CN101305011B - 吡啶衍生物及其在治疗精神障碍中的用途 - Google Patents
吡啶衍生物及其在治疗精神障碍中的用途 Download PDFInfo
- Publication number
- CN101305011B CN101305011B CN2006800418603A CN200680041860A CN101305011B CN 101305011 B CN101305011 B CN 101305011B CN 2006800418603 A CN2006800418603 A CN 2006800418603A CN 200680041860 A CN200680041860 A CN 200680041860A CN 101305011 B CN101305011 B CN 101305011B
- Authority
- CN
- China
- Prior art keywords
- alkyl
- compound
- solution
- mmol
- added
- 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
- 0 COC(C[C@]1NCCC1)=*C* Chemical compound COC(C[C@]1NCCC1)=*C* 0.000 description 7
- PXYNCQRQUOOTSQ-QMMMGPOBSA-N C(C1)CN2[C@@H]1CCNCC2 Chemical compound C(C1)CN2[C@@H]1CCNCC2 PXYNCQRQUOOTSQ-QMMMGPOBSA-N 0.000 description 1
- DAZREHXORNHICT-UHFFFAOYSA-N CC(C(C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)O)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CCN1C2COCC1)C2=O Chemical compound CC(C(C(C)(C)c1cc(C(F)(F)F)cc(C(F)(F)F)c1)O)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CCN1C2COCC1)C2=O DAZREHXORNHICT-UHFFFAOYSA-N 0.000 description 1
- WGIGVTCGIGERNO-AVJYQCBHSA-O CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(C1)[C@@H](COC)CN(CC2)C1C[SH+]2(O)OC)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(C1)[C@@H](COC)CN(CC2)C1C[SH+]2(O)OC)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 WGIGVTCGIGERNO-AVJYQCBHSA-O 0.000 description 1
- XDAVSKQFRCAXOY-SANMLTNESA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CCCN1[C@H]2CCC1)C2=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N(CCCN1[C@H]2CCC1)C2=O)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 XDAVSKQFRCAXOY-SANMLTNESA-N 0.000 description 1
- UMEVTBXNROQUQZ-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(C(NCC2)=O)N2CC1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(C(NCC2)=O)N2CC1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 UMEVTBXNROQUQZ-UHFFFAOYSA-N 0.000 description 1
- UXCBTZDZHHGJKO-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CO)N(CCC2)C2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c(cc1)c(C)cc1F)c1)cnc1N1CC(CO)N(CCC2)C2C1)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 UXCBTZDZHHGJKO-UHFFFAOYSA-N 0.000 description 1
- YFMZALAUALIBHT-UHFFFAOYSA-N CC(C)(C(N(C)c(c(-c1c(C)cccc1)c1)cnc1N(CC1)CC2N1CCOC2)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound CC(C)(C(N(C)c(c(-c1c(C)cccc1)c1)cnc1N(CC1)CC2N1CCOC2)=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1 YFMZALAUALIBHT-UHFFFAOYSA-N 0.000 description 1
- FJFVREVNXQAOGZ-PZORYLMUSA-N CC(C)(C)OC(N(CC1)CC(C(N[C@H](CO)C(OC)=O)=O)N1C(OC(C)(C)C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC(C(N[C@H](CO)C(OC)=O)=O)N1C(OC(C)(C)C)=O)=O FJFVREVNXQAOGZ-PZORYLMUSA-N 0.000 description 1
