AP909A - Piperidinylaminomethyl trifluoromethyl Cyclic ether compounds assubstance P antagonists. - Google Patents
Piperidinylaminomethyl trifluoromethyl Cyclic ether compounds assubstance P antagonists. Download PDFInfo
- Publication number
- AP909A AP909A APAP/P/1998/001402A AP9801402A AP909A AP 909 A AP909 A AP 909A AP 9801402 A AP9801402 A AP 9801402A AP 909 A AP909 A AP 909A
- Authority
- AP
- ARIPO
- Prior art keywords
- methoxy
- disorders
- methyl
- trifluoromethyl
- alkyl
- Prior art date
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- 239000005557 antagonist Substances 0.000 title claims description 7
- -1 Piperidinylaminomethyl trifluoromethyl Cyclic ether compounds Chemical class 0.000 title abstract description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 148
- 150000003839 salts Chemical class 0.000 claims abstract description 37
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 36
- 208000035475 disorder Diseases 0.000 claims abstract description 32
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 206010047700 Vomiting Diseases 0.000 claims abstract description 16
- 238000011282 treatment Methods 0.000 claims abstract description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 12
- 208000015114 central nervous system disease Diseases 0.000 claims abstract description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 11
- 208000018522 Gastrointestinal disease Diseases 0.000 claims abstract description 9
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract description 8
- 206010042496 Sunburn Diseases 0.000 claims abstract description 8
- 230000002411 adverse Effects 0.000 claims abstract description 8
- 241000590002 Helicobacter pylori Species 0.000 claims abstract description 7
- 230000000172 allergic effect Effects 0.000 claims abstract description 7
- 208000010668 atopic eczema Diseases 0.000 claims abstract description 7
- 229940037467 helicobacter pylori Drugs 0.000 claims abstract description 7
- 230000033115 angiogenesis Effects 0.000 claims abstract description 6
- 201000010099 disease Diseases 0.000 claims abstract description 3
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 6
- 238000000034 method Methods 0.000 claims description 42
- 208000019901 Anxiety disease Diseases 0.000 claims description 21
- 241000124008 Mammalia Species 0.000 claims description 16
- QDZOEBFLNHCSSF-PFFBOGFISA-N (2S)-2-[[(2R)-2-[[(2S)-1-[(2S)-6-amino-2-[[(2S)-1-[(2R)-2-amino-5-carbamimidamidopentanoyl]pyrrolidine-2-carbonyl]amino]hexanoyl]pyrrolidine-2-carbonyl]amino]-3-(1H-indol-3-yl)propanoyl]amino]-N-[(2R)-1-[[(2S)-1-[[(2R)-1-[[(2S)-1-[[(2S)-1-amino-4-methyl-1-oxopentan-2-yl]amino]-4-methyl-1-oxopentan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]amino]-3-(1H-indol-3-yl)-1-oxopropan-2-yl]pentanediamide Chemical compound C([C@@H](C(=O)N[C@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](CCCCN)NC(=O)[C@H]1N(CCC1)C(=O)[C@H](N)CCCNC(N)=N)C1=CC=CC=C1 QDZOEBFLNHCSSF-PFFBOGFISA-N 0.000 claims description 15
- 102100024304 Protachykinin-1 Human genes 0.000 claims description 15
- 101800003906 Substance P Proteins 0.000 claims description 15
- 230000036506 anxiety Effects 0.000 claims description 14
- 208000024714 major depressive disease Diseases 0.000 claims description 14
- 150000002431 hydrogen Chemical group 0.000 claims description 13
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- 230000000694 effects Effects 0.000 claims description 12
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
