PE20170697A1 - Indazoles sustituidos con benzilo como inhibidores de bub1 - Google Patents
Indazoles sustituidos con benzilo como inhibidores de bub1Info
- Publication number
- PE20170697A1 PE20170697A1 PE2017000480A PE2017000480A PE20170697A1 PE 20170697 A1 PE20170697 A1 PE 20170697A1 PE 2017000480 A PE2017000480 A PE 2017000480A PE 2017000480 A PE2017000480 A PE 2017000480A PE 20170697 A1 PE20170697 A1 PE 20170697A1
- Authority
- PE
- Peru
- Prior art keywords
- benzyl
- indazol
- ethanol
- amino
- alkyl
- Prior art date
Links
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical group C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 title 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical group [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 title 1
- 101000896657 Homo sapiens Mitotic checkpoint serine/threonine-protein kinase BUB1 Proteins 0.000 title 1
- 102100021691 Mitotic checkpoint serine/threonine-protein kinase BUB1 Human genes 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 101100326430 Caenorhabditis elegans bub-1 gene Proteins 0.000 abstract 1
- QVOGVAVHOLLLAZ-UHFFFAOYSA-N FC=1C=C(OCCO)C=C(C=1CN1N=C(C2=CC=CC=C12)C1=NC=C(C(=N1)NC1=C(C=NC=C1)OC)OC)F Chemical compound FC=1C=C(OCCO)C=C(C=1CN1N=C(C2=CC=CC=C12)C1=NC=C(C(=N1)NC1=C(C=NC=C1)OC)OC)F QVOGVAVHOLLLAZ-UHFFFAOYSA-N 0.000 abstract 1
- QRTAVTWIFZNXQN-UHFFFAOYSA-N FC=1C=C(OCCO)C=C(C=1CN1N=C(C2=CC=CC=C12)C1=NC=C(C(=N1)NC1=CC(=NC=C1)C)OC)F Chemical compound FC=1C=C(OCCO)C=C(C=1CN1N=C(C2=CC=CC=C12)C1=NC=C(C(=N1)NC1=CC(=NC=C1)C)OC)F QRTAVTWIFZNXQN-UHFFFAOYSA-N 0.000 abstract 1
- 108091000080 Phosphotransferase Proteins 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 102000020233 phosphotransferase Human genes 0.000 abstract 1
- 230000002062 proliferating effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/14—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 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
- A61K31/495—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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Se refiere a compuestos de formula I, en donde: V, W, Y y Z son CH o CR2; R1 es alquilo C1-C6, haloalquilo C1-C6, cicloalquilo C3-C6, entre otros; R2 es halogeno, alquilo C1-C3, haloalquilo C1-C3, entre otros; R3 es hidroxialquilo C2-C6 o R4; R4 es (alquilo C2-C6)-OC(=O)-C(H)(R5)-N(H)C(=O)-C(H)(R7)-NH2. Son compuestos preferidos: 2-2-{4-[(3-{4-[(3-cloropiridin-4-il)amino]-5-metoxipirimidin-2-il}-1H-indazol-1-il)metil]-3,5-difluorofenoxi}etanol, 2-{3,5-difluoro-4-[(3-{5-metoxi-4-[(2-metilpiridin-4-il)amino]pirimidin-2-il}-1H-indazol-1-il)metil]fenoxi}etanol, 2-{3,5-difluoro-4-[(3-{5-metoxi-4-[(3-metoxipiridin-4-il)amino]pirimidin-2-il}-1H-indazol-1-il)metil]fenoxi}etanol, entre otros. Dichos compuestos inhiben la quinasa Bub1 y son utiles en el tratamiento de trastornos proliferativos
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14185604 | 2014-09-19 | ||
| EP15176903 | 2015-07-15 | ||
| PCT/EP2015/071340 WO2016042084A1 (en) | 2014-09-19 | 2015-09-17 | Benzyl substituted indazoles as bub1 inhibitors |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20170697A1 true PE20170697A1 (es) | 2017-06-24 |
Family
ID=54140475
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2017000480A PE20170697A1 (es) | 2014-09-19 | 2015-09-17 | Indazoles sustituidos con benzilo como inhibidores de bub1 |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US10350206B2 (es) |
| EP (1) | EP3194379A1 (es) |
| JP (1) | JP6664385B2 (es) |
| KR (1) | KR20170049604A (es) |
| CN (1) | CN107001331A (es) |
| AP (1) | AP2017009803A0 (es) |
