AR042087A1 - Tieno (3,2b) piridin - 6- carbonitrilos y tieno (2,3-b) piridin- 5- carbonitrilos como inhibidores de proteinquinasas - Google Patents
Tieno (3,2b) piridin - 6- carbonitrilos y tieno (2,3-b) piridin- 5- carbonitrilos como inhibidores de proteinquinasasInfo
- Publication number
- AR042087A1 AR042087A1 ARP030104277A ARP030104277A AR042087A1 AR 042087 A1 AR042087 A1 AR 042087A1 AR P030104277 A ARP030104277 A AR P030104277A AR P030104277 A ARP030104277 A AR P030104277A AR 042087 A1 AR042087 A1 AR 042087A1
- Authority
- AR
- Argentina
- Prior art keywords
- nr4r4
- aryl
- alkenyl
- nr4c
- heteroaryl
- Prior art date
Links
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title 1
- 239000003909 protein kinase inhibitor Substances 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 8
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 1
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 abstract 1
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 208000001132 Osteoporosis Diseases 0.000 abstract 1
- 208000006011 Stroke Diseases 0.000 abstract 1
- 206010052779 Transplant rejections Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- RCCPEORTSYDPMB-UHFFFAOYSA-N hydroxy benzenecarboximidothioate Chemical compound OSC(=N)C1=CC=CC=C1 RCCPEORTSYDPMB-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 208000030761 polycystic kidney disease Diseases 0.000 abstract 1
- 206010039073 rheumatoid arthritis Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- 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
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- 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
-
- 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
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- 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
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Immunology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Physical Education & Sports Medicine (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Transplantation (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente proporciona compuestos de fórmula (1a)-(1f).Los mismos son de utilidad en el tratamiento del cáncer, accidente cerebrovascular, osteoporosis, enfermedad renal poliquística, enfermedad autoinmune, artritis reumatoidea, y rechazo a transplante y los procesos para producir dichos compuestos. Reivindicación 1: Un compuesto de fórmula (1a) o fórmula (1b) o un S-óxido o S-dióxido del mismo en el cual X es -NH-, -NR4, -O-, -S(O)m, -NHCH2-; m es un número entero entre 0-2; n es un número entero entre 2-5; q es un número entero entre 0-5; R1 es un anillo fenilo opcionalmente sustituido con de 1 a 4 sustituyentes seleccionados entre el grupo que consiste de -J, -NO2, -CN, -N3, -CHO, -CF3, -OCF3, -R4, -OR4, -S(O)mR4, NR4R4, -NR4S(O)mR4, -OR6OR4, -OR6NR4R4, -N(R4)R6OR4, -N(R4)R6NR4R4, -NR4C(O)R4, -C(O)R4, -C(O)OR4, -C(O)NR4R4, -OC(O)R4, -OC(O)OR4, -OC(O)NR4R4, -NR4C(O)R4, NR4C(O)OR4, -NR4C(O)NR4R4, -R5OR4, -R5NR4R4, -R5S(O)mR4, -R5C(O)R4, -R5C(O)OR4, -R5C(O)NR4R4, -R5OC(O)R4, -R5OC(O)OR4, -R5OC(O)NR4R4, -R5NR4C(O)R4, -R5NR4C(O)OR4, -R5NR4C(O)NR4R4, o YR7; R2 es -H, -R3, -J, -C(O)XR3, -CHO, en el cual el grupo R3 puede estar sustituido por uno o más grupos seleccionados entre -C(O)XR8, -CHO, -C(O)Q, 