ES2552320T3 - Nuevas piridín-2-onas y piridazín-3-onas sustituidas - Google Patents
Nuevas piridín-2-onas y piridazín-3-onas sustituidas Download PDFInfo
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- ES2552320T3 ES2552320T3 ES09769133.1T ES09769133T ES2552320T3 ES 2552320 T3 ES2552320 T3 ES 2552320T3 ES 09769133 T ES09769133 T ES 09769133T ES 2552320 T3 ES2552320 T3 ES 2552320T3
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- alkyl
- halogen
- alkoxy
- hydroxy
- optionally substituted
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- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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- A61P5/14—Drugs for disorders of the endocrine system of the thyroid hormones, e.g. T3, T4
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- 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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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Abstract
Compuesto según la fórmula III o IV:**Fórmula** en las que: R es H, -R1, -R1-R2-R3 , -R1-R3 o -R2-R3; en el que R1 es arilo, heteroarilo, cicloalquilo o heterocicloalquilo, y se sustituye opcionalmente con R1', en el que R1' es alquilo C1-6, hidroxi, hidroxialquilo C1-6, alcoxi C1-6, halógeno, nitro, amino, cicloalquilo, heterocicloalquilo, ciano o haloalquilo C1-6, R2 es -C(>=O), -C(>=O)O, -C(>=O)N(R2'), -(CH2)q o -S(>=O)2; en el que R2' es H o alquilo C1-6; y q es 1, 2 o 3, R3 es H o R4; en el que R4 es alquilo C1-6, alcoxi C1-6, heteroalquilo C1-6, arilo, ariloalquilo, alquiloarilo, heteroarilo, alquilheteroarilo, heteroaril-alquilo, cicloalquilo, alquil-cicloalquilo, cicloalquil-alquilo, heterocicloalquilo, alquil-heterocicloalquilo o heterocicloalquil-alquilo, y se sustituye opcionalmente con uno o más de entre alquilo C1-6, hidroxi, oxo, hidroxialquilo C1-6, alcoxi C1-6, halógeno, nitro, amino, ciano, alquilsulfonilo C1-6 o haloalquilo C1-6, X es CH o N, Y1 es H o alquilo C1-6, Y2 es Y2a o Y2b, en el que Y2a es H o halógeno, e Y2b es alquilo C1-6, sustituido opcionalmente con uno o más Y2b', e Y2b' es hidroxi, alcoxi C1-6 o halógeno, cada Y2' es, independientemente, Y2'a o Y2'b, en el que Y2'a es halógeno, e Y2'b es alquilo C1-6, sustituido opcionalmente con uno o más Y2'b', e Y2'b' es hidroxi, alcoxi C1-6 o halógeno, n es 0, 1, 2 ó 3, Y3 es H, halógeno o alquilo C1-6,en el que alquilo C1-6 se encuentra sustituido opcionalmente con uno o más sustituyentes seleccionados de entre el grupo que consiste de hidroxi, alcoxi C1-6, amino y halógeno, m es 0 ó 1; Y4 es Y4a, Y4b, Y4c o Y4d, en el que Y4a es H o halógeno, Y4b es alquilo C1-6, sustituido opcionalmente con uno o más sustituyentes seleccionados de entre el grupo que consiste de haloalquilo C1-6, halógeno, hidroxi, amino, ciano y alcoxi C1-6, Y4c es cicloalquilo C3-7, sustituido opcionalmente con uno o más sustituyentes seleccionados de entre el grupo que consiste de alquilo C1-6, haloalquilo C1-6, halógeno, hidroxi, amino y alcoxi C1-6, y Y4d es amino, sustituido opcionalmente con uno o más alquilos C1-6, o una sal farmacéuticamente aceptable del mismo.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US7527708P | 2008-06-24 | 2008-06-24 | |