- IIZGWFQKLVCLLA-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CC(C(O)=O)N1C(OC(C)(C)C)=O)=O Chemical compound CC(C)(C)OC(N(CC1)CC(C(O)=O)N1C(OC(C)(C)C)=O)=O IIZGWFQKLVCLLA-UHFFFAOYSA-N 0.000 description 1
- PXRKWLBROJKTLG-YHMJZVADSA-N CC(C)(C)OC(N(CCOC1)C1C(N[C@H](CO)C(OC)=O)=O)=O Chemical compound CC(C)(C)OC(N(CCOC1)C1C(N[C@H](CO)C(OC)=O)=O)=O PXRKWLBROJKTLG-YHMJZVADSA-N 0.000 description 1
- KVXXEKIGMOEPSA-UHFFFAOYSA-N CC(C)(C)OC(N(CCOC1)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCOC1)C1C(O)=O)=O KVXXEKIGMOEPSA-UHFFFAOYSA-N 0.000 description 1
- CTDIKDIZNAGMFK-UHFFFAOYSA-N CC(C)(C)OC(N(CCSC1)C1C(O)=O)=O Chemical compound CC(C)(C)OC(N(CCSC1)C1C(O)=O)=O CTDIKDIZNAGMFK-UHFFFAOYSA-N 0.000 description 1
- MCFFCQNSBLVXKS-OAHLLOKOSA-N CC(C)(C)OC(N1[C@@H](CNC(OCc2ccccc2)=O)CCC1)=O Chemical compound CC(C)(C)OC(N1[C@@H](CNC(OCc2ccccc2)=O)CCC1)=O MCFFCQNSBLVXKS-OAHLLOKOSA-N 0.000 description 1
- NFRFKIUDOXVXNV-GFCCVEGCSA-N CCOC([C@@H](COC1)N(Cc2ccccc2)C1=O)=O Chemical compound CCOC([C@@H](COC1)N(Cc2ccccc2)C1=O)=O NFRFKIUDOXVXNV-GFCCVEGCSA-N 0.000 description 1
- DOPPZLDDCUSBAF-OEMAIJDKSA-N CCOC([C@H]1COCCCC(Cc2ccccc2)C1)=O Chemical compound CCOC([C@H]1COCCCC(Cc2ccccc2)C1)=O DOPPZLDDCUSBAF-OEMAIJDKSA-N 0.000 description 1
- YIFCZNGSHKDPMH-UHFFFAOYSA-N CN(CCSC1)C1C(NC(CO)C(OC)=O)=O Chemical compound CN(CCSC1)C1C(NC(CO)C(OC)=O)=O YIFCZNGSHKDPMH-UHFFFAOYSA-N 0.000 description 1
- ANSUDRATXSJBLY-GSVOUGTGSA-N COC([C@@H](CO)N)=O Chemical compound COC([C@@H](CO)N)=O ANSUDRATXSJBLY-GSVOUGTGSA-N 0.000 description 1
- LTQSJQPTKFNKTH-UHFFFAOYSA-N FCC(CN(CCC1)C1C1)N1P Chemical compound FCC(CN(CCC1)C1C1)N1P LTQSJQPTKFNKTH-UHFFFAOYSA-N 0.000 description 1
- YEJJVVXWENVTAU-UHFFFAOYSA-N FCC1NCC(CCC2)N2C1 Chemical compound FCC1NCC(CCC2)N2C1 YEJJVVXWENVTAU-UHFFFAOYSA-N 0.000 description 1
- DPVSPOJGBBOZGB-UHFFFAOYSA-N O=C(CN1)N(CCNC2)C2C1=O Chemical compound O=C(CN1)N(CCNC2)C2C1=O DPVSPOJGBBOZGB-UHFFFAOYSA-N 0.000 description 1
- QXKAIPFKHPAPLY-ZETCQYMHSA-N O=C1NCCN(CCC2)[C@@H]2C1 Chemical compound O=C1NCCN(CCC2)[C@@H]2C1 QXKAIPFKHPAPLY-ZETCQYMHSA-N 0.000 description 1
- JNTSDSBEAXSUAU-LWOQYNTDSA-N OC[C@H](C(N1C2COCC1)=O)NC2=O Chemical compound OC[C@H](C(N1C2COCC1)=O)NC2=O JNTSDSBEAXSUAU-LWOQYNTDSA-N 0.000 description 1
- OPEBSOKNWMAPLB-JAMMHHFISA-N OC[C@H]1NCC(COCC2)N2C1 Chemical compound OC[C@H]1NCC(COCC2)N2C1 OPEBSOKNWMAPLB-JAMMHHFISA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5383—1,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
-
- 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
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/34—Tobacco-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Gynecology & Obstetrics (AREA)
- Rheumatology (AREA)
- Reproductive Health (AREA)
- Psychology (AREA)
- Child & Adolescent Psychology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0518472.6 | 2005-09-09 | ||
