ZA200601990B - 1-(2-Amino-benzol)-piperazine derivatives as glycine uptake inhibitors for the treatment of psychoses - Google Patents
1-(2-Amino-benzol)-piperazine derivatives as glycine uptake inhibitors for the treatment of psychoses Download PDFInfo
- Publication number
- ZA200601990B ZA200601990B ZA200601990A ZA200601990A ZA200601990B ZA 200601990 B ZA200601990 B ZA 200601990B ZA 200601990 A ZA200601990 A ZA 200601990A ZA 200601990 A ZA200601990 A ZA 200601990A ZA 200601990 B ZA200601990 B ZA 200601990B
- Authority
- ZA
- South Africa
- Prior art keywords
- alkyl
- phenyl
- piperazine
- fluoro
- piperazin
- Prior art date
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- 208000028017 Psychotic disease Diseases 0.000 title claims description 9
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 title description 14
- 239000004471 Glycine Substances 0.000 title description 7
- 239000003112 inhibitor Substances 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims description 127
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 127
- 229910052736 halogen Inorganic materials 0.000 claims description 103
- 150000002367 halogens Chemical group 0.000 claims description 103
- 229910052739 hydrogen Inorganic materials 0.000 claims description 77
- 239000001257 hydrogen Substances 0.000 claims description 77
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 49
- 125000001072 heteroaryl group Chemical group 0.000 claims description 45
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 36
- 125000001424 substituent group Chemical group 0.000 claims description 32
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 28
- GLUUGHFHXGJENI-UHFFFAOYSA-N diethylenediamine Natural products C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 24
- 125000005842 heteroatom Chemical group 0.000 claims description 24
- 150000002431 hydrogen Chemical class 0.000 claims description 23
- 229910052757 nitrogen Inorganic materials 0.000 claims description 23
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 22
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 229910052760 oxygen Inorganic materials 0.000 claims description 21
- 150000003839 salts Chemical class 0.000 claims description 21
- 239000002253 acid Substances 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 19
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 201000000980 schizophrenia Diseases 0.000 claims description 13
- -1 (Cs-Cs)-cycloalkyl Chemical group 0.000 claims description 12
- NEFFMZJKQNSKMQ-UHFFFAOYSA-N 1-[3-fluoro-4-[4-(2-morpholin-4-yl-5-nitrobenzoyl)piperazin-1-yl]phenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCOCC2)CC1 NEFFMZJKQNSKMQ-UHFFFAOYSA-N 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 7
- 208000024827 Alzheimer disease Diseases 0.000 claims description 6
- 206010012289 Dementia Diseases 0.000 claims description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 201000010099 disease Diseases 0.000 claims description 6
- 239000003814 drug Substances 0.000 claims description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 6
- 208000006096 Attention Deficit Disorder with Hyperactivity Diseases 0.000 claims description 5
- ARXNIOQXGVZLSL-UHFFFAOYSA-N [4-(4-methoxyphenyl)piperazin-1-yl]-(2-morpholin-4-yl-5-nitrophenyl)methanone Chemical compound C1=CC(OC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCOCC2)CC1 ARXNIOQXGVZLSL-UHFFFAOYSA-N 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 230000001771 impaired effect Effects 0.000 claims description 5