| AU (1) | AU2015316796A1 (es) |
| BR (1) | BR112017005444A2 (es) |
| CA (1) | CA2961589A1 (es) |
| CL (1) | CL2017000654A1 (es) |
| CO (1) | CO2017002532A2 (es) |
| CR (1) | CR20170100A (es) |
| CU (1) | CU20170029A7 (es) |
| DO (1) | DOP2017000078A (es) |
| EA (1) | EA032401B1 (es) |
| EC (1) | ECSP17016797A (es) |
| IL (1) | IL251071A0 (es) |
| MA (1) | MA39484A (es) |
| MX (1) | MX2017003664A (es) |
| NI (1) | NI201700034A (es) |
| PE (1) | PE20170697A1 (es) |
| PH (1) | PH12017500509A1 (es) |
| SG (1) | SG11201702082VA (es) |
| TN (1) | TN2017000092A1 (es) |
| TW (1) | TW201615636A (es) |
| UY (1) | UY36311A (es) |
| WO (1) | WO2016042084A1 (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UA111754C2 (uk) | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
| UA125503C2 (uk) | 2012-06-13 | 2022-04-13 | Інсайт Холдинґс Корпорейшн | Заміщені трициклічні сполуки як інгібітори fgfr |
| WO2014172644A2 (en) | 2013-04-19 | 2014-10-23 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| HK1223098A1 (zh) | 2013-06-21 | 2017-07-21 | Bayer Pharma Aktiengesellschaft | 杂芳基取代的吡唑 |
| US9765058B2 (en) | 2013-06-21 | 2017-09-19 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
| US9682974B2 (en) | 2013-10-30 | 2017-06-20 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted pyrazoles |
| HRP20181499T1 (hr) | 2014-02-06 | 2018-11-30 | Heptares Therapeutics Limited | Bičiklički aza spojevi kao agonisti muskarinskih m1 receptora |
| US10428044B2 (en) | 2014-06-17 | 2019-10-01 | Bayer Pharma Aktiengesellschaft | 3-amino-1,5,6,7-tetrahydro-4H-indol-4-ones |
| EA032401B1 (ru) | 2014-09-19 | 2019-05-31 | Байер Фарма Акциенгезельшафт | Бензилзамещенные индазолы в качестве ингибиторов bub1 |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| UA121669C2 (uk) | 2015-02-20 | 2020-07-10 | Інсайт Корпорейшн | Біциклічні гетероцикли як інгібітори fgfr |
| TWI808055B (zh) | 2016-05-11 | 2023-07-11 | 美商滬亞生物國際有限公司 | Hdac 抑制劑與 pd-1 抑制劑之組合治療 |
| TWI794171B (zh) | 2016-05-11 | 2023-03-01 | 美商滬亞生物國際有限公司 | Hdac抑制劑與pd-l1抑制劑之組合治療 |
| WO2018122168A1 (en) | 2016-12-29 | 2018-07-05 | Bayer Pharma Aktiengesellschaft | Combinations of bub1 kinase and parp inhibitors |
| WO2018158175A1 (en) | 2017-02-28 | 2018-09-07 | Bayer Pharma Aktiengesellschaft | Combination of bub1 inhibitors |
| EP3609883B1 (en) | 2017-04-11 | 2022-06-29 | Sunshine Lake Pharma Co., Ltd. | Fluorine-substituted indazole compounds and uses thereof |
| WO2018206547A1 (en) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and atr inhibitors |
| WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CN112566912A (zh) | 2018-05-04 | 2021-03-26 | 因赛特公司 | Fgfr抑制剂的盐 |
| SI3788047T1 (sl) | 2018-05-04 | 2024-11-29 | Incyte Corporation | Trdne oblike inhibitorja fgfr in postopki priprave le-teh |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| US11591329B2 (en) | 2019-07-09 | 2023-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| US12122767B2 (en) | 2019-10-01 | 2024-10-22 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| EP4045151A1 (en) | 2019-10-14 | 2022-08-24 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CA3163875A1 (en) | 2019-12-04 | 2021-06-10 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| EP4069695A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Derivatives of an fgfr inhibitor |
| WO2021146424A1 (en) | 2020-01-15 | 2021-07-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| US12065494B2 (en) | 2021-04-12 | 2024-08-20 | Incyte Corporation | Combination therapy comprising an FGFR inhibitor and a Nectin-4 targeting agent |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| CA3220155A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
