FR15C0049I2 - Dérivés de 4-phenylpyridine et leur utilisation comme antagonistes du recepteur NK-1 - Google Patents
Dérivés de 4-phenylpyridine et leur utilisation comme antagonistes du recepteur NK-1Info
- Publication number
- FR15C0049I2 FR15C0049I2 FR15C0049C FR15C0049C FR15C0049I2 FR 15C0049 I2 FR15C0049 I2 FR 15C0049I2 FR 15C0049 C FR15C0049 C FR 15C0049C FR 15C0049 C FR15C0049 C FR 15C0049C FR 15C0049 I2 FR15C0049 I2 FR 15C0049I2
- Authority
- FR
- France
- Prior art keywords
- receptor antagonists
- phenylpyridine derivatives
- phenylpyridine
- derivatives
- antagonists
- 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.)
- Active
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
- C07D213/30—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
-
- 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
- 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
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
- A61P25/04—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
- 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
- A61P25/24—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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
-
- 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
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/38—Radicals substituted by singly-bound nitrogen atoms having only hydrogen or hydrocarbon radicals attached to the substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/40—Acylated substituent nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
-
- 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
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Rheumatology (AREA)
- Addiction (AREA)
- Ophthalmology & Optometry (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Immunology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99103504 | 1999-02-24 | ||
EP99123689 | 1999-11-29 | ||
EP00102260A EP1035115B1 (fr) | 1999-02-24 | 2000-02-15 | Dérivés de 4-phenylpyridine et leur utilisation comme antagonistes du recepteur NK-1 |
Publications (2)
Publication Number | Publication Date |
---|---|
FR15C0049I1 FR15C0049I1 (fr) | 2015-08-28 |
FR15C0049I2 true FR15C0049I2 (fr) | 2016-02-12 |
Family
ID=26152908
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR0002170A Expired - Fee Related FR2790473B1 (fr) | 1999-02-24 | 2000-02-22 | Nouveaux composes et medicaments les contenant |
FR15C0049C Active FR15C0049I2 (fr) | 1999-02-24 | 2015-07-08 | Dérivés de 4-phenylpyridine et leur utilisation comme antagonistes du recepteur NK-1 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR0002170A Expired - Fee Related FR2790473B1 (fr) | 1999-02-24 | 2000-02-22 | Nouveaux composes et medicaments les contenant |
Country Status (55)
Families Citing this family (110)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU3979099A (en) * | 1998-05-11 | 1999-11-29 | Philadelphia Health & Education Corporation | (mct-1), a human oncogene |
WO2000050398A2 (fr) | 1999-02-24 | 2000-08-31 | F. Hoffmann-La Roche Ag | Derives de pyridinyl et de phenyle |
US6291465B1 (en) * | 1999-03-09 | 2001-09-18 | Hoffmann-La Roche Inc. | Biphenyl derivatives |
US6303790B1 (en) * | 1999-11-29 | 2001-10-16 | Hoffman-La Roche Inc. | Process for the preparation of pyridine derivatives |
EP1103545B1 (fr) * | 1999-11-29 | 2003-11-05 | F. Hoffmann-La Roche Ag | 2-(3,5-Bis-trifluorométhyl-phényl)-N-méthyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-isobutyramide |
AUPQ514600A0 (en) | 2000-01-18 | 2000-02-10 | James Cook University | Brain injury treatment |
JP3938651B2 (ja) * | 2000-04-13 | 2007-06-27 | セントラル硝子株式会社 | 光学活性α−メチル−ビス−3、5−(トリフルオロメチル)ベンジルアミンの製造方法 |
