EA200701978A1 - Способ получения опиоидных модуляторов - Google Patents
Способ получения опиоидных модуляторовInfo
- Publication number
- EA200701978A1 EA200701978A1 EA200701978A EA200701978A EA200701978A1 EA 200701978 A1 EA200701978 A1 EA 200701978A1 EA 200701978 A EA200701978 A EA 200701978A EA 200701978 A EA200701978 A EA 200701978A EA 200701978 A1 EA200701978 A1 EA 200701978A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- obtaining
- opioid modulators
- modulators
- opioid
- agonists
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 208000018522 Gastrointestinal disease Diseases 0.000 abstract 1
- 208000027520 Somatoform disease Diseases 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 208000027753 pain disease Diseases 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
-
- 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
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
-
- 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
- A61P1/10—Laxatives
-
- 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
- A61P1/12—Antidiarrhoeals
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/11—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/14—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being saturated and containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/26—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (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)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Optical Modulation, Optical Deflection, Nonlinear Optics, Optical Demodulation, Optical Logic Elements (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Настоящее изобретение относится к новым способам получения опиоидных модуляторов (агонистов и антагонистов) и промежуточных продуктов их синтеза. Опиоидные модуляторы применяют при лечении и профилактике как боли, так и желудочно-кишечных нарушений.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US66178405P | 2005-03-14 | 2005-03-14 | |
PCT/US2006/008450 WO2006099060A2 (en) | 2005-03-14 | 2006-03-06 | Process for the preparation of opioid modulators |
Publications (2)
Publication Number | Publication Date |
---|---|
EA200701978A1 true EA200701978A1 (ru) | 2008-04-28 |
EA015512B1 EA015512B1 (ru) | 2011-08-30 |
Family
ID=36646011
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200701978A EA015512B1 (ru) | 2005-03-14 | 2006-03-06 | Способ получения опиоидных модуляторов |
EA200701979A EA014366B1 (ru) | 2005-03-14 | 2006-03-06 | Способ получения опиоидных модуляторов |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200701979A EA014366B1 (ru) | 2005-03-14 | 2006-03-06 | Способ получения опиоидных модуляторов |
Country Status (30)
Country | Link |
---|---|
US (4) | US7629488B2 (ru) |
EP (2) | EP1858850B1 (ru) |
JP (3) | JP5384933B2 (ru) |
KR (2) | KR20070112255A (ru) |
CN (2) | CN101175725B (ru) |
AR (2) | AR053170A1 (ru) |
AU (2) | AU2006223394B2 (ru) |
BR (2) | BRPI0607792A2 (ru) |
CA (2) | CA2601674A1 (ru) |
CR (1) | CR9438A (ru) |
CY (1) | CY1116104T1 (ru) |
DK (1) | DK1858850T3 (ru) |
EA (2) | EA015512B1 (ru) |
ES (1) | ES2535048T3 (ru) |
HR (1) | HRP20150417T1 (ru) |
HU (1) | HUE024912T2 (ru) |
IL (3) | IL185974A0 (ru) |
ME (1) | ME02110B (ru) |
MX (2) | MX2007011412A (ru) |
MY (1) | MY145333A (ru) |
NI (1) | NI200700237A (ru) |
NO (2) | NO340604B1 (ru) |
NZ (1) | NZ590570A (ru) |
PL (1) | PL1858850T3 (ru) |