1,3-dioxolano, -R8, -(C(R9)2)qXR8, -(C(R9)2)qQ, -X(C(R9)2)nXR8, -X(C(R9)2)nQ, o -X(C(R9)2)qR8; R3 es un alquilo C1-6, cis-alquenilo de C2-6, trans-alquenilo de C2-6, alquinilo de C2-6, arilo o heteroarilo; R4 es H, alquilo C1-6, cis-alquenilo C2-6, un trans-alquenilo C2-6, o un alquinilo C2-6; R5 es un grupo divalente que comprende alquilo C1-6, alquenilo C2-6, y alquinilo C2-6; R6 es un grupo alquilo divalente de C2-6; R7 es un anillo cicloalquilo de C3-7, un anillo arilo o heteroarilo, un arilo o heteroarilo fusionado con uno a tres anillos arilo o heteroarilo, en el cual cualquiera de los anillos arilo, cicloalquilo, o heteroarilo puede estar opcionalmente sustituido con de 12 a 4 sustituyentes seleccionados entre el grupo que consiste de -H, -arilo, -CH2-arilo, -NH-arilo, -O-arilo, -S(O)m-arilo, -J,-NO2, -CN, -N3, -CHO, -CF3, -OCF3, -R4, -OR4, -S(O)mR4, NR4R4, -NR4S(O)mR4, -OR6OR4, -OR6NR4R4, -N(R4)R6OR4, -N(R4)R6NR4R4, -NR4C(O)R4, -C(O)R4, -C(O)OR4, -C(O)NR4R4, -OC(O)R4, -OC(O)OR4, -OC(O)NR4R4, -NR4C(O)R4, NR4C(O)OR4, -NR4C(O)NR4R4, -R5OR4, -R5NR4R4, -R5S(O)mR4, -R5C(O)R4, -R5C(O)OR4, -R5C(O)NR4R4, -R5C(O)R4, -R5C(O)OR4, -R5C(O)NR4R4, R5OC(O)R4, -R5OC(O)OR4, -R5OC(O)NR4R4, -R5NR4C(O)R4, -R5NR4C(O)OR4, o -R5NR4C(O)NR4R4; R8 es -h, alquilo C1-6, cis-alquenilo de C2-6, trans-alquenilo de C2-6, alquinilo de C2-6, arilo o heteroarilo; R9 es -R4 o -F; Y es -C(O)-, -C(O)O-, -OC(O)-, -C(O)NH-, -NHC(O), -NHSO2-, -SO2NH-, -C(OH)H-, -X(C(R9)2)q-, -(C(R9)2)q,-(C(R9)2)qX-, -C:::C-, cis y trans- -CH=CH- y cicloalquilo de C3-10; Q es NZZ´ en el cual Z y Z´ pueden ser iguales o diferentes y pueden ser H, alquilo C1-6, alquenilo de C2-6, alquinilo de C2-6, arilo o heteroarilo, y Z y Z´ junto con el N al cual están unidos pueden formar un anillo heterocíclico que puede tener un heteroátomo adicional seleccionado entre N, O, y S, opcionalmente sustituidos con -R4 sobre un C o un N, o sobre el N por un grupo -(C(R9)2)nR3, -C(R9)2)nZ"Z"´, o sobre el C por un grupo -(C(R9)2)qXR3, -(C(R9)2)qNZ"Z"´, Z" y Z"´ junto con el N al cual están unidos pueden formar un anillo heterocíclico que puede contener un heteroátomo adicional seleccionado entre N, O y S; Z"´ y Z" pueden seleccionarse entre H, alquilo de C1-6, alquenilo de C2-6, alquinilo de C2-6, arilo o heteroarilo; y J es F, Cl, Br, y I, o una sal de los mismos aceptable desde el punto de vista farmacéutico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US42886202P | 2002-11-25 | 2002-11-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR042087A1 true AR042087A1 (es) | 2005-06-08 |
Family
ID=32393469
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030104277A AR042087A1 (es) | 2002-11-25 | 2003-11-19 | Tieno (3,2b) piridin - 6- carbonitrilos y tieno (2,3-b) piridin- 5- carbonitrilos como inhibidores de proteinquinasas |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6987116B2 (es) |
| EP (1) | EP1565474A2 (es) |
| JP (1) | JP2006509760A (es) |
| KR (1) | KR20050086770A (es) |
| CN (1) | CN1714092A (es) |
| AR (1) | AR042087A1 (es) |
| AU (1) | AU2003290802A1 (es) |
| BR (1) | BR0316534A (es) |
| CA (1) | CA2502614A1 (es) |
| CL (1) | CL2003002287A1 (es) |
| EC (1) | ECSP055802A (es) |
| MX (1) | MXPA05004744A (es) |
| NI (1) | NI200500089A (es) |
| NO (1) | NO20051928L (es) |
| NZ (1) | NZ540104A (es) |
| RU (1) | RU2005120018A (es) |
| TW (1) | TW200412950A (es) |
