NZ525091A - Piperazinyl susbtituted piperidinyl compounds as antagonists of tachykinins - Google Patents
Piperazinyl susbtituted piperidinyl compounds as antagonists of tachykininsInfo
- Publication number
- NZ525091A NZ525091A NZ525091A NZ52509101A NZ525091A NZ 525091 A NZ525091 A NZ 525091A NZ 525091 A NZ525091 A NZ 525091A NZ 52509101 A NZ52509101 A NZ 52509101A NZ 525091 A NZ525091 A NZ 525091A
- Authority
- NZ
- New Zealand
- Prior art keywords
- phenyl
- methyl
- bis
- fluoro
- trifluoromethyl
- Prior art date
Links
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
- A61K31/495—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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
-
- 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
- C07D401/02—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 two hetero rings
- C07D401/04—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 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
- A61P1/08—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
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- 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
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0025354.2A GB0025354D0 (en) | 2000-10-17 | 2000-10-17 | Chemical compounds |
| PCT/GB2001/004580 WO2002032867A1 (en) | 2000-10-17 | 2001-10-12 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ525091A true NZ525091A (en) | 2005-04-29 |
Family
ID=9901397
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ525091A NZ525091A (en) | 2000-10-17 | 2001-10-12 | Piperazinyl susbtituted piperidinyl compounds as antagonists of tachykinins |
Country Status (29)
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9923748D0 (en) | 1999-10-07 | 1999-12-08 | Glaxo Group Ltd | Chemical compounds |
| USRE39921E1 (en) | 1999-10-07 | 2007-11-13 | Smithkline Beecham Corporation | Chemical compounds |
| GB0025354D0 (en) * | 2000-10-17 | 2000-11-29 | Glaxo Group Ltd | Chemical compounds |
| GB0108595D0 (en) | 2001-04-05 | 2001-05-23 | Glaxo Group Ltd | Chemical compounds |
| GB0119797D0 (en) | 2001-08-14 | 2001-10-03 | Glaxo Group Ltd | Chemical compounds |
| GB0203022D0 (en) * | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| GB0203020D0 (en) | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| EP1472222A1 (en) | 2002-02-08 | 2004-11-03 | Glaxo Group Limited | Piperidylcarboxamide derivatives and their use in the treatment of tachykinim-mediated diseases |
| TWI283241B (en) * | 2002-05-29 | 2007-07-01 | Tanabe Seiyaku Co | Novel piperidine compound |
| JP4079727B2 (ja) | 2002-09-06 | 2008-04-23 | セントラル硝子株式会社 | 光学活性１−（フルオロ、トリフルオロメチルまたはトリフルオロメトキシ置換フェニル）アルキルアミンｎ−モノアルキル誘導体とその製造方法 |
| AU2003298369B2 (en) | 2002-12-23 | 2009-08-27 | Janssen Pharmaceutica N.V. | Substituted 4-(4-piperidin-4-yl-piperazin-1-yl)-azepane derivatives and their use as neurokinin antagonists |
| EP1581517B1 (en) * | 2002-12-23 | 2007-02-21 | Janssen Pharmaceutica N.V. | Substituted 1-piperidin-4-yl-4-azetidin-3-yl-piperazine derivatives and their use as neurokinin antagonists |
| JO2696B1 (en) * | 2002-12-23 | 2013-03-03 | شركة جانسين فارماسوتيكا ان. في | Derivatives of 1-piperdine-4-yl-4-biprolidine-3-yl-piperazine substituted and used as quinine antagonists |
| JO2485B1 (en) * | 2002-12-23 | 2009-01-20 | شركة جانسين فارماسوتيكا ان. في | 1-Piperidine-3-Yl-4-Piperidine-4-Yl-Piperazine derivatives substituted and used as quinine antagonists |
| EP1594574A2 (en) * | 2003-01-27 | 2005-11-16 | Glaxo Group Limited | Nk1 receptor antagonists for the treatment of functional dyspepsia |
| FR2853648B1 (fr) * | 2003-04-11 | 2006-08-18 | Fournier Lab Sa | Nouveaux derives de benzenesulfonamides et leur utilisation en therapeutique |
