AR053652A1 - Derivados de indol como inhibidores de proteina quinasas. composiciones farmaceuticas - Google Patents
Derivados de indol como inhibidores de proteina quinasas. composiciones farmaceuticasInfo
- Publication number
- AR053652A1 AR053652A1 ARP050104664A ARP050104664A AR053652A1 AR 053652 A1 AR053652 A1 AR 053652A1 AR P050104664 A ARP050104664 A AR P050104664A AR P050104664 A ARP050104664 A AR P050104664A AR 053652 A1 AR053652 A1 AR 053652A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- halo
- substituted
- heteroaryl
- alkoxy
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
-
- 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
- A61K31/41—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
- A61K31/4164—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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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/06—Antiabortive agents; Labour repressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- 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
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- 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
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Abstract
Composiciones farmacéuticas que comprenden dichos compuestos. Reivindicacion 1: Un compuesto de la formula (1), en la cual: U, V y W son independientemente seleccionados entre CR5 y N, donde R5 es seleccionado entre hidrogeno y alquilo C1-6; Q es seleccionado entre NR5, NNR5 y CR5, donde R5 es seleccionado entre hidrogeno y alquilo C1-6; L1 es seleccionado entre -NR5C(O)-, -NR5C(O)NR5-, -C(O)NR5-, -NR5- y heteroarilo C5-10; donde R5 es seleccionado entre hidrogeno y alquilo C1-6; L2 es seleccionado entre un enlace, -O-, -NR5C(O)-, -NR5C(O)NR5-, -C(O)NR5- y -NR5-, donde R5 es seleccionado entre hidrogeno y alquilo C1-6; n es seleccionado entre 0 y 1; m es seleccionado entre 0, 1, 2, 3 y 4; R1 es seleccionado entre arilo C6-10, heteroarilo C5-10, cicloalquilo C3-12 y heterocicloalquilo C3-8; donde cualquier arilo, heteroarilo, cicloalquilo o heterocicloalquilo de R1 está optativamente sustituido con uno a tres radicales independientemente seleccionados entre halo, amino, nitro, ciano, alquilo C1-6, alquilo C1-6 sustituido con halo, alcoxi C1-6, alcoxi C1-6 sustituido con halo, arilC6-10-alquiloC0-4, heteroarilC5-10-alquiloC0-4, cicloalquilC3-12-alquiloC0-4 y heterocicloalquilC3-8-alquiloC0-4, donde un metileno de cualquiera de los grupos alquilo puede ser optativamente reemplazado por oxígeno; donde cualquier sustituyente arilo, heteroarilo, cicloalquilo o heterocicloalquilo de R1 puede ser optativamente sustituido con 1 a 3 radicales independientemente seleccionados entre alquilo C1-6, alcoxi C1-6, alquilo C1-6 sustituido con halo, alcoxi C1-6 sustituido con halo y alquilo C1-6 sustituido con hidroxi; R2 es seleccionado entre halo, amino, nitro, ciano, alquilo C1-6, alquilo C1-6 sustituido con halo, alcoxi C1-6, alcoxi C1-6 sustituido con halo, aril-C6-10- alquiloC0-4, cicloalquilC3-12-alquiloC0-4 y heteroarilC5-10-alquiloC0-4; donde cualquier arilo, heteroarilo, cicloalquilo o heterocicloalquilo de R2 está optativamente sustituido con uno o tres radicales independientemente seleccionados entre halo, amino, nitro, ciano, alquilo C1-6, alcoxi C1-6, alquilo C1-6 sustituido con halo y alcoxi C1-6 sustituido con halo; R3 es seleccionado entre hidrogeno y alquilo C1-6; y R4 es seleccionado entre