EG27104A - Pharmaceutical compounds - Google Patents
Pharmaceutical compoundsInfo
- Publication number
- EG27104A EG27104A EGNA2006000065A EG27104A EG 27104 A EG27104 A EG 27104A EG NA2006000065 A EGNA2006000065 A EG NA2006000065A EG 27104 A EG27104 A EG 27104A
- Authority
- EG
- Egypt
- Prior art keywords
- pharmaceutical compounds
- pharmaceutical
- compounds
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/38—Nitrogen atoms
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4152—1,2-Diazoles having oxo groups directly attached to the heterocyclic ring, e.g. antipyrine, phenylbutazone, sulfinpyrazone
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- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
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- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
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- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A61K31/4196—1,2,4-Triazoles
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- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/622—Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/626—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B
- C04B35/63—Preparing or treating the powders individually or as batches ; preparing or treating macroscopic reinforcing agents for ceramic products, e.g. fibres; mechanical aspects section B using additives specially adapted for forming the products, e.g.. binder binders
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D231/40—Acylated on said nitrogen atom
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- 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
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| GBGB0317127.9A GB0317127D0 (en) | 2003-07-22 | 2003-07-22 | Pharmaceutical compounds |
| US56976304P | 2004-05-10 | 2004-05-10 | |
| PCT/GB2004/003179 WO2005012256A1 (fr) | 2003-07-22 | 2004-07-22 | Composes 1h-pyrazole 3,4-disubstitues et leur utilisation en tant que kinases dependant des cyclines (cdk) et modulateurs de la glycogene synthase kinase-3 (gsk-3) |
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Families Citing this family (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL1651612T3 (pl) | 2003-07-22 | 2012-09-28 | Astex Therapeutics Ltd | Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3) |
| CA2548374C (fr) | 2003-12-23 | 2014-05-27 | Astex Therapeutics Limited | Derives de pyrazole servant de modulateurs de proteine kinase |
| TW200533657A (en) | 2004-02-17 | 2005-10-16 | Esteve Labor Dr | Substituted pyrazoline compounds, their preparation and use as medicaments |
| WO2006070202A1 (fr) * | 2004-12-30 | 2006-07-06 | Astex Therapeutics Limited | Dérivés de pyrazole ayant une activité de modulation des kinases |
| US20080139620A1 (en) * | 2005-01-21 | 2008-06-12 | Astex Therapeutics Limited | Pyrazole Derivatives For The Inhibition Of Cdk's And Gsk's |
| AR054425A1 (es) * | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico. |
| CN101146532B (zh) * | 2005-01-21 | 2012-05-09 | 阿斯泰克斯治疗有限公司 | 药物化合物 |
| MX2007008809A (es) * | 2005-01-21 | 2007-09-07 | Astex Therapeutics Ltd | Combinaciones de inhibidores de pirazol cinasa y otros agentes antitumor. |
| AU2006207325B2 (en) * | 2005-01-21 | 2012-08-16 | Astex Therapeutics Limited | Pharmaceutical compounds |
| CN101146791B (zh) * | 2005-01-21 | 2013-01-09 | 阿斯泰克斯治疗有限公司 | 作为激酶抑制剂的4-(2,6-二氯-苯甲酰基氨基)-1h-吡唑-3-甲酸哌啶-4-基酰胺的酸加成盐 |
| US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
| WO2008007113A2 (fr) * | 2006-07-14 | 2008-01-17 | Astex Therapeutics Limited | Combinaisons pharmaceutiques |
| AR052660A1 (es) * | 2005-01-21 | 2007-03-28 | Astex Therapeutics Ltd | Derivados de pirazol para inhibir la cdk's y gsk's |
| JPWO2006085685A1 (ja) * | 2005-02-09 | 2008-06-26 | 武田薬品工業株式会社 | ピラゾール化合物 |
| WO2006093271A1 (fr) * | 2005-03-03 | 2006-09-08 | Mitsubishi Rayon Co., Ltd. | Particules de polymère, composition de résine contenant celles-ci et corps moulé |
| CN101193862B (zh) | 2005-04-13 | 2013-08-21 | 阿斯特克斯治疗有限公司 | 羟基苯甲酰胺衍生物和其作为hsp90抑制剂的用途 |
| WO2006136829A2 (fr) * | 2005-06-21 | 2006-12-28 | Astex Therapeutics Limited | Composes pharmaceutiques |
| EP1902032A1 (fr) | 2005-06-22 | 2008-03-26 | Astex Therapeutics Limited | Composes pharmaceutiques |
| WO2006136837A2 (fr) | 2005-06-23 | 2006-12-28 | Astex Therapeutics Limited | Composes pharmaceutiques |
| US7897589B2 (en) * | 2005-07-15 | 2011-03-01 | Laboratorios Del Dr. Esteve, S.A. | Substituted pyrazoline compounds, their preparation and use as medicaments |
| EP1743892A1 (fr) | 2005-07-15 | 2007-01-17 | Laboratorios del Dr. Esteve S.A. | Composés pyrazoline substitués, leur préparation et utilisation comme médicaments |
| EP1757587A1 (fr) * | 2005-07-15 | 2007-02-28 | Laboratorios Del Dr. Esteve, S.A. | Composés de pyrazoline substituée, leur préparation et leur usage comme médicaments |