| WO2004089901A2 (en) * | 2003-03-31 | 2004-10-21 | Janssen Pharmaceutica N.V. | Phospholipase c inhibitors for use in treating inflammatory disorders |
| US20040235855A1 (en) * | 2003-03-31 | 2004-11-25 | Bharat Lagu | Phospholipase C inhibitors for use in treating inflammatory disorders |
| US7262197B2 (en) | 2003-03-31 | 2007-08-28 | Janssen Pharmaceutica, N.V | Phospholipase C inhibitors for use in treating inflammatory disorders |
| GB0308968D0 (en) * | 2003-04-17 | 2003-05-28 | Glaxo Group Ltd | Medicaments |
| ATE395062T1 (de) * | 2003-06-10 | 2008-05-15 | Janssen Pharmaceutica Nv | Kombination von opioiden und einem piperazin- derivat für die behandlung von schmerzen |
| BRPI0410630A (pt) * | 2003-06-19 | 2006-06-13 | Pfizer Prod Inc | antagonista de nk1 |
| JO2525B1 (en) * | 2004-04-08 | 2010-03-17 | شركة جانسين فارماسوتيكا ان. في | Derived 4-alkyl-and-4-canoelperidine derivatives and their use as anti-neroquin |
| WO2006062110A1 (ja) * | 2004-12-06 | 2006-06-15 | Banyu Pharmaceutical Co., Ltd. | ピペラジン誘導体 |
| GB0426942D0 (en) * | 2004-12-08 | 2005-01-12 | Glaxo Group Ltd | Medicament |
| EP1858896B1 (en) | 2005-03-08 | 2010-08-18 | Janssen Pharmaceutica NV | Diaza-spiro-[4.4]-nonane derivatives as neurokinin (nk1) antagonists |
| GB0514705D0 (en) * | 2005-07-18 | 2005-08-24 | Glaxo Group Ltd | Chemical compounds |
| GB0514707D0 (en) * | 2005-07-18 | 2005-08-24 | Glaxo Group Ltd | Chemical compounds |
| GB0514704D0 (en) * | 2005-07-18 | 2005-08-24 | Glaxo Group Ltd | Chemical compounds |
| JP4904945B2 (ja) | 2006-06-30 | 2012-03-28 | セントラル硝子株式会社 | 光学活性１−（フルオロ、トリフルオロメチルまたはトリフルオロメトキシ置換フェニル）アルキルアミンｎ−モノアルキル誘導体の製造方法 |
| AU2008208920A1 (en) | 2007-01-24 | 2008-07-31 | Glaxo Group Limited | Pharmaceutical compositions comprising 3, 5-diamin0-6- (2, 3-dichl0phenyl) -l, 2, 4-triazine or R(-) -2, 4-diamino-5- (2, 3-dichlorophenyl) -6-fluoromethyl pyrimidine and an NK1 |
| WO2009035652A1 (en) | 2007-09-13 | 2009-03-19 | Concert Pharmaceuticals, Inc. | Synthesis of deuterated catechols and benzo[d][1,3] dioxoles and derivatives thereof |
| GB0812849D0 (en) * | 2008-07-14 | 2008-08-20 | Glaxo Wellcome Mfg Pte Ltd | Novel compounds |
| US9782397B2 (en) | 2011-07-04 | 2017-10-10 | Irbm Science Park S.P.A. | Treatment of corneal neovascularization |
| MX2014010012A (es) | 2012-02-22 | 2014-09-12 | Leo Pharma As | Nuevos compuestos antagonistas del receptor de neurocinina 1. |
| WO2015024203A1 (en) * | 2013-08-20 | 2015-02-26 | Leo Pharma A/S | Novel neurokinin 1 receptor antagonist compounds ii |
| EA201992414A1 (ru) | 2017-04-10 | 2020-03-16 | Чейс Терапьютикс Корпорейшн | Комбинация nk1-антагониста и способ лечения синуклеинопатий |
| IL271464B1 (en) | 2017-06-30 | 2024-04-01 | Chase Therapeutics Corp | NK-1 antagonist preparations and methods for use in the treatment of depression |
| CN111116514B (zh) * | 2020-01-10 | 2024-03-19 | 广州科锐特生物科技有限公司 | 一种1-环丙甲酰基哌嗪盐酸盐的制备方法 |
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| US4219554A (en) | 1974-05-09 | 1980-08-26 | Toyama Chemical Company, Limited | Novel penicillins and cephalosporins and process for producing same |
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| GB0025354D0 (en) * | 2000-10-17 | 2000-11-29 | Glaxo Group Ltd | Chemical compounds |
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-
2000
- 2000-10-17 GB GBGB0025354.2A patent/GB0025354D0/en not_active Ceased
-
2001
- 2001-10-12 SI SI200130206T patent/SI1326832T1/xx unknown
- 2001-10-12 ES ES08151841T patent/ES2346108T3/es not_active Expired - Lifetime
- 2001-10-12 EP EP01976453A patent/EP1326832B1/en not_active Expired - Lifetime
- 2001-10-12 AT AT04077714T patent/ATE355271T1/de active
- 2001-10-12 MX MXPA03003536A patent/MXPA03003536A/es active IP Right Grant
- 2001-10-12 ES ES01976453T patent/ES2227287T3/es not_active Expired - Lifetime