Family Cites Families (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5011472A (en) | 1988-09-06 | 1991-04-30 | Brown University Research Foundation | Implantable delivery system for biological factors |
| US5470862A (en) | 1995-02-03 | 1995-11-28 | Ohmeda Pharmaceutical Products Division Inc. | Substituted pyrazolyl compounds and methods employing such compounds |
| DE59713007D1 (de) | 1996-10-14 | 2009-06-25 | Bayer Healthcare Ag | Neue heterocyclylmethyl-substituierte pyrazolderivate und ihre verwendung in der behandlung von herz-kreislauf-erkrankungen |
| DE19834047A1 (de) | 1998-07-29 | 2000-02-03 | Bayer Ag | Substituierte Pyrazolderivate |
| DE19846514A1 (de) | 1998-10-09 | 2000-04-20 | Bayer Ag | Neue Heterocyclyl-methyl-substituierte Pyrazole |
| AU2002359714B2 (en) | 2001-12-18 | 2006-12-21 | Merck Sharp & Dohme Corp. | Heteroaryl substituted pyrazole modulators of metabotropic glutamate receptor-5 |
| US7166293B2 (en) | 2002-03-29 | 2007-01-23 | Carlsbad Technology, Inc. | Angiogenesis inhibitors |
| WO2004024159A1 (en) | 2002-09-10 | 2004-03-25 | Scios Inc. | INHIBITORS OF TFGβ |
| DE10244810A1 (de) | 2002-09-26 | 2004-04-08 | Bayer Ag | Neue Morpholin-überbrückte Indazolderivate |
| US8748601B2 (en) | 2003-04-11 | 2014-06-10 | The Regents Of The University Of California | Selective serine/threonine kinase inhibitors |
| WO2005070900A1 (en) | 2004-01-22 | 2005-08-04 | Altana Pharma Ag | N-4-(6- (heteo) aryl-pyrimidin-4-ylaminophenyl) -bezenesulfonamides as kinase inhibitors |
| WO2007065010A2 (en) | 2005-12-02 | 2007-06-07 | Hif Bio, Inc. | Anti-angiogenesis compounds |
| DE102006043443A1 (de) | 2006-09-15 | 2008-03-27 | Bayer Healthcare Ag | Neue aza-bicyclische Verbindungen und ihre Verwendung |
| EP2148877A2 (en) | 2007-05-18 | 2010-02-03 | Bayer Schering Pharma AG | Inhibitors of hypoxia inducible factor (hif) useful for treating hyper-proliferative disorders and diseases associated with angiogenesis |
| JP2010111624A (ja) | 2008-11-06 | 2010-05-20 | Shionogi & Co Ltd | Ttk阻害作用を有するインダゾール誘導体 |
| ES2630026T3 (es) | 2008-12-18 | 2017-08-17 | Nerviano Medical Sciences S.R.L. | Derivados indazólicos sustituidos activos como inhibidores de cinasa |
| US20120232062A1 (en) | 2009-10-20 | 2012-09-13 | Eiger Biopharmaceuticals, Inc. | Azaindazoles to treat flaviviridae virus infection |
| PH12012501023A1 (en) | 2009-11-27 | 2014-12-19 | Adverio Pharma Gmbh | Method for producing methyl - {4, 6-diamino -2-[1- (2-fluorobenzyl) -1h- pyrazolo [3,4-b] pyridino -3-yl] pyrimidino -5-yl} methyl carbamate and its purification for use thereof as pharmaceutical substance |
| WO2011115804A1 (en) | 2010-03-17 | 2011-09-22 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
| RU2639876C2 (ru) | 2010-03-30 | 2017-12-25 | Версеон Корпорейшн | Мультизамещенные ароматические соединения в качестве ингибиторов тромбина |
| CN103313976B (zh) | 2010-06-30 | 2016-11-23 | 铁木医药有限公司 | sGC刺激物 |
| UA111754C2 (uk) * | 2011-10-06 | 2016-06-10 | Байєр Фарма Акцієнгезелльшафт | Заміщені бензиліндазоли для застосування як інгібіторів bub1-кінази для лікування гіперпроліферативних захворювань |
| EP2794596B1 (en) | 2011-12-21 | 2017-05-31 | Bayer Intellectual Property GmbH | Substituted benzylpyrazoles |
| CA2861804C (en) | 2011-12-27 | 2021-10-26 | Ironwood Pharmaceuticals, Inc. | 2-benzyl,3(pyrimidin-2-yl)substituted pyrazoles useful as sgc stimulators |
| EP2847180B1 (en) | 2012-05-11 | 2017-01-04 | Bayer Pharma Aktiengesellschaft | Substituted cycloalkenopyrazoles as bub1 inhibitors for the treatment of cancer |