| EP1743890A1 (fr) * | 2005-07-15 | 2007-01-17 | Laboratorios Del Dr. Esteve, S.A. | Dérivés 4,5-dihydro-1H-pyrazole, leur, préparation et utilisation comme médicaments. |
| EP2275096A3 (fr) | 2005-08-26 | 2011-07-13 | Braincells, Inc. | Neurogenese par modulation des recepteurs muscariniques |
| EP2258358A3 (fr) | 2005-08-26 | 2011-09-07 | Braincells, Inc. | Neurogenèse avec un inhibiteur de l'acetylcholinestérase |
| AU2006304787A1 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by PDE inhibition |
| CA2625210A1 (fr) | 2005-10-31 | 2007-05-10 | Braincells, Inc. | Modulation de la neurogenese dont la mediation est assuree par recepteur gaba |
| US20100216734A1 (en) | 2006-03-08 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis by nootropic agents |
| JP2009536617A (ja) | 2006-04-11 | 2009-10-15 | バーテックス ファーマシューティカルズ インコーポレイテッド | タンパク質キナーゼの阻害剤として有用なチアゾール、イミダゾール、およびピラゾール |
| CA2651152A1 (fr) * | 2006-05-05 | 2007-11-15 | Astex Therapeutics Limited | (1-methanesulfonyl-piperidin-4-yl)-amide de l'acide 4-(2,6-dichloro-benzoylamino)-1h-pyrazole-3-carboxylique pour le traitement du cancer |
| WO2007129062A1 (fr) * | 2006-05-08 | 2007-11-15 | Astex Therapeutics Limited | Combinaisons pharmaceutiques de dérivés de diazole pour le traitement du cancer |
| AU2007249399A1 (en) | 2006-05-09 | 2007-11-22 | Braincells, Inc. | Neurogenesis by modulating angiotensin |
| JP4884072B2 (ja) * | 2006-05-12 | 2012-02-22 | 三井化学アグロ株式会社 | 複素環誘導体ならびにその殺虫剤としての使用方法 |
| JP2009542608A (ja) * | 2006-06-29 | 2009-12-03 | アステックス・セラピューティクス・リミテッド | 医薬組合せ剤 |
| JP2009543770A (ja) * | 2006-07-14 | 2009-12-10 | アステックス・セラピューティクス・リミテッド | Cdk及びgskの阻害のためのピラゾール誘導体の組合せ剤 |
| WO2008007123A2 (fr) * | 2006-07-14 | 2008-01-17 | Astex Therapeutics Limited | Composés pharmaceutiques |
| US20090318430A1 (en) * | 2006-07-21 | 2009-12-24 | Astex Therapeutics Limited | Medical use of cyclin dependent kinases inhibitors |
| US20100184806A1 (en) | 2006-09-19 | 2010-07-22 | Braincells, Inc. | Modulation of neurogenesis by ppar agents |
| AR063028A1 (es) | 2006-10-06 | 2008-12-23 | Banyu Pharma Co Ltd | Derivados heterociclicos de piridin-2-carboxamida activadores de glucoquinasas, utiles para el tratamiento de diabetes y obesidad y composiciones farmaceuticas que los contienen. |
| GB0620259D0 (en) | 2006-10-12 | 2006-11-22 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| US8916552B2 (en) * | 2006-10-12 | 2014-12-23 | Astex Therapeutics Limited | Pharmaceutical combinations |
| JP5410285B2 (ja) * | 2006-10-12 | 2014-02-05 | アステックス、セラピューティックス、リミテッド | 医薬化合物 |
| US9730912B2 (en) | 2006-10-12 | 2017-08-15 | Astex Therapeutics Limited | Pharmaceutical compounds |
| JP5528807B2 (ja) | 2006-10-12 | 2014-06-25 | アステックス、セラピューティックス、リミテッド | 複合薬剤 |
| BRPI0717618A2 (pt) | 2006-10-21 | 2013-10-22 | Abbott Gmbh & Co Kg | Compostos heterocíclicos e uso dos mesmos como inibidores de glicogênio sintase quinase 3 |
| KR100832747B1 (ko) * | 2006-10-27 | 2008-05-27 | 한국화학연구원 | 아미노피라졸 유도체, 이의 제조 방법 및 이를 함유하는허혈성 질환의 예방 또는 치료용 조성물 |
| FR2908409B1 (fr) * | 2006-11-10 | 2009-01-09 | Sanofi Aventis Sa | Pyrazoles substituees,compositions les contenant,procede de fabrication et utilisation |
| GB0704932D0 (en) | 2007-03-14 | 2007-04-25 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| WO2009036022A1 (fr) * | 2007-09-10 | 2009-03-19 | Board Of Regents, The University Of Texas System | Amélioration de la distribution d'acide nucléique à médiation par polysaccharide |
| EP2070924A1 (fr) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Nouveaux dérivés de 2-hetarylthiazol-4-amides d'acide carboxylique, leur fabrication et leur utilisation en tant que médicament |
| EP2070925A1 (fr) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Nouveaux dérivés de 2-thiazol-4-amides d'acide carboxylique substitués, leur fabrication et leur utilisation en tant que médicament |
| EP2070916A1 (fr) | 2007-12-10 | 2009-06-17 | Bayer Schering Pharma Aktiengesellschaft | Dérivés de 2-aryl-thiazol-4-amides d'acide carboxylique, leur fabrication et leur utilisation en tant que médicament |
| EP2085397A1 (fr) * | 2008-01-21 | 2009-08-05 | Esteve Quimica, S.A. | Forme cristalline d'abacavir |
| GB0806527D0 (en) | 2008-04-11 | 2008-05-14 | Astex Therapeutics Ltd | Pharmaceutical compounds |
| EP2151234A1 (fr) * | 2008-07-28 | 2010-02-10 | Laboratorios Del. Dr. Esteve, S.A. | Formulation pharmaceutique comprenant un composé récepteur CB1 dans une solution solide et/ou une dispersion solide |
| US20100216805A1 (en) | 2009-02-25 | 2010-08-26 | Braincells, Inc. | Modulation of neurogenesis using d-cycloserine combinations |
| CA2784807C (fr) | 2009-12-29 | 2021-12-14 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinase raf de type ii |
| EP2594555B1 (fr) * | 2010-07-02 | 2018-03-07 | ASKA Pharmaceutical Co., Ltd. | COMPOSÉ HÉTÉROCYCLIQUE, ET INHIBITEUR DE DÉGRADATION DE p27 KIP1 |
| CN103119035B (zh) | 2010-09-27 | 2015-09-30 | 雅培股份有限两合公司 | 杂环化合物和它们作为糖原合成酶激酶-3抑制剂的用途 |