KR100501608B1 (ko) * | 2000-07-14 | 2005-07-18 | 에프. 호프만-라 로슈 아게 | 4-페닐-피리딘 유도체의 nk1 수용체의 길항성선구약물로서의 n-산화물 |
TWI287003B (en) | 2000-07-24 | 2007-09-21 | Hoffmann La Roche | 4-phenyl-pyridine derivatives |
TWI259180B (en) * | 2000-08-08 | 2006-08-01 | Hoffmann La Roche | 4-Phenyl-pyridine derivatives |
DK1349541T3 (da) * | 2000-12-14 | 2007-01-08 | Hoffmann La Roche | Selvemulgerende lipidmatrix (SELM) |
US6531597B2 (en) * | 2001-02-13 | 2003-03-11 | Hoffmann-La Roche Inc. | Process for preparation of 2-phenyl acetic acid derivatives |
US7112593B2 (en) | 2001-03-27 | 2006-09-26 | Eisai Co., Ltd. | N-aryl-substituted cyclic amine derivative and medicine containing the same as active ingredient |
DK1385577T3 (da) * | 2001-04-23 | 2006-08-21 | Hoffmann La Roche | Anvendelse af NK-1-receptorantagonister mod godartet prostatahyperplasi |
ES2632544T3 (es) * | 2001-06-07 | 2017-09-14 | Analgesic Neuropharmaceuticals, Llc | Tratamiento de dolor neuropático con el antagonista del receptor de N-metil-D-aspartato (NMDA) dextrometorfano |
US20030083345A1 (en) * | 2001-07-10 | 2003-05-01 | Torsten Hoffmann | Method of treatment and/or prevention of brain, spinal or nerve injury |
US6849624B2 (en) * | 2001-07-31 | 2005-02-01 | Hoffmann-La Roche Inc. | Aromatic and heteroaromatic substituted amides |
WO2003022254A1 (fr) * | 2001-09-10 | 2003-03-20 | F. Hoffmann-La Roche Ag | Formulations thixotropes huileuses |
US7390813B1 (en) | 2001-12-21 | 2008-06-24 | Xenon Pharmaceuticals Inc. | Pyridylpiperazines and aminonicotinamides and their use as therapeutic agents |
BR0314126A (pt) | 2002-09-20 | 2005-06-28 | Pfizer Prod Inc | Ligandos de amida acìclica e sulfonamida para o receptor de estrogênio |
US7244748B2 (en) * | 2002-12-06 | 2007-07-17 | Purdue Research Foundation | Pyridines for treating injured mammalian nerve tissue |
US8729107B2 (en) * | 2002-12-06 | 2014-05-20 | Purdue Research Foundation | Pyridines for treating injured mammalian nerve tissue |
EP1592428B1 (fr) | 2003-01-31 | 2007-07-11 | F. Hoffmann-La Roche AG | Nouvelle modification cristalline de 2-(3,5-bis-trifluoromethyl-phenyl)-n- 6-(1,1-dioxo-1lamda-6-thiomorpholin-4-yl)-4(4-fluoro-2-methyl-phenyl)-pyridine-3-yl|-n-methyl-isobutyramide |
RU2347777C2 (ru) * | 2003-07-03 | 2009-02-27 | Ф.Хоффманн-Ля Рош Аг | Двойные агонисты nk1/nk3 для лечения шизофрении |
US7288658B2 (en) * | 2003-07-15 | 2007-10-30 | Hoffmann-La Roche Inc. | Process for preparation of pyridine derivatives |
EP3042895A1 (fr) | 2003-07-30 | 2016-07-13 | Xenon Pharmaceuticals Inc. | Dérivés de la pipérazine et leur utilisation en tant qu'agents thérapeutiques |
CA2572645C (fr) * | 2004-07-06 | 2011-01-18 | F. Hoffmann-La Roche Ag | Procede pour la preparation de derives pyridines carboxamide utilises comme intermediaires dans la synthese d'antagonistes de recepteurs nk-1 |
WO2006014168A1 (fr) * | 2004-07-06 | 2006-02-09 | Xenon Pharmaceuticals Inc. | Dérivés de nicotinamide et utilisation de ceux-ci comme agents thérapeutiques |
KR100881240B1 (ko) * | 2004-07-06 | 2009-02-05 | 에프. 호프만-라 로슈 아게 | Nk-1 수용체 길항제의 합성에 있어서 중간체로서사용되는 카르복스아미드 피리딘 유도체의 제조 방법 |
WO2006013205A1 (fr) * | 2004-08-04 | 2006-02-09 | Solvay Pharmaceuticals B.V. | Antagonistes des récepteurs de la neurokinine-1 pour le traitement des états sensibles à une élévation de la testostérone |
US20060030556A1 (en) * | 2004-08-04 | 2006-02-09 | Solvay Pharmaceuticals B.V. | Neurokinin-1 receptor antagonists for the treatment of conditions responsive to testosterone elevation, including testosterone deficiency |
US20060030600A1 (en) * | 2004-08-06 | 2006-02-09 | Patrick Schnider | Dual NK1/NK3 receptor antagonists for the treatment of schizophrenia |
