PE20121683A1 - DERIVADOS (HETEROCICLO-TETRAHIDRO-PIRIDIN)-(PIPERAZINIL)-1-ALCANONA Y (HETEROCICLO-DIHIDRO-PIRROLIDIN)-(PIPERAZINIL)-1-ALCANONA COMO INHIBIDORES DE p75 - Google Patents
DERIVADOS (HETEROCICLO-TETRAHIDRO-PIRIDIN)-(PIPERAZINIL)-1-ALCANONA Y (HETEROCICLO-DIHIDRO-PIRROLIDIN)-(PIPERAZINIL)-1-ALCANONA COMO INHIBIDORES DE p75Info
- Publication number
- PE20121683A1 PE20121683A1 PE2012000828A PE2012000828A PE20121683A1 PE 20121683 A1 PE20121683 A1 PE 20121683A1 PE 2012000828 A PE2012000828 A PE 2012000828A PE 2012000828 A PE2012000828 A PE 2012000828A PE 20121683 A1 PE20121683 A1 PE 20121683A1
- Authority
- PE
- Peru
- Prior art keywords
- heterociclo
- piperazinil
- atoms
- inhibitores
- alcanona
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 101000801254 Homo sapiens Tumor necrosis factor receptor superfamily member 16 Proteins 0.000 abstract 1
- 206010033645 Pancreatitis Diseases 0.000 abstract 1
- 238000006471 dimerization reaction Methods 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 208000010125 myocardial infarction Diseases 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
Classifications
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- A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
- A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
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- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- Pain & Pain Management (AREA)
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- Urology & Nephrology (AREA)
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Abstract
SE REFIERE A UN COMPUESTO DE FORMULA (I): DONDE n ES 1 O 2; m ES 0 O 1; A REPRESENTA UN GRUPO HETEROCICLICO CONDENSADO DE FORMULA (Y); B ES H; -W- ES UN HETEROCICLO NITROGENADO TAL COMO (a), ENTRE OTROS; 1-2 REPRESENTA 1 O 2; R2 ES (b), ENTRE OTROS; U COMPLETA ES UN NUCLEO DE 6 ATOMOS, AROMATICO O SATURADO QUE CONTIENE 1 O 2 ATOMOS DE N, OPCIONALMENTE SUSTITUIDO O U COMPLETA ES UN NUCLEO DE 5 ATOMOS, AROMATICO O SATURADO, QUE CONTIENE UN ATOMO DE N, DE OXIGENO, ENTRE OTROS OPCIONALMENTE SUSTITUIDO; X Y X1 ES CH O N; R Y R1 ES H, HALOGENO, ENTRE OTROS; R3 Y R4 SON H O UN GRUPO ALQUILO C1-C6; R5 Y R6 SON INDEPENDIENTEMENTE H, HALOGENO, ALCOXI (C1-C4), ENTRE OTROS. ES COMPUESTO PREFERIDO: 1-(4-BENZO[b]TIOFEN-7-IL-3,6-DIHIDRO-2H-PIRIDIN-1-IL)-2-(3,5-DIMETIL-2,3,5,6-TETRAHIDRO-[1,2´]BIPIRAZINIL-4-IL)-ETANONA; ENTRE OTROS. REFERIDO ADEMAS A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS INHIBEN LA DIMERIZACION DEL RECEPTOR p75NTR SIENDO UTILES PARA EL TRATAMIENTO DE ESQUIZOFRENIA, EPILEPSIA, DEPRESION, INFARTO DE MIOCARDIO, PANCREATITIS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0906025A FR2953836B1 (fr) | 2009-12-14 | 2009-12-14 | Nouveaux derives (heterocycle-tetrahydro-pyridine)-(piperazinyl)-1-alcanone et (heterocycle-dihydro-pyrrolidine)-(piperazinyl)-1-alcanone et leur utilisation comme inhibiteurs de p75 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20121683A1 true PE20121683A1 (es) | 2012-12-06 |
Family
ID=41693508
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2012000828A PE20121683A1 (es) | 2009-12-14 | 2010-12-13 | DERIVADOS (HETEROCICLO-TETRAHIDRO-PIRIDIN)-(PIPERAZINIL)-1-ALCANONA Y (HETEROCICLO-DIHIDRO-PIRROLIDIN)-(PIPERAZINIL)-1-ALCANONA COMO INHIBIDORES DE p75 |
Country Status (38)
| Country | Link |
|---|---|
| US (2) | US8518947B2 (es) |
| EP (1) | EP2513088B1 (es) |
| JP (1) | JP5760005B2 (es) |
| KR (1) | KR101730205B1 (es) |
| CN (1) | CN102656162B (es) |
| AR (1) | AR079442A1 (es) |
| AU (1) | AU2010338111B2 (es) |
| BR (1) | BR112012014310B1 (es) |
| CA (1) | CA2784153C (es) |
| CL (1) | CL2012001580A1 (es) |
| CO (1) | CO6501125A2 (es) |
| CR (1) | CR20120315A (es) |
