PE20050336A1 - Compuestos triciclicos como inhibidores de la proteina farnesil transferasa - Google Patents
Compuestos triciclicos como inhibidores de la proteina farnesil transferasaInfo
- Publication number
- PE20050336A1 PE20050336A1 PE2004000760A PE2004000760A PE20050336A1 PE 20050336 A1 PE20050336 A1 PE 20050336A1 PE 2004000760 A PE2004000760 A PE 2004000760A PE 2004000760 A PE2004000760 A PE 2004000760A PE 20050336 A1 PE20050336 A1 PE 20050336A1
- Authority
- PE
- Peru
- Prior art keywords
- methyl
- alkyl
- cycloalkyl
- group
- inhibitors
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 102000004357 Transferases Human genes 0.000 title abstract 2
- 108090000992 Transferases Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000004169 proteins and genes Human genes 0.000 title abstract 2
- 108090000623 proteins and genes Proteins 0.000 title abstract 2
- 229950008696 farnesil Drugs 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 3
- -1 ISOPROPYL Chemical class 0.000 abstract 2
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003254 radicals Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
SE REFIERE A COMPUESTOS DERIVADOS DE LA FORMULA I, EN DONDE R1 ES UN GRUPO a ENTRE OTROS, DONDE n ES 1-6; X ES O, S o N; R2, R3, R4 Y R5 SON H, Br, Cl o F; R5A ES H, ALQUILO C1-C6 o CICLOALQUILO C3-C6; R6 Y R7 SON H, ALQUILO C1-C4 o CICLOALQUILO C3-C7, ENTRE OTROS; R8 SE SELECCIONA DEL GRUPO CONSISTENTE EN LOS RADICALES 2.0, 3.0, ENTRE OTROS; R9 ES ALQUILO C1-C6, ARILO, HETEROARILO, CICLOALQUILO, ENTRE OTROS, CON LA CONDICION DE QUE EL ATOMO DE C, MEDIANTE EL CUAL DICHO GRUPO R9 ESTA UNIDO AL SUSTITUYENTE X, NO ESTA SUSTITUIDO CON UN GRUPO -OH, NH2, NH(ALQUILO C1-C6)2 o N(ALQUILO C1-C6)2; R10 ES ARILO, HETEROARILO, CICLOALQUILO, HETEROCICLOALQUILO, ENTRE OTROS; R11 ES ALQUILO, ARILO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ESTER ISOPROPILICO DEL ACIDO 4-{8-CLORO-6-[[(1-METOXI-CICLOPROPANOCARBONIL)-AMINO]-(3-METIL-3H-IMIDAZOL-4-IL)-METIL]-11H-BENZO[5,6]CICLOHEPTA[1,2-b]PIRIDIN-11-IL-PIPERAZIN}-1-CARBOXILICO; ESTER ISOPROPILICO DEL ACIDO 4-{8-CLORO-6-[[(1-HIDROXI-CICLOPROPANOCARBONIL)-AMINO]-(3-METIL-3H-IMIDAZOL-4-IL)-METIL]-11H-BENZO[5,6]CICLOHEPTA[1,2-b]PIRIDIN-11-IL-PIPERAZIN}-1-CARBOXILICO; ESTER CICLOPENTILICO DEL ACIDO 4-{6-[(BICICLOPROPIL-1-ILOXICARBONILAMINO)-(3-METIL-3H-IMIDAZOL-4-IL)-METIL]-8-CLORO-11H-BENZO[5,6]CICLOHEPTA[1,2-b]PIRIDIN-11-IL}-PIPERAZIN-1-CARBOXILICO; ENTRE OTROS. TAMBIEN SE REFIERE A UN KIT Y UNA COMPOSICION FARMACEUTICA. ESTOS COMPUESTOS SON INHIBIDORES DE LA PROTEINA FARNESILO TRANSFERASA Y SON UTILES EN EL TRATAMIENTO DE TUMORES
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US49326903P | 2003-08-07 | 2003-08-07 | |
| US49850903P | 2003-08-28 | 2003-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20050336A1 true PE20050336A1 (es) | 2005-05-30 |
Family
ID=34138747
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2004000760A PE20050336A1 (es) | 2003-08-07 | 2004-08-05 | Compuestos triciclicos como inhibidores de la proteina farnesil transferasa |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US7557107B2 (es) |