| UA (1) | UA81000C2 (es) |
| WO (1) | WO2004048386A2 (es) |
| ZA (1) | ZA200504238B (es) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7276519B2 (en) * | 2002-11-25 | 2007-10-02 | Wyeth | Thieno[3,2-b]pyridine-6-carbonitriles and thieno[2,3-b]pyridine-5-carbonitriles as protein kinase inhibitors |
| FR2862647B1 (fr) | 2003-11-25 | 2008-07-04 | Aventis Pharma Sa | Derives de pyrazolyle, procede de preparation et intermediaires de ce procede a titre de medicaments et de compositions pharmaceutiques les renfermant |
| US7459562B2 (en) | 2004-04-23 | 2008-12-02 | Bristol-Myers Squibb Company | Monocyclic heterocycles as kinase inhibitors |
| TW200538453A (en) | 2004-04-26 | 2005-12-01 | Bristol Myers Squibb Co | Bicyclic heterocycles as kinase inhibitors |
| US7432373B2 (en) | 2004-06-28 | 2008-10-07 | Bristol-Meyers Squibb Company | Processes and intermediates useful for preparing fused heterocyclic kinase inhibitors |
| US7173031B2 (en) | 2004-06-28 | 2007-02-06 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
| US7439246B2 (en) | 2004-06-28 | 2008-10-21 | Bristol-Myers Squibb Company | Fused heterocyclic kinase inhibitors |
| CA2573538C (en) | 2004-07-30 | 2014-11-25 | Methylgene Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| GB0423653D0 (en) * | 2004-10-25 | 2004-11-24 | Piramed Ltd | Pharmaceutical compounds |
| AU2006343808B2 (en) | 2005-05-20 | 2012-03-29 | Mirati Therapeutics, Inc. | Inhibitors of VEGF receptor and HGF receptor signaling |
| CA2608726C (en) * | 2005-05-20 | 2013-07-09 | Methylgene Inc. | Inhibitors of vegf receptor and hgf receptor signaling |
| WO2007035428A1 (en) | 2005-09-15 | 2007-03-29 | Bristol-Myers Squibb Company | Met kinase inhibitors |
| PE20070619A1 (es) * | 2005-09-27 | 2007-07-02 | Wyeth Corp | TIENO(2,3-b)PIRIDIN-5-CARBONITRILOS COMO INHIBIDORES DE PROTEINAS QUINASA |
| US7547782B2 (en) | 2005-09-30 | 2009-06-16 | Bristol-Myers Squibb Company | Met kinase inhibitors |
| US8003662B2 (en) * | 2006-01-30 | 2011-08-23 | Array Biopharma, Inc. | Heterobicyclic thiophene compounds and methods of use |
| GB0601962D0 (en) | 2006-01-31 | 2006-03-15 | Ucb Sa | Therapeutic agents |
| WO2007089716A2 (en) * | 2006-02-01 | 2007-08-09 | The Regents Of The University Of California | Use of aminopyrimidine compounds in the treatment of immune disorders |
| US20090099356A1 (en) * | 2006-02-08 | 2009-04-16 | Wyeth | Preparation of 7-alkenyl-3 quinolinecarbonitriles via a palladium mediated coupling reaction |
| US20110053931A1 (en) * | 2006-06-08 | 2011-03-03 | John Gaudino | Quinoline compounds and methods of use |
| EP2069359B1 (en) * | 2006-08-21 | 2014-11-12 | Genentech, Inc. | Aza-benzothiophenyl compounds and methods of use |
| KR101428116B1 (ko) * | 2006-08-21 | 2014-08-07 | 제넨테크, 인크. | 아자-벤조푸라닐 화합물 및 사용 방법 |
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| GB0714384D0 (en) * | 2007-07-23 | 2007-09-05 | Ucb Pharma Sa | theraputic agents |
| RU2346947C1 (ru) * | 2007-08-13 | 2009-02-20 | Государственное образовательное учреждение высшего профессионального образования "Кубанский государственный технологический университет" (ГОУВПО "КубГТУ") | Способ получения фурилгетарилметанов, содержащих тиено[2,3-b]пиридиновый фрагмент |
| EP2183254B1 (en) * | 2007-08-29 | 2017-06-21 | MethylGene Inc. | Inhibitors of protein tyrosine kinase activity |