| GB0518472A GB0518472D0 (en) | 2005-09-09 | 2005-09-09 | Novel compounds |
| GB0611153A GB0611153D0 (en) | 2006-06-06 | 2006-06-06 | Novel compounds |
| GB0611153.8 | 2006-06-06 | ||
| PCT/EP2006/008845 WO2007028654A1 (en) | 2005-09-09 | 2006-09-07 | Pyridine derivatives and their use in the treatment of psychotic disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101305011A CN101305011A (zh) | 2008-11-12 |
| CN101305011B true CN101305011B (zh) | 2011-03-02 |
Family
ID=37546936
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2006800418603A Active CN101305011B (zh) | 2005-09-09 | 2006-09-07 | 吡啶衍生物及其在治疗精神障碍中的用途 |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US7683056B2 (https=) |
| EP (2) | EP1928886B1 (https=) |
| JP (1) | JP5121716B2 (https=) |
| KR (1) | KR101292348B1 (https=) |
| CN (1) | CN101305011B (https=) |
| AR (1) | AR058805A1 (https=) |
| AT (1) | ATE505472T1 (https=) |
| AU (1) | AU2006289281B2 (https=) |
| BR (1) | BRPI0615787B8 (https=) |
| CA (1) | CA2621564C (https=) |
| CR (1) | CR9847A (https=) |
| CY (1) | CY1111907T1 (https=) |
| DE (1) | DE602006021323D1 (https=) |
| DK (1) | DK1928886T3 (https=) |
| EA (1) | EA013909B1 (https=) |
| HR (1) | HRP20110457T1 (https=) |
| IL (1) | IL189578A (https=) |
| JO (1) | JO2722B1 (https=) |
| MA (1) | MA29780B1 (https=) |
| MY (1) | MY145713A (https=) |
| NO (1) | NO340921B1 (https=) |
| NZ (1) | NZ565983A (https=) |
| PE (1) | PE20070614A1 (https=) |
| PL (1) | PL1928886T3 (https=) |
| PT (1) | PT1928886E (https=) |
| SI (1) | SI1928886T1 (https=) |
| TW (1) | TWI378101B (https=) |
| WO (1) | WO2007028654A1 (https=) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007039123A2 (en) * | 2005-09-22 | 2007-04-12 | Smithkline Beecham Corporation | Combination therapy comprising an nk-3 antagonist and an antipsychotic agent |
| EP1943216B1 (en) * | 2005-10-10 | 2010-06-30 | Glaxo Group Limited | Prolinamide derivatives as sodium channel modulators |
| TW200730494A (en) * | 2005-10-10 | 2007-08-16 | Glaxo Group Ltd | Novel compounds |
| EP1945632B1 (en) | 2005-11-08 | 2013-09-18 | Vertex Pharmaceuticals Incorporated | Heterocyclic modulators of atp-binding cassette transporters |
| US7754739B2 (en) | 2007-05-09 | 2010-07-13 | Vertex Pharmaceuticals Incorporated | Modulators of CFTR |
| EP2117538A1 (en) | 2007-01-24 | 2009-11-18 | Glaxo Group Limited | Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-) |
| CA2684105C (en) | 2007-05-03 | 2011-09-06 | Pfizer Limited | Pyridine derivatives |
| US8969386B2 (en) | 2007-05-09 | 2015-03-03 | Vertex Pharmaceuticals Incorporated | Modulators of CFTR |
| SI2225230T1 (sl) | 2007-12-07 | 2017-03-31 | Vertex Pharmaceuticals Incorporated | Trdne oblike 3-(6-(1-2,2-difluorobenzo(d)(1,3)dioxol-5-il)ciklopropan- karboksamido)-3-metilpiridin-2-il) benzojske kisline |