- BBNAKYQCUWPKCG-UHFFFAOYSA-N 1-[3-fluoro-4-[4-(2-morpholin-4-yl-5-nitrobenzoyl)piperazin-1-yl]phenyl]propan-1-one Chemical compound FC1=CC(C(=O)CC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCOCC2)CC1 BBNAKYQCUWPKCG-UHFFFAOYSA-N 0.000 claims description 4
- AWKVHISJBMJMNQ-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-(4-methylpiperazin-1-yl)-5-nitrobenzoyl]piperazin-1-yl]phenyl]propan-1-one Chemical compound FC1=CC(C(=O)CC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCN(C)CC2)CC1 AWKVHISJBMJMNQ-UHFFFAOYSA-N 0.000 claims description 4
- KPFUQGKMXCDEJE-UHFFFAOYSA-N 4-morpholin-4-yl-3-(4-phenylpiperazine-1-carbonyl)benzenesulfonamide Chemical compound C1CN(C=2C=CC=CC=2)CCN1C(=O)C1=CC(S(=O)(=O)N)=CC=C1N1CCOCC1 KPFUQGKMXCDEJE-UHFFFAOYSA-N 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzenecarbonitrile Natural products N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 4
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 125000003107 substituted aryl group Chemical group 0.000 claims description 4
- SDHZEMOLXNOMQA-UHFFFAOYSA-N 1-[3-fluoro-4-[4-(5-nitro-2-piperidin-1-ylbenzoyl)piperazin-1-yl]phenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCCCC2)CC1 SDHZEMOLXNOMQA-UHFFFAOYSA-N 0.000 claims description 3
- MAGBVRGFYGCXEG-UHFFFAOYSA-N 1-[3-fluoro-4-[4-(5-nitro-2-pyrrolidin-1-ylbenzoyl)piperazin-1-yl]phenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCCC2)CC1 MAGBVRGFYGCXEG-UHFFFAOYSA-N 0.000 claims description 3
- LMTCLQMTWFYOFU-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-(2-methylpiperidin-1-yl)-5-nitrobenzoyl]piperazin-1-yl]phenyl]ethanone Chemical compound CC1CCCCN1C1=CC=C([N+]([O-])=O)C=C1C(=O)N1CCN(C=2C(=CC(=CC=2)C(C)=O)F)CC1 LMTCLQMTWFYOFU-UHFFFAOYSA-N 0.000 claims description 3
- FNSJBNAZKYMGGW-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-(2-methylpyrrolidin-1-yl)-5-nitrobenzoyl]piperazin-1-yl]phenyl]ethanone Chemical compound CC1CCCN1C1=CC=C([N+]([O-])=O)C=C1C(=O)N1CCN(C=2C(=CC(=CC=2)C(C)=O)F)CC1 FNSJBNAZKYMGGW-UHFFFAOYSA-N 0.000 claims description 3
- HSLYJFYYXRBFMV-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-(3-methylpiperidin-1-yl)-5-nitrobenzoyl]piperazin-1-yl]phenyl]ethanone Chemical compound C1C(C)CCCN1C1=CC=C([N+]([O-])=O)C=C1C(=O)N1CCN(C=2C(=CC(=CC=2)C(C)=O)F)CC1 HSLYJFYYXRBFMV-UHFFFAOYSA-N 0.000 claims description 3
- PPSXUJHLEZNINP-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-(4-methylpiperidin-1-yl)-5-nitrobenzoyl]piperazin-1-yl]phenyl]propan-1-one Chemical compound FC1=CC(C(=O)CC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCC(C)CC2)CC1 PPSXUJHLEZNINP-UHFFFAOYSA-N 0.000 claims description 3
- JXGMFYDRDWHQGN-UHFFFAOYSA-N 1-[3-fluoro-4-[4-[2-[3-(hydroxymethyl)pyrrolidin-1-yl]-5-nitrobenzoyl]piperazin-1-yl]phenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CC(CO)CC2)CC1 JXGMFYDRDWHQGN-UHFFFAOYSA-N 0.000 claims description 3
- ZYJAISCYKPGCDV-UHFFFAOYSA-N 1-[4-[4-[2-(azepan-1-yl)-5-methylsulfonylbenzoyl]piperazin-1-yl]-3-fluorophenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)S(C)(=O)=O)N2CCCCCC2)CC1 ZYJAISCYKPGCDV-UHFFFAOYSA-N 0.000 claims description 3
- POCDLGSDUIFCGG-UHFFFAOYSA-N 1-[4-[4-[2-(azepan-1-yl)-5-nitrobenzoyl]piperazin-1-yl]-3-fluorophenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCCCCC2)CC1 POCDLGSDUIFCGG-UHFFFAOYSA-N 0.000 claims description 3