CN101083982A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 用于治疗硬脂酰CoA去饱和酶介导的疾病的杂环衍生物 |
AU2005286728A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase |
WO2006034440A2 (fr) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Derives heterocycliques et leur utilisation en tant qu'agents therapeutiques |
US7829712B2 (en) | 2004-09-20 | 2010-11-09 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-CoA-desaturase |
TW200626139A (en) | 2004-09-20 | 2006-08-01 | Xenon Pharmaceuticals Inc | Heterocyclic derivatives and their use as therapeutic agents |
WO2006034441A1 (fr) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Derives heterocycliques et leur utilisation en tant qu'inhibiteurs de la stearoyl-coa desaturase |
CN101084211A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为治疗剂的用途 |
US7569725B2 (en) * | 2004-10-21 | 2009-08-04 | Britsol-Myers Squibb Company | Anthranilic acid derivatives as inhibitors of 17β-hydroxysteroid dehydrogenase 3 |
WO2006060174A1 (fr) * | 2004-11-15 | 2006-06-08 | Honeywell International Inc. | Mousses polymeres a base d'isocyanate avec des materiaux a nano-echelle |
DE602006008900D1 (de) * | 2005-02-22 | 2009-10-15 | Hoffmann La Roche | Nk1-antagonisten |
AU2006216566A1 (en) * | 2005-02-24 | 2006-08-31 | Janssen Pharmaceutica N.V. | Novel pyridine derivatives as potassium ion channel openers |
EP2281556A1 (fr) | 2005-02-25 | 2011-02-09 | F. Hoffmann-La Roche AG | Comprimés avec une meilleure dispersibilité de substance des médicaments |
DK1863767T3 (da) * | 2005-03-23 | 2009-05-04 | Hoffmann La Roche | Metabolitter til NK-I-antagonister til emesis |
EP2029138A1 (fr) | 2005-06-03 | 2009-03-04 | Xenon Pharmaceuticals Inc. | Derives aminothiazole utilises en tant qu'inhibiteurs de la stearoyle-coa desaturase humaine |
KR20080053297A (ko) * | 2005-08-11 | 2008-06-12 | 버텍스 파마슈티칼스 인코포레이티드 | 낭포성 섬유종 트랜스막 전도도 조정자의 조절자 |
JO2722B1 (en) | 2005-09-09 | 2013-09-15 | سميث كلاين بيتشام كوربوريشن | New vehicles |
ES2335922T3 (es) * | 2005-09-23 | 2010-04-06 | F.Hoffmann-La Roche Ag | Nueva formulacion de dosificacion. |
EP1945632B1 (fr) | 2005-11-08 | 2013-09-18 | Vertex Pharmaceuticals Incorporated | Modulateurs hétérocycliques de transporteurs à cassette liant l' atp |
US7671221B2 (en) * | 2005-12-28 | 2010-03-02 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
US7872022B2 (en) * | 2006-04-03 | 2011-01-18 | Hoffmann-La Roche Inc. | Serotonin transporter (SERT) inhibitors for the treatment of depression and anxiety |
US7645789B2 (en) | 2006-04-07 | 2010-01-12 | Vertex Pharmaceuticals Incorporated | Indole derivatives as CFTR modulators |
SI3091011T1 (en) | 2006-04-07 | 2018-06-29 | Vertex Pharmaceuticals Incorporated | Modulators of ATP conveyor belt conveyors |
US7754739B2 (en) * | 2007-05-09 | 2010-07-13 | Vertex Pharmaceuticals Incorporated | Modulators of CFTR |
CA2686838C (fr) | 2007-05-09 | 2017-03-14 | Vertex Pharmaceuticals Incorporated | Modulateurs de cftr |
RS60229B1 (sr) | 2007-12-07 | 2020-06-30 | Vertex Pharma | Čvrsti oblici 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-il) ciklopropankarboksamido)-3-metilpiridin-2-il) benzojeve kiseline |
ES2625957T3 (es) * | 2007-12-07 | 2017-07-21 | Vertex Pharmaceuticals Incorporated | Procedimiento para producir ácidos cicloalquilcarboxiamido-piridinabenzoicos |
EP2249650A4 (fr) * | 2008-02-19 | 2012-01-11 | Glaxosmithkline Llc | Anilinopyridines utilisées comme inhibiteurs de fak |
CA2716109C (fr) | 2008-02-28 | 2016-07-19 | Vertex Pharmaceuticals Incorporated | Derives heteroaryles convenant comme modulateurs du cftr |