| US9090592B2 (en) | 2010-12-30 | 2015-07-28 | AbbVie Deutschland GmbH & Co. KG | Heterocyclic compounds and their use as glycogen synthase kinase-3 inhibitors |
| WO2013074986A1 (fr) | 2011-11-17 | 2013-05-23 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de la kinase c-jun-n-terminale (jnk) |
| CA2862832A1 (fr) * | 2012-01-09 | 2013-07-18 | X-Rx, Inc. | Derives de benzhydrol-pyrazole presentant une activite inhibitrice de kinase et utilisations de ceux-ci |
| WO2013126283A1 (fr) | 2012-02-20 | 2013-08-29 | E. I. Du Pont De Nemours And Company | Pyrazoles fongicides |
| PH12017500997A1 (en) | 2012-04-04 | 2018-02-19 | Samumed Llc | Indazole inhibitors of the wnt signal pathway and therapeutic uses thereof |
| CN103012428A (zh) * | 2013-01-08 | 2013-04-03 | 中国药科大学 | 4-(五元杂环并嘧啶/吡啶取代)氨基-1H-3-吡唑甲酰胺类CDK/Aurora双重抑制剂及其用途 |
| WO2014145205A2 (fr) | 2013-03-15 | 2014-09-18 | St. Jude Children's Research Hospital | Procédés et compositions de modulateurs de la transcription de p27kip1 |
| WO2014165851A1 (fr) | 2013-04-05 | 2014-10-09 | The Children's Hospital Of Philadelphia | Régulation positive transitoire de myc dans des lymphomes à cellules b |
| GB201313664D0 (en) * | 2013-07-31 | 2013-09-11 | Univ Cardiff | Bcl-3 inhibitors |
| FR3011239A1 (fr) * | 2013-10-01 | 2015-04-03 | Univ Claude Bernard Lyon | Nouveaux derives comprenant un groupe pyrazole et un groupe indole, utiles en tant qu'inhibiteurs de la kinase gsk3 |
| US10047070B2 (en) | 2013-10-18 | 2018-08-14 | Dana-Farber Cancer Institute, Inc. | Polycyclic inhibitors of cyclin-dependent kinase 7 (CDK7) |
| ES2676734T3 (es) | 2013-10-18 | 2018-07-24 | Syros Pharmaceuticals, Inc. | Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas |
| US9830586B2 (en) * | 2014-03-31 | 2017-11-28 | Ncr Corporation | Electronic payments |
| EP3236959B1 (fr) | 2014-12-23 | 2025-09-24 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de la kinase cycline-dépendante 7 (cdk7) |
| WO2016140501A1 (fr) * | 2015-03-04 | 2016-09-09 | Kainos Medicine, Inc. | N-oxyde de pyridine pour activateur d'inhibiteurs d'homologue 2 de zeste |
| US10155765B2 (en) | 2015-03-12 | 2018-12-18 | Merck Sharp & Dohme Corp. | Carboxamide inhibitors of IRAK4 activity |
| WO2016160617A2 (fr) | 2015-03-27 | 2016-10-06 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de kinases cycline-dépendantes |
| JP6902025B2 (ja) | 2015-06-18 | 2021-07-14 | ティン セラピューティックス エルエルシー | 聴覚損失の予防および治療のための方法および組成物 |
| JP7028766B2 (ja) | 2015-09-09 | 2022-03-02 | ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド | サイクリン依存性キナーゼの阻害剤 |
| EP3356345B1 (fr) | 2015-09-30 | 2023-11-08 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Dérivés d'hétéroaryle en tant qu'inhibiteurs de la sepiapterine reductase |
| EP3370721A4 (fr) | 2015-11-06 | 2019-05-22 | Samumed, LLC | Traitement de l'ostéoarthrite |
| AR108325A1 (es) | 2016-04-27 | 2018-08-08 | Samumed Llc | Isoquinolin-3-il carboxamidas y preparación y uso de las mismas |
| EP3464285B1 (fr) | 2016-06-01 | 2022-09-21 | BioSplice Therapeutics, Inc. | Procédé de préparation de n-(5-(3-(7-(3-fluorophényl))-3 h-imidazo[4,5-c]pyridin-2-yl)-1h-indazol-5-yl)pyridin-3-yl)-3-méthylbutanamide |
| RU2769251C2 (ru) | 2016-08-23 | 2022-03-29 | Эйсай Ар Энд Ди Менеджмент Ко., Лтд. | Комбинированная терапия для лечения гепатоцеллюлярной карциномы |
| EP3595725B1 (fr) | 2017-03-16 | 2023-05-03 | Eisai R&D Management Co., Ltd. | Traitement en combinaison pour le traitement du cancer du sein |
| CN109705090B (zh) * | 2017-10-25 | 2023-06-20 | 上海君实生物医药科技股份有限公司 | 3,4-二取代的1h-吡唑化合物的酒石酸加成盐及其晶型 |
| MA52360B1 (fr) | 2018-04-26 | 2025-05-30 | Pfizer Inc. | Dérivés de 2-amino-pyridine ou de 2-amino-pyrimidine utilisés en tant qu'inhibiteurs de kinases dépendantes des cyclines |
| CN112367991A (zh) * | 2018-06-25 | 2021-02-12 | 达纳-法伯癌症研究所股份有限公司 | Taire家族激酶抑制剂及其用途 |
| WO2020006115A1 (fr) * | 2018-06-26 | 2020-01-02 | Betty Tam | Méthodes de traitement du cancer à l'aide d'un inhibiteur de clk |
| WO2020033413A2 (fr) * | 2018-08-07 | 2020-02-13 | Tosk, Inc. | Modulateurs de ras gtpase |
| EP3902542A4 (fr) | 2018-12-28 | 2022-09-07 | Dana-Farber Cancer Institute, Inc. | Inhibiteurs de la kinase dépendante des cyclines 7 et leurs utilisations |
| WO2020146779A1 (fr) * | 2019-01-11 | 2020-07-16 | The Regents Of The University Of California | Inhibiteurs de mtorc1 pour activer l'autophagie |
| WO2020150545A1 (fr) * | 2019-01-17 | 2020-07-23 | Samumed, Llc | DÉRIVÉS DE PYRAZOLE UTILISÉS COMME MODULATEURS DE LA VOIE DE SIGNALISATION WNT/β-CATÉNINE |
| EP3911317A2 (fr) * | 2019-01-17 | 2021-11-24 | BioSplice Therapeutics, Inc. | Procédés de traitement de troubles du cartilage par inhibition de clk et dyrk |
| US11390626B2 (en) | 2019-01-29 | 2022-07-19 | Tosk, Inc. | Pyrazolopyrimidine modulators of RAS GTPase |
| US20240350492A1 (en) | 2020-07-10 | 2024-10-24 | Ting Therapeutics Llc | Methods for the Prevention and Treatment of Hearing Loss |