- IDAZYBJHLCJTMV-UHFFFAOYSA-N 1-[4-[4-[2-(cyclopropylmethylamino)-5-nitrobenzoyl]piperazin-1-yl]-3-fluorophenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)NCC2CC2)CC1 IDAZYBJHLCJTMV-UHFFFAOYSA-N 0.000 claims description 3
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- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 3
- BOAKVQQGHGRPEQ-UHFFFAOYSA-N (2-morpholin-4-yl-5-nitrophenyl)-[4-[2-nitro-4-(trifluoromethyl)phenyl]piperazin-1-yl]methanone Chemical compound C1CN(C=2C(=CC(=CC=2)C(F)(F)F)[N+]([O-])=O)CCN1C(=O)C1=CC([N+](=O)[O-])=CC=C1N1CCOCC1 BOAKVQQGHGRPEQ-UHFFFAOYSA-N 0.000 claims description 2
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- NGZOCXDYNQRWLP-UHFFFAOYSA-N 1-[3-fluoro-4-[4-(5-nitro-2-pyrrolidin-1-ylbenzoyl)piperazin-1-yl]phenyl]propan-1-one Chemical compound FC1=CC(C(=O)CC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCCC2)CC1 NGZOCXDYNQRWLP-UHFFFAOYSA-N 0.000 claims description 2
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- APRUQAPYORBONL-UHFFFAOYSA-N 1-[4-[4-[2-(2,5-dihydropyrrol-1-yl)-5-nitrobenzoyl]piperazin-1-yl]-3-fluorophenyl]ethanone Chemical compound FC1=CC(C(=O)C)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CC=CC2)CC1 APRUQAPYORBONL-UHFFFAOYSA-N 0.000 claims description 2
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- UDPKBPQKKRZMNY-UHFFFAOYSA-N 3-[4-[2-fluoro-4-(trifluoromethyl)phenyl]piperazine-1-carbonyl]-n-methyl-4-morpholin-4-ylbenzenesulfonamide Chemical compound C1CN(C=2C(=CC(=CC=2)C(F)(F)F)F)CCN1C(=O)C1=CC(S(=O)(=O)NC)=CC=C1N1CCOCC1 UDPKBPQKKRZMNY-UHFFFAOYSA-N 0.000 claims description 2
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- FFUKJOFYKAUWMW-UHFFFAOYSA-N [4-(4-methoxyphenyl)piperazin-1-yl]-(5-nitro-2-pyrrolidin-1-ylphenyl)methanone Chemical compound C1=CC(OC)=CC=C1N1CCN(C(=O)C=2C(=CC=C(C=2)[N+]([O-])=O)N2CCCC2)CC1 FFUKJOFYKAUWMW-UHFFFAOYSA-N 0.000 claims description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
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- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
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| PT1663232E (pt) * | 2003-09-09 | 2007-12-12 | Hoffmann La Roche | Derivados de 1- (2-amino-benzol) -piperazina como inibidores de absorção de glicina para o tratamento de psicoses |
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| US7829712B2 (en) | 2004-09-20 | 2010-11-09 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-CoA-desaturase |
| AR051091A1 (es) | 2004-09-20 | 2006-12-20 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa |
| CA2580762A1 (fr) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Derives heterocycliques et leur utilisation comme agents therapeutiques |
| AU2005286648A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
| CA2580857A1 (fr) | 2004-09-20 | 2006-09-28 | Xenon Pharmaceuticals Inc. | Derives heterocycliques et leur utilisation en tant qu'agents therapeutiques |
| EP1807085B1 (fr) * | 2004-09-20 | 2013-08-21 | Xenon Pharmaceuticals Inc. | Dérivés hétérocycliques et leur utilisation en tant qu'agents thérapeutiques |
| EP2289510A1 (fr) | 2004-09-20 | 2011-03-02 | Xenon Pharmaceuticals Inc. | Dérivés hétérocycliques pour le traitement des maladies induites par des enzymes stearoyl-coa desaturase |
| HRP20090264T1 (hr) | 2004-12-09 | 2009-06-30 | F. Hoffmann - La Roche Ag | Derivati fenil-piperazin metanona |
| WO2006063709A1 (fr) | 2004-12-15 | 2006-06-22 | F.Hoffmann-La Roche Ag | Utilisation de phenylmethanones substituees bicycliques et tricycliques comme inhibiteurs des transporteurs de la glycine i (glyt-1) pour traiter la maladie d'alzheimer |