hidrogeno, -XR6, -XNR5XR6, -XOXR6 y -XNR5XR5R6, donde cada X es independientemente seleccionado entre un enlace y alquileno C1-4 donde cualquier alquileno de X puede ser optativamente sustituido con hidroxi, R5 es seleccionado entre hidrogeno y alquilo C1-6; R6 es seleccionado entre arilo C6-10, heteroarilo C5-10, cicloalquilo C3-12 y heterocicloalquilo C3-8, donde cualquier arilo, heteroarilo, cicloalquilo o heterocicloalquilo de R6 puede ser optativamente sustituido con 1 a 3 radicales independientemente seleccionados entre alquilo C1-6, hidroxi, ciano, -NR5S(O)0-2R5, -S(O)0-2NR5R5, -NR5S(O)0-2NR5R5, -C(O) NR5XNR5R5, -XNR5XNR5R5, -C(O)R7, -C(O)NR5XOR5, -C(O)NR5R5, -C(O)NR5R7, -C(O)NR5XR7 y -XC(O)OR5; donde cada X es independientemente seleccionado entre un enlace y alquileno C1-4 donde cualquier alquileno de X puede ser optativamente sustituido con hidroxi, donde cada R5 es seleccionado entre hidrogeno y alquilo C1-6 y R7 es seleccionado entre heteroarilC5-10- alquiloC0-4 y heterocicloalquilC3-10-alquiloC0-4; donde cualquier heteroarilo o heterocicloalquilo de R7 está optativamente sustituido con un radical seleccionado del grupo constituido por dietil-amino-etilo, dimetil-amino, amino, alquilo C1-6, pirimidinilo, pirazinilo, alquilo C1-6 sustituido con halo y -C(O)OR5; así como las sales, hidratos, solvatos e isomero farmacéuticamente aceptables del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62678504P | 2004-11-09 | 2004-11-09 | |
US70964805P | 2005-08-19 | 2005-08-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR053652A1 true AR053652A1 (es) | 2007-05-16 |
Family
ID=36337126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP050104664A AR053652A1 (es) | 2004-11-09 | 2005-11-07 | Derivados de indol como inhibidores de proteina quinasas. composiciones farmaceuticas |
Country Status (17)
Country | Link |
---|---|
US (1) | US8101608B2 (es) |
EP (1) | EP1814545A4 (es) |
JP (1) | JP4917041B2 (es) |
KR (1) | KR20070084066A (es) |
AR (1) | AR053652A1 (es) |
AU (1) | AU2005304719B2 (es) |
BR (1) | BRPI0517968A (es) |
CA (1) | CA2583737C (es) |
GT (1) | GT200500321A (es) |
IL (1) | IL182687A0 (es) |
MA (1) | MA29216B1 (es) |
MX (1) | MX2007005547A (es) |
NO (1) | NO20072887L (es) |
RU (1) | RU2406725C2 (es) |
TN (1) | TNSN07176A1 (es) |
TW (1) | TW200631577A (es) |
WO (1) | WO2006052936A2 (es) |
Families Citing this family (38)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2005118551A2 (en) | 2004-05-28 | 2005-12-15 | Ligand Pharmaceuticals Inc. | Thrombopoietin activity modulating compounds and methods |
JP4728340B2 (ja) | 2004-10-25 | 2011-07-20 | リガンド・ファーマシューティカルズ・インコーポレイテッド | トロンボポエチン活性を変調する化合物および変調方法 |
CA2602453A1 (en) * | 2005-07-13 | 2007-01-18 | Allergan, Inc. | Kinase inhibitors |
EP1902025A1 (en) | 2005-07-13 | 2008-03-26 | Allergan, Inc. | Kinase inhibitors |
US7749530B2 (en) | 2005-07-13 | 2010-07-06 | Allergan, Inc. | Kinase inhibitors |
UA93548C2 (uk) | 2006-05-05 | 2011-02-25 | Айерем Елелсі | Сполуки та композиції як модулятори хеджхогівського сигнального шляху |
DE102006024834B4 (de) * | 2006-05-24 | 2010-07-01 | Schebo Biotech Ag | Neue Indol-Pyrrol-Derivate und deren Verwendungen |
WO2008022013A1 (en) * | 2006-08-11 | 2008-02-21 | Allergan, Inc. | Kinase inhibitors |
US7928136B2 (en) | 2006-09-11 | 2011-04-19 | Curis, Inc. | Substituted 2-indolinone as PTK inhibitors containing a zinc binding moiety |
ES2565683T3 (es) | 2006-09-15 | 2016-04-06 | Xcovery, Inc. | Compuestos inhibidores de quinasa |