| US12180220B2 (en) | 2020-10-14 | 2024-12-31 | Tosk, Inc. | Heteroaryl modulators of RAS GTPase |
| CN115124527B (zh) * | 2022-05-31 | 2024-03-12 | 武汉智汇农耀科技有限公司 | 一种杂环酰胺-氮杂吲哚类化合物及其制备方法和应用、一种除草剂 |
Family Cites Families (164)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2917432A (en) | 1954-10-05 | 1959-12-15 | Burroughs Wellcome Co | Leukemia treatment |
| US3046301A (en) | 1959-10-29 | 1962-07-24 | Burroughs Wellcome Co | Method of making chlorambucil |
| GB1354939A (en) | 1971-10-28 | 1974-06-05 | Ici Ltd | Process for the manufacture of 1,1,2-triphenylalk-1-enes |
| US4005063A (en) | 1973-10-11 | 1977-01-25 | Abbott Laboratories | [Des-gly]10 -GnRH nonapeptide anide analogs in position 6 having ovulation-inducing activity |
| GB1524747A (en) | 1976-05-11 | 1978-09-13 | Ici Ltd | Polypeptide |
| US4282361A (en) * | 1978-03-16 | 1981-08-04 | Massachusetts Institute Of Technology | Synthesis for 7-alkylamino-3-methylpyrazolo [4,3-d]pyrimidines |
| DE2845574A1 (de) | 1978-10-19 | 1980-04-24 | Deutsches Krebsforsch | Durch heterocyclische ringe oder alkylreste substituierte analoga von ccnu und verfahren zu deren herstellung |
| ATE28864T1 (de) | 1982-07-23 | 1987-08-15 | Ici Plc | Amide-derivate. |
| US4666828A (en) | 1984-08-15 | 1987-05-19 | The General Hospital Corporation | Test for Huntington's disease |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4801531A (en) | 1985-04-17 | 1989-01-31 | Biotechnology Research Partners, Ltd. | Apo AI/CIII genomic polymorphisms predictive of atherosclerosis |
| US4978672A (en) | 1986-03-07 | 1990-12-18 | Ciba-Geigy Corporation | Alpha-heterocyclc substituted tolunitriles |
| JPS6425763A (en) * | 1987-04-24 | 1989-01-27 | Mitsubishi Chem Ind | Pyrazoles and insecticide and acaricide containing said pyrazoles as active ingredient |
| US5164196A (en) | 1987-05-19 | 1992-11-17 | Ventech Research, Inc. | Crotoxin complex as cytotoxic agent |
| EP0308020A3 (fr) | 1987-09-18 | 1990-12-05 | Merck & Co. Inc. | Les acides 5-(aryl et hétéroaryl)-6-(aryl et hétéroaryl)-1,2-dihydro-2-oxo-3-pyridinecarboxyliques et leurs dérivés |
| US5002755A (en) | 1988-02-18 | 1991-03-26 | Vanderbilt University | Method of controlling nephrotoxicity of anti-tumor plaintum compounds |
| US5272057A (en) | 1988-10-14 | 1993-12-21 | Georgetown University | Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase |
| US5192659A (en) | 1989-08-25 | 1993-03-09 | Genetype Ag | Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes |
| JPH05507480A (ja) | 1990-05-26 | 1993-10-28 | ビイク グルデン ロンベルク ヒエーミツシエ フアブリーク ゲゼルシヤフト ミツト ベシユレンクテル ハフツング | 医薬品抵抗性の克服の際に使用するための1,4―ジヒドロピリジン |
| FR2665898B1 (fr) | 1990-08-20 | 1994-03-11 | Sanofi | Derives d'amido-3 pyrazole, procede pour leur preparation et compositions pharmaceutiques les contenant. |
| IL100110A0 (en) | 1990-12-26 | 1992-08-18 | American Cyanamid Co | Insecticidal and synergistic miticidal compositions |
| CZ290470B6 (cs) | 1991-10-18 | 2002-07-17 | Monsanto Technology Llc | 5 či 6 členné aromáty jako fungicidy pro kontrolu stéblolamu rostlin, způsob kontroly a fungicidní směs k provedení tohoto způsobu |
| DE69329503T2 (de) | 1992-11-13 | 2001-05-03 | Idec Pharma Corp | Therapeutische Verwendung von chimerischen und markierten Antikörpern, die gegen ein Differenzierung-Antigen gerichtet sind, dessen Expression auf menschliche B Lymphozyt beschränkt ist, für die Behandlung von B-Zell-Lymphoma |
| BR9307659A (pt) | 1992-12-17 | 1999-06-29 | Pfizer | Pirazóis e pirazolopirimidinas tendo atividade antagonista crf |
| JP3156026B2 (ja) | 1993-12-27 | 2001-04-16 | 株式会社大塚製薬工場 | ホスホン酸ジエステル誘導体 |
| US5773001A (en) | 1994-06-03 | 1998-06-30 | American Cyanamid Company | Conjugates of methyltrithio antitumor agents and intermediates for their synthesis |
| ATE262902T1 (de) | 1994-11-10 | 2004-04-15 | Millennium Pharm Inc | Verwendung von pyrazole verbindungen zur behandlung von glomerulonephritis, krebs, atherosklerose oder restenose |
| US5502068A (en) | 1995-01-31 | 1996-03-26 | Synphar Laboratories, Inc. | Cyclopropylpyrroloindole-oligopeptide anticancer agents |
| GB9514380D0 (en) | 1995-07-13 | 1995-09-13 | Knoll Ag | Therapeutic agents |
| US6218529B1 (en) | 1995-07-31 | 2001-04-17 | Urocor, Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate, breast and bladder cancer |
| WO1998004689A1 (fr) | 1995-07-31 | 1998-02-05 | Urocor, Inc. | Biomarqueurs et cibles de diagnostic, de pronostic et de traitement du cancer de la prostate |
| US5675024A (en) | 1995-11-22 | 1997-10-07 | Allergan | Aryl or heteroaryl amides of tetrahydronaphthalene, chroman, thiochroman and 1,2,3,4,-tetrahydroquinoline carboxylic acids, having an electron withdrawing substituent in the aromatic or heteroaromatic moiety, having retinoid-like biological activity |
| US5663357A (en) | 1995-11-22 | 1997-09-02 | Allergan | Substituted heteroarylamides having retinoid-like biological activity |