| PE20061156A1 (es) | 2004-12-23 | 2006-12-16 | Glaxo Group Ltd | Derivados de benzamida como agentes inhibidores del transportador de glicina |
| JP2008525398A (ja) * | 2004-12-23 | 2008-07-17 | グラクソ グループ リミテッド | グリシン輸送阻害剤 |
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| US7485637B2 (en) * | 2005-01-04 | 2009-02-03 | Hoffmann-La Roche Inc. | Benzoyl-tetrahydropiperidine derivatives |
| CA2593453A1 (fr) * | 2005-01-06 | 2006-07-13 | F. Hoffmann-La Roche Ag | Phenyl methanones sulfanyl substituees utilisees comme inhibiteurs du transporteur de glycine 1 (glyt-1) pour le traitement de troubles neurologiques et neuropsychiatriques |
| AU2005324024B2 (en) * | 2005-01-07 | 2011-02-17 | F. Hoffmann-La Roche Ag | [4-(Heteroaryl) piperazin-1-yl]-(2,5-substituted -phenyl)methanone derivatives as glycine transporter 1 (GlyT-1) inhibitors for the treatment of neurological and neuropsychiatric disorders |
| AU2006207650B2 (en) * | 2005-01-18 | 2011-01-27 | F. Hoffmann-La Roche Ag | 2, 5-disubstituted phenyl methanone derivatives as glycine transporter 1 (GlyT-I) inhibitors for the treatment of neurological and neuropsychiatry disorders |
| BRPI0607241A2 (pt) * | 2005-01-26 | 2009-08-25 | Hoffmann La Roche | derivados de fenil metanona e o uso dos mesmos como inibidores do transportador de glicina 1 |
| DE602006010665D1 (en) * | 2005-02-07 | 2010-01-07 | Hoffmann La Roche | Heterocyclsche substituierte phenylmethanone als inhibitoren des glycintransporters 1 |
| GB0505085D0 (en) * | 2005-03-11 | 2005-04-20 | Glaxo Group Ltd | Compounds |
| GB0505084D0 (en) * | 2005-03-11 | 2005-04-20 | Glaxo Group Ltd | Compounds |
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| AU2006343359A1 (en) | 2005-06-03 | 2007-11-15 | Xenon Pharmaceuticals Inc. | Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors |
| CN101007794B (zh) * | 2006-01-26 | 2010-09-01 | 中国科学院上海药物研究所 | N,n'-二取代哌嗪类衍生物及其制备方法、药物组合物和用途 |
| MX2009014235A (es) | 2007-08-22 | 2010-04-27 | Abbott Gmbh & Co Kg | 4-bencilaminoquinolonas, composiciones farmaceuticas que las contiene y su uso. |
| JP5441705B2 (ja) | 2007-10-15 | 2014-03-12 | 武田薬品工業株式会社 | アミド化合物およびその用途 |
| WO2009102761A1 (fr) | 2008-02-12 | 2009-08-20 | Bristol-Myers Squibb Company | 1,2,3-triazoles en tant qu'inhibiteurs de 11-bêta-hydroxysteroïde déshydrogénase type i |
| MX2010010773A (es) | 2008-04-01 | 2011-04-11 | Abbott Gmbh & Co Kg | Tetrahidroisoquinolinas, composiciones farmaceuticas que las contienen y su uso en terapia. |
| CN101597278B (zh) | 2008-06-04 | 2013-04-17 | 中国中化股份有限公司 | 酰胺类化合物及其制备与应用 |
| AR075442A1 (es) | 2009-02-16 | 2011-03-30 | Abbott Gmbh & Co Kg | Derivados de aminotetralina, composiciones farmaceuticas que las contienen y sus usos en terapia |
| TW201038569A (en) | 2009-02-16 | 2010-11-01 | Abbott Gmbh & Co Kg | Heterocyclic compounds, pharmaceutical compositions containing them, and their use in therapy |
| CN102711764A (zh) * | 2009-08-24 | 2012-10-03 | 纽若斯丹公司 | 神经刺激性哌嗪的合成 |
| TWI525090B (zh) | 2010-04-27 | 2016-03-11 | Mitsubishi Tanabe Pharma Corp | Novel amide derivatives and their use as pharmaceuticals |
| US8153653B2 (en) * | 2010-06-22 | 2012-04-10 | Hoffmann-La Roche Inc. | Amido-tropane derivatives |
