HRP20100263T1 - Ciklopropil amini kao modulatori histaminskog h3 receptora - Google Patents
Ciklopropil amini kao modulatori histaminskog h3 receptora Download PDFInfo
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- HRP20100263T1 HRP20100263T1 HR20100263T HRP20100263T HRP20100263T1 HR P20100263 T1 HRP20100263 T1 HR P20100263T1 HR 20100263 T HR20100263 T HR 20100263T HR P20100263 T HRP20100263 T HR P20100263T HR P20100263 T1 HRP20100263 T1 HR P20100263T1
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- cyclopropyl
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Abstract
Spoj, naznačen time, da je izabran iz skupine koju čine: (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon, (4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon, (4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te (4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon, te njihovi enantiomeri, hidrati, solvati i farmaceutski prihvatljive soli. Patent sadrži još 27 patentnih zahtjeva.
Claims (28)
1. Spoj, naznačen time, da je izabran iz skupine koju čine:
(4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon,
(4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon,
(4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te
(4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon,
te njihovi enantiomeri, hidrati, solvati i farmaceutski prihvatljive soli.
2. Spoj u skladu sa zahtjevom 1, naznačen time, da je (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon ili njegov enantiomer, hidrat, solvat ili farmaceutski prihvatljiva sol.
3. Spoj u skladu sa zahtjevom 1, naznačen time, da je (4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon ili njegov enantiomer, hidrat, solvat ili farmaceutski prihvatljiva sol.
4. Spoj u skladu sa zahtjevom 1, naznačen time, da je (4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon ili njegov enantiomer, hidrat, solvat ili farmaceutski prihvatljiva sol.
5. Spoj u skladu sa zahtjevom 1, naznačen time, da je (4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon ili njegov enantiomer, hidrat, solvat ili farmaceutski prihvatljiva sol.
6. Spoj u skladu sa zahtjevom 2, naznačen time, da je izabran iz skupine koju čine (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon i (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon dihidroklorid.
7. Spoj u skladu sa zahtjevom 6, naznačen time, da je (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon.
8. Spoj u skladu sa zahtjevom 6, naznačen time, da je (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon dihidroklorid.
9. Spoj u skladu sa zahtjevom 2, naznačen time, da je (4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon citratna sol.
10. Spoj u skladu sa zahtjevom 1, naznačen time, da je (4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon citratna sol, (4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon citratna sol ili (4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon citratna sol.
11. Farmaceutski pripravak, naznačen time, da sadrži farmaceutski prihvatljivu podlogu i učinkovitu količinu najmanje jednog spoja izabranog iz skupine koju čine:
(4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon,
(4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon,
(4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te
(4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon,
te njihovi enantiomeri, hidrati, solvati i farmaceutski prihvatljive soli.
12. Najmanje jedan spoj izabran iz skupine koju čine:
(4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon,
(4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon,
(4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te
(4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon,
te njihovi enantiomeri, hidrati, solvati i farmaceutski prihvatljive soli, naznačen time, da se koristi u liječenju ili prevenciji CNS poremećaja izabranog iz skupine koju čine: neurološki poremećaji uključujući i poremećaje spavanje/buđenje i napetost/opreznost (na primjer nesanica i promjena vremenskih zona (jet lag)), hiperaktivni poremećaji s deficitom pozornosti (ADHD), poremećaji učenja i pamćenja, kognitivna disfunkcija, migrena, neurogena upala, demencija, blago kognitivno oštećenje (pre-demencija), Alzheimer-ova bolest, epilepsija, narkolepsija s ili bez pridružene katapleksije, katapleksija, poremećaji homeostaze spavanje/buđenje, idiopatska somnolencija (pospanost), pretjerana dnevna pospanost (EDS), poremećaji cirkadijskog ritma, poremećaji spavanje/umor, umor, iscrpljenost povezana s apnejom u snu, poremećaj sna zbog perimenopauzalnih hormonalnih pomaka, umor povezan s Parkinsonovom bolesti, MS-povezan umor, umor povezan s depresijom, umor izazvan s kemoterapijom, poremećaji hranjenja, debljina, bolest putovanja, vertigo, šizofrenija, zlouporaba supstancija, bipolarni poremećaji, manični poremećaji i depresija kod sisavaca.