| US20090118276A1 (en) * | 2007-11-02 | 2009-05-07 | Wyeth | Thienopyrimidines, thienopyridines, and pyrrolopyrimidines as b-raf inhibitors |
| EP2240494B1 (en) * | 2008-01-21 | 2016-03-30 | UCB Biopharma SPRL | Thieno-pyridine derivatives as mek inhibitors |
| AR070317A1 (es) * | 2008-02-06 | 2010-03-31 | Osi Pharm Inc | Furo (3,2-c) piridina y tieno (3,2-c) piridinas |
| KR20100137495A (ko) * | 2008-03-05 | 2010-12-30 | 메틸진 인코포레이티드 | 단백질 티로신 키나아제 활성의 억제제 |
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| PE20110570A1 (es) * | 2008-07-01 | 2011-08-26 | Genentech Inc | Heterociclos biciclicos sustituidos |
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| JP6280546B2 (ja) | 2012-06-26 | 2018-02-14 | デル マー ファーマシューティカルズ | ジアンヒドロガラクチトール、ジアセチルジアンヒドロガラクチトール、ジブロモズルシトール、又はこれらの類似体若しくは誘導体を用いた、遺伝子多型又はahi1の調節不全若しくは変異を有する患者におけるチロシンキナーゼインヒビター抵抗性悪性腫瘍を処置するための方法 |
| ME03780B (me) | 2013-01-15 | 2021-04-20 | Incyte Holdings Corp | Jedinjenja tiazolkarboksamida i piridinkarboksamida korisna kao inhibitori pim kinaze |
| KR101468207B1 (ko) * | 2013-02-14 | 2014-12-01 | 한국화학연구원 | 신규한 싸이에노[3,2-b]피리딜 우레아 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 포함하는 유로텐신-Ⅱ 수용체 활성 관련 질환의 예방 또는 치료용 약학적 조성물 |
| EA201690458A1 (ru) | 2013-08-23 | 2016-07-29 | Инсайт Корпорейшн | Фуро- и тиенопиридинкарбоксамиды, используемые в качестве ингибиторов pim-киназы |
| AR105967A1 (es) | 2015-09-09 | 2017-11-29 | Incyte Corp | Sales de un inhibidor de pim quinasa |
| WO2017059251A1 (en) | 2015-10-02 | 2017-04-06 | Incyte Corporation | Heterocyclic compounds useful as pim kinase inhibitors |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
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| PE20220139A1 (es) | 2019-02-13 | 2022-01-27 | Ptc Therapeutics Inc | Compuestos de tioeno[3,2-b] piridin-7-amina para tratar la disautonomia familiar |
| CN113195469B (zh) * | 2019-02-19 | 2024-05-24 | 四川科伦博泰生物医药股份有限公司 | 含氮并环化合物、其制备方法及用途 |
| US11358971B2 (en) | 2019-07-03 | 2022-06-14 | H. Lundbeck A/S | Prodrugs of modulators of the NMDA receptor |
| US11466027B2 (en) | 2019-07-03 | 2022-10-11 | H. Lundbeck A/S | Modulators of the NMDA receptor |
| CN114269753B (zh) * | 2019-09-29 | 2024-03-05 | 四川科伦博泰生物医药股份有限公司 | 一种含氮并环类化合物,包含其的药物组合物,其制备方法及其用途 |
| WO2022169866A1 (en) * | 2021-02-05 | 2022-08-11 | Ptc Therapeutics Inc. | Methods for treating spinocerebellar ataxia type 3 |
| EP4483954A1 (en) * | 2023-06-29 | 2025-01-01 | Masarykova Univerzita | Substituted thieno [3,2-b]pyridines as inhibitors of protein kinases |
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| US45A (en) * | 1836-10-11 | Machine fob shelling cokm | ||
| EP0126970A3 (en) | 1983-04-27 | 1985-11-06 | Beecham Group Plc | Anxiolytic and anti-depressant thienopyridine derivatives |
| AR004010A1 (es) * | 1995-10-11 | 1998-09-30 | Glaxo Group Ltd | Compuestos heterociclicos |
| ID23978A (id) * | 1997-11-11 | 2000-06-14 | Pfizer Prod Inc | Turunan-turunan tienopirimidin dan tienopiridin yang berguna sebagai zat-zat anti kangker |
| EP1950201A1 (en) * | 1998-09-29 | 2008-07-30 | Wyeth Holdings Corporation | Substituted 3-cyanoquinolines as protein tyrosine kinases inhibitors |
| JP3270834B2 (ja) * | 1999-01-27 | 2002-04-02 | ファイザー・プロダクツ・インク | 抗がん剤として有用なヘテロ芳香族二環式誘導体 |
| GB9906566D0 (en) * | 1999-03-23 | 1999-05-19 | Zeneca Ltd | Chemical compounds |
