CN101048414B - 用于治疗精神障碍的稠合的三环衍生物 - Google Patents
用于治疗精神障碍的稠合的三环衍生物 Download PDFInfo
- Publication number
- CN101048414B CN101048414B CN2005800372427A CN200580037242A CN101048414B CN 101048414 B CN101048414 B CN 101048414B CN 2005800372427 A CN2005800372427 A CN 2005800372427A CN 200580037242 A CN200580037242 A CN 200580037242A CN 101048414 B CN101048414 B CN 101048414B
- Authority
- CN
- China
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- compound according
- methyl
- ethyl
- 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.)
- Expired - Fee Related
Links
- FNSPIBDKXKNHEJ-UHFFFAOYSA-N C=CCc1cccc-2c1OCc1nnn[n]-21 Chemical compound C=CCc1cccc-2c1OCc1nnn[n]-21 FNSPIBDKXKNHEJ-UHFFFAOYSA-N 0.000 description 1
- RQLAJTRGFNEHAY-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1c1c(ccc(C=O)n2)c2ccc1)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1c1c(ccc(C=O)n2)c2ccc1)=O RQLAJTRGFNEHAY-UHFFFAOYSA-N 0.000 description 1
- PUOXMWOHHZDZBP-UHFFFAOYSA-N CC(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3cccc4nc(C)ccc34)c1OC2)=O Chemical compound CC(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3cccc4nc(C)ccc34)c1OC2)=O PUOXMWOHHZDZBP-UHFFFAOYSA-N 0.000 description 1
- ODTPYCQBNJPZCM-UHFFFAOYSA-N CC1=C(C)N2c(cccc3CCN(CC4)CCN4c4cccc5nc(C)ccc45)c3OCC2N1 Chemical compound CC1=C(C)N2c(cccc3CCN(CC4)CCN4c4cccc5nc(C)ccc45)c3OCC2N1 ODTPYCQBNJPZCM-UHFFFAOYSA-N 0.000 description 1
- QYAGFASLMAXKSP-UHFFFAOYSA-N CC1=NNC2N1c1cccc(CC=O)c1C=C2 Chemical compound CC1=NNC2N1c1cccc(CC=O)c1C=C2 QYAGFASLMAXKSP-UHFFFAOYSA-N 0.000 description 1
- YJVSDYVIMIJRJE-UHFFFAOYSA-N CC1Nc2cccc(C(CC3)(CCN3C(OC(C)(C)C)=O)O)c2C=C1 Chemical compound CC1Nc2cccc(C(CC3)(CCN3C(OC(C)(C)C)=O)O)c2C=C1 YJVSDYVIMIJRJE-UHFFFAOYSA-N 0.000 description 1
- CVAJBXBSKCQEEL-UHFFFAOYSA-N CCOC(c(nc1)c(COc2c3CCN(CC4)CCN4c4cccc5c4ccc(C)n5)[n]1-c2ccc3F)=O Chemical compound CCOC(c(nc1)c(COc2c3CCN(CC4)CCN4c4cccc5c4ccc(C)n5)[n]1-c2ccc3F)=O CVAJBXBSKCQEEL-UHFFFAOYSA-N 0.000 description 1
- HSHJRPHSLZOOEP-UHFFFAOYSA-N CCOC(c(nc1)c2[n]1-c(cccc1C(C)C=O)c1OC2)=O Chemical compound CCOC(c(nc1)c2[n]1-c(cccc1C(C)C=O)c1OC2)=O HSHJRPHSLZOOEP-UHFFFAOYSA-N 0.000 description 1
- DMBCLEUWZUWYHZ-UHFFFAOYSA-N CN(C)C(c1nc2cccc(N3CCNCC3)c2cc1)=O Chemical compound CN(C)C(c1nc2cccc(N3CCNCC3)c2cc1)=O DMBCLEUWZUWYHZ-UHFFFAOYSA-N 0.000 description 1
- LTSBBMPKGJHJNN-UHFFFAOYSA-N CNC(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3c(ccc(C(F)F)n4)c4ccc3)c1OC2)=O Chemical compound CNC(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3c(ccc(C(F)F)n4)c4ccc3)c1OC2)=O LTSBBMPKGJHJNN-UHFFFAOYSA-N 0.000 description 1
- ZQBMKMZGWKGAHQ-UHFFFAOYSA-N COC(Cc(cc1)nc2c1c(CC=C)ccc2)=O Chemical compound COC(Cc(cc1)nc2c1c(CC=C)ccc2)=O ZQBMKMZGWKGAHQ-UHFFFAOYSA-N 0.000 description 1