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- 206010027599 migraine Diseases 0.000 claims description 8
- 208000016285 Movement disease Diseases 0.000 claims description 7
- 208000027866 inflammatory disease Diseases 0.000 claims description 7
- 201000000980 schizophrenia Diseases 0.000 claims description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
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- 208000013200 Stress disease Diseases 0.000 claims description 6
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- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 231100000872 sexual dysfunction Toxicity 0.000 claims description 6
- 208000011117 substance-related disease Diseases 0.000 claims description 6
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 5
- 239000003937 drug carrier Substances 0.000 claims description 5
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims description 4
- AZXGYKQBRXSPHY-LLVKDONJSA-N (1r)-6-methoxy-1-methyl-1-(trifluoromethyl)-3,4-dihydroisochromene Chemical compound C=1([C@](OCC2)(C)C(F)(F)F)C2=CC(OC)=CC=1 AZXGYKQBRXSPHY-LLVKDONJSA-N 0.000 claims description 3
- GPWNWKWQOLEVEQ-UHFFFAOYSA-N 2,4-diaminopyrimidine-5-carbaldehyde Chemical compound NC1=NC=C(C=O)C(N)=N1 GPWNWKWQOLEVEQ-UHFFFAOYSA-N 0.000 claims description 3
- NBUDNQJPOCYIIN-UHFFFAOYSA-N 5-methoxy-1-(trifluoromethyl)-1,3-dihydro-2-benzofuran Chemical compound COC1=CC=C2C(C(F)(F)F)OCC2=C1 NBUDNQJPOCYIIN-UHFFFAOYSA-N 0.000 claims description 3
- AZXGYKQBRXSPHY-UHFFFAOYSA-N 6-methoxy-1-methyl-1-(trifluoromethyl)-3,4-dihydroisochromene Chemical compound C1COC(C(F)(F)F)(C)C=2C1=CC(OC)=CC=2 AZXGYKQBRXSPHY-UHFFFAOYSA-N 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- AZXGYKQBRXSPHY-NSHDSACASA-N (1s)-6-methoxy-1-methyl-1-(trifluoromethyl)-3,4-dihydroisochromene Chemical compound C=1([C@@](OCC2)(C)C(F)(F)F)C2=CC(OC)=CC=1 AZXGYKQBRXSPHY-NSHDSACASA-N 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- RDOKLDFJIBLNAR-UHFFFAOYSA-N 6-methoxy-1-methyl-1-(trifluoromethyl)-3,4-dihydroisochromene-7-carbaldehyde Chemical compound C1COC(C)(C(F)(F)F)C2=C1C=C(OC)C(C=O)=C2 RDOKLDFJIBLNAR-UHFFFAOYSA-N 0.000 claims description 2
- GPWGSWJZRDEAJI-UHFFFAOYSA-N 6-methoxy-3-(trifluoromethyl)-2,3-dihydro-1-benzofuran-5-carbaldehyde Chemical compound C1=C(C=O)C(OC)=CC2=C1C(C(F)(F)F)CO2 GPWGSWJZRDEAJI-UHFFFAOYSA-N 0.000 claims description 2
- FGGKIMGMRFUCLN-UHFFFAOYSA-N 6-methoxy-3-methyl-3-(trifluoromethyl)-1h-2-benzofuran Chemical compound COC1=CC=C2C(C(F)(F)F)(C)OCC2=C1 FGGKIMGMRFUCLN-UHFFFAOYSA-N 0.000 claims description 2
- XIRBHTNKLIOEGN-UHFFFAOYSA-N 6-methoxy-3-phenyl-3-(trifluoromethyl)-1h-2-benzofuran Chemical compound C=1C(OC)=CC=C2C=1COC2(C(F)(F)F)C1=CC=CC=C1 XIRBHTNKLIOEGN-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 230000002265 prevention Effects 0.000 claims 2
- RDOKLDFJIBLNAR-LBPRGKRZSA-N (1s)-6-methoxy-1-methyl-1-(trifluoromethyl)-3,4-dihydroisochromene-7-carbaldehyde Chemical compound C1CO[C@](C)(C(F)(F)F)C2=C1C=C(OC)C(C=O)=C2 RDOKLDFJIBLNAR-LBPRGKRZSA-N 0.000 claims 1
- UTEFTKTYELSUJY-UHFFFAOYSA-N 6-methoxy-3-phenyl-3-(trifluoromethyl)-1h-2-benzofuran-5-carbaldehyde Chemical compound C1=2C=C(C=O)C(OC)=CC=2COC1(C(F)(F)F)C1=CC=CC=C1 UTEFTKTYELSUJY-UHFFFAOYSA-N 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract description 18
- 239000000543 intermediate Substances 0.000 abstract description 5
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- 239000000730 antalgic agent Substances 0.000 abstract 1