| AU703203B2 (en) * | 1996-01-30 | 1999-03-18 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| AU706497B2 (en) | 1996-04-03 | 1999-06-17 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
| WO1997036881A1 (fr) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibiteurs de la farnesyl-proteine transferase |
| WO1997036897A1 (fr) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibiteurs de la farnesyl-proteine transferase |
| AU2381397A (en) | 1996-04-19 | 1997-11-12 | Novo Nordisk A/S | Modulators of molecules with phosphotyrosine recognition units |
| DE69733756T2 (de) | 1996-05-03 | 2006-06-01 | Abbott Laboratories, Abbott Park | Antiangiogenische peptiden, dafür kodierende polynukleotide und verfahren zur hemmung der angiogenesis |
| EP0915825B1 (fr) | 1996-06-21 | 2004-05-06 | Allergan, Inc. | Derives de tetrahydronaphtalene et de dihydronaphtalene substitues ayant une activite biologique de type retinoide et/ou antagoniste du retinoide |
| WO1998008845A1 (fr) | 1996-08-27 | 1998-03-05 | Novartis Ag | 1,2,4,6-thiatriazines s-substituees desherbantes |
| TW523506B (en) | 1996-12-18 | 2003-03-11 | Ono Pharmaceutical Co | Sulfonamide or carbamide derivatives and drugs containing the same as active ingredients |
| US6020357A (en) | 1996-12-23 | 2000-02-01 | Dupont Pharmaceuticals Company | Nitrogen containing heteroaromatics as factor Xa inhibitors |
| IL130286A0 (en) | 1996-12-23 | 2000-06-01 | Du Pont Pharm Co | Nitrogen containing heteroaromatics as factor Xa inhibitors |
| US6306393B1 (en) | 1997-03-24 | 2001-10-23 | Immunomedics, Inc. | Immunotherapy of B-cell malignancies using anti-CD22 antibodies |
| NZ338075A (en) * | 1997-04-25 | 2000-10-27 | Pfizer Ltd | Pyrazolopyrimidinones which inhibit type 5 cyclic guanosine 3',5'-monophosphate phosphodiesterase (cGMP PED5) for the treatment of sexual dysfunction |
| EP1019394A1 (fr) * | 1997-05-22 | 2000-07-19 | G.D. Searle & Co. | DERIVES DE PYRAZOLE COMME INHIBITEURS DE KINASE p38 |
| BR9810151A (pt) | 1997-06-19 | 2000-08-08 | Du Pont Pharm Co | Composto, composição farmacêutica e método para tratamento ou prevenção de uma desordem tromoboembólica |
| EE200000289A (et) | 1997-10-27 | 2001-06-15 | Agouron Pharmaceuticals, Inc. | Asendatud 4-amino-tiasool-2-üüli ühendid kui tsükliinisõltuvusega kinaaside inhibiitorid |
| WO1999032477A1 (fr) | 1997-12-19 | 1999-07-01 | Schering Aktiengesellschaft | Derives d'$i(ortho)-anthranilamide comme anticoagulants |
| CA2314401A1 (fr) | 1997-12-22 | 1999-07-01 | Du Pont Pharmaceuticals Company | Heteroaromatiques contenant de l'azote, presentant des groupes p1 a substitution ortho, et utilises en tant qu'inhibiteurs du facteur xa |
| WO1999067235A1 (fr) | 1998-06-25 | 1999-12-29 | Sumitomo Pharmaceuticals Co., Ltd. | Composes cycliques a cinq elements |
| WO2000006169A1 (fr) | 1998-07-29 | 2000-02-10 | Merck & Co., Inc. | Antagonistes des recepteurs de l'integrine |
| JP2000186092A (ja) | 1998-12-22 | 2000-07-04 | Kyowa Hakko Kogyo Co Ltd | Ucn−01の製造法 |
| CA2348740A1 (fr) | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Inhibiteurs de la thrombine ou du facteur xa |
| WO2000059902A2 (fr) | 1999-04-02 | 2000-10-12 | Du Pont Pharmaceuticals Company | Sulfonyles aryles faisant office d'inhibiteurs du facteur xa |
| CA2366932C (fr) | 1999-04-15 | 2009-08-25 | Bristol-Myers Squibb Company | Inhibiteurs cycliques de proteine tyrosine kinase |
| US6166244A (en) | 1999-05-07 | 2000-12-26 | Allergan Sales, Inc. | Oxygen, sulfur and nitrogen substituted cyclohexene and cyclohexane derivatives having retinoid-like biological activity |
| JP2003500390A (ja) | 1999-05-24 | 2003-01-07 | シーオーアール セラピューティクス インコーポレイテッド | Xa因子阻害剤 |
| FR2795726A1 (fr) | 1999-06-30 | 2001-01-05 | Aventis Cropscience Sa | Nouveaux pyrazoles fongicides |
| PE20010306A1 (es) | 1999-07-02 | 2001-03-29 | Agouron Pharma | Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa |
| US6127382A (en) | 1999-08-16 | 2000-10-03 | Allergan Sales, Inc. | Amines substituted with a tetrahydroquinolinyl group an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity |
| US6093838A (en) | 1999-08-16 | 2000-07-25 | Allergan Sales, Inc. | Amines substituted with a dihydro-benzofuranyl or with a dihydro-isobenzofuranyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity |
| AU6936500A (en) | 1999-08-24 | 2001-03-19 | Regents Of The University Of California, The | Non-quinoline inhibitors of malaria parasites |
| NZ517828A (en) | 1999-09-17 | 2003-10-31 | Millennium Pharm Inc | Inhibitors having activity against mammalian factor Xa |
| HK1052497B (zh) | 1999-09-17 | 2007-03-02 | 千禧药品公司 | 苯甲酸胺和相关的因子xa抑制剂 |
| US6632815B2 (en) * | 1999-09-17 | 2003-10-14 | Millennium Pharmaceuticals, Inc. | Inhibitors of factor Xa |
| WO2002034721A1 (fr) | 2000-10-20 | 2002-05-02 | Bristol-Myers Squibb Pharma Company | Semi-carbazides acyle et utilisations de celles-ci comme inhibiteurs de kinase dependante des cyclines (cdk) |