- NTJMTWKWUQAHAL-JOCHJYFZSA-N C[C@H](C1)N(CCc2c(C)ccc-3c2CCc2c(C(NC)=O)nc[n]-32)CCN1c1cccc2nc(C)ccc12 Chemical compound C[C@H](C1)N(CCc2c(C)ccc-3c2CCc2c(C(NC)=O)nc[n]-32)CCN1c1cccc2nc(C)ccc12 NTJMTWKWUQAHAL-JOCHJYFZSA-N 0.000 description 1
- UHCNEUWWWYPKNN-HXUWFJFHSA-N C[C@H](C1)N(CCc2c3OCc4c(C(NC)=O)nc[n]4-c3ccc2)CCN1c1c(ccc(C)n2)c2ccc1 Chemical compound C[C@H](C1)N(CCc2c3OCc4c(C(NC)=O)nc[n]4-c3ccc2)CCN1c1c(ccc(C)n2)c2ccc1 UHCNEUWWWYPKNN-HXUWFJFHSA-N 0.000 description 1
- DUQVLRKBBSVOFJ-GOSISDBHSA-N C[C@H](C1)N(CCc2cccc-3c2CCc2c(C(O)=O)nn[n]-32)CCN1c1cc(F)cc2nc(C)ccc12 Chemical compound C[C@H](C1)N(CCc2cccc-3c2CCc2c(C(O)=O)nn[n]-32)CCN1c1cc(F)cc2nc(C)ccc12 DUQVLRKBBSVOFJ-GOSISDBHSA-N 0.000 description 1
- WORTVYIFSBJLQF-LJQANCHMSA-N C[C@H](C1)N(CCc2cccc-3c2CCc2nnn[n]-32)CCN1c1cccc2nc(C)ccc12 Chemical compound C[C@H](C1)N(CCc2cccc-3c2CCc2nnn[n]-32)CCN1c1cccc2nc(C)ccc12 WORTVYIFSBJLQF-LJQANCHMSA-N 0.000 description 1
- RKWZRKZRPIUILS-UHFFFAOYSA-N Cc(cc1)c(CCN(CC2)CCN2c2cccc3c2ccc(C)n3)c(CC2)c1-[n]1c2c(C(N)=O)nc1 Chemical compound Cc(cc1)c(CCN(CC2)CCN2c2cccc3c2ccc(C)n3)c(CC2)c1-[n]1c2c(C(N)=O)nc1 RKWZRKZRPIUILS-UHFFFAOYSA-N 0.000 description 1
- ZWTFYZPXEGVODH-UHFFFAOYSA-O Cc(cc1)nc2c1c(C1CCN(CCC(C=CCC3N4NC)=C3C=CC4=C[NH3+])CC1)ccc2 Chemical compound Cc(cc1)nc2c1c(C1CCN(CCC(C=CCC3N4NC)=C3C=CC4=C[NH3+])CC1)ccc2 ZWTFYZPXEGVODH-UHFFFAOYSA-O 0.000 description 1
- ZAUKNTWEYFEWDD-UHFFFAOYSA-N Cc(cc1)nc2c1c(N1CCN(CCc3cccc(N45)c3OCC4=NN(C)C5=O)CC1)ccc2 Chemical compound Cc(cc1)nc2c1c(N1CCN(CCc3cccc(N45)c3OCC4=NN(C)C5=O)CC1)ccc2 ZAUKNTWEYFEWDD-UHFFFAOYSA-N 0.000 description 1
- KKCLFVGCIPPQTB-UHFFFAOYSA-N Cc(cc1)nc2c1c(N1CCN(CCc3cccc-4c3CCc3c(C(O)=O)nc[n]-43)CC1)ccc2 Chemical compound Cc(cc1)nc2c1c(N1CCN(CCc3cccc-4c3CCc3c(C(O)=O)nc[n]-43)CC1)ccc2 KKCLFVGCIPPQTB-UHFFFAOYSA-N 0.000 description 1
- LHWYHPOPXMPQGV-UHFFFAOYSA-N Cc1ccc(c(N2CCN(CCc3cccc-4c3OCc3ncc[n]-43)CC2)ccc2)c2n1 Chemical compound Cc1ccc(c(N2CCN(CCc3cccc-4c3OCc3ncc[n]-43)CC2)ccc2)c2n1 LHWYHPOPXMPQGV-UHFFFAOYSA-N 0.000 description 1
- PMKSAFPTOHNNKR-UHFFFAOYSA-N Cc1nc2cccc(N3CCN(Cc4cccc-5c4OCc4ncc[n]-54)CC3)c2cc1 Chemical compound Cc1nc2cccc(N3CCN(Cc4cccc-5c4OCc4ncc[n]-54)CC3)c2cc1 PMKSAFPTOHNNKR-UHFFFAOYSA-N 0.000 description 1
- OEUPEDBVXDZNTC-UHFFFAOYSA-N Cc1nnc2[n]1-c(cccc1CCN(CC3)CCC3c3cccc4c3ccc(C)n4)c1OC2 Chemical compound Cc1nnc2[n]1-c(cccc1CCN(CC3)CCC3c3cccc4c3ccc(C)n4)c1OC2 OEUPEDBVXDZNTC-UHFFFAOYSA-N 0.000 description 1
- GWQTVIRNHUDPMH-UHFFFAOYSA-N FC(c(cc1)nc2c1c(N1CCN(CCc3c(ccc4nnn[n]44)c4ccc3)CC1)ccc2)F Chemical compound FC(c(cc1)nc2c1c(N1CCN(CCc3c(ccc4nnn[n]44)c4ccc3)CC1)ccc2)F GWQTVIRNHUDPMH-UHFFFAOYSA-N 0.000 description 1