| DE60009888T2 (de) * | 1999-04-21 | 2005-04-21 | Wyeth Corp | Substituierte 3-cyano-[1.7], [1.5] und [1.8]naphthyridininhibitoren von tyrosin kinasen |
| WO2001047892A1 (en) * | 1999-12-29 | 2001-07-05 | Wyeth | Tricyclic protein kinase inhibitors |
| AR035851A1 (es) * | 2000-03-28 | 2004-07-21 | Wyeth Corp | 3-cianoquinolinas, 3-ciano-1,6-naftiridinas y 3-ciano-1,7-naftiridinas como inhibidoras de proteina quinasas |
| WO2001094353A1 (en) * | 2000-06-06 | 2001-12-13 | Pfizer Products Inc. | Thiophene derivatives useful as anticancer agents |
| US20020004511A1 (en) * | 2000-06-28 | 2002-01-10 | Luzzio Michael Joseph | Thiophene derivatives useful as anticancer agents |
| AU2001295791A1 (en) * | 2000-11-02 | 2002-05-15 | Astrazeneca Ab | 4-substituted quinolines as antitumor agents |
| EP1418917A1 (en) | 2001-08-10 | 2004-05-19 | Novartis AG | Use of c-src inhibitors alone or in combination with sti571 for the treatment of leukaemia |
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- 2003-11-07 CL CL200302287A patent/CL2003002287A1/es unknown
- 2003-11-14 KR KR1020057009358A patent/KR20050086770A/ko not_active Withdrawn
- 2003-11-14 BR BR0316534-5A patent/BR0316534A/pt not_active IP Right Cessation
- 2003-11-14 MX MXPA05004744A patent/MXPA05004744A/es active IP Right Grant
- 2003-11-14 RU RU2005120018/04A patent/RU2005120018A/ru not_active Application Discontinuation
- 2003-11-14 NZ NZ540104A patent/NZ540104A/en unknown
- 2003-11-14 UA UAA200506270A patent/UA81000C2/uk unknown
- 2003-11-14 CN CNA2003801039013A patent/CN1714092A/zh active Pending
- 2003-11-14 CA CA002502614A patent/CA2502614A1/en not_active Abandoned
- 2003-11-14 JP JP2004555437A patent/JP2006509760A/ja active Pending
- 2003-11-14 WO PCT/US2003/036206 patent/WO2004048386A2/en not_active Ceased
- 2003-11-14 EP EP03783385A patent/EP1565474A2/en not_active Withdrawn
- 2003-11-14 AU AU2003290802A patent/AU2003290802A1/en not_active Withdrawn
- 2003-11-17 TW TW092132143A patent/TW200412950A/zh unknown
- 2003-11-19 AR ARP030104277A patent/AR042087A1/es not_active Application Discontinuation
- 2003-11-21 US US10/719,359 patent/US6987116B2/en not_active Expired - Fee Related
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- 2005-04-26 NI NI200500089A patent/NI200500089A/es unknown
- 2005-05-19 EC EC2005005802A patent/ECSP055802A/es unknown
- 2005-05-24 ZA ZA200504238A patent/ZA200504238B/xx unknown
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| CA2502614A1 (en) | 2004-06-10 |
| ZA200504238B (en) | 2009-09-30 |
| US20040138251A1 (en) | 2004-07-15 |
| CN1714092A (zh) | 2005-12-28 |
| US6987116B2 (en) | 2006-01-17 |
| NZ540104A (en) | 2007-05-31 |
| MXPA05004744A (es) | 2005-08-03 |
| EP1565474A2 (en) | 2005-08-24 |
| UA81000C2 (en) | 2007-11-26 |
| ECSP055802A (es) | 2005-08-11 |
| NO20051928L (no) | 2005-08-19 |
| TW200412950A (en) | 2004-08-01 |
| NO20051928D0 (no) | 2005-04-20 |
| WO2004048386A3 (en) | 2004-10-07 |
| NI200500089A (es) | 2006-01-11 |
| AU2003290802A1 (en) | 2004-06-18 |
| BR0316534A (pt) | 2005-10-04 |
| CL2003002287A1 (es) | 2005-01-14 |
| JP2006509760A (ja) | 2006-03-23 |
| WO2004048386A2 (en) | 2004-06-10 |
| KR20050086770A (ko) | 2005-08-30 |
| WO2004048386A9 (en) | 2005-07-14 |
| RU2005120018A (ru) | 2006-05-10 |
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