PT (1) | PT1858850E (ru) |
RS (1) | RS53873B1 (ru) |
SI (1) | SI1858850T1 (ru) |
TW (3) | TWI500595B (ru) |
WO (2) | WO2006099060A2 (ru) |
ZA (2) | ZA200708809B (ru) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7041681B2 (en) * | 2002-04-29 | 2006-05-09 | Janssen Pharmaceutica N.V. | Compounds as opioid receptor modulators |
ME02221B (me) * | 2004-03-15 | 2016-02-20 | Janssen Pharmaceutica Nv | Postupak za proizvodnju intermedijara jedinjenja korisnih kao modulatori opioidnih receptora |
KR20070112255A (ko) * | 2005-03-14 | 2007-11-22 | 얀센 파마슈티카 엔.브이. | 오피오이드 조절체의 제조 방법 |
HUE028538T2 (en) * | 2007-07-09 | 2016-12-28 | Forest Tosara Ltd | New Crystals and Procedure 5 - ({[2-Amino-3- (4-carbamoyl-2,6-dimethylphenyl) propionyl] - [1- (4-phenyl-1H-imidazol-2-yl) ethyl] ] -amino} -methyl) -2-methoxybenzoic acid |
TWI468375B (zh) * | 2008-10-27 | 2015-01-11 | Janssen Pharmaceutica Nv | 製備經保護之l-丙胺酸衍生物之方法 |
IS2977B (is) | 2015-02-23 | 2017-07-15 | Actavis Group Ptc Ehf. | Aðferð til framleiðslu á milliefnum sem eru nytsamleg við nýsmíði á elúxadólíni |
WO2017043626A1 (ja) * | 2015-09-11 | 2017-03-16 | 株式会社カネカ | 光学活性4-カルバモイル-2,6-ジメチルフェニルアラニン誘導体の製造法 |
CN105777584B (zh) * | 2016-03-28 | 2018-01-02 | 成都伊诺达博医药科技有限公司 | 丙氨酸衍生物的制备方法 |
CN105693554B (zh) * | 2016-04-06 | 2017-08-08 | 成都伊诺达博医药科技有限公司 | 丙氨酸衍生物的制备方法 |
US10822308B2 (en) * | 2016-06-23 | 2020-11-03 | Sun Pharmaceutical Industries Limited | Processes for the preparation of eluxadoline |
WO2018047131A1 (en) * | 2016-09-09 | 2018-03-15 | Sun Pharmaceutical Industries Limited | Amorphous eluxadoline |
US10479769B2 (en) | 2016-09-20 | 2019-11-19 | Sun Pharmaceutical Industries Limited | Processes for the preparation of eluxadoline |
CN106866463B (zh) * | 2017-01-24 | 2018-08-28 | 富乐马鸿凯(大连)医药有限公司 | 艾沙度林中间体的制备方法 |
WO2018138274A1 (en) | 2017-01-27 | 2018-08-02 | Quimica Sintetica, S. A. | Eluxadoline crystalline forms and processes for their preparation |
WO2018138272A1 (en) | 2017-01-27 | 2018-08-02 | Quimica Sintetica, S. A. | Eluxadoline crystalline form and process for the preparation thereof |
CN111377832A (zh) * | 2018-12-27 | 2020-07-07 | 江苏联昇化学有限公司 | 一种伊卢多啉中间体制备的新方法 |
US20230312542A1 (en) | 2020-03-31 | 2023-10-05 | Mitsubishi Tanabe Pharma Corporation | Hydroxypyrrolidine derivative and medicinal application thereof |
CN114163348A (zh) * | 2020-11-27 | 2022-03-11 | 成都泰蓉生物科技有限公司 | 一种氨酰基取代的l-苯丙氨酸的合成方法 |
CN114507252B (zh) * | 2022-02-21 | 2023-10-27 | 广西大学 | 新型芳基硅烷化合物的合成方法 |
Family Cites Families (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5430129A (en) * | 1977-08-09 | 1979-03-06 | Mitsubishi Gas Chem Co Inc | Preparation of toluic acid amide |
JPS5528959A (en) * | 1978-08-22 | 1980-02-29 | Sumitomo Chem Co Ltd | Production of amide derivative |
FR2584401B1 (fr) * | 1985-07-04 | 1987-11-20 | Ile De France | Nouveau benzamide, son procede de preparation et son application dans le domaine therapeutique |
JP2727243B2 (ja) * | 1988-12-27 | 1998-03-11 | 日本化薬株式会社 | 2−アシルアミノ桂皮酸誘導体の製造法 |
US5684175A (en) * | 1993-02-05 | 1997-11-04 | Napro Biotherapeutics, Inc. | C-2' hydroxyl-benzyl protected, N-carbamate protected (2R, 3S)- 3-phenylisoserine and production process therefor |
JP3493206B2 (ja) * | 1993-03-19 | 2004-02-03 | ダイセル化学工業株式会社 | 光学活性β−アミノ酸類の製法 |
JP3486922B2 (ja) * | 1993-08-23 | 2004-01-13 | 住友化学工業株式会社 | 酸アミドの製造法 |