- HLNAFVKSXBALRO-UHFFFAOYSA-N O=C(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3cccc4c3ccc(CF)n4)c1OC2)N1CCOCC1 Chemical compound O=C(c(nc1)c2[n]1-c(cccc1CCN(CC3)CCN3c3cccc4c3ccc(CF)n4)c1OC2)N1CCOCC1 HLNAFVKSXBALRO-UHFFFAOYSA-N 0.000 description 1
- ZZGQSAVCPDVORI-UHFFFAOYSA-N O=C1Nc2cccc(OS(C(F)(F)F)(=O)=O)c2CC1 Chemical compound O=C1Nc2cccc(OS(C(F)(F)F)(=O)=O)c2CC1 ZZGQSAVCPDVORI-UHFFFAOYSA-N 0.000 description 1
- SQBDZSLWMXYFEG-UHFFFAOYSA-N O=CCc1cccc-2c1CCc1nnn[n]-21 Chemical compound O=CCc1cccc-2c1CCc1nnn[n]-21 SQBDZSLWMXYFEG-UHFFFAOYSA-N 0.000 description 1
- MRWXWBMSSMFYAL-UHFFFAOYSA-N Oc1c(CCN(CC2)CCN2c2c(ccc(C(F)(F)F)n3)c3ccc2)c(F)ccc1Br Chemical compound Oc1c(CCN(CC2)CCN2c2c(ccc(C(F)(F)F)n3)c3ccc2)c(F)ccc1Br MRWXWBMSSMFYAL-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed 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
- A61K31/435—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
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4738—Quinolines; Isoquinolines 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/12—Drugs for genital or sexual disorders; Contraceptives for climacteric disorders
-
- 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
- A61P25/18—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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Anesthesiology (AREA)
- Pain & Pain Management (AREA)
- Gynecology & Obstetrics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0419315A GB0419315D0 (en) | 2004-08-31 | 2004-08-31 | Compounds |
| GB0419315.7 | 2004-08-31 | ||
| GB0507386A GB0507386D0 (en) | 2005-04-12 | 2005-04-12 | Compounds |
| GB0507386.1 | 2005-04-12 | ||
| GB0515010A GB0515010D0 (en) | 2005-07-21 | 2005-07-21 | Compounds |
| GB0515010.7 | 2005-07-21 | ||
| PCT/EP2005/009379 WO2006024517A1 (en) | 2004-08-31 | 2005-08-29 | Fused tricyclic derivatives for the treatment of psychotic disorders |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101048414A CN101048414A (zh) | 2007-10-03 |
| CN101048414B true CN101048414B (zh) | 2011-09-07 |
Family
ID=35106764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2005800372427A Expired - Fee Related CN101048414B (zh) | 2004-08-31 | 2005-08-29 | 用于治疗精神障碍的稠合的三环衍生物 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20120022056A1 (https=) |
| EP (1) | EP1786822A1 (https=) |
| JP (1) | JP2008511574A (https=) |
| KR (1) | KR20070057885A (https=) |
| CN (1) | CN101048414B (https=) |
| AR (1) | AR053307A1 (https=) |
| AU (1) | AU2005279278A1 (https=) |
| BR (1) | BRPI0514377A (https=) |
| CA (1) | CA2578781A1 (https=) |
| IL (1) | IL181387A (https=) |
| MA (1) | MA28871B1 (https=) |
| MX (1) | MX2007002548A (https=) |
| NO (1) | NO20071326L (https=) |
| NZ (1) | NZ553506A (https=) |
| PE (1) | PE20060653A1 (https=) |
| TW (1) | TW200619221A (https=) |