| AU1028601A (en) | 1999-11-05 | 2001-05-14 | Smithkline Beecham Plc | Isoquinoline and quinazoline derivatives having a combined 5ht1a, 5ht1b and 5ht1d receptor activity |
| YU54202A (sh) | 2000-01-18 | 2006-01-16 | Agouron Pharmaceuticals Inc. | Jedinjenja indazola, farmaceutske smeše i postupci za stimulisanje i inhibiranje ćelijske proliferacije |
| HN2001000008A (es) | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| EP1259887A4 (fr) | 2000-01-25 | 2003-08-13 | Vistaprint Usa Inc | Gestion d'impressions |
| IL145757A (en) | 2000-02-05 | 2007-12-03 | Vertex Pharma | History of pyrazole and pharmaceutical preparations containing them |
| CA2399791A1 (fr) | 2000-02-11 | 2001-08-16 | Bristol-Myers Squibb Company | Modulateurs de recepteurs aux cannabinoides, leurs procedes de preparation et utilisations de modulateurs de recepteurs aux cannabinoides pour le traitement de maladies respiratoires et non respiratoires |
| ES2254385T3 (es) | 2000-02-29 | 2006-06-16 | Millennium Pharmaceuticals, Inc. | Benzamidas e inhibidores relacionados del factor xa. |
| US20040087798A1 (en) * | 2000-03-14 | 2004-05-06 | Akira Yamada | Novel amide compounds |
| MY138097A (en) | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| US6613917B1 (en) | 2000-03-23 | 2003-09-02 | Allergan, Inc. | Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity |
| CA2401748A1 (fr) | 2000-03-29 | 2001-10-04 | Cyclacel Limited | 4-heteroaryle-pyrimidines substituees en 2 et leur utilisation dans le traitement de troubles proliferants |
| JP2004501083A (ja) * | 2000-04-18 | 2004-01-15 | アゴーロン・ファーマシューティカルズ・インコーポレイテッド | プロテインキナーゼを阻害するためのピラゾール |
| WO2001081345A1 (fr) | 2000-04-20 | 2001-11-01 | Mitsubishi Pharma Corporation | Composes d'amides aromatiques |
| JP2004507455A (ja) | 2000-04-25 | 2004-03-11 | ブリストル−マイヤーズ スクイブ カンパニー | サイクリン依存性キナーゼ阻害剤としての、5−チオ−、スルフィニル−およびスルホニルピラゾロ[3,4−b]−ピリジンの用途 |
| HK1053833A1 (zh) | 2000-04-27 | 2003-11-07 | Abbott Laboratories | 取代苯基法呢基转移酶抑制剂 |
| US6414013B1 (en) | 2000-06-19 | 2002-07-02 | Pharmacia & Upjohn S.P.A. | Thiophene compounds, process for preparing the same, and pharmaceutical compositions containing the same background of the invention |
| AU2001273040A1 (en) | 2000-06-27 | 2002-01-08 | Du Pont Pharmaceuticals Company | Factor xa inhibitors |
| IL153645A0 (en) | 2000-07-31 | 2003-07-06 | Smithkline Beecham Plc | Carboxamide compounds and their use as antagonists of a human 11cby receptor |
| EP1313710A1 (fr) * | 2000-08-31 | 2003-05-28 | Pfizer Products Inc. | Derives pyrazole et leur utilisation en tant qu'inhibiteurs des proteines kinases |
| JP2004509115A (ja) | 2000-09-15 | 2004-03-25 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
| US6455559B1 (en) * | 2001-07-19 | 2002-09-24 | Pharmacia Italia S.P.A. | Phenylacetamido-pyrazole derivatives, process for their preparation and their use as antitumor agents |
| PT1355905E (pt) | 2000-12-21 | 2007-05-31 | Vertex Pharma | Compostos de pirazole úteis como inibidores de proteínaquinase |
| DE10064823A1 (de) | 2000-12-22 | 2002-06-27 | Knoll Ag | Integrinrezeptorliganden |
| US6995162B2 (en) * | 2001-01-12 | 2006-02-07 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| US7105682B2 (en) * | 2001-01-12 | 2006-09-12 | Amgen Inc. | Substituted amine derivatives and methods of use |
| US6878714B2 (en) | 2001-01-12 | 2005-04-12 | Amgen Inc. | Substituted alkylamine derivatives and methods of use |
| GB0102687D0 (en) | 2001-02-02 | 2001-03-21 | Pharmacia & Upjohn Spa | Oxazolyl-pyrazole derivatives active as kinase inhibitors,process for their preparation and pharmaceutical compositions comprising them |
| MY130778A (en) | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
| EP1372631A4 (fr) | 2001-02-28 | 2005-07-27 | Brian C Giles | Methode et formule pour un effet antitumoral et antimetastatique |
| PL364660A1 (en) | 2001-03-05 | 2004-12-13 | E.I.Du Pont De Nemours And Company | Heterocyclic diamide invertebrate pest control agents |
| DE10110750A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Neuartige Aminodicarbonsäurederivate mit pharmazeutischen Eigenschaften |
| GB0106661D0 (en) * | 2001-03-16 | 2001-05-09 | Pfizer Ltd | Pharmaceutically active compounds |
| ES2241994T3 (es) * | 2001-03-16 | 2005-11-01 | Pfizer Inc. | Compuestos pirazolo(4,3-d)pirimidinona como inhibidores de gmpc. |
| JPWO2002074298A1 (ja) * | 2001-03-21 | 2004-07-08 | 小野薬品工業株式会社 | Il−6産生阻害剤 |
| MXPA03009441A (es) | 2001-04-16 | 2004-02-12 | Schering Corp | Ciclobuteno-1,2-dionas 3,4-disustituidas como ligandos del receptor de quimocina cxc. |
| US6905669B2 (en) | 2001-04-24 | 2005-06-14 | Supergen, Inc. | Compositions and methods for reestablishing gene transcription through inhibition of DNA methylation and histone deacetylase |
| WO2002092002A2 (fr) | 2001-05-11 | 2002-11-21 | The Burnham Institute | Methodes de criblage, methodes diagnostiques et therapeutiques relatives a riz |
| WO2002094183A2 (fr) | 2001-05-18 | 2002-11-28 | Tap Pharmaceutical Products Inc. | Methode de traitement d'une tumeur, utilisant des derives de fumagillol |