MX9705710A (es) * | 1995-01-27 | 1997-10-31 | Novo Nordisk As | Compuestos con propiedades de liberacion de la hormona del crecimiento. |
JPH09295939A (ja) * | 1995-09-26 | 1997-11-18 | Takeda Chem Ind Ltd | リン酸アミド誘導体、その製造法および用途 |
OA11901A (en) * | 1998-03-11 | 2006-04-10 | Searle & Co | Halogenated amidino amino acid derivatives useful as nitric oxide synthase inhibitors. |
DE60006032T2 (de) * | 1999-05-28 | 2004-06-17 | Pfizer Products Inc., Groton | 3-(3-Hydroxyphenyl)-3-amino-propionamidderivate |
CA2422617C (en) * | 2000-10-30 | 2011-07-12 | Janssen Pharmaceutica N.V. | Tripeptidyl peptidase inhibitors |
US7041681B2 (en) * | 2002-04-29 | 2006-05-09 | Janssen Pharmaceutica N.V. | Compounds as opioid receptor modulators |
ME02221B (me) * | 2004-03-15 | 2016-02-20 | Janssen Pharmaceutica Nv | Postupak za proizvodnju intermedijara jedinjenja korisnih kao modulatori opioidnih receptora |
KR20070112255A (ko) * | 2005-03-14 | 2007-11-22 | 얀센 파마슈티카 엔.브이. | 오피오이드 조절체의 제조 방법 |
-
2006
- 2006-03-06 KR KR1020077023282A patent/KR20070112255A/ko not_active Application Discontinuation
- 2006-03-06 CA CA002601674A patent/CA2601674A1/en not_active Abandoned
- 2006-03-06 EP EP06737611.1A patent/EP1858850B1/en active Active
- 2006-03-06 EA EA200701978A patent/EA015512B1/ru unknown
- 2006-03-06 JP JP2008501919A patent/JP5384933B2/ja not_active Expired - Fee Related
- 2006-03-06 PL PL06737611T patent/PL1858850T3/pl unknown
- 2006-03-06 MX MX2007011412A patent/MX2007011412A/es active IP Right Grant
- 2006-03-06 WO PCT/US2006/008450 patent/WO2006099060A2/en active Application Filing
- 2006-03-06 MX MX2007011409A patent/MX2007011409A/es unknown
- 2006-03-06 DK DK06737611.1T patent/DK1858850T3/en active
- 2006-03-06 ME MEP-2015-31A patent/ME02110B/me unknown
- 2006-03-06 PT PT67376111T patent/PT1858850E/pt unknown
- 2006-03-06 WO PCT/US2006/008240 patent/WO2006098982A1/en active Application Filing
- 2006-03-06 US US11/368,564 patent/US7629488B2/en active Active
- 2006-03-06 EA EA200701979A patent/EA014366B1/ru not_active IP Right Cessation
- 2006-03-06 CN CN2006800163712A patent/CN101175725B/zh not_active Expired - Fee Related
- 2006-03-06 CA CA2601481A patent/CA2601481C/en active Active
- 2006-03-06 CN CNA2006800166320A patent/CN101175726A/zh active Pending
- 2006-03-06 RS RS20150121A patent/RS53873B1/en unknown
- 2006-03-06 JP JP2008501912A patent/JP2008533141A/ja not_active Withdrawn
- 2006-03-06 HU HUE06737611A patent/HUE024912T2/en unknown
- 2006-03-06 BR BRPI0607792-7A patent/BRPI0607792A2/pt not_active IP Right Cessation
- 2006-03-06 NZ NZ590570A patent/NZ590570A/en not_active IP Right Cessation
- 2006-03-06 EP EP06737413A patent/EP1863764A1/en not_active Withdrawn
- 2006-03-06 KR KR1020077022664A patent/KR101280929B1/ko active IP Right Grant
- 2006-03-06 BR BRPI0607793-5A patent/BRPI0607793A2/pt not_active Application Discontinuation
- 2006-03-06 SI SI200631907T patent/SI1858850T1/sl unknown
- 2006-03-06 AU AU2006223394A patent/AU2006223394B2/en not_active Ceased
- 2006-03-06 ES ES06737611.1T patent/ES2535048T3/es active Active
- 2006-03-06 AU AU2006223482A patent/AU2006223482A1/en not_active Abandoned
- 2006-03-06 US US11/368,588 patent/US20060211861A1/en not_active Abandoned
- 2006-03-14 AR ARP060100974A patent/AR053170A1/es not_active Application Discontinuation
- 2006-03-14 TW TW101129655A patent/TWI500595B/zh not_active IP Right Cessation
- 2006-03-14 TW TW095108513A patent/TW200700388A/zh unknown