CN101522026A (zh) * | 2006-10-06 | 2009-09-02 | Irm责任有限公司 | 蛋白激酶抑制剂及其应用方法 |
GEP20135925B (en) | 2007-03-14 | 2013-10-10 | Exelixis Patent Co Llc | Inhibitors of hedgehog pathway |
CA2960659C (en) | 2007-11-09 | 2021-07-13 | The Salk Institute For Biological Studies | Use of tam receptor inhibitors as immunoenhancers and tam activators as immunosuppressors |
CL2009000400A1 (es) * | 2008-02-22 | 2010-09-10 | Irm Llc | Compuestos heterociclicos derivados de 3-fenil-1,6- naftiridin-2-ona; moduladores de la actividad cinasa; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como trastornos alergicos, trastornos autoinmunes, neoplasias, rechazo en trasplante de organos, entre otras. |
JP5305704B2 (ja) * | 2008-03-24 | 2013-10-02 | 富士フイルム株式会社 | 新規化合物、光重合性組成物、カラーフィルタ用光重合性組成物、カラーフィルタ、及びその製造方法、固体撮像素子、並びに、平版印刷版原版 |
JP2011520809A (ja) * | 2008-05-05 | 2011-07-21 | アムジエン・インコーポレーテツド | γセクレターゼモジュレーターとしての尿素化合物 |
WO2009139834A1 (en) * | 2008-05-13 | 2009-11-19 | Poniard Pharmaceuticals, Inc. | Bioactive compounds for treatment of cancer and neurodegenerative diseases |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
EA029131B1 (ru) | 2008-05-21 | 2018-02-28 | Ариад Фармасьютикалз, Инк. | Фосфорсодержащие производные в качестве ингибиторов киназы |
CA2729012A1 (en) | 2008-06-27 | 2009-12-30 | Amgen Inc. | Ang-2 inhibition to treat multiple sclerosis |
CN102115472B (zh) * | 2010-01-04 | 2013-12-04 | 深圳市天和医药科技开发有限公司 | 3-(2-吡咯亚甲基)氮杂吲哚啉-2-酮衍生物及其制法与应用 |
GB201014374D0 (en) * | 2010-08-27 | 2010-10-13 | Univ Greenwich | Novel hybrid compounds |
WO2012151561A1 (en) | 2011-05-04 | 2012-11-08 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
EP2838538B1 (en) * | 2012-04-20 | 2017-03-15 | Annji Pharmaceutical Co., Ltd. | Cyclopropanecarboxylate esters of purine analogues |
WO2013169401A1 (en) | 2012-05-05 | 2013-11-14 | Ariad Pharmaceuticals, Inc. | Compounds for inhibiting cell proliferation in egfr-driven cancers |
CA2879542A1 (en) | 2012-07-25 | 2014-01-30 | Salk Institute For Biological Studies | Regulating the interaction between tam ligands and lipid membranes with exposed phosphatidylserine |
WO2014066840A1 (en) * | 2012-10-26 | 2014-05-01 | Regents Of The University Of Minnesota | Aurora kinase inhibitors |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
WO2016161572A1 (en) | 2015-04-08 | 2016-10-13 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
US10487054B2 (en) | 2017-04-21 | 2019-11-26 | Regents Of The University Of Minnesota | Therapeutic compounds |
MX2022001863A (es) | 2019-08-12 | 2022-05-30 | Deciphera Pharmaceuticals Llc | Metodos para tratar los tumores del estroma gastrointestinal. |
WO2021030405A1 (en) | 2019-08-12 | 2021-02-18 | Deciphera Pharmaceuticals, Llc | Ripretinib for treating gastrointestinal stromal tumors |
KR20220123058A (ko) | 2019-12-30 | 2022-09-05 | 데시페라 파마슈티칼스, 엘엘씨. | 1-(4-브로모-5-(1-에틸-7-(메틸아미노)-2-옥소-1,2-디히드로-1,6-나프티리딘-3-일)-2-플루오로페닐)-3-페닐우레아의 조성물 |
MX2022008103A (es) | 2019-12-30 | 2022-09-19 | Deciphera Pharmaceuticals Llc | Formulaciones de inhibidores de la cinasa amorfa y metodos de estas. |
CN114853735B (zh) * | 2022-07-06 | 2022-10-21 | 北京鑫开元医药科技有限公司 | 靶向泛素化降解trk的化合物及其制备方法、组合物和用途 |
CN114853736B (zh) * | 2022-07-06 | 2022-10-21 | 北京鑫开元医药科技有限公司 | 具有trk抑制活性的化合物、制备方法、组合物及其用途 |
US11779572B1 (en) | 2022-09-02 | 2023-10-10 | Deciphera Pharmaceuticals, Llc | Methods of treating gastrointestinal stromal tumors |