GB0808747D0 (en) | 2008-05-14 | 2008-06-18 | Glaxo Wellcome Mfg Pte Ltd | Novel compounds |
GB0814340D0 (en) * | 2008-08-05 | 2008-09-10 | Smithkline Beecham Corp | Anhydrous crystol form fo a pyridine derivative |
US8796269B2 (en) * | 2009-08-27 | 2014-08-05 | Nerre Therapeutics Limited | Crystalline 2-(3,5-Bis(trifluoromethyl)phenyl)-N-(4-(4-fluoro-2-methylphenyl)-6-((7S,9aS)-7-(hydroxymethyl)hexahydropyrazino[2,1-c][1,4]oxazin-8(1H)-yl)pyridin-3-yl)-N,2-dimethyl-propanamide of the formula (I), their use in therapy, and process for the preparation of the same |
EP2722045B1 (fr) | 2009-11-18 | 2016-07-06 | Helsinn Healthcare SA | Compositions pour traiter les nausées et vomissements à médiation centrale |
PT2361090E (pt) | 2009-11-18 | 2014-09-03 | Helsinn Healthcare Sa | Composições para o tratamento centrado de náusea e vómito mediado |
TW201143768A (en) * | 2009-12-15 | 2011-12-16 | Lundbeck & Co As H | Pyridone derivatives as NK3 antagonists |
US8802868B2 (en) | 2010-03-25 | 2014-08-12 | Vertex Pharmaceuticals Incorporated | Solid forms of (R)-1(2,2-difluorobenzo[D][1,3]dioxo1-5-yl)-N-(1-(2,3-dihydroxypropyl-6-fluoro-2-(1-hydroxy-2-methylpropan2-yl)-1H-Indol-5-yl)-Cyclopropanecarboxamide |
DK3150198T3 (da) | 2010-04-07 | 2021-11-01 | Vertex Pharma | Farmaceutiske sammensætninger af 3-(6-(1-(2,2-difluorbenzo[d][1,3]dioxol-5-yl)-cyclopropancarboxamido)-3-methylpyriodin-2-yl)benzoesyre og indgivelse deraf |
AR081069A1 (es) | 2010-04-07 | 2012-06-06 | Vertex Pharma | Formas solidas del acido 3-(6-(1-(2,2-difluorbenzo[d][1,3]dioxol-5-il)ciclopropancarboxamido)-3-metilpiridin-2-il)benzoico |
US9035072B2 (en) | 2010-04-22 | 2015-05-19 | Vertex Pharmaceuticals Incorporated | Process of producing cycloalkylcarboxamido-indole compounds |
EP2560488B1 (fr) * | 2010-04-23 | 2015-10-28 | Cytokinetics, Inc. | Aminopyridines et aminotriazines, leurs compositions et leurs procédés d'utilisation |
AR081331A1 (es) | 2010-04-23 | 2012-08-08 | Cytokinetics Inc | Amino- pirimidinas composiciones de las mismas y metodos para el uso de los mismos |
AR081626A1 (es) | 2010-04-23 | 2012-10-10 | Cytokinetics Inc | Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos |
US8987307B2 (en) | 2011-03-03 | 2015-03-24 | Hoffmann-La Roche Inc. | 3-amino-pyridines as GPBAR1 agonists |
WO2013019635A1 (fr) * | 2011-07-29 | 2013-02-07 | Tempero Pharmaceuticals, Inc. | Composés et méthodes |
WO2013019621A1 (fr) * | 2011-07-29 | 2013-02-07 | Tempero Pharmaceuticals, Inc. | Composés et méthodes |
PL2744497T3 (pl) | 2011-10-18 | 2016-10-31 | Terapeutyczne połączenia netupitantu i palonosetronu | |
CA2852991C (fr) | 2011-11-08 | 2019-12-31 | Vertex Pharmaceuticals Incorporated | Modulateurs de transporteurs de cassette de liaison a l'atp |
US8426450B1 (en) * | 2011-11-29 | 2013-04-23 | Helsinn Healthcare Sa | Substituted 4-phenyl pyridines having anti-emetic effect |
EP2872122A1 (fr) | 2012-07-16 | 2015-05-20 | Vertex Pharmaceuticals Incorporated | Compositions pharmaceutiques de (r)-1-(2,2-diflurorbenzo[d][1,3]dioxol-5-yl)-n-(1-(2,3-dihydroxypropyl)-6-fluoro-2-(1-hydroxy-2-methylpropan-2-yl)-1h-indol-5-yl) cyclopropanecarboxamide et son administration |
AU2014347644B2 (en) * | 2013-11-08 | 2018-06-14 | Kissei Pharmaceutical Co., Ltd. | Carboxymethyl piperidine derivative |
MX2016006118A (es) | 2013-11-12 | 2016-07-21 | Vertex Pharma | Proceso para preparar composiciones farmaceuticas para el tratamiento de enfermedades mediadas por regulador de la conductancia transmembrana de la fibrosis quistica (cftr). |
PT3925607T (pt) | 2014-04-15 | 2023-09-26 | Vertex Pharma | Composições farmacêuticas para o tratamento de doenças mediadas pelo regulador de condutância transmembranar da fibrose quística |
