AR065901A1 - Derivados de pirrolipirimidina - Google Patents
Derivados de pirrolipirimidinaInfo
- Publication number
- AR065901A1 AR065901A1 ARP080101351A ARP080101351A AR065901A1 AR 065901 A1 AR065901 A1 AR 065901A1 AR P080101351 A ARP080101351 A AR P080101351A AR P080101351 A ARP080101351 A AR P080101351A AR 065901 A1 AR065901 A1 AR 065901A1
- Authority
- AR
- Argentina
- Prior art keywords
- 4alkyl
- optionally substituted
- groups
- ring
- atom
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Rheumatology (AREA)
- Dermatology (AREA)
- Oncology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Biomedical Technology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Estos compuestos son utiles como inhibidores de la cinasa JAK3. Reivindicacion 1: Un compuesto caracterizado por la formula (1) donde Cy1 representa fenilo o un heterociclo aromático de 5 o 6 miembros unido al grupo NH a través de un átomo de C,que pueden estar opcionalmente fusionados a un anillo de 5 o 6 miembros carbocíclico o heterocíclico saturado, parcialmente insaturado o aromático, donde Cy1 puede contener de 1 a 4 heteroátomos seleccionados de entre N, O y S, donde uno o másátomos de C o S del anillo opcional de 5 o 6 miembros fusionado pueden estar oxidados formando grupos CO, SO o SO2, y donde Cy1 puede estar opcionalmente sustituidos por uno o más R1; Cy2 representa un heterociclo monocíclico de 3 a 7 miembros obicíclico de 6 a 11 miembros, donde el anillo que contiene el átomo de N que se une a la pirrolopirimidina es saturado o parcialmente insaturado, donde Cy2 contiene de 1 a 4 heteroátomos seleccionados de entre N, O y S, donde uno o más átomos de C oS pueden estar opcionalmente oxidados formando grupos CO, SO o SO2, y donde Cy2 puede estar opcionalmente sustituido por uno o más R2; cada R1 y R2 representan independientemente C1-4alquilo, C2-4alquenilo, C2-4alquinilo, halogeno, -CN, -NO2, -COR3,-CO2R3, -CONR3R3, -COCONR3R3, -OR3, -OCOR4, -OCONR4R4, -OCO2R4, -SR3, -SOR4, -SO2R4, -SO2NR3R3, -SO2NR5COR4, -NR3R3, -NR5COR3, -NR5CONR3R3, -NR5CO2R4, -NR5SO2R4, -C(N-OH)R4 o Cy3, donde los grupos C1-4alquilo, C2-4alquenilo y C2-4alquinilo puedenestar opcionalmente sustituidos por uno o más R6 y Cy3 puede estar opcionalmente sustituido por uno o más R7; R3 representa hidrogeno o R4; R4 representa C1-4alquilo, C2-4alquenilo, C2-4alquinilo o Cy4, donde los grupos C1-4alquilo, C2-4alquenilo yC2-4alquinilo pueden estar opcionalmente sustituidos por uno o más R6 y Cy4 puede estar opcionalmente sustituido por uno o más R8; R5 representa hidrogeno o C1-4alquilo; R6 representa halogeno, -CN, -NO2, -COR9, -CO2R9, -CONR9R9, -OR9, -OCOR10, -OCONR10R10, -OCO2R10, -SR9, -SOR10, -SO2R10, -SO2NR9R9, -SO2NR5COR10, -NR9R9, -NR5COR9, -NR5CONR9R9, -NR5CO2R10, -NR5SO2R10, -C(=N-OH)R10 o Cy4, donde Cy4 puede estar opcioanlmente sustituido por uno o más R8; R7 representa C1.4alquilo que puedeestar opcionalmente sustituido por uno o más R11, o bien R7 representa cualquiera de los significados descritos para R12; R8 representa C1-4alquilo, haloC1-4alquilo, C1-4alcoxiC1-4alquilo, hidroxiC1-4alquilo, cianoC1-4alquilo o cualquiera de lossignificados descritos para R12; R9 representa hidrogeno o R10; R10 representa C1-4alquilo, haloC1-4alquilo, C1-4alcoxiC1-4alquilo, hidroxiC1-4alquilo, cianoC1-4alquilo, Cy5-C1-4alquilo