13. Najmanje jedan spoj izabran iz skupine koju čine:
(4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon,
(4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon,
(4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te
(4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon,
te njihovi enantiomeri, hidrati, solvati i farmaceutski prihvatljive soli, naznačen time, da se koristi u liječenju ili prevenciji alergijskih reakcija gornjih dišnih puteva, astme, svrbeža, nazalne kongestije ili alergijskog rinitisa kod sisavaca.
14. Najmanje jedan spoj u skladu sa zahtjevom 1 te b) jedan ili više histaminskih H1 ili H2 antagonista, naznačeni time, da se koriste u liječenju ili prevenciji alergijskog rinitisa, nazalne kongestije i alergijske kongestije.
15. Najmanje jedan spoj u skladu sa zahtjevom 1 te b) jedan ili više blokatora ponovnog vezivanja neurotransmitera, naznačeni time, da se koriste u liječenju ili prevenciji depresije, poremećaja raspoloženja ili šizofrenije.
16. Najmanje jedan spoj u skladu sa zahtjevom 1 te b) modafinil, naznačeni time, da se koriste u liječenju ili prevenciji narkolepsije, pretjerane dnevne pospanosti (EDS), Alzheimer-ove bolesti, depresije, poremećaja deficita pozornosti, MS-povezanog umora, omamljenosti nakon anestezije, kognitivnog oštećenja, šizofrenije, spazma povezanog sa cerebralnom paralizom, slabljenja pamćenja zbog dobi, idiopatske somnolencije ili jet-lag.
17. Spoj u skladu sa zahtjevom 1, naznačen time, da je izotopno označen tako da se može prepoznati pomoću PET ili SPECT.
18. Spoj u skladu sa zahtjevom 1 koji je 18F-označen ili 11C-označen, naznačen time, da se koristi u postupku proučavanja poremećaja posredovanih histaminom, a navedeni postupak obuhvaća korak uporabe navedenog spoja kao molekularne probe pozitron emisijske tomografije (PET).
19. Farmaceutski pripravak u skladu sa zahtjevom 11, naznačen time, da nadalje sadrži topiramat.
20. Spoj izabran iz skupine koju čine:
(4-ciklopropil-piperazin-1-il)-(4-morfolin-4-ilmetil-fenil)-metanon,
(4-ciklopropil-piperazin-1-il)-[4-(4-fluoro-piperidin-1-ilmetil)-fenil]-metanon,
(4-ciklopropil-piperazin-1-il)-(4-tiomorfolin-4-ilmetil-fenil)-metanon, te
(4-ciklopropil-piperazin-1-il)-[4-(2-hidroksimetil-morfolin-4-ilmetil)-fenil]-metanon,
te njihove farmaceutski prihvatljive soli, naznačen time, da se koristi u liječenju pojedinca koji pati od bolesti ili mu je dijagnosticirana bolest izabrana iz skupine koju čine: kognitivni poremećaji, poremećaji spavanja, psihijatrijski poremećaji i ostali poremećaji.
21. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: demencija, Alzheimer-ova bolest, kognitivna disfunkcija, blago kognitivno oštećenje, pre-demencija, hiperaktivni poremećaj s deficitom pozornosti, poremećaji deficita pozornosti te poremećaji učenja i pamćenja.
22. Spoj u skladu sa zahtjevom 21, naznačen time, da je bolest izabrana iz skupine koju čine: smanjena sposobnost učenja, smanjena sposobnost pamćenja i gubitak pamćenja.
23. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: insomnija, poremećeno spavanje, narkolepsija s ili bez pridružene katapleksije, katapleksija, poremećaj homeostaze spavanje/budnost, idiopatska somnolencija, pretjerana dnevna pospanost, poremećaji cirkadijskog ritma, umor, letargija i jet-lag.
24. Spoj u skladu sa zahtjevom 23, naznačen time, da je bolest izabrana iz skupine koju čine: apneja u snu, perimenopauzalni hormonalni pomaci, Parkinsonova bolest, multipla skleroza, depresija, kemoterapija te poremećaj zbog rada u smjenama.
25. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: šizofrenija, bipolarni poremećaji, manični poremećaji, depresija, opsesivno-konvulzivni poremećaj i post-traumatski stresni poremećaj.
26. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: bolest putovanja, vertigo, epilepsija, migrena, neurogena upala, poremećaji hranjenja, debljina i poremećaji zlouporabe supstancija.
27. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: depresija, poremećeno spavanje, umor, letargija, kognitivno oštećenje, smanjena sposobnost pamćenja, gubitak pamćenja, smanjena sposobnost učenja, poremećaji deficita pozornosti i poremećaji hranjenja.
28. Spoj u skladu sa zahtjevom 20, naznačen time, da je bolest izabrana iz skupine koju čine: slabljenje pamćenja zbog dobi, poremećaj REM-ponašanja, benigni posturalni vertigo, tinitus, poremećaji pokreta, sindrom nemirnih nogu, poremećaji povezani s očima, makularna degeneracija i retinitis pigmentosis.
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| US71765905P | 2005-09-16 | 2005-09-16 | |
| PCT/US2006/035877 WO2007035425A2 (en) | 2005-09-16 | 2006-09-14 | Cyclopropyl amines as modulators of the histamine h3 receptor |
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| HRP20100263T1 true HRP20100263T1 (hr) | 2010-06-30 |
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| MY (1) | MY145305A (hr) |
| NO (1) | NO340949B1 (hr) |
| NZ (1) | NZ566533A (hr) |
| PL (1) | PL1948607T3 (hr) |
| PT (1) | PT1948607E (hr) |
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| SI (1) | SI1948607T1 (hr) |
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| UA (1) | UA96424C2 (hr) |
| WO (1) | WO2007035425A2 (hr) |
| ZA (1) | ZA200803337B (hr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2561791A1 (en) * | 2004-03-31 | 2005-10-20 | Janssen Pharmaceutica, N.V. | Non-imidazole heterocyclic compounds |
| PT1948607E (pt) | 2005-09-16 | 2010-06-02 | Janssen Pharmaceutica Nv | Ciclopropilaminas como moduladores do receptor h3 de histamina |
| BRPI0618076A2 (pt) * | 2005-10-31 | 2011-08-16 | Janssen Pharmaceutica Nv | processos para a preparação de derivados de ciclopropil-amida |
| US7795426B2 (en) * | 2005-10-31 | 2010-09-14 | Janssen Pharmaceutica Nv | Processes for the preparation of cyclopropyl-amide derivatives |
| JP5285603B2 (ja) * | 2006-05-30 | 2013-09-11 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ヒスタミンh3受容体のモジュレーターとしての置換ピリジルアミド化合物 |
| US9108948B2 (en) * | 2006-06-23 | 2015-08-18 | Abbvie Inc. | Cyclopropyl amine derivatives |
| NZ611323A (en) * | 2006-06-23 | 2014-10-31 | Abbvie Bahamas Ltd | Cyclopropyl amine derivatives as histamin h3 receptor modulators |
| US20080045507A1 (en) * | 2006-06-29 | 2008-02-21 | Allison Brett D | Substituted benzamide modulators of the histamine h3 receptor |
| TW200823204A (en) * | 2006-10-17 | 2008-06-01 | Arena Pharm Inc | Biphenyl sulfonyl and phenyl-heteroaryl sulfonyl modulators of the histamine H3-receptor useful for the treatment of disorders related thereto |
| BRPI0721088B8 (pt) * | 2006-12-14 | 2021-05-25 | Janssen Pharmaceutica Nv | processo para a preparação de derivados de piperazinil e diazepanil benzamida |
| SA08290520B1 (ar) | 2007-08-22 | 2012-02-22 | استرازينيكا ايه بي | مشتقات سيكلو بروبيل أميد وتركيبات صيدلية تحتوي عليها لعلاج حالة مرضية سببها مستقبلات هيستامين h3 |
| EP2222664B1 (en) | 2007-11-20 | 2014-10-29 | Janssen Pharmaceutica, N.V. | Cycloalkyloxy- and heterocycloalkyloxypyridine compounds as modulators of the histamine h3 receptor |
| TW201039825A (en) | 2009-02-20 | 2010-11-16 | Astrazeneca Ab | Cyclopropyl amide derivatives 983 |
| US9186353B2 (en) * | 2009-04-27 | 2015-11-17 | Abbvie Inc. | Treatment of osteoarthritis pain |