EP3140007A1 (fr) * | 2014-05-05 | 2017-03-15 | Apicore US LLC | Procédés de fabrication de nétupitant et d'intermédiaires de celui-ci |
TWI649307B (zh) * | 2014-05-07 | 2019-02-01 | 日商橘生藥品工業股份有限公司 | Cyclohexylpyridine derivative |
TW201613888A (en) | 2014-09-26 | 2016-04-16 | Helsinn Healthcare Sa | Crystalline forms of an NK-1 antagonist |
BR112017010406B1 (pt) | 2014-11-18 | 2021-03-09 | Vertex Pharmaceuticals Incorporated | processo de realização de teste de alta produtividade de cromatografia líquida de alta eficiência |
AU2016226006B2 (en) | 2015-03-04 | 2021-03-04 | Vanda Pharmaceuticals Inc. | Method of treatment with tradipitant |
CN105061303A (zh) * | 2015-08-03 | 2015-11-18 | 成都欣捷高新技术开发有限公司 | 一种制备奈妥吡坦关键中间体n-甲基-4-(2-甲基苯基)-6-(4-甲基-1-哌嗪基)-3-吡啶胺的新方法 |
EP4019018A1 (fr) | 2015-09-11 | 2022-06-29 | Chase Pharmaceuticals Corporation | Combinaisons muscariniques et leur utilisation pour lutter contre des troubles hypocholinergiques du système nerveux central |
EP3388423B1 (fr) * | 2015-12-07 | 2020-05-27 | Kissei Pharmaceutical Co., Ltd. | Antagoniste du récepteur nk1 |
TWI773657B (zh) * | 2015-12-18 | 2022-08-11 | 美商亞德利克斯公司 | 作爲非全身tgr5促效劑之經取代之4-苯基吡啶化合物 |
US12084472B2 (en) | 2015-12-18 | 2024-09-10 | Ardelyx, Inc. | Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists |
CN106892864A (zh) * | 2015-12-21 | 2017-06-27 | 上海科胜药物研发有限公司 | 一种奈妥皮坦游离碱的晶型a及其制备方法 |
EA201891472A1 (ru) * | 2015-12-22 | 2018-12-28 | Такеда Фармасьютикал Компани Лимитед | Тройные модуляторы эндосомальных рецепторов, сопряженных с g-белком |
IL312486B1 (en) | 2017-04-10 | 2025-01-01 | Chase Therapeutics Corp | NK1 antagonist combination and method for treating synucleinopathies |
MA49524A (fr) | 2017-06-30 | 2021-05-26 | Chase Therapeutics Corp | Compositions d'antagoniste de nk-1 et méthodes destinées à être utilisées dans le traitement de la dépression |
CN109384712B (zh) * | 2017-08-14 | 2021-05-07 | 北京宽厚医药科技有限公司 | 靶向nk1受体拮抗剂及其在化疗所致恶心、呕吐治疗中的应用 |
EP3672964A4 (fr) | 2017-08-21 | 2021-05-26 | Leiutis Pharmaceuticals Pvt. Ltd. | Nouvelles formulations à triple combinaison pour une thérapie antiémétique |
US10821099B2 (en) | 2018-09-28 | 2020-11-03 | Vanda Pharmaceuticals Inc. | Use of tradipitant in motion sickness |
JP7468964B2 (ja) * | 2018-09-28 | 2024-04-16 | バンダ・ファーマシューティカルズ・インコーポレイテッド | 動揺病におけるトラジピタントの使用 |
WO2020132716A1 (fr) * | 2018-12-24 | 2020-07-02 | Eustralis Pharmaceuticals Limited (Trading As Pressura Neuro) | Fabrication d'un composé chimique, nouvelle forme de sel, et utilisations thérapeutiques associées |
CN112174881B (zh) * | 2019-07-04 | 2022-06-21 | 上海森辉医药有限公司 | 一种奈妥匹坦的衍生物及其制备方法 |
JP2023519570A (ja) | 2020-04-03 | 2023-05-11 | ネッレ セラピューティクス リミテッド | 新規使用 |
CA3177477A1 (fr) | 2020-06-02 | 2021-12-09 | Nerre Therapeutics Limited | Antagonistes du recepteur de la neurokinine (nk)-1 destines a etre utilises dans le traitement d'etats de fibrose pulmonaire favorises par une lesion mecanique des poumons |
US12097197B2 (en) | 2021-12-21 | 2024-09-24 | Slayback Pharma Llc | Stable liquid compositions of netupitant and palonosetron |
EP4385500A1 (fr) | 2022-12-12 | 2024-06-19 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Combinaison de doses fixes comprenant du nétupitant et du palonosétron |
WO2024126398A1 (fr) | 2022-12-12 | 2024-06-20 | Alfred E. Tiefenbacher (Gmbh & Co. Kg) | Combinaison de doses fixes comprenant du netupitant et du palonosétron |
EP4385497A1 (fr) | 2022-12-12 | 2024-06-19 | Alfred E. Tiefenbacher (GmbH & Co. KG) | Combinaison de doses fixes sans antioxydant de nétupitant et de palonosétron |