o Cy4, donde Cy4 puede estar opcionalmente sustituido por uno omás R8; R11 representa halogeno, -CN, -NO2, -COR9, -CO2R9, -CONR9R9, -OR9, -OCOR10, -OCONR10R10, -OCOR2R10, -SR9, -SOR10, -SO2R10, -SO2NR9R9, -SO2NR5COR10, -NR9R9, -NR5COR9, -NR5CONR9R9, -NR5CO2R10, -NR5SO2R10, o -C(=N-OH)R10; R12 representahalogeno, -CN, -NO2, -COR13, -CO2R13, -CONR13R13, -OR13, -OCOR14, -OCONR14R14, -OCOR2R14, -SR13, -SOR14, -SO2R14, -SO2NR13R13, -SO2NR5COR14, -NR13R13, -NR5COR13, -NR5CONR13R13, -NR5CO2R14, -NR5SO2R14 o -C(=N-OH)R14; R13 representa hidrogeno o R14;R14 representa C1-4alquilo, haloC1-4alquilo, C1-4alcoxiC1-4alquilo, o hidroxiC1-4alquilo; o bien dos grupos R13 o dos grupos R14 sobre un mismo átomo de N pueden estar unidos completando, junto con el átomo de N, un anillo saturado de 5 a 6 átomos,que puede contener adicionalmente uno o dos heteroátomos seleccionados de entre N, S y O y que puede estar opcionalmente sustituido por uno o más grupos C1-4alquilo; cada Cy3 y Cy4 representan independientemente un anillo monocíclico de 3 a 7miembros o bicíclico de 6 a 11 miembros que puede ser carbocíclico o heterocíclico en cuyo caso puede contener de 1 a 4 heteroátomos seleccionados de entre N, S y O, donde Cy3 y Cy4 puede ser saturado, parcialmente insaturado o aromático, y puedeestar unido al resto de la molécula a través de cualquier átomo de C o N disponible, y donde uno o más átomos de C o S del anillo pueden estar opcionalmente oxidados formando grupos CO, SO o SO2; Cy5 representa un anillo seleccionado de entre (a)-(c); y R15 representa hidrogeno o C1-4 alquilo; o una sal del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP07380088 | 2007-04-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR065901A1 true AR065901A1 (es) | 2009-07-08 |
Family
ID=38475914
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP080101351A AR065901A1 (es) | 2007-04-02 | 2008-03-31 | Derivados de pirrolipirimidina |
Country Status (16)
Country | Link |
---|---|
US (1) | US20110160185A9 (es) |
EP (1) | EP2142550A1 (es) |
JP (1) | JP2010523522A (es) |
KR (1) | KR20100015353A (es) |
CN (1) | CN101679440A (es) |
AR (1) | AR065901A1 (es) |
AU (1) | AU2008234822A1 (es) |
BR (1) | BRPI0809992A2 (es) |
CA (1) | CA2682646A1 (es) |
CL (1) | CL2008000946A1 (es) |
IL (1) | IL201073A0 (es) |
MX (1) | MX2009010595A (es) |
PE (1) | PE20090996A1 (es) |
RU (1) | RU2009140319A (es) |
TW (1) | TW200904442A (es) |
WO (1) | WO2008119792A1 (es) |
Families Citing this family (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009026107A1 (en) | 2007-08-17 | 2009-02-26 | Portola Pharmaceuticals, Inc. | Protein kinase inhibitors |
US8138339B2 (en) | 2008-04-16 | 2012-03-20 | Portola Pharmaceuticals, Inc. | Inhibitors of protein kinases |
NZ589315A (en) | 2008-04-16 | 2012-11-30 | Portola Pharm Inc | 2,6-diamino-pyrimidin-5-yl-carboxamides as Spleen tryosine kinase (syk) or Janus kinase (JAK) inhibitors |
BRPI0910668A2 (pt) | 2008-04-22 | 2019-09-24 | Portola Pharmaceutiacals Inc | inibidores de proteína quinases |
AR073397A1 (es) * | 2008-09-23 | 2010-11-03 | Palau Pharma Sa | Derivados de (r) -3- (n,n-dimetilamino) pirrolidina |
AU2009324210A1 (en) | 2008-12-05 | 2010-06-10 | F. Hoffmann-La Roche Ag | Pyrrolopyrazinyl urea kinase inhibitors |