| EP (1) | EP1660477B1 (es) |
| JP (1) | JP2007501791A (es) |
| KR (1) | KR20060057599A (es) |
| AR (1) | AR045447A1 (es) |
| AT (1) | ATE417041T1 (es) |
| AU (1) | AU2004263493A1 (es) |
| BR (1) | BRPI0413384A (es) |
| CA (1) | CA2535210A1 (es) |
| DE (1) | DE602004018332D1 (es) |
| EC (1) | ECSP066349A (es) |
| ES (1) | ES2317047T3 (es) |
| IL (1) | IL173514A0 (es) |
| MX (1) | MXPA06001483A (es) |
| PE (1) | PE20050336A1 (es) |
| RU (1) | RU2006106768A (es) |
| TW (1) | TW200510384A (es) |
| WO (1) | WO2005014577A1 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7342016B2 (en) * | 2000-08-30 | 2008-03-11 | Schering Corporation | Farnesyl protein transferase inhibitors as antitumor agents |
| KR101086533B1 (ko) | 2002-05-24 | 2011-11-23 | 쉐링 코포레이션 | 중화 사람 항-ｉｇｆｒ 항체, 이를 제조하는 방법 및 이를 포함하는 조성물 |
| US20040082588A1 (en) * | 2002-09-30 | 2004-04-29 | Schering Corporation | Methods for treating disorders of calcium homeostasis |
| TW200526684A (en) * | 2003-11-21 | 2005-08-16 | Schering Corp | Anti-IGFR1 antibody therapeutic combinations |
| US20060205810A1 (en) * | 2004-11-24 | 2006-09-14 | Schering Corporation | Platinum therapeutic combinations |
| EP1831200A2 (en) * | 2004-12-21 | 2007-09-12 | Schering Corporation | Novel farnesyl protein transferase inhibitors as antitumor agents |
| AU2006235487B2 (en) * | 2005-04-12 | 2011-12-22 | Elan Pharma International Limited | Nanoparticulate quinazoline derivative formulations |
| MX2007012896A (es) * | 2005-04-15 | 2007-12-10 | Schering Corp | Metodos y composiciones para tratamiento o prevencion de cancer. |
| CA2637572A1 (en) * | 2006-01-19 | 2007-07-26 | Schering Corporation | Piperazine derivatives as farnesyl protein transferase inhibitors |
| EP1854465A1 (en) | 2006-05-12 | 2007-11-14 | Alexander Tobias Teichmann | Use of 4,17 beta-dihydroxyandrost-4-ene-3-one for treating cancers |
| CA2683109A1 (en) * | 2006-10-11 | 2008-04-17 | Fusion Antibodies Limited | Combination therapy |
| MX2010004450A (es) | 2007-10-22 | 2010-05-05 | Schering Corp | Derivados heterociclo biciclicos y su uso como moduladores de la actividad de gpr119. |
| GB0807018D0 (en) | 2008-04-17 | 2008-05-21 | Fusion Antibodies Ltd | Antibodies and treatment |
| BR112014032346A2 (pt) | 2012-06-26 | 2017-06-27 | Del Mar Pharmaceuticals | métodos para tratamento de malignidades resistentes ao inibidor de tirosina-quinase em pacientes com polimorfismos genéticos ou desregulações de ahi1 mutações empregando dianidrogalactitol, diacetildianidrogalactitol, dibromodulcitol, ou análogos ou derivados destes |
| CN105492011A (zh) | 2013-04-08 | 2016-04-13 | 丹尼斯·M·布朗 | 不理想给药化学化合物的治疗增效 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL111235A (en) * | 1993-10-15 | 2001-03-19 | Schering Plough Corp | Medicinal preparations for inhibiting protein G activity and for the treatment of malignant diseases, containing tricyclic compounds, some such new compounds and a process for the preparation of some of them |