WO2024126408A1 (fr) | 2022-12-12 | 2024-06-20 | Alfred E. Tiefenbacher (Gmbh & Co. Kg) | Association de dose fixe sans antioxydant de netupitant et de palonosétron |
Family Cites Families (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1557420A (en) | 1977-03-10 | 1979-12-12 | Soc D Etudes Prod Chimique | Preparation of isobutyramide derivatives |
KR810001320B1 (ko) | 1977-03-17 | 1981-10-14 | 삐에르 위브 | 신규한 이소부티라미드류의 제조방법 |
KR810001697B1 (ko) | 1978-02-06 | 1981-10-27 | 삐에르 위브 | 이소부티라미드 유도체의 신규한 제조방법 |
EP0089765A3 (fr) | 1982-03-17 | 1984-05-23 | Smith Kline & French Laboratories Limited | Dérivés de pyridine |
US4745123A (en) * | 1986-02-18 | 1988-05-17 | Warner-Lambert Company | Substituted tetrahydro-3-pyridine-carboxylic acid, ester, and amide cholinergic agents |
GB8607313D0 (en) | 1986-03-25 | 1986-04-30 | Ici Plc | Pharmaceutical compositions |
GB8607312D0 (en) | 1986-03-25 | 1986-04-30 | Ici Plc | Therapeutic agents |
CA1339423C (fr) | 1988-09-14 | 1997-09-02 | Yuji Ono | Pyridines et leur emploi en pharmacie |
US4994456A (en) | 1989-03-01 | 1991-02-19 | Nisshin Flour Milling Co., Ltd. | Pyridinecarboxylic acid amide derivatives and pharmaceutical compositions comprising same |
US4973597A (en) | 1989-06-30 | 1990-11-27 | Eli Lilly And Company | Anticonvulsant agents |
HU207047B (en) | 1989-11-07 | 1993-03-01 | Richter Gedeon Vegyeszet | Process for producing new pyridine derivatives and pharmaceutical copositions comprising same |
US5364943A (en) | 1991-11-27 | 1994-11-15 | Pfizer Inc. | Preparation of substituted piperidines |
GB9021056D0 (en) | 1990-09-27 | 1990-11-07 | Pfizer Ltd | Antiarrhythmic agents |
GB9214120D0 (en) | 1991-07-25 | 1992-08-12 | Ici Plc | Therapeutic amides |
US5719147A (en) * | 1992-06-29 | 1998-02-17 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
AU4718093A (en) | 1992-07-31 | 1994-03-03 | Merck Sharp & Dohme Limited | Substituted amines as tachykinin receptor antagonists |
US5387595A (en) | 1992-08-26 | 1995-02-07 | Merck & Co., Inc. | Alicyclic compounds as tachykinin receptor antagonists |
GB9305672D0 (en) | 1993-03-19 | 1993-05-05 | Wyeth John & Brother Ltd | Amide derivatives |
NZ264063A (en) | 1993-08-13 | 1995-11-27 | Nihon Nohyaku Co Ltd | N-(2-phenylpyrid-3-yl)- and n-(4-phenylpyrimidin-5-yl)-n'-phenylurea derivatives and pharmaceutical compositions |
IL111960A (en) | 1993-12-17 | 1999-12-22 | Merck & Co Inc | Morpholines and thiomorpholines their preparation and pharmaceutical compositions containing them |
JP3071467B2 (ja) | 1993-12-29 | 2000-07-31 | メルク シヤープ エンド ドーム リミテツド | 置換モルホリン誘導体およびその治療剤としての使用 |
IL112778A0 (en) | 1994-03-04 | 1995-05-26 | Merck & Co Inc | Substituted heterocycles, their preparation and pharmaceutical compositions containing them |
JPH10501228A (ja) | 1994-06-06 | 1998-02-03 | ワーナー−ランバート・コンパニー | タキキニン(nk▲下1▼)受容体アンタゴニスト |
US6294537B1 (en) | 1995-03-17 | 2001-09-25 | Sanofi-Synthelabo | Compounds which are specific antagonists of the human NK3 receptor and their use as medicinal products and diagnostic tools |
TW394773B (en) * | 1995-03-24 | 2000-06-21 | Takeda Chemical Industries Ltd | Cyclic compounds for antagonizing tachykinin receptor, substance p receptor and neurokinin a receptor, their production and pharmaceutical composition |
AR004735A1 (es) * | 1995-11-24 | 1999-03-10 | Smithkline Beecham Spa | Quinoleina 4-amido sustituida, un procedimiento para su preparacion, una composicion farmaceutica que los contiene y el uso de los mismos para lapreparacion de un medicamento. |
KR100313641B1 (ko) | 1996-03-29 | 2002-02-19 | 디. 제이. 우드, 스피겔 알렌 제이 | 6-페닐피리딜-2-아민유도체 |
AU4885097A (en) | 1996-11-08 | 1998-06-03 | Sankyo Company Limited | Arylureas or arylmethylcarbamoyl derivatives |
