN(C)/C=C(/c1ccc(C)c(O)c1C1)\O[C@@H]1C1CCN(Cc2ccc(C(F)(F)F)cc2)CC1 Chemical compound CCN(C)/C=C(/c1ccc(C)c(O)c1C1)\O[C@@H]1C1CCN(Cc2ccc(C(F)(F)F)cc2)CC1 PVKYISGSUZAXQS-FDJRJZQMSA-N 0.000 description 1
- ZQHIZUHWKITBPZ-ZEQRLZLVSA-N CCNC[C@@H](c1ccc(C)c(O)c1C1)O[C@@H]1C1CCN(Cc2ccccc2)CC1 Chemical compound CCNC[C@@H](c1ccc(C)c(O)c1C1)O[C@@H]1C1CCN(Cc2ccccc2)CC1 ZQHIZUHWKITBPZ-ZEQRLZLVSA-N 0.000 description 1
- AKNRIMCEXFATKY-BKUYFWCQSA-N Cc(c(O)c1CC(C(CC2)CCN2C(Oc2c(C(F)(F)F)cccc2)=O)O2)ccc1/C2=C/N Chemical compound Cc(c(O)c1CC(C(CC2)CCN2C(Oc2c(C(F)(F)F)cccc2)=O)O2)ccc1/C2=C/N AKNRIMCEXFATKY-BKUYFWCQSA-N 0.000 description 1
- MBWROEPUMJSIIK-IRXDYDNUSA-N Cc(ccc1c2C[C@@H](C3CCN(C)CC3)O[C@H]1CNC)c2O Chemical compound Cc(ccc1c2C[C@@H](C3CCN(C)CC3)O[C@H]1CNC)c2O MBWROEPUMJSIIK-IRXDYDNUSA-N 0.000 description 1
- BAHPHSJGRDWLDW-GOTSBHOMSA-N Cc(ccc1c2C[C@@H](C3CCN(Cc4cc(OC)ccc4)CC3)O[C@H]1CN)c2O Chemical compound Cc(ccc1c2C[C@@H](C3CCN(Cc4cc(OC)ccc4)CC3)O[C@H]1CN)c2O BAHPHSJGRDWLDW-GOTSBHOMSA-N 0.000 description 1
- BVIGEHJQWMSXJX-VXKWHMMOSA-N Cc(ccc1c2C[C@@H](C3CCN(Cc4cccc(C(F)(F)F)c4)CC3)O[C@H]1CN)c2O Chemical compound Cc(ccc1c2C[C@@H](C3CCN(Cc4cccc(C(F)(F)F)c4)CC3)O[C@H]1CN)c2O BVIGEHJQWMSXJX-VXKWHMMOSA-N 0.000 description 1
- 0 Cc1ccc([C@@](C*)O[C@@](C2)C3CCNCC3)c2c1OC Chemical compound Cc1ccc([C@@](C*)O[C@@](C2)C3CCNCC3)c2c1OC 0.000 description 1
- MOYUDENLEICFRW-IRXDYDNUSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(N(C)C)=O)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(N(C)C)=O)c2c1O MOYUDENLEICFRW-IRXDYDNUSA-N 0.000 description 1
- OVWTWTOZFMYVSD-OALUTQOASA-N Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(N3CCOCC3)=O)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(N3CCOCC3)=O)c2c1O OVWTWTOZFMYVSD-OALUTQOASA-N 0.000 description 1
- SDEIHBIEJRKIES-DQEYMECFSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(Oc3cc(cccc4)c4cc3)=O)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(Oc3cc(cccc4)c4cc3)=O)c2c1O SDEIHBIEJRKIES-DQEYMECFSA-N 0.000 description 1
- POAZCUQXIWLLCB-SFTDATJTSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(c(cc3)ccc3Br)=O)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C(CC3)CCN3C(c(cc3)ccc3Br)=O)c2c1O POAZCUQXIWLLCB-SFTDATJTSA-N 0.000 description 1
- ISPLQTPMNBBWRZ-VMPREFPWSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(CC(c4ccccc4)c4ccccc4)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(CC(c4ccccc4)c4ccccc4)CC3)c2c1O ISPLQTPMNBBWRZ-VMPREFPWSA-N 0.000 description 1
- LNLHKRLPAWEOJX-VXKWHMMOSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(CC4CCCCC4)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(CC4CCCCC4)CC3)c2c1O LNLHKRLPAWEOJX-VXKWHMMOSA-N 0.000 description 1
- GHRLRZIGFWTIRF-VXKWHMMOSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(c(Cl)c4)ccc4Cl)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(c(Cl)c4)ccc4Cl)CC3)c2c1O GHRLRZIGFWTIRF-VXKWHMMOSA-N 0.000 description 1