| EP2639224B1 (en) | 2007-12-07 | 2016-08-24 | Vertex Pharmaceuticals Incorporated | Process for producing cycloalkylcarboxiamido-pyridine benzoic acids |
| EP2098526B1 (en) * | 2008-02-22 | 2014-01-15 | Neurotune AG | Nitrogen-containing bicyclic compounds active on chronic pain conditions |
| NZ720282A (en) | 2008-02-28 | 2017-12-22 | Vertex Pharma | Heteroaryl derivatives as cftr modulators |
| FR2928150A1 (fr) | 2008-02-29 | 2009-09-04 | Vetoquinol Sa Sa | Nouveaux derives 7-substitues de 3-carboxy-oxadiazino-quinolones, leur preparation et leur application comme anti-bacteriens |
| WO2009119528A1 (ja) * | 2008-03-24 | 2009-10-01 | 武田薬品工業株式会社 | 複素環化合物 |
| GB0808747D0 (en) | 2008-05-14 | 2008-06-18 | Glaxo Wellcome Mfg Pte Ltd | Novel compounds |
| EP2145891A1 (en) | 2008-07-09 | 2010-01-20 | Vetoquinol S.A. | 9-substituted-5-carboxy-oxadiazino-quinolone derivatives, their preparation and their application as anti-bacterials |
| GB0814340D0 (en) * | 2008-08-05 | 2008-09-10 | Smithkline Beecham Corp | Anhydrous crystol form fo a pyridine derivative |
| US20110034469A1 (en) | 2009-08-04 | 2011-02-10 | Takeda Pharmaceutical Company Limited | Heterocyclic Compound |
| PL2470545T3 (pl) * | 2009-08-27 | 2014-03-31 | Nerre Therapeutics Ltd | Bezwodne postaci pochodnej pirydyny |
| WO2011054773A1 (en) | 2009-11-03 | 2011-05-12 | Glaxosmithkline Llc | Novel lactam compounds |
| HRP20211752T1 (hr) | 2010-04-07 | 2022-02-18 | Vertex Pharmaceuticals Incorporated | Farmaceutski pripravci 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioksol-5-il)ciklopropankarboksamido)-3-metilpiridin-2-il)benzojeve kiseline i njihova primjena |
| ES2529233T3 (es) | 2010-07-09 | 2015-02-18 | Convergence Pharmaceuticals Limited | Compuestos tetrazol como bloqueadores de canales de calcio |
| US8648118B2 (en) | 2010-12-17 | 2014-02-11 | Boehringer Ingelheim International Gmbh | Bicyclic ring system substituted amide functionalised phenols as medicaments |
| CN102617503B (zh) * | 2011-03-03 | 2014-05-07 | 上海常丰生物医药科技有限公司 | (s)-3-吗啉基羧酸的合成方法 |
| WO2013049164A1 (en) * | 2011-09-29 | 2013-04-04 | Abbvie Inc. | SUBSTITUTED OCTAHYDROPYRROLO[1,2-a]PYRAZINES AS CALCIUM CHANNEL BLOCKERS |
| UY34349A (es) | 2011-09-29 | 2013-04-05 | Abb Vie Inc | OCTAHIDROPIRROLO[1,2-a]PIRAZINA SULFONAMIDAS SUSTITUIDAS COMO BLOQUEADORES DE CANALES DE CALCIO |
| WO2013112804A1 (en) | 2012-01-25 | 2013-08-01 | Vertex Pharmaceuticals Incorporated | Formulations of 3-(6-(1-(2.2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid |
| JP2016503007A (ja) | 2012-12-12 | 2016-02-01 | アッヴィ・インコーポレイテッド | 疼痛治療におけるカルシウムチャネル遮断薬として有用なジアゼピン誘導体 |
| CA2930008A1 (en) | 2013-11-08 | 2015-05-14 | Kissei Pharmaceutical Co., Ltd. | Carboxymethyl piperidine derivative |