| WO (1) | WO2006024517A1 (https=) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0316915D0 (en) | 2003-07-18 | 2003-08-20 | Glaxo Group Ltd | Compounds |
| US7898642B2 (en) | 2004-04-14 | 2011-03-01 | Asml Netherlands B.V. | Lithographic apparatus and device manufacturing method |
| JP4324221B2 (ja) * | 2005-08-26 | 2009-09-02 | 株式会社医薬分子設計研究所 | Pparアゴニスト活性を有する誘導体 |
| JP2009523820A (ja) * | 2006-01-23 | 2009-06-25 | アミラ ファーマシューティカルス,インコーポレーテッド | 5−リポキシゲナーゼの三環系抑制剤 |
| US7501438B2 (en) | 2006-07-07 | 2009-03-10 | Forest Laboratories Holdings Limited | Pyridoimidazole derivatives |
| CA2662080C (en) | 2006-09-07 | 2012-07-17 | F. Hoffmann-La Roche Ag | A process for the manufacture of snac (salcaprozate sodium) |
| JP2010504367A (ja) | 2006-09-26 | 2010-02-12 | グラクソ グループ リミテッド | 性機能障害、認知障害、精神病性障害、不安、鬱病などを処置するための5ht1a受容体モジュレーターとしての5−{2−[4−(2−メチル−5−キノリニル)−l−ピペリジニル]エチル}キノリノン誘導体 |
| AU2008223348A1 (en) * | 2007-03-07 | 2008-09-12 | Alantos Pharmaceuticals Holding, Inc. | Metalloprotease inhibitors containing a heterocyclic moiety |
| EP2070933A1 (en) | 2007-12-07 | 2009-06-17 | Laboratorios del Dr. Esteve S.A. | Tricyclic triazolic compounds |
| GB0800840D0 (en) | 2008-01-17 | 2008-02-27 | Glaxo Group Ltd | Novel salt |
| DK2268644T3 (da) | 2008-03-05 | 2011-10-10 | Boehringer Ingelheim Int | Tricycliske pyridinderivater, medikamenter indeholdende sådanne forbindelser, deres anvendelse og fremgangsmåde til deres fremstilling |
| WO2010111626A2 (en) * | 2009-03-27 | 2010-09-30 | Takeda Pharmaceutical Company Limited | Poly (adp-ribose) polymerase (parp) inhibitors |
| EA201201160A1 (ru) | 2010-02-19 | 2013-04-30 | Бёрингер Ингельхайм Интернациональ Гмбх | Трициклические производные пиридина, лекарственные средства, содержащие такие соединения, их применение и способ их получения |
| AU2011261375B2 (en) | 2010-06-04 | 2016-09-22 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
| WO2012154731A1 (en) * | 2011-05-08 | 2012-11-15 | Vanderbilt University | Substituted 1h-pyrrolo[3,2-c]quinolin-4(5h)-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m4 |
| JP5947382B2 (ja) | 2011-08-17 | 2016-07-06 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | フロ[3,4−c]キノリン誘導体、このような化合物を含む薬物、それらの使用及びそれらの調製方法 |
| EP2792679A1 (en) * | 2013-04-19 | 2014-10-22 | Laboratorios Del. Dr. Esteve, S.A. | Tricyclic triazolic compounds |
| JP6523267B2 (ja) * | 2013-06-24 | 2019-05-29 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツングMerck Patent Gesellschaft mit beschraenkter Haftung | Fshrの調節剤としてのイミダゾール化合物及びその使用 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0887349A1 (en) * | 1997-06-26 | 1998-12-30 | Akzo Nobel N.V. | Tetrahydroimidazo (2,1-a)isoquinoline derivatives |