| WO2011102795A1 (en) | 2010-02-18 | 2011-08-25 | Astrazeneca Ab | New crystalline form of a cyclopropyl benzamide derivative |
| BR112012020780A2 (pt) * | 2010-02-18 | 2016-05-03 | Astrazeneca Ab | forma sólida, composição farmacêutica, e, uso de uma forma sólida. |
| LT3789038T (lt) | 2010-05-14 | 2022-12-12 | The Board Of Trustees Of The Leland Stanford Junior University | Humanizuoti ir chimeriniai monokloniniai antikūnai prieš cd47 |
| US8853390B2 (en) | 2010-09-16 | 2014-10-07 | Abbvie Inc. | Processes for preparing 1,2-substituted cyclopropyl derivatives |
| US20130339859A1 (en) | 2012-06-15 | 2013-12-19 | Muzik LLC | Interactive networked headphones |
| US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
| US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
| US10088921B2 (en) | 2014-10-10 | 2018-10-02 | Muzik Inc. | Devices for sharing user interactions |
| EP4251148A1 (en) | 2020-11-27 | 2023-10-04 | Richter Gedeon Nyrt. | Histamine h3 receptor antagonists/inverse agonists for the treatment of autism spectrum disorder |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3714179A (en) | 1970-09-08 | 1973-01-30 | Searle & Co | 1-alkyl-2-furfurylthioimidazoles and congeners |
| US3886160A (en) | 1972-09-28 | 1975-05-27 | Searle & Co | 2-(2-Methyl-5-nitro-1-imidazolyl) ethyl-2-thiopseudoureas |
| FR2543139B1 (fr) * | 1983-03-22 | 1985-08-16 | Cerm Cent Europ Rech Mauvernay | Derives de (1-alcoxy 2-amino) ethyl pyridine ou pyrazine, leur preparation et leur application en therapeutique |
| EP0186817B1 (en) | 1984-12-10 | 1989-08-02 | Nissan Chemical Industries Ltd. | 3(2h)pyridazinone, process for its preparation and anti-allergic agent containing it |
| JP2813747B2 (ja) | 1989-05-22 | 1998-10-22 | 富士写真フイルム株式会社 | 画像形成法 |
| US5030644A (en) | 1989-07-31 | 1991-07-09 | Merck & Co., Inc. | Imidazole compounds and their use as transglutaminase inhibitors |
| US5569659A (en) | 1991-09-11 | 1996-10-29 | Mcneilab, Inc. | 4-arylpiperazines and 4-arylpiperidines |
| NZ240863A (en) | 1991-09-11 | 1995-04-27 | Mcneilab Inc | Substituted 4-aryl piperidine and 4-aryl piperazine derivatives, preparation and pharmaceutical compositions thereof |
| US5217986A (en) | 1992-03-26 | 1993-06-08 | Harbor Branch Oceanographic Institution, Inc. | Anti-allergy agent |
| US5352707A (en) | 1992-03-26 | 1994-10-04 | Harbor Branch Oceanographic Institution, Inc. | Method for treating airway congestion |
| RU2124511C1 (ru) | 1993-05-14 | 1999-01-10 | Фармасьютикал Ко., Лтд | Производные пиперазина |
| US5681954A (en) | 1993-05-14 | 1997-10-28 | Daiichi Pharmaceutical Co., Ltd. | Piperazine derivatives |
| US5464788A (en) | 1994-03-24 | 1995-11-07 | Merck & Co., Inc. | Tocolytic oxytocin receptor antagonists |
| EP0794779A4 (en) | 1994-12-22 | 1998-04-29 | Smithkline Beecham Corp | FIBRINOGENIC RECEPTOR ANTAGONISTS |
| IL117149A0 (en) | 1995-02-23 | 1996-06-18 | Schering Corp | Muscarinic antagonists |
| US5889006A (en) | 1995-02-23 | 1999-03-30 | Schering Corporation | Muscarinic antagonists |
| US6011029A (en) | 1996-02-26 | 2000-01-04 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
| JPH1059954A (ja) | 1996-08-14 | 1998-03-03 | Takeda Chem Ind Ltd | 環状アミン誘導体およびそれを含んでなる医薬 |