| US5874442A (en) | 1995-12-22 | 1999-02-23 | Schering-Plough Corporation | Tricyclic amides useful for inhibition of G-protein function and for treatment of proliferative disease |
| PL185597B1 (pl) * | 1995-12-22 | 2003-06-30 | Schering Corp | Tricykliczne amidy, środek farmaceutyczny i ich zastosowania |
| JP2003525239A (ja) | 2000-02-29 | 2003-08-26 | 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 | タキサン化合物とのファルネシルタンパク質トランスフェラーゼ阻害剤の組み合わせ剤 |
| US20030229099A1 (en) | 2000-08-30 | 2003-12-11 | Zhu Hugh Y. | Novel farnesyl protein transferase inhibitors as antitumor agents |
| AR033680A1 (es) * | 2000-08-30 | 2004-01-07 | Schering Corp | Compuestos triciclicos utiles como inhibidores de la farnesil proteino transferasa y su uso para la manufactura de medicamentos como agentes antitumorales |
| US7342016B2 (en) | 2000-08-30 | 2008-03-11 | Schering Corporation | Farnesyl protein transferase inhibitors as antitumor agents |
| CA2468996A1 (en) * | 2001-12-03 | 2003-06-12 | Schering Corporation | Use of fpt inhibitors and at least two antineoplastic agents in the treatment of cancer |
| US20040082588A1 (en) * | 2002-09-30 | 2004-04-29 | Schering Corporation | Methods for treating disorders of calcium homeostasis |
| EP1831200A2 (en) | 2004-12-21 | 2007-09-12 | Schering Corporation | Novel farnesyl protein transferase inhibitors as antitumor agents |
-
2004
- 2004-08-04 AU AU2004263493A patent/AU2004263493A1/en not_active Abandoned
- 2004-08-04 AT AT04779960T patent/ATE417041T1/de not_active IP Right Cessation
- 2004-08-04 TW TW093123372A patent/TW200510384A/zh unknown
- 2004-08-04 KR KR1020067002512A patent/KR20060057599A/ko not_active Withdrawn
- 2004-08-04 US US10/911,340 patent/US7557107B2/en not_active Expired - Fee Related
- 2004-08-04 EP EP04779960A patent/EP1660477B1/en not_active Expired - Lifetime
- 2004-08-04 BR BRPI0413384-6A patent/BRPI0413384A/pt not_active IP Right Cessation
- 2004-08-04 MX MXPA06001483A patent/MXPA06001483A/es active IP Right Grant
- 2004-08-04 ES ES04779960T patent/ES2317047T3/es not_active Expired - Lifetime
- 2004-08-04 CA CA002535210A patent/CA2535210A1/en not_active Abandoned
- 2004-08-04 JP JP2006522672A patent/JP2007501791A/ja active Pending
- 2004-08-04 WO PCT/US2004/025042 patent/WO2005014577A1/en not_active Ceased
- 2004-08-04 RU RU2006106768/04A patent/RU2006106768A/ru not_active Application Discontinuation
- 2004-08-04 DE DE602004018332T patent/DE602004018332D1/de not_active Expired - Lifetime
- 2004-08-05 PE PE2004000760A patent/PE20050336A1/es not_active Application Discontinuation
- 2004-08-06 AR ARP040102806A patent/AR045447A1/es not_active Application Discontinuation
-
2006
- 2006-02-02 IL IL173514A patent/IL173514A0/en unknown
- 2006-02-06 EC EC2006006349A patent/ECSP066349A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2535210A1 (en) | 2005-02-17 |
| DE602004018332D1 (de) | 2009-01-22 |
| EP1660477B1 (en) | 2008-12-10 |
| HK1087122A1 (en) | 2006-10-06 |
| AU2004263493A1 (en) | 2005-02-17 |
| ATE417041T1 (de) | 2008-12-15 |