| ES2290305T3 (es) | 2001-05-21 | 2008-02-16 | E.I. Du Pont De Nemours And Company | Agentes de control de plagas de invertebrados que contienen un anillo heterociclico no aromatico. |
| US20030236198A1 (en) | 2001-06-13 | 2003-12-25 | Genesoft, Inc. | Antipathogenic benzamide compounds |
| JP4342939B2 (ja) | 2001-08-03 | 2009-10-14 | バーテックス ファーマシューティカルズ インコーポレイテッド | ピラゾール誘導キナーゼインヒビターおよびその使用 |
| US6916798B2 (en) | 2001-08-03 | 2005-07-12 | Vertex Pharmaceuticals Incorporated | Inhibitors of GSK-3 and uses thereof |
| US20030078232A1 (en) | 2001-08-08 | 2003-04-24 | Elfatih Elzein | Adenosine receptor A3 agonists |
| AUPR738301A0 (en) | 2001-08-30 | 2001-09-20 | Starpharma Limited | Chemotherapeutic agents |
| AU2002331766A1 (en) | 2001-08-31 | 2003-03-18 | University Of Connecticut | Novel pyrazole analogs acting on cannabinoid receptors |
| CN101851173A (zh) | 2001-09-14 | 2010-10-06 | 梅特希尔基因公司 | 组蛋白脱乙酰化酶抑制剂 |
| JP2005505595A (ja) | 2001-10-12 | 2005-02-24 | シェーリング コーポレイション | Cxc−ケモカインレセプターアンタゴニストとしての3,4−二置換マレイミド化合物 |
| HN2002000317A (es) * | 2001-11-02 | 2003-05-21 | Pfizer | Inhibidores de pde9 para tratamiento de trastornos cardiovasculares |
| CA2466375A1 (fr) | 2001-11-08 | 2003-05-15 | Pharmacia & Upjohn Company | Composes heteroaryles substitues azabicycliques pour le traitement de maladies |
| WO2003048081A2 (fr) | 2001-12-04 | 2003-06-12 | Bristol-Myers Squibb Company | Glycinamides en tant qu'inhibiteurs du facteur xa |
| US20030166932A1 (en) | 2002-01-04 | 2003-09-04 | Beard Richard L. | Amines substituted with a dihydronaphthalenyl, chromenyl, or thiochromenyl group, an aryl or heteroaryl group and an alkyl group, having retinoid-like biological activity |
| KR20060111716A (ko) | 2002-01-22 | 2006-10-27 | 워너-램버트 캄파니 엘엘씨 | 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온 |
| US7205307B2 (en) | 2002-02-14 | 2007-04-17 | Icagen, Inc. | Pyrimidines as novel openers of potassium ion channels |
| CA2632078C (fr) | 2002-03-04 | 2012-08-14 | Sloan-Kettering Institute For Cancer Research | Procedes d'induction de differenciation terminale |
| EP1485093B1 (fr) | 2002-03-12 | 2010-11-03 | Merck Sharp & Dohme Corp. | Modulateurs de tetrazole di-aryle substitues du recepteur 5 de glutamate metabotropique |
| DE60237425D1 (de) * | 2002-03-28 | 2010-10-07 | Univerzita Palackeho V Olomouc | PyrazoloÄ4,3-dÜpyrimidine, Verfahren zu ihrer Herstellung und therapeutische Anwendung |
| US6995168B2 (en) | 2002-05-31 | 2006-02-07 | Euro-Celtique S.A. | Triazaspiro compounds useful for treating or preventing pain |
| AU2003249369A1 (en) | 2002-06-21 | 2004-01-06 | Cellular Genomics, Inc. | Certain amino-substituted monocycles as kinase modulators |
| ATE425753T1 (de) | 2002-08-02 | 2009-04-15 | Genesoft Pharmaceuticals Inc | Biaryl-verbindungen mit antiinfektiver wirkung |
| GB0218625D0 (en) | 2002-08-10 | 2002-09-18 | Astex Technology Ltd | Pharmaceutical compounds |
| ATE378336T1 (de) | 2002-09-19 | 2007-11-15 | Schering Corp | Imidazopyridine als hemmstoffe cyclin abhängiger kinasen |
| US6737382B1 (en) | 2002-10-23 | 2004-05-18 | Nippon Soda Co. Ltd. | Insecticidal aminothiazole derivatives |
| WO2004039795A2 (fr) | 2002-10-29 | 2004-05-13 | Fujisawa Pharmaceutical Co., Ltd. | Composes amide |
| US20050026877A1 (en) | 2002-12-03 | 2005-02-03 | Novacea, Inc. | Pharmaceutical compositions comprising active vitamin D compounds |
| US7144911B2 (en) | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
| US7202257B2 (en) | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
| SG2012000667A (en) | 2003-01-08 | 2015-03-30 | Univ Washington | Antibacterial agents |
| US7169797B2 (en) * | 2003-02-14 | 2007-01-30 | Abbott Laboratories | Protein-tyrosine phosphatase inhibitors and uses thereof |
| US7320989B2 (en) * | 2003-02-28 | 2008-01-22 | Encysive Pharmaceuticals, Inc. | Pyridine, pyrimidine, quinoline, quinazoline, and naphthalene urotensin-II receptor antagonists |
| TW200505902A (en) | 2003-03-20 | 2005-02-16 | Schering Corp | Cannabinoid receptor ligands |
| PL1618092T3 (pl) | 2003-05-01 | 2011-02-28 | Bristol Myers Squibb Co | Związki amidopirazolowe z podstawnikami arylowymi jako inhibitory kinazy |
| WO2004099127A1 (fr) | 2003-05-07 | 2004-11-18 | Novo Nordisk A/S | Composes utilises comme inhibiteurs de kinase |
| WO2004099148A1 (fr) | 2003-05-09 | 2004-11-18 | Pharmacia & Upjohn Company Llc | Derives pyrimidiques substitues |
| WO2005000309A2 (fr) | 2003-06-27 | 2005-01-06 | Ionix Pharmaceuticals Limited | Composes chimiques |
| EP1642594A1 (fr) | 2003-06-27 | 2006-04-05 | Ono Pharmaceutical Co., Ltd. | Remede contre des maladies des voies urinaires |
| TWI372050B (en) | 2003-07-03 | 2012-09-11 | Astex Therapeutics Ltd | (morpholin-4-ylmethyl-1h-benzimidazol-2-yl)-1h-pyrazoles |
| PL1651612T3 (pl) | 2003-07-22 | 2012-09-28 | Astex Therapeutics Ltd | Związki 3,4-pochodne 1h-pirazolu i ich zastosowanie jako kinazy zależne od cyklin (cdk) i modulatory kinazy syntazy glikogenu-3 (gsk-3) |