- CJRBLZJWKCATMO-VXKWHMMOSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(cc4)cc(C(F)(F)F)c4F)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(cc4)cc(C(F)(F)F)c4F)CC3)c2c1O CJRBLZJWKCATMO-VXKWHMMOSA-N 0.000 description 1
- WFMVDHNJDJZDSV-VXKWHMMOSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(cccc4)c4Cl)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc(cccc4)c4Cl)CC3)c2c1O WFMVDHNJDJZDSV-VXKWHMMOSA-N 0.000 description 1
- WZOIZYRTPCTDBG-ZEQRLZLVSA-N Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc4c[nH]c5ccccc45)CC3)c2c1O Chemical compound Cc1ccc([C@H](CN)O[C@@H](C2)C3CCN(Cc4c[nH]c5ccccc45)CC3)c2c1O WZOIZYRTPCTDBG-ZEQRLZLVSA-N 0.000 description 1
- QKOIEBXTHJUZTJ-GOTSBHOMSA-N Cc1ccc([C@H](CNC)O[C@@H](C2)C3CCN(Cc(cc4)cc(F)c4F)CC3)c2c1O Chemical compound Cc1ccc([C@H](CNC)O[C@@H](C2)C3CCN(Cc(cc4)cc(F)c4F)CC3)c2c1O QKOIEBXTHJUZTJ-GOTSBHOMSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- 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
-
- 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
- A61P25/24—Antidepressants
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Otolaryngology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US56655704P | 2004-04-29 | 2004-04-29 | |
| PCT/US2005/014487 WO2005111025A1 (en) | 2004-04-29 | 2005-04-27 | 3-piperidinylisochroman-5-ols as dopamine agonists |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2007535548A JP2007535548A (ja) | 2007-12-06 |
| JP2007535548A5 JP2007535548A5 (enExample) | 2008-03-27 |
| JP4685861B2 true JP4685861B2 (ja) | 2011-05-18 |
Family
ID=34967397
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007510941A Expired - Fee Related JP4685861B2 (ja) | 2004-04-29 | 2005-04-27 | ドーパミンアゴニストとしての3−ピペリジニルイソクロマン−5−オール |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7919508B2 (enExample) |
| EP (1) | EP1749001B1 (enExample) |
| JP (1) | JP4685861B2 (enExample) |
| AR (1) | AR050245A1 (enExample) |
| AT (1) | ATE459618T1 (enExample) |
| DE (1) | DE602005019719D1 (enExample) |
| DK (1) | DK1749001T3 (enExample) |
| ES (1) | ES2342083T3 (enExample) |
| PT (1) | PT1749001E (enExample) |
| TW (1) | TW200607802A (enExample) |
| WO (1) | WO2005111025A1 (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MX370104B (es) * | 2013-10-22 | 2019-12-02 | Chiesi Farm Spa | Proceso para la preparacion de un inhibidor de fosfodiesterasa (pde4). |
| CA2946990A1 (en) * | 2014-04-28 | 2015-11-05 | Pfizer Inc. | Heterocyclic compounds and their use as dopamine d1 ligands |
| HRP20201469T1 (hr) * | 2014-10-08 | 2020-12-11 | UCB Biopharma SRL | Derivati tetrahidroizokinolina |
| JP7187437B2 (ja) * | 2016-07-29 | 2022-12-12 | サノビオン ファーマシューティカルズ インク | 化合物および組成物ならびにそれらの使用 |