| US5869479A (en) | 1997-08-14 | 1999-02-09 | Schering Corporation | Treatment of upper airway allergic responses |
| AU9650398A (en) | 1997-11-07 | 1999-05-31 | Daiichi Pharmaceutical Co., Ltd. | Piperazine-cyclodextrin complexes |
| GB9803536D0 (en) | 1998-02-19 | 1998-04-15 | Black James Foundation | Histamine H,receptor ligands |
| EP0978512A1 (en) | 1998-07-29 | 2000-02-09 | Societe Civile Bioprojet | Non-imidazole aryloxy (or arylthio) alkylamines as histamine H3-receptor antagonists and their therapeutic applications |
| CN1468227A (zh) | 2000-08-08 | 2004-01-14 | ����-������ҩƷ��˾ | 非咪唑芳氧基烷基胺 |
| DE60126785T2 (de) | 2000-08-08 | 2007-10-25 | Ortho-Mcneil Pharmaceutical, Inc. | Nicht-imidazol aryloxypiperidine als h3 rezeptor liganden |
| US7179912B2 (en) | 2000-09-01 | 2007-02-20 | Icos Corporation | Materials and methods to potentiate cancer treatment |
| WO2002024695A2 (en) | 2000-09-22 | 2002-03-28 | Ortho Mcneil Pharmaceutical, Inc. | Octahydro-indolizines and quinolizines and hexahydro-pyrrolizines |
| US6642226B2 (en) | 2001-02-06 | 2003-11-04 | Hoffman-La Roche Inc. | Substituted phenyl-piperidine methanone compounds |
| EP1379493A2 (en) | 2001-03-23 | 2004-01-14 | Eli Lilly and Company | Non-imidazole aryl alkylamines compounds as histamine h3 receptor antagonists, preparation and therapeutic uses |
| WO2003000314A2 (en) | 2001-06-20 | 2003-01-03 | The Regents Of The University Of California | Hemodialysis system and method |
| ATE449090T1 (de) | 2001-07-02 | 2009-12-15 | High Point Pharmaceuticals Llc | Substituierte piperazin- und diazepanderivate zur verwendung als histamin h3 rezeptormodulatoren |
| JP4619655B2 (ja) | 2001-09-14 | 2011-01-26 | ハイ・ポイント・ファーマスーティカルズ、エルエルシー | 新規アミノアゼチジン、−ピロリジンおよび−ピペリジン誘導体 |
| EP1434765B1 (en) | 2001-09-14 | 2009-12-02 | High Point Pharmaceuticals, LLC | Substituted piperidines with selective binding to histamine h3-receptor |
| WO2003031432A1 (en) | 2001-10-12 | 2003-04-17 | Novo Nordisk A/S | Substituted piperidines and their use for the treatment of diseases related to the histamine h3 receptor |
| MXPA04005562A (es) | 2001-12-10 | 2005-04-19 | Johnson & Johnson | Fenilalquinos. |
| WO2003055866A1 (en) | 2001-12-21 | 2003-07-10 | Bayer Pharmaceuticals Corporation | Quinazoline and quinoline derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents |
| MXPA04007416A (es) | 2002-02-01 | 2004-10-11 | Novo Nordisk As | Amidas de azetidinas, pirrolidinas, piperidinas y azepanos sustituidos como aminoalquilo. |
| IL162859A0 (en) * | 2002-02-05 | 2005-11-20 | Novo Nordisk As | Novel aryl-and heteroarylpiperazines |
| MXPA05004384A (es) | 2002-10-23 | 2005-10-18 | Johnson & Johnson | Piperacinil y diacepanil benzamidas y benztioamidas. |
| WO2005035534A1 (ja) | 2003-10-08 | 2005-04-21 | Ono Pharmaceutical Co., Ltd. | 複素ビシクロ環および複素トリシクロ環化合物およびその医薬 |
| GB0324159D0 (en) | 2003-10-15 | 2003-11-19 | Glaxo Group Ltd | Novel compounds |
| BRPI0519288A2 (pt) | 2004-12-24 | 2009-01-06 | Astrazeneca Ab | compostos heterocÍclicos como antagonistas de ccr2b |
| PT1948607E (pt) | 2005-09-16 | 2010-06-02 | Janssen Pharmaceutica Nv | Ciclopropilaminas como moduladores do receptor h3 de histamina |
| US7514433B2 (en) | 2006-08-03 | 2009-04-07 | Hoffmann-La Roche Inc. | 1H-indole-6-yl-piperazin-1-yl-methanone derivatives |
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