| CY (1) | CY1116960T1 (es) |
| DK (1) | DK2513088T3 (es) |
| DO (1) | DOP2012000146A (es) |
| EA (1) | EA024403B1 (es) |
| EC (1) | ECSP12011971A (es) |
| ES (1) | ES2548872T3 (es) |
| FR (1) | FR2953836B1 (es) |
| GT (1) | GT201200178A (es) |
| HR (1) | HRP20151036T1 (es) |
| HU (1) | HUE027940T2 (es) |
| IL (1) | IL220273A (es) |
| MA (1) | MA33916B1 (es) |
| MX (1) | MX2012006863A (es) |
| NI (1) | NI201200103A (es) |
| NZ (1) | NZ600576A (es) |
| PE (1) | PE20121683A1 (es) |
| PH (1) | PH12012501170A1 (es) |
| PL (1) | PL2513088T3 (es) |
| PT (1) | PT2513088E (es) |
| SG (1) | SG181711A1 (es) |
| SI (1) | SI2513088T1 (es) |
| TN (1) | TN2012000166A1 (es) |
| TW (1) | TWI475021B (es) |
| UY (1) | UY33104A (es) |
| WO (1) | WO2011080445A1 (es) |
| ZA (1) | ZA201204339B (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2953839A1 (fr) * | 2009-12-14 | 2011-06-17 | Sanofi Aventis | Nouveaux derives d'(heterocycle-piperidine condensee)-(piperazinyl)-1alcanone ou d'(heterocycle-pyrrolidine condensee)-(piperazinyl)-1alcanone et leur utilisation comme inhibiteurs de p75 |
| EP2606894A1 (en) * | 2011-12-20 | 2013-06-26 | Sanofi | Novel therapeutic use of p75 receptor antagonists |
| US11752149B2 (en) | 2019-12-02 | 2023-09-12 | Pipeline Therapeutics, Inc. | Muscarinic acetylcholine M1 receptor antagonists |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2744448B1 (fr) | 1996-02-02 | 1998-04-24 | Pf Medicament | Nouvelles piperidines derivees d'aryl piperazine, ainsi que leur procede de preparation, les compositions pharmaceutiques et leur utilisation comme medicaments |
| AU749271B2 (en) | 1997-07-01 | 2002-06-20 | Agouron Pharmaceuticals, Inc. | Glucagon antagonists/inverse agonists |
| DE19826841A1 (de) | 1998-06-16 | 1999-12-23 | Merck Patent Gmbh | Arylalkanoylpyridazine |
| GB9905010D0 (en) | 1999-03-04 | 1999-04-28 | Merck Sharp & Dohme | Therapeutic agents |
| EP1165522A1 (en) | 1999-04-06 | 2002-01-02 | Krenitsky Pharmaceuticals, Inc. | Neurotrophic thio substituted pyrimidines |
| US6468990B1 (en) | 1999-05-17 | 2002-10-22 | Queen's University At Kingston | Method of inhibiting binding of nerve growth factor to p75 NTR receptor |
| FR2803593B1 (fr) | 2000-01-06 | 2002-02-15 | Sanofi Synthelabo | Nouvelles tetrahydropyridines, procede pour leur preparation et compositions pharmaceutiques les contenant |
| GB0117577D0 (en) * | 2001-02-16 | 2001-09-12 | Aventis Pharm Prod Inc | Novel heterocyclic substituted carbonyl derivatives and their use as dopamine D receptor ligands |
| UA77526C2 (en) | 2002-06-07 | 2006-12-15 | Sanofi Aventis | Substituted derivatives of 1-piperazineacylpiperidine, a method for the preparation thereof and their use in therapy |
| FR2862968B1 (fr) | 2003-12-01 | 2006-08-04 | Sanofi Synthelabo | Derives de 4-[(arylmethyl)aminomethyl]piperidine, leur preparation et leur application en therapeutique |
| FR2862967B1 (fr) | 2003-12-01 | 2006-08-04 | Sanofi Synthelabo | Derives de (4-phenylpiperazin-1-yl)acylpiperidine, leur preparation et leur application en therapeutique |
| TW200615268A (en) * | 2004-08-02 | 2006-05-16 | Osi Pharm Inc | Aryl-amino substituted pyrrolopyrimidine multi-kinase inhibiting compounds |
| CN104387382A (zh) * | 2008-03-24 | 2015-03-04 | 梅迪维新技术公司 | 吡啶并[3,4-b]吲哚和应用方法 |
| FR2932482B1 (fr) | 2008-06-13 | 2010-10-08 | Sanofi Aventis | Nouveaux derives de (phenyl-3,6-dihydro-2h-pyridinyl)- (piperazinyl ponte)-1-alcanone et leur utilisation comme inhibiteurs de p75 |
| FR2932481B1 (fr) | 2008-06-13 | 2010-10-08 | Sanofi Aventis | Derives de 4-{2-°4-phenyl-3,6-dihydro-2h-pyridin-1-yl!-2- oxo-alkyl}-1-piperazin-2-one, leur preparation et leur application en therapeutique. |
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