US5972938A (en) | 1997-12-01 | 1999-10-26 | Merck & Co., Inc. | Method for treating or preventing psychoimmunological disorders |
WO2000050398A2 (fr) * | 1999-02-24 | 2000-08-31 | F. Hoffmann-La Roche Ag | Derives de pyridinyl et de phenyle |
US6303790B1 (en) * | 1999-11-29 | 2001-10-16 | Hoffman-La Roche Inc. | Process for the preparation of pyridine derivatives |
EP1103545B1 (fr) * | 1999-11-29 | 2003-11-05 | F. Hoffmann-La Roche Ag | 2-(3,5-Bis-trifluorométhyl-phényl)-N-méthyl-N-(6-morpholin-4-yl-4-o-tolyl-pyridin-3-yl)-isobutyramide |
-
2000
- 2000-02-15 DK DK03026298.4T patent/DK1394150T3/da active
- 2000-02-15 AT AT03026298T patent/ATE496032T1/de active
- 2000-02-15 ES ES03026298T patent/ES2359235T3/es not_active Expired - Lifetime
- 2000-02-15 EP EP03026298A patent/EP1394150B1/fr not_active Expired - Lifetime
- 2000-02-15 SE SE00102260T patent/SE1035115T5/xx unknown
- 2000-02-15 AT AT00102260T patent/ATE277905T1/de active
- 2000-02-15 DK DK00102260T patent/DK1035115T3/da active
- 2000-02-15 DE DE60014216T patent/DE60014216T2/de not_active Expired - Lifetime
- 2000-02-15 EP EP00102260A patent/EP1035115B1/fr not_active Expired - Lifetime
- 2000-02-15 PT PT03026298T patent/PT1394150E/pt unknown
- 2000-02-15 ES ES00102260T patent/ES2226622T3/es not_active Expired - Lifetime
- 2000-02-15 PT PT00102260T patent/PT1035115E/pt unknown
- 2000-02-15 SI SI200030506T patent/SI1035115T1/xx unknown
- 2000-02-15 DE DE60045564T patent/DE60045564D1/de not_active Expired - Lifetime
- 2000-02-18 GB GB0003908A patent/GB2347422A/en not_active Withdrawn
- 2000-02-18 PE PE2000000125A patent/PE20001467A1/es not_active IP Right Cessation
- 2000-02-18 NZ NZ502948A patent/NZ502948A/en not_active IP Right Cessation
- 2000-02-21 IL IL134654A patent/IL134654A/en active Protection Beyond IP Right Term
- 2000-02-21 GE GEAP20005227A patent/GEP20022676B/en unknown
- 2000-02-21 CZ CZ20000609A patent/CZ300596B6/cs not_active IP Right Cessation
- 2000-02-21 HU HU0000748A patent/HU227629B1/hu unknown
- 2000-02-22 MY MYPI20000648A patent/MY123648A/en unknown
- 2000-02-22 RS RSP-2008/0562A patent/RS20080562A/sr unknown
- 2000-02-22 GT GT200000017A patent/GT200000017A/es unknown
- 2000-02-22 SK SK5052-2008A patent/SK287912B6/sk not_active IP Right Cessation
- 2000-02-22 IS IS5381A patent/IS2116B/is unknown
- 2000-02-22 FR FR0002170A patent/FR2790473B1/fr not_active Expired - Fee Related
- 2000-02-22 TN TNTNSN00032A patent/TNSN00032A1/fr unknown
- 2000-02-22 UA UA2000021039A patent/UA71547C2/uk unknown
- 2000-02-22 MY MYPI20044751A patent/MY147451A/en unknown
- 2000-02-22 AR ARP000100737A patent/AR029614A1/es active IP Right Grant
- 2000-02-22 PA PA20008491101A patent/PA8491101A1/es unknown
- 2000-02-22 RS RS20080562A patent/RS53869B1/en unknown
- 2000-02-22 US US09/507,456 patent/US6297375B1/en not_active Expired - Lifetime
- 2000-02-22 JO JO200014A patent/JO2294B1/en active
- 2000-02-22 RS YUP-95/00A patent/RS50194B/sr unknown
- 2000-02-22 ME MEP-2009-57A patent/ME00593B/me unknown
- 2000-02-22 DE DE10008042A patent/DE10008042A1/de not_active Withdrawn
- 2000-02-22 EG EG20000206A patent/EG23817A/xx active
- 2000-02-22 SK SK235-2000A patent/SK287911B6/sk not_active IP Right Cessation
- 2000-02-23 IT IT2000MI000328A patent/IT1320763B1/it active
- 2000-02-23 HR HR20000097A patent/HRP20000097B1/xx not_active IP Right Cessation
- 2000-02-23 ES ES200000418A patent/ES2171109B2/es not_active Expired - Fee Related
- 2000-02-23 CN CNB001024019A patent/CN1142144C/zh not_active Expired - Lifetime
- 2000-02-23 EA EA200000155A patent/EA003673B1/ru active Protection Beyond IP Right Term