- 230000002485 urinary effect Effects 0.000 abstract 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 102
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 69
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 69
- 239000000243 solution Substances 0.000 description 49
- 239000000203 mixture Substances 0.000 description 41
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 40
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 36
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 36
- 238000005160 1H NMR spectroscopy Methods 0.000 description 34
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 34
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- 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
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/76—Benzo[c]pyrans
-
- 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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
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- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Immunology (AREA)
- Heart & Thoracic Surgery (AREA)
- Dermatology (AREA)
- Reproductive Health (AREA)
- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Cardiology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Vascular Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IB9701466 | 1997-11-19 | ||
| PCT/IB1998/001704 WO1999025714A1 (en) | 1997-11-19 | 1998-10-26 | Piperidinylaminomethyl trifluoromethyl cyclic ether compounds as substance p antagonists |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AP9801402A0 AP9801402A0 (en) | 1998-12-31 |
| AP909A true AP909A (en) | 2000-12-04 |
Family
ID=11004634
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| APAP/P/1998/001402A AP909A (en) | 1997-11-19 | 1998-11-19 | Piperidinylaminomethyl trifluoromethyl Cyclic ether compounds assubstance P antagonists. |
Country Status (39)
| Country | Link |
|---|---|
| US (2) | US20030208079A1 (cs) |
| EP (1) | EP1032571B1 (cs) |
| JP (2) | JP3394239B2 (cs) |
| KR (1) | KR100366902B1 (cs) |
| CN (1) | CN1173974C (cs) |
| AP (1) | AP909A (cs) |
| AR (1) | AR016422A1 (cs) |
| AT (1) | ATE219078T1 (cs) |
| AU (1) | AU734218B2 (cs) |
| BG (1) | BG63969B1 (cs) |
| CA (1) | CA2310627C (cs) |
| CO (1) | CO4771153A1 (cs) |
| CZ (1) | CZ297315B6 (cs) |
| DE (1) | DE69806045T2 (cs) |
| DK (1) | DK1032571T3 (cs) |
| DZ (1) | DZ2655A1 (cs) |
| EA (1) | EA002621B1 (cs) |
| ES (1) | ES2177058T3 (cs) |
| HR (1) | HRP20000313B1 (cs) |
| HU (1) | HUP0101112A3 (cs) |
| ID (1) | ID24240A (cs) |
| IL (1) | IL135631A0 (cs) |
| IS (1) | IS2202B (cs) |
| MA (1) | MA26567A1 (cs) |
| MY (1) | MY120558A (cs) |
| NO (2) | NO20002544L (cs) |
| NZ (1) | NZ503912A (cs) |
| OA (1) | OA11380A (cs) |
| PA (1) | PA8463001A1 (cs) |
| PE (1) | PE20000021A1 (cs) |
| PL (1) | PL193484B1 (cs) |
| PT (1) | PT1032571E (cs) |
| RS (1) | RS49792B (cs) |
| SK (1) | SK283460B6 (cs) |
| TN (1) | TNSN98210A1 (cs) |
| TR (1) | TR200001463T2 (cs) |
| TW (1) | TW426667B (cs) |
| UA (1) | UA59417C2 (cs) |
| WO (1) | WO1999025714A1 (cs) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9812662D0 (en) * | 1998-06-11 | 1998-08-12 | Merck Sharp & Dohme | Therapeutic use |
| GB9812617D0 (en) * | 1998-06-11 | 1998-08-12 | Merck Sharp & Dohme | Therapeutic use |
| IL145945A0 (en) * | 1999-05-06 | 2002-07-25 | Pfizer Prod Inc | Substituted benzolactam compounds |
| RS49964B (sr) | 1999-05-17 | 2008-09-29 | Pfizer Products Inc., | Postupak za dobijanje 2-fenil-3-aminopiridina,njegovih supstituisanih fenil derivata, i njegovih soli |