- 2006-03-14 TW TW095108512A patent/TWI414518B/zh not_active IP Right Cessation
- 2006-03-14 AR ARP060100973A patent/AR054745A1/es active IP Right Grant
- 2006-03-14 MY MYPI20061110A patent/MY145333A/en unknown
-
2007
- 2007-09-13 NI NI200700237A patent/NI200700237A/es unknown
- 2007-09-16 IL IL185974A patent/IL185974A0/en unknown
- 2007-09-16 IL IL185972A patent/IL185972A/en active IP Right Grant
- 2007-10-12 ZA ZA200708809A patent/ZA200708809B/xx unknown
- 2007-10-12 ZA ZA200708810A patent/ZA200708810B/xx unknown
- 2007-10-12 CR CR9438A patent/CR9438A/es not_active Application Discontinuation
- 2007-10-15 NO NO20075269A patent/NO340604B1/no not_active IP Right Cessation
- 2007-10-15 NO NO20075268A patent/NO20075268L/no not_active Application Discontinuation
-
2009
- 2009-10-16 US US12/580,641 patent/US20100036132A1/en not_active Abandoned
- 2009-11-25 US US12/625,973 patent/US20100152460A1/en not_active Abandoned
-
2010
- 2010-11-18 IL IL209402A patent/IL209402A/en active IP Right Grant
-
2013
- 2013-07-16 JP JP2013147688A patent/JP5802242B2/ja not_active Expired - Fee Related
-
2015
- 2015-02-19 CY CY20151100172T patent/CY1116104T1/el unknown
- 2015-04-14 HR HRP20150417TT patent/HRP20150417T1/hr unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA200701978A1 (ru) | Способ получения опиоидных модуляторов | |
CY1112238T1 (el) | Αναστολεις μιτωτικης κινεσινης και μεθοδοι χρησης αυτων | |
CY1111927T1 (el) | Νεες ενωσεις ως διαμορφωτες υποδοχεα οπιοειδων | |
MA32975B1 (fr) | Antagonistes de c5ar | |
TW200612905A (en) | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders | |
MY147767A (en) | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders | |
MX2009008104A (es) | Hepcidina, antagonistas de hepcidina y metodos de uso. | |
EA201101475A1 (ru) | Способы применения рецептора gpr119 для идентификации соединений, которые можно использовать для увеличения костной массы субъекта | |
NO20064325L (no) | Heteroarylaminopyrazolderivativer nyttige for behandling av diabetes | |
ATE538650T1 (de) | Cannabinoid-rezeptor-antagonisten / inverse agonisten zur behandlung von übergewicht | |
NO20055741L (no) | Nye kjemiske forbindelser | |
ATE469897T1 (de) | Indazolcarbonsäureamidverbindungen | |
MY147217A (en) | Antibody molecules having specificity for human il-06 | |
EA201170356A1 (ru) | Полиморфные и аморфные формы лакозамида и аморфные композиции | |
NO20055563L (no) | Midler for behandlingen av lavere abdominale lidelser | |
NO20076186L (no) | Mitotiske kinesininhibitorer og fremgangsmater for anvendelse derav | |
ATE466841T1 (de) | 1-phenethylpiperidinderivate und ihre verwendung als opioidrezeptor-liganden | |
EA201190313A1 (ru) | Замещенные пиперидины | |
ATE450256T1 (de) | Verwendung von zusammensetzungen enthaltend kappa-opioidrezeptor-antagonisten zur behandlung von dissoziativen störungen | |
EA200801211A1 (ru) | Производные 9-хлор-15-простагландина, способ их получения и использования в лекарственных препаратах | |
EA200701688A1 (ru) | Замещённые пирролы, содержащие их композиции, способ получения и применение | |
EA201001872A1 (ru) | Новые способы получения производных циклопропиламида | |
EA200970122A1 (ru) | Фармацевтически приемлемые солевые и полиморфные формы малеата флюпиртина | |
DE602004019541D1 (de) | Cycloalkyläbü kondensierte indole | |
EA200700191A1 (ru) | Композиции, содержащие никорандил, способ получения и применение |