| US6143767A (en) * | 1996-08-14 | 2000-11-07 | Pfizer Inc | Piperidinylamino tricyclic compounds as substance P antagonists |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6919334B2 (en) * | 2002-09-12 | 2005-07-19 | Wyeth | Antidepressant azaheterocyclymethyl derivatives of 4,5-dihydroimidazo[1,4,5-de][1,4]benzoxazine |
| GB0227240D0 (en) * | 2002-11-21 | 2002-12-31 | Glaxo Group Ltd | Compounds |
-
2005
- 2005-08-26 PE PE2005000983A patent/PE20060653A1/es not_active Application Discontinuation
- 2005-08-29 AR ARP050103607A patent/AR053307A1/es not_active Application Discontinuation
- 2005-08-29 AU AU2005279278A patent/AU2005279278A1/en not_active Abandoned
- 2005-08-29 JP JP2007528777A patent/JP2008511574A/ja active Pending
- 2005-08-29 TW TW094129416A patent/TW200619221A/zh unknown
- 2005-08-29 KR KR1020077007190A patent/KR20070057885A/ko not_active Ceased
- 2005-08-29 EP EP05778196A patent/EP1786822A1/en not_active Withdrawn
- 2005-08-29 NZ NZ553506A patent/NZ553506A/en not_active IP Right Cessation
- 2005-08-29 MX MX2007002548A patent/MX2007002548A/es active IP Right Grant
- 2005-08-29 BR BRPI0514377-2A patent/BRPI0514377A/pt not_active IP Right Cessation
- 2005-08-29 CN CN2005800372427A patent/CN101048414B/zh not_active Expired - Fee Related
- 2005-08-29 US US11/574,450 patent/US20120022056A1/en not_active Abandoned
- 2005-08-29 WO PCT/EP2005/009379 patent/WO2006024517A1/en not_active Ceased
- 2005-08-29 CA CA002578781A patent/CA2578781A1/en not_active Abandoned
-
2007
- 2007-02-15 IL IL181387A patent/IL181387A/en not_active IP Right Cessation
- 2007-03-12 NO NO20071326A patent/NO20071326L/no not_active Application Discontinuation
- 2007-03-23 MA MA29771A patent/MA28871B1/fr unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6143767A (en) * | 1996-08-14 | 2000-11-07 | Pfizer Inc | Piperidinylamino tricyclic compounds as substance P antagonists |
| EP0887349A1 (en) * | 1997-06-26 | 1998-12-30 | Akzo Nobel N.V. | Tetrahydroimidazo (2,1-a)isoquinoline derivatives |
Also Published As
| Publication number | Publication date |
|---|---|
| US20120022056A1 (en) | 2012-01-26 |
| EP1786822A1 (en) | 2007-05-23 |
| WO2006024517A1 (en) | 2006-03-09 |
| PE20060653A1 (es) | 2006-09-27 |
| IL181387A (en) | 2011-10-31 |
| KR20070057885A (ko) | 2007-06-07 |
| NO20071326L (no) | 2007-05-03 |
| CN101048414A (zh) | 2007-10-03 |
| MA28871B1 (fr) | 2007-09-03 |
| AR053307A1 (es) | 2007-05-02 |
| AU2005279278A1 (en) | 2006-03-09 |
| TW200619221A (en) | 2006-06-16 |
| CA2578781A1 (en) | 2006-03-09 |
| NZ553506A (en) | 2010-02-26 |
| IL181387A0 (en) | 2007-07-04 |
| BRPI0514377A (pt) | 2008-06-24 |
| MX2007002548A (es) | 2007-04-24 |
| JP2008511574A (ja) | 2008-04-17 |
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