- 2001-10-12 PT PT04077714T patent/PT1524266E/pt unknown
- 2001-10-12 EP EP06122021A patent/EP1752449A1/en not_active Withdrawn
- 2001-10-12 CZ CZ20031082A patent/CZ299824B6/cs not_active IP Right Cessation
- 2001-10-12 PL PL361180A patent/PL203071B1/pl unknown
- 2001-10-12 DE DE60127002T patent/DE60127002T2/de not_active Expired - Lifetime
- 2001-10-12 DE DE60142197T patent/DE60142197D1/de not_active Expired - Lifetime
- 2001-10-12 AT AT01976453T patent/ATE278669T1/de active
- 2001-10-12 AU AU9572301A patent/AU9572301A/xx active Pending
- 2001-10-12 KR KR1020037005286A patent/KR100847414B1/ko not_active IP Right Cessation
- 2001-10-12 IL IL15516501A patent/IL155165A0/xx active IP Right Grant
- 2001-10-12 EP EP08151841A patent/EP1921064B1/en not_active Expired - Lifetime
- 2001-10-12 JP JP2002536051A patent/JP3940359B2/ja not_active Expired - Fee Related
- 2001-10-12 US US10/398,264 patent/US7119092B2/en not_active Expired - Fee Related
- 2001-10-12 DK DK04077714T patent/DK1524266T3/da active
- 2001-10-12 SI SI200130727T patent/SI1524266T1/sl unknown
- 2001-10-12 AT AT08151841T patent/ATE468324T1/de not_active IP Right Cessation
- 2001-10-12 ES ES04077714T patent/ES2282794T3/es not_active Expired - Lifetime
- 2001-10-12 PT PT01976453T patent/PT1326832E/pt unknown
- 2001-10-12 NZ NZ525091A patent/NZ525091A/en not_active IP Right Cessation
- 2001-10-12 CN CNB018175325A patent/CN1231468C/zh not_active Expired - Fee Related
- 2001-10-12 AU AU2001295723A patent/AU2001295723B2/en not_active Ceased
- 2001-10-12 EP EP04077714A patent/EP1524266B1/en not_active Expired - Lifetime
- 2001-10-12 DE DE60106287T patent/DE60106287T2/de not_active Expired - Lifetime
- 2001-10-12 HU HU0301459A patent/HU228146B1/hu not_active IP Right Cessation
- 2001-10-12 DK DK01976453T patent/DK1326832T3/da active
- 2001-10-12 CA CA002425876A patent/CA2425876C/en not_active Expired - Fee Related
- 2001-10-12 WO PCT/GB2001/004580 patent/WO2002032867A1/en active Application Filing
- 2001-10-12 BR BR0114637-8A patent/BR0114637A/pt not_active Application Discontinuation
- 2001-10-15 TW TW090125397A patent/TWI299730B/zh not_active IP Right Cessation
- 2001-10-15 MY MYPI20014779A patent/MY124957A/en unknown
- 2001-10-15 AR ARP010104833A patent/AR034268A1/es not_active Application Discontinuation
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2003
- 2003-03-31 IL IL155165A patent/IL155165A/en not_active IP Right Cessation
- 2003-04-07 NO NO20031561A patent/NO324468B1/no not_active IP Right Cessation
- 2003-04-10 ZA ZA200302801A patent/ZA200302801B/en unknown
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2004
- 2004-01-13 HK HK04100241A patent/HK1058788A1/xx not_active IP Right Cessation
- 2004-11-22 US US10/994,605 patent/US7060702B2/en not_active Expired - Lifetime
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2005
- 2005-05-23 HK HK05104289A patent/HK1075889A1/xx not_active IP Right Cessation
- 2005-08-24 AU AU2005204234A patent/AU2005204234B2/en not_active Ceased
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2006
- 2006-02-21 US US11/358,631 patent/US7294630B2/en not_active Expired - Fee Related
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2007
- 2007-05-21 CY CY20071100689T patent/CY1107634T1/el unknown
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2008
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2009
- 2009-04-09 AU AU2009201407A patent/AU2009201407B2/en not_active Ceased
- 2009-12-03 US US12/630,037 patent/US20100081667A1/en not_active Abandoned
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Free format text: PATENT RENEWED FOR 7 YEARS UNTIL 12 OCT 2021 BY THOMSON REUTERS Effective date: 20140912 |
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| EXPY | Patent expired |