| EP3490607A4 (en) * | 2016-07-29 | 2020-04-08 | Sunovion Pharmaceuticals Inc. | COMPOUNDS AND COMPOSITIONS, AND USES THEREOF |
| JP7471818B2 (ja) | 2016-08-18 | 2024-04-22 | ヴィダック ファーマ リミテッド | ピペラジン誘導体、医薬組成物、及びその使用方法 |
| SG11202000669VA (en) | 2017-08-02 | 2020-02-27 | Sunovion Pharmaceuticals Inc | Isochroman compounds and uses thereof |
| CN111196781B (zh) * | 2018-11-16 | 2023-07-28 | 湖南中南制药有限责任公司 | 一种改进的制备五氟利多的方法 |
| KR20210139376A (ko) | 2019-03-14 | 2021-11-22 | 선오비온 파마슈티컬스 인코포레이티드 | 이소크로마닐 화합물의 염, 및 이의 결정성 형태, 제조방법, 치료 용도 및 약제학적 조성물 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4994486A (en) * | 1989-05-31 | 1991-02-19 | Abbott Laboratories | Dopaminergic compounds |
| JPH04505619A (ja) * | 1989-05-31 | 1992-10-01 | アボツト・ラボラトリーズ | ドーパミン作用物質 |
| JP2001512436A (ja) * | 1997-02-07 | 2001-08-21 | アベンティス・ファーマスーティカルズ・インコーポレイテッド | 抗精神病剤として有用な(4−ピペリジニル)−1h−2−ベンゾピラン誘導体 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6004982A (en) * | 1997-09-15 | 1999-12-21 | Hoechst Marion Roussel, Inc. | 4-piperidinyl) H-2-benzopyran derivatives useful as antipsychotic agents |
-
2005
- 2005-04-27 ES ES05740005T patent/ES2342083T3/es not_active Expired - Lifetime
- 2005-04-27 DK DK05740005.3T patent/DK1749001T3/da active
- 2005-04-27 JP JP2007510941A patent/JP4685861B2/ja not_active Expired - Fee Related
- 2005-04-27 AT AT05740005T patent/ATE459618T1/de active
- 2005-04-27 EP EP05740005A patent/EP1749001B1/en not_active Expired - Lifetime
- 2005-04-27 WO PCT/US2005/014487 patent/WO2005111025A1/en not_active Ceased
- 2005-04-27 PT PT05740005T patent/PT1749001E/pt unknown
- 2005-04-27 DE DE602005019719T patent/DE602005019719D1/de not_active Expired - Lifetime
- 2005-04-28 AR ARP050101668A patent/AR050245A1/es not_active Application Discontinuation
- 2005-04-29 TW TW094113776A patent/TW200607802A/zh unknown
-
2006
- 2006-10-24 US US11/552,169 patent/US7919508B2/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4994486A (en) * | 1989-05-31 | 1991-02-19 | Abbott Laboratories | Dopaminergic compounds |
| JPH04505619A (ja) * | 1989-05-31 | 1992-10-01 | アボツト・ラボラトリーズ | ドーパミン作用物質 |
| JP2001512436A (ja) * | 1997-02-07 | 2001-08-21 | アベンティス・ファーマスーティカルズ・インコーポレイテッド | 抗精神病剤として有用な(4−ピペリジニル)−1h−2−ベンゾピラン誘導体 |
Also Published As
| Publication number | Publication date |
|---|---|
| DK1749001T3 (da) | 2010-06-28 |
| JP2007535548A (ja) | 2007-12-06 |
| US7919508B2 (en) | 2011-04-05 |
| PT1749001E (pt) | 2010-05-31 |
| AR050245A1 (es) | 2006-10-11 |
| WO2005111025A1 (en) | 2005-11-24 |
| DE602005019719D1 (de) | 2010-04-15 |
| TW200607802A (en) | 2006-03-01 |
| ES2342083T3 (es) | 2010-07-01 |
| ATE459618T1 (de) | 2010-03-15 |
| EP1749001B1 (en) | 2010-03-03 |
| US20070099955A1 (en) | 2007-05-03 |
| EP1749001A1 (en) | 2007-02-07 |
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