SI2440558T1 (sl) * | 2009-06-08 | 2015-10-30 | Takeda Pharmaceutical Company Limited | Spojine dihidropirolonaftiridinona kot inhibitorji JAK |
TWI466885B (zh) * | 2009-07-31 | 2015-01-01 | Japan Tobacco Inc | 含氮螺環化合物及其醫藥用途 |
UA109775C2 (xx) * | 2009-10-29 | 2015-10-12 | N-вмісні гетероарильні похідні як інгібітори jak3-кінази | |
WO2012003829A1 (en) * | 2010-07-09 | 2012-01-12 | Leo Pharma A/S | Novel homopiperazine derivatives as protein tyrosine kinase inhibitors and pharmaceutical use thereof |
RU2563644C2 (ru) | 2010-08-20 | 2015-09-20 | Хатчисон Медифарма Лимитед | Пирролопиримидиновые соединения и их применения |
EP2611448A1 (en) * | 2010-09-01 | 2013-07-10 | Ambit Biosciences Corporation | 7-cyclylquinazoline derivatives and methods of use thereof |
WO2012030924A1 (en) * | 2010-09-01 | 2012-03-08 | Ambit Biosciences Corporation | Azolopyridine and azolopyrimidine compounds and methods of use thereof |
MX363551B (es) | 2011-11-23 | 2019-03-27 | Portola Pharmaceuticals Inc Star | Compuestos derivados de pirazina como inhibidores de cinasa. |
WO2014013014A1 (en) | 2012-07-18 | 2014-01-23 | Fundació Privada Centre De Regulació Genòmica (Crg) | Jak inhibitors for activation of epidermal stem cell populations |
DK2947084T3 (da) * | 2013-01-18 | 2020-11-02 | Guangzhou Maxinovel Pharmaceuticals Co | Fem- og seks-ledet heterocyklisk forbindelse og forberedelsesmetode, farmaceutisk sammensætning og anvendelse deraf |
KR101657616B1 (ko) * | 2013-05-24 | 2016-09-19 | 주식회사유한양행 | 피리미딘 고리를 포함하는 바이사이클릭 유도체 및 그의 제조방법 |
WO2015143692A1 (en) * | 2014-03-28 | 2015-10-01 | Changzhou Jiekai Pharmatech Co., Ltd. | Heterocyclic compounds as axl inhibitors |
CN105315285B (zh) * | 2014-07-25 | 2017-12-08 | 上海海雁医药科技有限公司 | 2,4‑二取代7H‑吡咯并[2,3‑d]嘧啶衍生物、其制法与医药上的用途 |
NO2721710T3 (es) | 2014-08-21 | 2018-03-31 | ||
CN105732636B (zh) * | 2014-12-30 | 2020-04-21 | 广东东阳光药业有限公司 | 杂芳化合物及其在药物中的应用 |
CN107801397B (zh) | 2015-02-13 | 2021-07-30 | 达纳-法伯癌症研究所公司 | Lrrk2抑制剂及其制备和使用方法 |
CN104876934B (zh) * | 2015-05-12 | 2017-08-11 | 山东大学 | 一种含氮杂环苯基哌啶类化合物及其制备方法与应用 |
AU2016267141B2 (en) * | 2015-05-28 | 2020-04-16 | Theravance Biopharma R&D Ip, Llc | Naphthyridine compounds as jak kinase inhibitors |
US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
AU2016340167B2 (en) | 2015-10-16 | 2021-06-24 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
US11773106B2 (en) | 2015-10-16 | 2023-10-03 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
JOP20190024A1 (ar) | 2016-08-26 | 2019-02-19 | Gilead Sciences Inc | مركبات بيروليزين بها استبدال واستخداماتها |
WO2018041989A1 (en) | 2016-09-02 | 2018-03-08 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for diagnosing and treating refractory celiac disease type 2 |
KR102526964B1 (ko) | 2018-02-26 | 2023-04-28 | 길리애드 사이언시즈, 인코포레이티드 | Hbv 복제 억제제로서의 치환된 피롤리진 화합물 |
CN110526915B (zh) * | 2018-05-25 | 2022-02-01 | 首药控股(北京)股份有限公司 | 一种间变性淋巴瘤激酶抑制剂的制备方法 |
US10744136B2 (en) | 2018-11-05 | 2020-08-18 | Avista Pharma Solutions, Inc. | Sulfonamide derivatives as JAK inhibitors |
JP2022527972A (ja) | 2019-04-02 | 2022-06-07 | アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル | 前悪性病変を有する患者において癌を予測及び予防する方法 |
US20220202820A1 (en) | 2019-04-16 | 2022-06-30 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Use of jak inhibitors for the treatment of painful conditions involving nav1.7 channels |