| JP6963896B2 (ja) | 2013-11-12 | 2021-11-10 | バーテックス ファーマシューティカルズ インコーポレイテッドVertex Pharmaceuticals Incorporated | Cftr媒介性疾患の処置のための医薬組成物を調製する方法 |
| TWI649307B (zh) | 2014-05-07 | 2019-02-01 | 日商橘生藥品工業股份有限公司 | Cyclohexylpyridine derivative |
| WO2016021562A1 (ja) * | 2014-08-06 | 2016-02-11 | キッセイ薬品工業株式会社 | シアノチオフェン誘導体 |
| PT3221692T (pt) | 2014-11-18 | 2021-09-10 | Vertex Pharma | Processo de realização de testagem de alta produtividade por cromatografia líquida de alta eficiência |
| ES2912881T3 (es) | 2014-12-23 | 2022-05-30 | Convergence Pharmaceuticals | Procedimiento para preparar derivados de alfa-carboxamida pirrolidina |
| SMT201900719T1 (it) * | 2015-05-18 | 2020-01-14 | Nerre Therapeutics Ltd | Antagonista del recettore nk-1/nk-3 per il trattamento delle vampate di calore |
| US11192856B2 (en) | 2017-10-05 | 2021-12-07 | Biogen Inc. | Process for preparing alpha-carboxamide pyrrolidine derivatives |
| AU2019233606B2 (en) | 2018-03-14 | 2024-10-03 | KaNDy Therapeutics Limited | Novel pharmaceutical formulation comprising dual NK-1/NK-3 receptor antagonists |
| US11583538B2 (en) | 2019-04-08 | 2023-02-21 | Venenum Biodesign, LLC | Substituted pyrrolo[1,2-a]pyrazines and pyrrolo[1,2-a][1,4]diazepines as TREX1 inhibitors |
| PE20221167A1 (es) | 2019-11-15 | 2022-07-25 | Kandy Therapeutics Ltd | Nuevo proceso quimico para la elaboracion de 6-cloro-4-(4-fluoro-2-metilfenil)piridin-3-amina, un intermediario clave de nt-814 |
| KR102682775B1 (ko) * | 2020-06-26 | 2024-07-08 | 홀로스메딕 주식회사 | 신규한 화합물의 제조방법 |
| WO2021261969A1 (ko) * | 2020-06-26 | 2021-12-30 | 홀로스메딕 주식회사 | 신규한 화합물의 제조방법 |
| WO2022075974A1 (en) * | 2020-10-06 | 2022-04-14 | Venenum Biodesign, LLC | Cyclic trex1 inhibitors |
| KR20240004329A (ko) * | 2021-04-05 | 2024-01-11 | 더 보드 어브 트러스티스 어브 더 리랜드 스탠포드 주니어 유니버시티 | 신경전달에 대한 거울상이성질체 선택적 작용 |
| EP4431512A1 (en) | 2023-03-16 | 2024-09-18 | Bayer Consumer Care AG | Novel dual nk-1/nk-3 receptor antagonists |
| WO2025242584A1 (en) | 2024-05-24 | 2025-11-27 | Bayer Consumer Care Ag | A stable soft gelatin capsule formulation for elinzanetant |
| WO2025242585A1 (en) | 2024-05-24 | 2025-11-27 | Bayer Consumer Care Ag | Crystalline forms of salts of elinzanetant and compositions containing salts of elinzanetant |
| WO2025242583A1 (en) | 2024-05-24 | 2025-11-27 | Bayer Consumer Care Ag | Novel formulation comprising elinzanetant in a solid dispersion |
| WO2025261856A1 (en) | 2024-06-18 | 2025-12-26 | Bayer Consumer Care Ag | Improved process for producing an elinzanetant precursor |
| US12533358B1 (en) | 2025-05-14 | 2026-01-27 | Bayer Consumer Care Ag | Methods of treatment with elinzanetant |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005002577A1 (en) * | 2003-07-03 | 2005-01-13 | F. Hoffmann-La Roche Ag | Dual nk1/nk3 antagonists for treating schizophrenia |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4921855A (en) | 1987-06-22 | 1990-05-01 | Fujisawa Pharmaceutical Co., Ltd. | New Histidyl amino acid derivatives, and pharmaceutical composition comprising the same |