US75277P | 2008-06-24 | ||
PCT/EP2009/057320 WO2009156284A1 (en) | 2008-06-24 | 2009-06-15 | Novel substituted pyridin-2-ones and pyridazin-3-ones |
Publications (1)
Publication Number | Publication Date |
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ES2552320T3 true ES2552320T3 (es) | 2015-11-27 |
Family
ID=40972952
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES09769133.1T Active ES2552320T3 (es) | 2008-06-24 | 2009-06-15 | Nuevas piridín-2-onas y piridazín-3-onas sustituidas |
Country Status (25)
Country | Link |
---|---|
US (4) | US7902194B2 (es) |
EP (1) | EP2297142B1 (es) |
JP (1) | JP5536049B2 (es) |
KR (1) | KR101299867B1 (es) |
CN (3) | CN103709148B (es) |
AR (1) | AR072272A1 (es) |
AU (1) | AU2009264400B2 (es) |
BR (1) | BRPI0914657A2 (es) |
CA (1) | CA2728016C (es) |
CL (1) | CL2010001483A1 (es) |
CO (1) | CO6382183A2 (es) |
CR (1) | CR11815A (es) |
EC (1) | ECSP10010709A (es) |
ES (1) | ES2552320T3 (es) |
HK (2) | HK1152940A1 (es) |
IL (1) | IL209141A0 (es) |
MA (1) | MA32487B1 (es) |
MX (1) | MX2010013191A (es) |
NZ (2) | NZ588819A (es) |
PE (1) | PE20100851A1 (es) |
RU (1) | RU2500680C2 (es) |
TW (1) | TWI396537B (es) |
UA (1) | UA103327C2 (es) |
WO (1) | WO2009156284A1 (es) |
ZA (1) | ZA201007816B (es) |
Families Citing this family (38)
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TW200900396A (en) * | 2007-04-10 | 2009-01-01 | Kudos Pharm Ltd | Phthalazinone derivatives |
PE20110164A1 (es) * | 2008-07-02 | 2011-03-28 | Hoffmann La Roche | Nuevas fenilpirazinonas como inhibidores de quinasa |
US8299077B2 (en) * | 2009-03-02 | 2012-10-30 | Roche Palo Alto Llc | Inhibitors of Bruton's tyrosine kinase |
CA2748414A1 (en) * | 2009-04-24 | 2010-10-28 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
RU2017112518A (ru) | 2010-05-07 | 2019-01-25 | Джилид Коннектикут, Инк. | Пиридоновые и азапиридоновые соединения и способы применения |
AR082590A1 (es) * | 2010-08-12 | 2012-12-19 | Hoffmann La Roche | Inhibidores de la tirosina-quinasa de bruton |
US8975260B2 (en) | 2010-09-01 | 2015-03-10 | Genetech, Inc | Pyridazinones, method of making, and method of use thereof |
KR20140052032A (ko) | 2011-08-17 | 2014-05-02 | 에프. 호프만-라 로슈 아게 | 브루톤 티로신 키나아제의 억제제 |
BR112014010391A2 (pt) * | 2011-11-03 | 2017-04-18 | Hoffmann La Roche | composto, composição farmacêutica, processo de produção de uma composição farmacêutica, método de tratamento, kit e uso de uma composição farmacêutica |
EP2773632B1 (en) * | 2011-11-03 | 2017-04-12 | F. Hoffmann-La Roche AG | 8-fluorophthalazin-1(2h)-one compounds as inhibitors of btk activity |
UA111756C2 (uk) | 2011-11-03 | 2016-06-10 | Ф. Хоффманн-Ля Рош Аг | Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона |
EA027561B1 (ru) | 2011-11-03 | 2017-08-31 | Ф.Хоффманн-Ля Рош Аг | Алкилированные соединения пиперазина в качестве ингибиторов тирозинкиназы брутона |
WO2013083666A1 (en) | 2011-12-09 | 2013-06-13 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
US9365566B2 (en) | 2012-03-27 | 2016-06-14 | Takeda Pharmaceutical Company Limited | Cinnoline derivatives |
AU2013293087B2 (en) | 2012-07-24 | 2017-08-31 | Pharmacyclics Llc | Mutations associated with resistance to inhibitors of Bruton's tyrosine kinase (BTK) |
AU2013299557B2 (en) | 2012-08-10 | 2017-06-22 | Boehringer Ingelheim International Gmbh | Heteroaromatic compounds as Bruton's tyrosine kinase (BTK) inhibitors |
BR112015005361A2 (pt) * | 2012-09-13 | 2017-07-04 | Hoffmann La Roche | inibidores de tirosina quinase de bruton |
US9458105B2 (en) * | 2012-11-16 | 2016-10-04 | Hoffmann-La Roche Inc. | Inhibitors of Bruton's tyrosine kinase |
WO2014135470A1 (en) | 2013-03-05 | 2014-09-12 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
JO3377B1 (ar) | 2013-03-11 | 2019-03-13 | Takeda Pharmaceuticals Co | مشتقات بيريدينيل وبيريدينيل مندمج |
CN104177338B (zh) * | 2013-05-22 | 2018-04-03 | 南京勇山生物科技有限公司 | 一类布鲁顿激酶抑制剂 |
EP3016943B1 (en) * | 2013-07-03 | 2019-08-21 | F. Hoffmann-La Roche AG | Heteroaryl pyridone and aza-pyridone amide compounds |
AU2014293011A1 (en) | 2013-07-26 | 2016-03-17 | Race Oncology Ltd. | Compositions to improve the therapeutic benefit of bisantrene |
JP6153667B2 (ja) | 2013-07-30 | 2017-06-28 | ギリアード コネチカット, インコーポレイテッド | Sky阻害剤の製剤 |
PL3027618T3 (pl) | 2013-07-30 | 2021-04-19 | Kronos Bio, Inc. | Polimorf inhibitorów syk |
KR101813830B1 (ko) | 2013-12-05 | 2017-12-29 | 에프. 호프만-라 로슈 아게 | 친전자성 작용기를 갖는 헤테로아릴 피리돈 및 아자-피리돈 화합물 |
WO2015086642A1 (en) * | 2013-12-13 | 2015-06-18 | F. Hoffmann-La Roche Ag | Inhibitors of bruton's tyrosine kinase |
TWI735853B (zh) | 2013-12-23 | 2021-08-11 | 美商克洛諾斯生技有限公司 | 脾酪胺酸激酶抑制劑 |
TW201702218A (zh) | 2014-12-12 | 2017-01-16 | 美國杰克森實驗室 | 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法 |
EP3402789B1 (en) * | 2016-01-13 | 2020-03-18 | Boehringer Ingelheim International Gmbh | Isoquinolones as btk inhibitors |
JP7305352B2 (ja) | 2016-03-31 | 2023-07-10 | 武田薬品工業株式会社 | イソキノリニルトリアゾロン錯体 |
MA46285A (fr) | 2016-09-19 | 2019-07-31 | Mei Pharma Inc | Polythérapie |
US11384082B2 (en) | 2017-08-25 | 2022-07-12 | Kronos Bio, Inc. | Hydrates of polymorphs of 6-(1H-indazol-6-YL)-N-(4-morpholinophenyl)-2,3-dihydroimidazo[1,2-A]pyrazin-8-amine bisemsylate as Syk inhibitors |
WO2019126731A1 (en) | 2017-12-22 | 2019-06-27 | Petra Pharma Corporation | Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors |
CN113950479A (zh) | 2019-02-22 | 2022-01-18 | 克洛诺斯生物股份有限公司 | 作为syk抑制剂的缩合吡嗪的固体形式 |
WO2020188015A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
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CA2375734A1 (en) * | 1999-06-03 | 2000-12-14 | Knoll Gmbh | Benzothiazinone and benzoxazinone compounds |
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