| US7557107B2 (en) | 2009-07-07 |
| ES2317047T3 (es) | 2009-04-16 |
| WO2005014577A1 (en) | 2005-02-17 |
| ECSP066349A (es) | 2006-08-30 |
| JP2007501791A (ja) | 2007-02-01 |
| BRPI0413384A (pt) | 2006-10-17 |
| AR045447A1 (es) | 2005-10-26 |
| RU2006106768A (ru) | 2007-09-20 |
| WO2005014577A9 (en) | 2006-03-23 |
| US20050059672A1 (en) | 2005-03-17 |
| TW200510384A (en) | 2005-03-16 |
| EP1660477A1 (en) | 2006-05-31 |
| MXPA06001483A (es) | 2006-05-15 |
| KR20060057599A (ko) | 2006-05-26 |
| IL173514A0 (en) | 2006-07-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20050336A1 (es) | Compuestos triciclicos como inhibidores de la proteina farnesil transferasa | |
| PE20220931A1 (es) | Inhibidores de shp2 fosfatasa de tipo pirazolo[3,4-b]pirazina | |
| PE20070218A1 (es) | COMPUESTOS DE CICLOALQUILO AMINO-HIDANTOINA Y USO DE ESTOS PARA LA MODULACION DE ß-SECRETASA | |
| AR046711A1 (es) | 5-7-diaminopirazolo[4,3d]pirimidinas como inhibidores de la pde-5,composiciones farmaceuticas que las contienen y usos en el tratamiento de hipertensiones | |
| PE20091095A1 (es) | Moduladores de gamma secretasa | |
| PE20020406A1 (es) | 7-OXO-PIRIDO[2,3-d]PIRIMIDINAS 2,6-DISUSTITUIDAS COMO INHIBIDORES DE LAS PROTEINAS CINASAS | |
| PE20121157A1 (es) | Compuestos heterociclicos como inhibidores de proteasas serinas | |
| DE60236600D1 (de) | Substituierte 1h-dihydropyrazole, ihre herstellung und verwendung | |
| PE20060570A1 (es) | Compuestos de quinazolina e isoquinolina piperidilo sustituidos como inhibidores de fosfodiesterasa pde-10 | |
| AR054560A1 (es) | Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer | |
| PE20140192A1 (es) | Derivados de bencimidazol como inhibidores de cinasa pi3 | |
| PE20040450A1 (es) | Heteroariloxi-aril-espiro-pirimidina-2,4,6-triona n-sustituida como inhibidores de metaloproteinasa | |
| AR045595A1 (es) | Composiciones utiles como inhibidores de proteinas quinasas | |
| AR086357A1 (es) | Derivados de indazol sustituidos activos como inhibidores de quinasas | |
| AR040773A1 (es) | Pirazoles utiles como inhibidores de gsk-3 | |
| PE20120058A1 (es) | Derivados de imidazopirazina como inhibidores de syk | |
| PE20091211A1 (es) | Derivados de pirazolopirimidina como moduladores de pde9a | |
| PE20130012A1 (es) | Derivados de pirazol como inhibidores de jak | |
| AR040349A1 (es) | Quinolinas sustituidas como antagonistas del receptor ccr5 | |
| PE20021004A1 (es) | Derivados de piperidina como inhibidores de la ccr5 | |
| PE20060334A1 (es) | Derivados de piridina como antagonistas del receptor a2b de adenosina | |
| PE20080404A1 (es) | Derivados bencil-amino-piperidina como inhibidores de cetp | |
| AR046200A1 (es) | Derivados de pirazina y su uso farmaceutico. procesos de preparacion y composiciones farmaceuticas | |
| CY1116885T1 (el) | Υποκατεστημενα παραγωγα κυκλοεξυλομεθυλιου | |
| CY1107747T1 (el) | Υποκατεστημενα τετρακυκλικα παραγωγα πυρρολοκινολονης χρησιμα ως αναστολεις της φωσφοδιεστερασης |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FC | Refusal |