| US5166203A (en) | 1990-08-30 | 1992-11-24 | Kanebo, Ltd. | Quinolinecarboxylic acid derivatives, antibacterial agent containing the same |
| SI1004583T1 (en) | 1998-11-23 | 2004-12-31 | Pfizer Products Inc. | Process and hydantoin intermediates for the synthesis of growth hormone secretagogues |
| PT1035115E (pt) | 1999-02-24 | 2005-01-31 | Hoffmann La Roche | Derivados de 4-fenilpiridina e a sua utilizacao como antagonistas do receptor nk-1 |
| DOP2000000107A (es) | 1999-12-01 | 2002-09-16 | Agouron Pharmaceutical Inc | Compuestos, composiciones y metodos para estimular el crecimiento y alongamiento de las neuronas |
| TWI259180B (en) | 2000-08-08 | 2006-08-01 | Hoffmann La Roche | 4-Phenyl-pyridine derivatives |
| GB0203020D0 (en) * | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| GB0203022D0 (en) * | 2002-02-08 | 2002-03-27 | Glaxo Group Ltd | Chemical compounds |
| TW200407324A (en) | 2002-05-17 | 2004-05-16 | Bristol Myers Squibb Co | Bicyclic modulators of androgen receptor function |
-
2006
- 2006-09-07 EA EA200800784A patent/EA013909B1/ru unknown
- 2006-09-07 EP EP06777183A patent/EP1928886B1/en active Active
- 2006-09-07 US US12/065,923 patent/US7683056B2/en active Active
- 2006-09-07 CN CN2006800418603A patent/CN101305011B/zh active Active
- 2006-09-07 KR KR1020087008441A patent/KR101292348B1/ko active Active
- 2006-09-07 WO PCT/EP2006/008845 patent/WO2007028654A1/en not_active Ceased
- 2006-09-07 DK DK06777183.2T patent/DK1928886T3/da active
- 2006-09-07 EP EP10190918A patent/EP2336136A1/en not_active Withdrawn
- 2006-09-07 NZ NZ565983A patent/NZ565983A/en not_active IP Right Cessation
- 2006-09-07 PE PE2006001077A patent/PE20070614A1/es not_active Application Discontinuation
- 2006-09-07 HR HR20110457T patent/HRP20110457T1/hr unknown
- 2006-09-07 MY MYPI20064110A patent/MY145713A/en unknown
- 2006-09-07 JO JO2006301A patent/JO2722B1/en active
- 2006-09-07 JP JP2008529564A patent/JP5121716B2/ja active Active
- 2006-09-07 DE DE602006021323T patent/DE602006021323D1/de active Active
- 2006-09-07 PT PT06777183T patent/PT1928886E/pt unknown
- 2006-09-07 CA CA2621564A patent/CA2621564C/en active Active
- 2006-09-07 AR ARP060103894A patent/AR058805A1/es active IP Right Grant
- 2006-09-07 BR BRPI0615787A patent/BRPI0615787B8/pt active IP Right Grant
- 2006-09-07 AU AU2006289281A patent/AU2006289281B2/en active Active
- 2006-09-07 PL PL06777183T patent/PL1928886T3/pl unknown
- 2006-09-07 AT AT06777183T patent/ATE505472T1/de active
- 2006-09-07 TW TW095132989A patent/TWI378101B/zh active
- 2006-09-07 SI SI200631047T patent/SI1928886T1/sl unknown