WO2024054793A1 (en) | 2022-09-09 | 2024-03-14 | University Of Rochester | Inhibition of efferocytosis as a treatment to prevent bone loss and increase bone density and strength |
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GB9718913D0 (en) * | 1997-09-05 | 1997-11-12 | Glaxo Group Ltd | Substituted oxindole derivatives |
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PT1082302E (pt) * | 1998-05-28 | 2004-04-30 | Biogen Inc | Um inibidor de amt-4: omepupa-v |
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AU5468499A (en) * | 1998-08-04 | 2000-02-28 | Sugen, Inc. | 3-methylidenyl-2-indolinone modulators of protein kinase |
EP1149093A1 (en) | 1998-12-17 | 2001-10-31 | F. Hoffmann-La Roche Ag | 4-aryloxindoles as inhibitors of jnk protein kinases |
GB9904933D0 (en) | 1999-03-04 | 1999-04-28 | Glaxo Group Ltd | Compounds |
ME00415B (me) | 2000-02-15 | 2011-10-10 | Pharmacia & Upjohn Co Llc | Pirol supstituisani 2-indol protein kinazni inhibitori |
AU2001268154A1 (en) * | 2000-06-02 | 2001-12-17 | Sugen, Inc. | Indolinone derivatives as protein kinase/phosphatase inhibitors |
US20030119839A1 (en) | 2001-12-13 | 2003-06-26 | Nan-Horng Lin | Protein kinase inhibitors |
TW200301123A (en) | 2001-12-21 | 2003-07-01 | Astrazeneca Uk Ltd | New use |
AU2003302665B2 (en) | 2002-11-15 | 2009-12-24 | Symphony Evolution, Inc. | Kinase modulators |
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2005
- 2005-11-04 GT GT200500321A patent/GT200500321A/es unknown
- 2005-11-07 AU AU2005304719A patent/AU2005304719B2/en not_active Ceased
- 2005-11-07 EP EP05851419A patent/EP1814545A4/en not_active Withdrawn
- 2005-11-07 US US11/718,886 patent/US8101608B2/en not_active Expired - Fee Related
- 2005-11-07 WO PCT/US2005/040372 patent/WO2006052936A2/en active Application Filing
- 2005-11-07 KR KR1020077010439A patent/KR20070084066A/ko active IP Right Grant
- 2005-11-07 JP JP2007540153A patent/JP4917041B2/ja not_active Expired - Fee Related
- 2005-11-07 AR ARP050104664A patent/AR053652A1/es unknown
- 2005-11-07 MX MX2007005547A patent/MX2007005547A/es active IP Right Grant
- 2005-11-07 CA CA2583737A patent/CA2583737C/en not_active Expired - Fee Related
- 2005-11-07 RU RU2007121505/04A patent/RU2406725C2/ru not_active IP Right Cessation
- 2005-11-07 BR BRPI0517968-8A patent/BRPI0517968A/pt not_active IP Right Cessation
- 2005-11-08 TW TW094139176A patent/TW200631577A/zh unknown
-
2007
- 2007-04-19 IL IL182687A patent/IL182687A0/en unknown
- 2007-05-08 TN TNP2007000176A patent/TNSN07176A1/fr unknown
- 2007-05-30 MA MA29953A patent/MA29216B1/fr unknown
- 2007-06-06 NO NO20072887A patent/NO20072887L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
MX2007005547A (es) | 2007-07-05 |
GT200500321A (es) | 2006-09-04 |
RU2406725C2 (ru) | 2010-12-20 |
AU2005304719B2 (en) | 2009-07-23 |
WO2006052936A3 (en) | 2006-10-26 |
JP2008519762A (ja) | 2008-06-12 |
TW200631577A (en) | 2006-09-16 |
CA2583737C (en) | 2011-09-20 |
EP1814545A4 (en) | 2009-06-10 |
RU2007121505A (ru) | 2008-12-20 |
WO2006052936A2 (en) | 2006-05-18 |
TNSN07176A1 (en) | 2008-11-21 |
CA2583737A1 (en) | 2006-05-18 |
KR20070084066A (ko) | 2007-08-24 |
US20080221192A1 (en) | 2008-09-11 |
NO20072887L (no) | 2007-08-03 |
US8101608B2 (en) | 2012-01-24 |
JP4917041B2 (ja) | 2012-04-18 |
BRPI0517968A (pt) | 2008-10-21 |
IL182687A0 (en) | 2007-09-20 |
AU2005304719A1 (en) | 2006-05-18 |
MA29216B1 (fr) | 2008-02-01 |
EP1814545A2 (en) | 2007-08-08 |
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