| WO2000071538A2 (en) | 1999-05-21 | 2000-11-30 | Pfizer Products Inc. | 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives |
| EP1219619B1 (en) * | 1999-10-07 | 2004-08-11 | Hisamitsu Pharmaceutical Co. Inc. | 3-amino-2-phenylpiperidine derivatives as substance p antagonists |
| ATE257477T1 (de) * | 1999-10-18 | 2004-01-15 | Pfizer Prod Inc | Verfahren zur herstellung von zyklischen piperidinylaminomethyl-trifluoromethyl- etherderivaten |
| CA2324116A1 (en) * | 1999-10-25 | 2001-04-25 | Susan Beth Sobolov-Jaynes | Nk-1 receptor antagonists and eletriptan for the treatment of migraine |
| IL142810A0 (en) * | 2000-05-03 | 2002-03-10 | Pfizer Prod Inc | Pharmaceutical uses for fluoroalkoxybenzylamino derivatives of nitrogen containing heterocycles |
| US20020049211A1 (en) * | 2000-09-06 | 2002-04-25 | Sobolov-Jaynes Susan Beth | Combination treatment for depression and anxiety |
| EP1192952A3 (en) * | 2000-09-28 | 2003-03-26 | Pfizer Products Inc. | Combination, for treating depression and anxiety, containing an NK-3 receptor antagonist and a CNS penetrant NK-1 receptor antagonist |
| JP2004525109A (ja) | 2001-02-15 | 2004-08-19 | キング・ファーマシューティカルズ・インコーポレイティッド | 安定化された甲状腺ホルモン医薬組成物、及びその製法 |
| US6555581B1 (en) | 2001-02-15 | 2003-04-29 | Jones Pharma, Inc. | Levothyroxine compositions and methods |
| US7101569B2 (en) | 2001-08-14 | 2006-09-05 | Franz G Andrew | Methods of administering levothyroxine pharmaceutical compositions |
| EP1288208B1 (en) | 2001-08-30 | 2006-07-12 | Pfizer Products Inc. | Process for the preparation of 2-(4-Alkyl-1-Piperazinyl)-Benzaldehyde and -Benzylidenyl compounds by Nucleophilc Aromatic Substitution of 2-Fluorobenzaldehyde with 4-Alkyl-1-Piperazine in Water as Solvent |
| US20040001895A1 (en) * | 2002-06-17 | 2004-01-01 | Pfizer Inc. | Combination treatment for depression and anxiety |
| JP2005537322A (ja) * | 2002-08-27 | 2005-12-08 | マーク エル． ウィッテン | タバコの煙の影響の改善 |
| US6911544B2 (en) * | 2002-10-23 | 2005-06-28 | Pfizer Inc. | Process for the preparation of (S,S)-cis-2-phenyl-3-aminopiperidine |
| US7122700B2 (en) | 2004-07-30 | 2006-10-17 | Xerox Corporation | Arylamine processes |
| DE102008000891A1 (de) | 2008-03-31 | 2009-10-01 | Robert Bosch Gmbh | Schutzsystem für Werkzeugmaschinen |
| NO2729147T3 (cs) | 2011-07-04 | 2018-02-03 | ||
| AU2019223237A1 (en) | 2018-02-26 | 2020-09-03 | Ospedale San Raffaele S.R.L. | NK-1 antagonists for use in the treatment of ocular pain |
| US20230134843A1 (en) | 2020-03-11 | 2023-05-04 | Ospedale San Raffaele S.R.L. | Treatment of stem cell deficiency |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996030367A1 (fr) * | 1995-03-27 | 1996-10-03 | Hisamitsu Pharmaceutical Co., Inc. | Derives de piperidine |
| WO1997008144A1 (en) * | 1995-08-24 | 1997-03-06 | Pfizer Pharmaceuticals Inc. | Substituted benzylaminopiperidine compounds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9317987D0 (en) * | 1993-08-26 | 1993-10-13 | Glaxo Group Ltd | Chemical compounds |
| RU2156250C2 (ru) * | 1995-04-24 | 2000-09-20 | Новартис Аг | Производные хромона, способ их получения и фармацевтическая композиция |
| ATE199552T1 (de) * | 1995-07-07 | 2001-03-15 | Pfizer | Substituierte benzolaktamverbindungen als substanz-p-antagonisten |
| US6329396B1 (en) * | 1996-06-10 | 2001-12-11 | Pfizer Inc. | Substituted benzylaminopiperidine compounds |
| WO2000071538A2 (en) * | 1999-05-21 | 2000-11-30 | Pfizer Products Inc. | 1-trifluoromethyl-4-hydroxy-7-piperidinyl-aminomethylchroman derivatives |