WO2020235902A1 (ko) * | 2019-05-17 | 2020-11-26 | 주식회사 보로노이 | 헤테로고리 융합 피리미딘 유도체 및 이의 용도 |
CN110183471B (zh) * | 2019-05-21 | 2022-02-15 | 江苏大学 | 一种哌嗪类衍生物及制备方法及应用 |
CN110317176A (zh) * | 2019-07-04 | 2019-10-11 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
WO2022216097A1 (ko) * | 2021-04-08 | 2022-10-13 | 주식회사 스탠다임 | 신규한 lrrk2 억제제 |
WO2023222565A1 (en) | 2022-05-16 | 2023-11-23 | Institut National de la Santé et de la Recherche Médicale | Methods for assessing the exhaustion of hematopoietic stems cells induced by chronic inflammation |
WO2024006916A1 (en) * | 2022-06-29 | 2024-01-04 | Aerie Pharmaceuticals, Inc. | Azetidinyl pyrimidines and uses thereof as jak inhibitors |
CN118005609A (zh) * | 2022-11-09 | 2024-05-10 | 沈阳药科大学 | 2-氨基嘧啶类化合物及其用途 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PA8474101A1 (es) * | 1998-06-19 | 2000-09-29 | Pfizer Prod Inc | Compuestos de pirrolo [2,3-d] pirimidina |
JP4666762B2 (ja) * | 1998-06-19 | 2011-04-06 | ファイザー・プロダクツ・インク | ピロロ[2.3−d]ピリミジン化合物 |
MX2007009429A (es) * | 2005-02-03 | 2008-03-18 | Vertex Pharma | Pirrolopirimidinas utiles como inhibidores de proteinas cinasas. |
GB0526246D0 (en) * | 2005-12-22 | 2006-02-01 | Novartis Ag | Organic compounds |
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2008
- 2008-03-31 CN CN200880015843A patent/CN101679440A/zh active Pending
- 2008-03-31 RU RU2009140319/04A patent/RU2009140319A/ru not_active Application Discontinuation
- 2008-03-31 US US12/594,228 patent/US20110160185A9/en not_active Abandoned
- 2008-03-31 BR BRPI0809992-8A2A patent/BRPI0809992A2/pt not_active IP Right Cessation
- 2008-03-31 KR KR1020097020666A patent/KR20100015353A/ko not_active Application Discontinuation
- 2008-03-31 PE PE2008000586A patent/PE20090996A1/es not_active Application Discontinuation
- 2008-03-31 CA CA002682646A patent/CA2682646A1/en not_active Abandoned
- 2008-03-31 WO PCT/EP2008/053842 patent/WO2008119792A1/en active Application Filing
- 2008-03-31 AR ARP080101351A patent/AR065901A1/es not_active Application Discontinuation
- 2008-03-31 JP JP2010501495A patent/JP2010523522A/ja not_active Withdrawn
- 2008-03-31 AU AU2008234822A patent/AU2008234822A1/en not_active Abandoned
- 2008-03-31 MX MX2009010595A patent/MX2009010595A/es not_active Application Discontinuation
- 2008-03-31 EP EP08735625A patent/EP2142550A1/en not_active Withdrawn
- 2008-04-01 CL CL200800946A patent/CL2008000946A1/es unknown
- 2008-04-01 TW TW097111869A patent/TW200904442A/zh unknown
-
2009
- 2009-09-21 IL IL201073A patent/IL201073A0/en unknown
Also Published As
Publication number | Publication date |
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IL201073A0 (en) | 2010-05-17 |
US20100113420A1 (en) | 2010-05-06 |
CA2682646A1 (en) | 2008-10-09 |
CL2008000946A1 (es) | 2008-10-10 |
BRPI0809992A2 (pt) | 2014-10-14 |
JP2010523522A (ja) | 2010-07-15 |
RU2009140319A (ru) | 2011-05-10 |
AU2008234822A1 (en) | 2008-10-09 |
PE20090996A1 (es) | 2009-07-15 |
US20110160185A9 (en) | 2011-06-30 |
CN101679440A (zh) | 2010-03-24 |
KR20100015353A (ko) | 2010-02-12 |
WO2008119792A1 (en) | 2008-10-09 |
EP2142550A1 (en) | 2010-01-13 |
TW200904442A (en) | 2009-02-01 |
MX2009010595A (es) | 2009-10-22 |
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