| SE0303396D0 (sv) | 2003-12-16 | 2003-12-16 | Astrazeneca Ab | Chemical compounds |
| RU2377988C2 (ru) | 2004-02-20 | 2010-01-10 | Новартис Вэксинес Энд Дайэгностикс, Инк. | Модуляция воспалительных и метастатических процессов |
| EP1725528B1 (fr) | 2004-03-11 | 2013-05-29 | 4Sc Ag | Sulfonylpyrroles inhibiteurs d'hdac |
| US20060084691A1 (en) | 2004-10-18 | 2006-04-20 | Bilal Piperdi | Combined treatment with bortezomib and an epidermal growth factor receptor kinase inhibitor |
| US8404718B2 (en) | 2005-01-21 | 2013-03-26 | Astex Therapeutics Limited | Combinations of pyrazole kinase inhibitors |
| AR054425A1 (es) * | 2005-01-21 | 2007-06-27 | Astex Therapeutics Ltd | Sales de adicion de piperidin 4-il- amida de acido 4-(2,6-dicloro-benzoilamino) 1h-pirazol-3-carboxilico. |
| US20080139620A1 (en) * | 2005-01-21 | 2008-06-12 | Astex Therapeutics Limited | Pyrazole Derivatives For The Inhibition Of Cdk's And Gsk's |
| AR052660A1 (es) * | 2005-01-21 | 2007-03-28 | Astex Therapeutics Ltd | Derivados de pirazol para inhibir la cdk's y gsk's |
| MX2007008809A (es) * | 2005-01-21 | 2007-09-07 | Astex Therapeutics Ltd | Combinaciones de inhibidores de pirazol cinasa y otros agentes antitumor. |
| CN101146532B (zh) * | 2005-01-21 | 2012-05-09 | 阿斯泰克斯治疗有限公司 | 药物化合物 |
| AU2006207325B2 (en) * | 2005-01-21 | 2012-08-16 | Astex Therapeutics Limited | Pharmaceutical compounds |
| WO2008007113A2 (fr) | 2006-07-14 | 2008-01-17 | Astex Therapeutics Limited | Combinaisons pharmaceutiques |
| CA2651152A1 (fr) | 2006-05-05 | 2007-11-15 | Astex Therapeutics Limited | (1-methanesulfonyl-piperidin-4-yl)-amide de l'acide 4-(2,6-dichloro-benzoylamino)-1h-pyrazole-3-carboxylique pour le traitement du cancer |
| WO2007129062A1 (fr) | 2006-05-08 | 2007-11-15 | Astex Therapeutics Limited | Combinaisons pharmaceutiques de dérivés de diazole pour le traitement du cancer |
| JP2009542608A (ja) | 2006-06-29 | 2009-12-03 | アステックス・セラピューティクス・リミテッド | 医薬組合せ剤 |
| WO2008007123A2 (fr) | 2006-07-14 | 2008-01-17 | Astex Therapeutics Limited | Composés pharmaceutiques |
| JP2009543770A (ja) | 2006-07-14 | 2009-12-10 | アステックス・セラピューティクス・リミテッド | Cdk及びgskの阻害のためのピラゾール誘導体の組合せ剤 |
| US20090318430A1 (en) | 2006-07-21 | 2009-12-24 | Astex Therapeutics Limited | Medical use of cyclin dependent kinases inhibitors |
| US8916552B2 (en) | 2006-10-12 | 2014-12-23 | Astex Therapeutics Limited | Pharmaceutical combinations |
-
2004
- 2004-07-22 PL PL04743512T patent/PL1651612T3/pl unknown
- 2004-07-22 JP JP2006520896A patent/JP4681548B2/ja not_active Expired - Fee Related
- 2004-07-22 PL PL10175329T patent/PL2256106T3/pl unknown
- 2004-07-22 EP EP20100175329 patent/EP2256106B1/fr not_active Expired - Lifetime
- 2004-07-22 AU AU2004261459A patent/AU2004261459B2/en not_active Ceased
- 2004-07-22 NZ NZ544756A patent/NZ544756A/xx not_active IP Right Cessation
- 2004-07-22 WO PCT/GB2004/003179 patent/WO2005012256A1/fr not_active Ceased
- 2004-07-22 MX MXPA06000794A patent/MXPA06000794A/es active IP Right Grant
- 2004-07-22 KR KR1020067001424A patent/KR101204247B1/ko not_active Expired - Fee Related
- 2004-07-22 CA CA2532965A patent/CA2532965C/fr not_active Expired - Fee Related
- 2004-07-22 BR BRPI0412259-3A patent/BRPI0412259B1/pt not_active IP Right Cessation
- 2004-07-22 EP EP04743512A patent/EP1651612B9/fr not_active Expired - Lifetime
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2006
- 2006-01-19 IL IL173271A patent/IL173271A/en active IP Right Grant
- 2006-01-20 TN TNP2006000019A patent/TNSN06019A1/en unknown
- 2006-01-20 EC EC2006006298A patent/ECSP066298A/es unknown
- 2006-01-20 US US11/336,599 patent/US7385059B2/en not_active Expired - Lifetime
- 2006-01-21 EG EGNA2006000065 patent/EG27104A/xx active
- 2006-01-27 MA MA28760A patent/MA27936A1/fr unknown
- 2006-02-17 IS IS8310A patent/IS2898B/is unknown
- 2006-02-21 NO NO20060855A patent/NO335069B1/no not_active IP Right Cessation
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2007
- 2007-10-19 US US11/875,482 patent/US7825140B2/en not_active Expired - Fee Related
- 2007-10-19 US US11/875,470 patent/US7745638B2/en not_active Expired - Fee Related
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2010
- 2010-09-08 US US12/877,499 patent/US8080666B2/en not_active Expired - Fee Related
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2011
- 2011-11-04 US US13/289,373 patent/US8779147B2/en not_active Expired - Fee Related
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2012
- 2012-07-04 CY CY20121100595T patent/CY1112903T1/el unknown
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2014
- 2014-05-19 US US14/281,360 patent/US9051278B2/en not_active Expired - Fee Related
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2015
- 2015-05-18 CY CY20151100448T patent/CY1116298T1/el unknown
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