| ATE257477T1 (de) * | 1999-10-18 | 2004-01-15 | Pfizer Prod Inc | Verfahren zur herstellung von zyklischen piperidinylaminomethyl-trifluoromethyl- etherderivaten |
-
1998
- 1998-10-21 TW TW087117444A patent/TW426667B/zh not_active IP Right Cessation
- 1998-10-26 ID IDW20000926A patent/ID24240A/id unknown
- 1998-10-26 CN CNB988112930A patent/CN1173974C/zh not_active Expired - Fee Related
- 1998-10-26 EA EA200000432A patent/EA002621B1/ru not_active IP Right Cessation
- 1998-10-26 CZ CZ20001834A patent/CZ297315B6/cs not_active IP Right Cessation
- 1998-10-26 NZ NZ503912A patent/NZ503912A/xx unknown
- 1998-10-26 CA CA002310627A patent/CA2310627C/en not_active Expired - Fee Related
- 1998-10-26 HU HU0101112A patent/HUP0101112A3/hu unknown
- 1998-10-26 AT AT98947726T patent/ATE219078T1/de not_active IP Right Cessation
- 1998-10-26 DE DE69806045T patent/DE69806045T2/de not_active Expired - Fee Related
- 1998-10-26 AU AU94549/98A patent/AU734218B2/en not_active Ceased
- 1998-10-26 RS YUP-294/00A patent/RS49792B/sr unknown
- 1998-10-26 HR HR960576A patent/HRP20000313B1/xx not_active IP Right Cessation
- 1998-10-26 SK SK723-2000A patent/SK283460B6/sk unknown
- 1998-10-26 PT PT98947726T patent/PT1032571E/pt unknown
- 1998-10-26 EP EP98947726A patent/EP1032571B1/en not_active Expired - Lifetime
- 1998-10-26 UA UA2000042374A patent/UA59417C2/uk unknown
- 1998-10-26 IL IL13563198A patent/IL135631A0/xx not_active IP Right Cessation
- 1998-10-26 JP JP2000521096A patent/JP3394239B2/ja not_active Expired - Fee Related
- 1998-10-26 WO PCT/IB1998/001704 patent/WO1999025714A1/en active IP Right Grant
- 1998-10-26 ES ES98947726T patent/ES2177058T3/es not_active Expired - Lifetime
- 1998-10-26 TR TR2000/01463T patent/TR200001463T2/xx unknown
- 1998-10-26 DK DK98947726T patent/DK1032571T3/da active
- 1998-11-11 PA PA19988463001A patent/PA8463001A1/es unknown
- 1998-11-16 PE PE1998001112A patent/PE20000021A1/es not_active Application Discontinuation
- 1998-11-17 AR ARP980105829A patent/AR016422A1/es unknown
- 1998-11-17 MY MYPI98005209A patent/MY120558A/en unknown
- 1998-11-17 MA MA25354A patent/MA26567A1/fr unknown
- 1998-11-18 DZ DZ980265A patent/DZ2655A1/xx active
- 1998-11-18 CO CO98067902A patent/CO4771153A1/es unknown
- 1998-11-18 TN TNTNSN98210A patent/TNSN98210A1/fr unknown
- 1998-11-19 AP APAP/P/1998/001402A patent/AP909A/en active
-
2000
- 2000-04-26 IS IS5470A patent/IS2202B/is unknown
- 2000-05-12 OA OA1200000138A patent/OA11380A/en unknown
- 2000-05-15 BG BG104437A patent/BG63969B1/bg unknown
- 2000-05-18 NO NO20002544A patent/NO20002544L/no not_active Application Discontinuation
- 2000-05-18 PL PL98340642A patent/PL193484B1/pl unknown
- 2000-05-18 KR KR10-2000-7005431A patent/KR100366902B1/ko not_active Expired - Fee Related
-
2002
- 2002-06-18 JP JP2002177452A patent/JP2003040777A/ja active Pending
-
2003
- 2003-04-21 US US10/419,425 patent/US20030208079A1/en not_active Abandoned
-
2004
- 2004-07-07 NO NO20042879A patent/NO20042879L/no not_active Application Discontinuation
- 2004-11-18 US US10/991,977 patent/US20050171354A1/en not_active Abandoned
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1996030367A1 (fr) * | 1995-03-27 | 1996-10-03 | Hisamitsu Pharmaceutical Co., Inc. | Derives de piperidine |
| WO1997008144A1 (en) * | 1995-08-24 | 1997-03-06 | Pfizer Pharmaceuticals Inc. | Substituted benzylaminopiperidine compounds |
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