| US9051280B2 (en) | 2010-08-13 | 2015-06-09 | AbbVie Deutschland GmbH & Co. KG | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8883839B2 (en) | 2010-08-13 | 2014-11-11 | Abbott Laboratories | Tetraline and indane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9045459B2 (en) | 2010-08-13 | 2015-06-02 | AbbVie Deutschland GmbH & Co. KG | Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8846743B2 (en) | 2010-08-13 | 2014-09-30 | Abbott Laboratories | Aminoindane derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8877794B2 (en) | 2010-08-13 | 2014-11-04 | Abbott Laboratories | Phenalkylamine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US8609672B2 (en) | 2010-08-27 | 2013-12-17 | University Of The Pacific | Piperazinylpyrimidine analogues as protein kinase inhibitors |
| US9309200B2 (en) | 2011-05-12 | 2016-04-12 | AbbVie Deutschland GmbH & Co. KG | Benzazepine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| CA2844275A1 (fr) | 2011-08-05 | 2013-02-14 | AbbVie Deutschland GmbH & Co. KG | Derives d'aminochromane, d'aminothiochromane et d'amino-1,2,3,4-tetrahydroquinoleine, compositions pharmaceutiques contenant ceux-ci et leur utilisation therapeutique |
| JP5800786B2 (ja) * | 2011-10-26 | 2015-10-28 | 田辺三菱製薬株式会社 | 新規アミド誘導体を有効成分として含有する医薬組成物 |
| MX2014006004A (es) | 2011-11-18 | 2015-04-16 | Abbvie Deutschland | Derivados de aminobenzociclohepteno, aminotetralina, aminoindano y fenalcilamina n-sustituidas, composiciones farmaceuticas que los contienen, y su uso en terapia. |
| US9365512B2 (en) | 2012-02-13 | 2016-06-14 | AbbVie Deutschland GmbH & Co. KG | Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9650334B2 (en) | 2013-03-15 | 2017-05-16 | Abbvie Inc. | Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| US9656955B2 (en) | 2013-03-15 | 2017-05-23 | Abbvie Inc. | Pyrrolidine derivatives, pharmaceutical compositions containing them, and their use in therapy |
| CA2924689A1 (fr) | 2013-10-17 | 2015-04-23 | AbbVie Deutschland GmbH & Co. KG | Derives d'aminochromane, d'aminothiochromane et d'amino-1,2,3,4-tetrahydroquinoleine, compositions pharmaceutiques contenant ceux-ci et leur utilisation therapeutique |
| MX2016004934A (es) | 2013-10-17 | 2016-12-20 | Abbvie Deutschland | Derivados de aminotetralina y aminoindano, composiciones farmaceuticas que los contienen, y su uso en terapia. |
| MA39888A (fr) | 2014-04-24 | 2017-03-01 | Dart Neuroscience Cayman Ltd | Composés de 2,4,5,6-tétrahydropyrrolo[3,4-c] pyrazole et 4,5,6,7-tétrahydro-2 h-pyrazolo [4,3-c] pyridine utilisés comme inhibiteurs de glyt1 |
| US9550754B2 (en) | 2014-09-11 | 2017-01-24 | AbbVie Deutschland GmbH & Co. KG | 4,5-dihydropyrazole derivatives, pharmaceutical compositions containing them, and their use in therapy |
| TWI601712B (zh) | 2014-11-05 | 2017-10-11 | 達特神經科學(開曼)有限責任公司 | 作為glyt1抑制劑之經取代之氮雜環丁基化合物 |
| MX2020013085A (es) | 2018-06-05 | 2021-03-02 | Crinetics Pharmaceuticals Inc | Antagonistas del receptor de subtipo 2 de melanocortina (mc2r) y usos de los mismos. |
| US12479825B2 (en) | 2019-11-07 | 2025-11-25 | Crinetics Pharmaceuticals, Inc. | Melanocortin subtype-2 receptor (MC2R) antagonists and uses thereof |
| EP4077307B1 (fr) | 2019-12-18 | 2025-03-12 | Crinetics Pharmaceuticals, Inc. | Antagonistes du récepteur du sous-type 2 de la mélanocortine (mc2r) à pipéridine à double substitution gem et leurs utilisations |
| WO2021133563A1 (fr) | 2019-12-23 | 2021-07-01 | Crinetics Pharmaceuticals, Inc. | Antagonistes du récepteur du sous-type 2 de la mélanocortine à base de pipéridine spirocyclique (mc2r) et leurs utilisations |