- 2000-02-23 BR BRPI0000908A patent/BRPI0000908B8/pt not_active IP Right Cessation
- 2000-02-23 ZA ZA200000894A patent/ZA200000894B/xx unknown
- 2000-02-23 SG SG200001033A patent/SG91856A1/en unknown
- 2000-02-23 NO NO20000885A patent/NO315554B1/no not_active IP Right Cessation
- 2000-02-23 SV SV2000000024A patent/SV2002000024A/es active IP Right Grant
- 2000-02-23 CA CA2299139A patent/CA2299139C/fr not_active Expired - Lifetime
- 2000-02-23 MA MA25913A patent/MA26722A1/fr unknown
- 2000-02-23 KR KR10-2000-0008674A patent/KR100384904B1/ko active Protection Beyond IP Right Term
- 2000-02-24 OA OA1200000052A patent/OA11680A/fr unknown
- 2000-02-24 TR TR2000/00520A patent/TR200000520A3/tr unknown
- 2000-02-24 PL PL338598A patent/PL217311B1/pl unknown
- 2000-02-24 BG BG104187A patent/BG64554B1/bg unknown
- 2000-02-24 JP JP2000047003A patent/JP3399900B2/ja not_active Expired - Lifetime
- 2000-02-24 AU AU19468/00A patent/AU767048B2/en not_active Expired
- 2000-02-25 TW TW089103387A patent/TWI288746B/zh not_active IP Right Cessation
-
2001
- 2001-03-12 HK HK01101744A patent/HK1031223A1/xx unknown
- 2001-07-10 US US09/901,982 patent/US6479483B2/en not_active Expired - Lifetime
-
2007
- 2007-09-24 AR ARP070104196A patent/AR062949A2/es active IP Right Grant
-
2008
- 2008-06-27 HR HRP20080306AA patent/HRP20080306B1/hr not_active IP Right Cessation
-
2009
- 2009-12-10 UY UY0001032314A patent/UY32314A/es not_active Application Discontinuation
-
2011
- 2011-02-10 CY CY20111100162T patent/CY1111317T1/el unknown
-
2015
- 2015-06-17 LU LU92745C patent/LU92745I2/fr unknown
- 2015-07-08 FR FR15C0049C patent/FR15C0049I2/fr active Active
- 2015-08-28 NL NL300758C patent/NL300758I2/nl unknown
- 2015-10-21 LT LTPA2015036C patent/LTC1035115I2/lt unknown
- 2015-10-29 CY CY2015042C patent/CY2015042I1/el unknown
- 2015-10-29 BE BE2015C057C patent/BE2015C057I2/fr unknown
- 2015-10-29 CY CY2015041C patent/CY2015041I1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
FR15C0049I2 (fr) | Dérivés de 4-phenylpyridine et leur utilisation comme antagonistes du recepteur NK-1 | |
MA26773A1 (fr) | Derives de 3-phenylpyridine et leur utilisation comme recepteurs antagonistes nk-1 | |
FR13C0001I2 (fr) | Derives de quinuclidine et leur utilisation comme ligands des recepteurs m3 muscariniques | |
FR17C1056I1 (fr) | Pd-1, recepteur de b7-4, et son utilisation | |
BR9712248A (pt) | Antagonista receptores de vitronectina | |
MA26762A1 (fr) | Derives de pyrrolidine- antagonistes du recepteur ccr-3 | |
CY2010003I2 (el) | Αγωνιστες των βητα-2 αδρενεργικων υποδοχεων | |
DE60118569D1 (de) | 4-phenylpyridin-derivate als neurokinin-1-rezeptor-antagonisten | |
ATE305920T1 (de) | Bradykinin receptorantagoniste | |
NO20001514D0 (no) | Vitronectin-reseptor-antagonist | |
NO20001515D0 (no) | Vitronektin reseptor-antagonist | |
MA26907A1 (fr) | Cyclohexylamines bicycliques et leur utilisation comme antagonistes de recepteurs de nmda. | |
NO971136D0 (no) | Aminoalkyl- og acylaminoaklyleter, fremgangsmåte for fremstilling derav og anvendelse som bradykinin-reseptor antagonister | |
EP1248607A4 (fr) | Antagonistes des recepteurs de l'urotensine ii | |
PT1146874E (pt) | Antagonista de receptor da vitronectina | |
BR9709911A (pt) | Derivados de indola úteis como antagonistas receptores de 5-ht-2c | |
IL142362A0 (en) | Ureidopiperidine derivatives as selective human nk3 receptor antagonists | |
GB9708766D0 (en) | Fibrinogen receptor antagonist | |
GB9603245D0 (en) | Fibrinogen receptor antagonist | |
ZA986620B (en) | Fibrinogen receptor antagonist | |
HUP9901033A3 (en) | 4-substituted piperidine analogs and their use as subtype selective nmda receptor antagonists |