-
2008
- 2008-02-18 IL IL189578A patent/IL189578A/en active IP Right Grant
- 2008-03-17 MA MA30749A patent/MA29780B1/fr unknown
- 2008-03-28 CR CR9847A patent/CR9847A/es not_active Application Discontinuation
- 2008-04-07 NO NO20081728A patent/NO340921B1/no unknown
-
2009
- 2009-12-14 US US12/636,849 patent/US7919491B2/en active Active
-
2011
- 2011-02-23 US US13/032,740 patent/US8097618B2/en active Active
- 2011-07-04 CY CY20111100641T patent/CY1111907T1/el unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2005002577A1 (en) * | 2003-07-03 | 2005-01-13 | F. Hoffmann-La Roche Ag | Dual nk1/nk3 antagonists for treating schizophrenia |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN101305011B (zh) | 吡啶衍生物及其在治疗精神障碍中的用途 | |
| TWI811353B (zh) | 作為parp7抑制劑的嗒酮 | |
| JP2009507801A5 (https=) | ||
| CN107207514B (zh) | 稠环杂芳基化合物及其作为trk抑制剂的用途 | |
| TWI794232B (zh) | 激酶抑制劑及其用途 | |
| KR20230019855A (ko) | Kras g12c 단백질의 억제제 및 그의 용도 | |
| WO2024083256A1 (zh) | pan-KRAS降解剂及其制备方法和应用 | |
| TW201605859A (zh) | 作為酪蛋白激酶1δ/ε抑制劑之新穎經取代之吡唑并-哌 | |
| CN110691784A (zh) | 抑制mcl-1蛋白的化合物 | |
| CN111433207B (zh) | 作为αV整合素抑制剂的吡咯并吡嗪衍生物 | |
| TWI902994B (zh) | Irak4抑制劑、藥物組成物及其用途 | |
| KR102281284B1 (ko) | 피페라진 유도체 및 약제로서의 이의 용도 | |
| CN105541693A (zh) | 芳杂环类衍生物及其在药物上的应用 | |
| TW201602116A (zh) | 作為β-分泌酶抑制劑之橋接二環胺基噻嗪二氧化物化合物及其使用方法 | |
| CN111201226A (zh) | 环状被取代的咪唑并[4,5-c]喹啉衍生物 | |
| CN115151551B (zh) | 作为mcl-1抑制剂的大环吲哚衍生物 | |
| HK40104906A (zh) | 作为髓样细胞上表达的触发受体2激动剂的杂环化合物和使用方法 | |
| TW202610655A (zh) | Kras抑制劑 | |
| CN117295749A (zh) | 作为mcl-1抑制剂的大环2-烯丙基四氢呋喃 | |
| HK1242314B (zh) | 稠环杂芳基化合物及其作为trk抑制剂的用途 | |
| HK1242314A1 (en) | Fused ring heteroaryl compounds and their use as trk inhibitors |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| ASS | Succession or assignment of patent right |
Owner name: NIL MEDICAL CO., LTD. Free format text: FORMER OWNER: SMITHKLINE BEECHAM CORP. Effective date: 20130702 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| C56 | Change in the name or address of the patentee |
Owner name: SMITHKLINE BEECHAM CORP. Free format text: FORMER NAME: SMITHKLINE BEECHAN CORP. |
|
| CP01 | Change in the name or title of a patent holder |
Address after: American Pennsylvania Patentee after: GLAXOSMITHKLINE LLC Address before: American Pennsylvania Patentee before: SMITHKLINE BEECHAM Corp. |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20130702 Address after: Steve Niki Patentee after: NERRE THERAPEUTICS LTD. Address before: American Pennsylvania Patentee before: GLAXOSMITHKLINE LLC |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20210222 Address after: Hakuhoku County, England Patentee after: Kandi Medical Co.,Ltd. Address before: Steve Niki Patentee before: NeRRe Therapeutics Ltd. |
|
| TR01 | Transfer of patent right |