| WO2022149618A1 (fr) * | 2021-01-06 | 2022-07-14 | 中外製薬株式会社 | Procédé d'alkylation d'un groupe fonctionnel acide |
| JP2024510260A (ja) | 2021-03-19 | 2024-03-06 | クリネティックス ファーマシューティカルズ,インク. | 疾患の治療のためのメラノコルチンサブタイプ-2受容体(mc2r)アンタゴニスト |
| CN114409621B (zh) * | 2022-02-09 | 2023-09-08 | 江苏省原子医学研究所 | 一种靶向多巴胺d3受体的诊疗药物及其应用 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2423847A1 (de) * | 1973-05-28 | 1975-01-02 | Ciba Geigy Ag | Neue sulfamoylbenzoesaeureamide |
| DE2611705A1 (de) * | 1976-03-18 | 1977-09-22 | Josef Dipl Chem Dr Rer N Klosa | N-5-(nitrofurfuryliden-)-1-amino- hydantoin enthaltende kristalloesungsmittel |
| IT1176613B (it) * | 1984-08-14 | 1987-08-18 | Ravizza Spa | Derivati piperazinici farmacologicamente attivi e processo per la loro preparazione |
| IL138228A0 (en) * | 1998-03-06 | 2001-10-31 | Janssen Pharmaceutica Nv | Glycine transport inhibitors |
| RS53252B (sr) * | 2003-08-11 | 2014-08-29 | F.Hoffmann-La Roche Ag. | Piperazin sa or-supstituisanom fenil grupom i njihova upotreba kao inhibitora glyt1 |
| DK1703909T3 (da) * | 2003-09-09 | 2009-06-22 | Hoffmann La Roche | 1-benzoyl-piperazinderivater som glycinoptagelsesinhibitorer til behandling af psykoser |
| PT1663232E (pt) * | 2003-09-09 | 2007-12-12 | Hoffmann La Roche | Derivados de 1- (2-amino-benzol) -piperazina como inibidores de absorção de glicina para o tratamento de psicoses |
| US7191925B2 (en) * | 2003-09-16 | 2007-03-20 | Aris Sandra M | Clean carry apparatus |
-
2004
- 2004-08-30 PT PT04764631T patent/PT1663232E/pt unknown
- 2004-08-30 AT AT04764631T patent/ATE374610T1/de active
- 2004-08-30 WO PCT/EP2004/009665 patent/WO2005023260A1/fr not_active Ceased
- 2004-08-30 JP JP2006525694A patent/JP4563386B2/ja not_active Expired - Fee Related
- 2004-08-30 AU AU2004269889A patent/AU2004269889B2/en not_active Ceased
- 2004-08-30 CN CN2004800321632A patent/CN1874777B/zh not_active Expired - Fee Related
- 2004-08-30 CA CA2537292A patent/CA2537292C/fr not_active Expired - Fee Related
- 2004-08-30 NZ NZ545454A patent/NZ545454A/en unknown
- 2004-08-30 BR BRPI0414209A patent/BRPI0414209B8/pt not_active IP Right Cessation
- 2004-08-30 EP EP04764631A patent/EP1663232B1/fr not_active Expired - Lifetime
- 2004-08-30 KR KR1020067004792A patent/KR100774630B1/ko not_active Expired - Fee Related
- 2004-08-30 ES ES04764631T patent/ES2294529T3/es not_active Expired - Lifetime
- 2004-08-30 RU RU2006111583/04A patent/RU2354653C2/ru not_active IP Right Cessation
- 2004-08-30 MX MXPA06002727A patent/MXPA06002727A/es active IP Right Grant
- 2004-08-30 DE DE602004009323T patent/DE602004009323T2/de not_active Expired - Lifetime
- 2004-08-30 PL PL04764631T patent/PL1663232T3/pl unknown
- 2004-08-30 DK DK04764631T patent/DK1663232T3/da active
- 2004-09-02 US US10/933,103 patent/US7427612B2/en not_active Expired - Lifetime
- 2004-09-03 TW TW093126741A patent/TWI295287B/zh not_active IP Right Cessation
- 2004-09-07 AR ARP040103200A patent/AR045602A1/es not_active Application Discontinuation
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2006
- 2006-02-16 IL IL173768A patent/IL173768A0/en active IP Right Grant
- 2006-02-17 NO NO20060768A patent/NO20060768L/no not_active Application Discontinuation
- 2006-03-08 ZA ZA200601990A patent/ZA200601990B/en unknown
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2008
- 2008-07-22 US US12/177,386 patent/US7595314B2/en not_active Expired - Lifetime
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