| WO2014047111A1 (en) | 2012-09-18 | 2014-03-27 | Ironwood Pharmaceuticals, Inc. | Sgc stimulators |
| EP2897953B8 (en) | 2012-09-19 | 2019-06-26 | Cyclerion Therapeutics, Inc. | Sgc stimulators |
| WO2014047662A2 (en) | 2012-09-24 | 2014-03-27 | Whitehead Institute For Biomedical Research | Indazole derivatives and uses thereof |
| JP2016514719A (ja) | 2013-03-21 | 2016-05-23 | バイエル ファーマ アクチエンゲゼルシャフト | ヘテロアリール置換インダゾール |
| CN105051030A (zh) | 2013-03-21 | 2015-11-11 | 拜耳制药股份公司 | 二氨基杂芳基取代的吲唑 |
| EP2976336A1 (en) | 2013-03-21 | 2016-01-27 | Bayer Pharma Aktiengesellschaft | 3-heteroaryl substituted indazoles |
| WO2014202588A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted pyrazoles |
| CA2916097A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
| WO2014202586A1 (en) | 2013-06-21 | 2014-12-24 | Bayer Pharma Aktiengesellschaft | Diaminoheteroaryl substituted pyrazoles |
| US9765058B2 (en) | 2013-06-21 | 2017-09-19 | Bayer Pharma Aktiengesellschaft | Substituted benzylpyrazoles |
| HK1223098A1 (zh) | 2013-06-21 | 2017-07-21 | Bayer Pharma Aktiengesellschaft | 杂芳基取代的吡唑 |
| US9682974B2 (en) | 2013-10-30 | 2017-06-20 | Bayer Pharma Aktiengesellschaft | Heteroaryl substituted pyrazoles |
| CN106659791A (zh) | 2014-09-19 | 2017-05-10 | 雀巢产品技术援助有限公司 | 用α‑淀粉酶抑制剂为伴侣动物治疗癌症 |
| CR20170102A (es) | 2014-09-19 | 2017-07-17 | Glaxosmithkline Ip Dev Ltd | Nuevos activadores de la guanilato ciclasa soluble y su uso |
| JP2017529353A (ja) | 2014-09-19 | 2017-10-05 | バイエル ファーマ アクチエンゲゼルシャフト | Bub1キナーゼ阻害薬としてのベンジル置換インダゾール類 |
| JP2017530963A (ja) | 2014-09-19 | 2017-10-19 | バイエル ファーマ アクチエンゲゼルシャフト | ベンジル置換インダゾール類 |
| PT3733662T (pt) | 2014-09-19 | 2023-08-18 | Forma Therapeutics Inc | Derivados piridin-2(1h)-ona-quinolinona como inibidores de isocitrato desidrogenase mutante |
| EA032401B1 (ru) | 2014-09-19 | 2019-05-31 | Байер Фарма Акциенгезельшафт | Бензилзамещенные индазолы в качестве ингибиторов bub1 |
| JP2017535514A (ja) | 2014-09-19 | 2017-11-30 | バイエル ファーマ アクチエンゲゼルシャフト | Bub1キナーゼ阻害薬としてのベンジル置換インダゾール類 |
| WO2017148995A1 (en) | 2016-03-04 | 2017-09-08 | Bayer Pharma Aktiengesellschaft | 1-(pyrimidin-2-yl)-1h-indazoles having bub1 kinase inhibiting activity |
| WO2017157991A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | 1-alkyl-pyrazoles and -indazoles as bub1 inhibitors for the treatment of hyperproliferative diseases |
| WO2017157992A1 (en) | 2016-03-18 | 2017-09-21 | Bayer Pharma Aktiengesellschaft | Annulated pyrazoles as bub1 kinase inhibitors for treating proliferative disorders |
| WO2018122168A1 (en) | 2016-12-29 | 2018-07-05 | Bayer Pharma Aktiengesellschaft | Combinations of bub1 kinase and parp inhibitors |
| WO2018158175A1 (en) | 2017-02-28 | 2018-09-07 | Bayer Pharma Aktiengesellschaft | Combination of bub1 inhibitors |
| WO2018206547A1 (en) | 2017-05-12 | 2018-11-15 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and atr inhibitors |
| WO2018215282A1 (en) | 2017-05-26 | 2018-11-29 | Bayer Pharma Aktiengesellschaft | Combination of bub1 and pi3k inhibitors |
-
2015
- 2015-09-17 EA EA201790649A patent/EA032401B1/ru not_active IP Right Cessation
- 2015-09-17 SG SG11201702082VA patent/SG11201702082VA/en unknown
- 2015-09-17 CA CA2961589A patent/CA2961589A1/en not_active Abandoned
- 2015-09-17 WO PCT/EP2015/071340 patent/WO2016042084A1/en not_active Ceased
- 2015-09-17 PE PE2017000480A patent/PE20170697A1/es unknown
- 2015-09-17 TN TN2017000092A patent/TN2017000092A1/en unknown
- 2015-09-17 US US15/512,494 patent/US10350206B2/en not_active Expired - Fee Related
- 2015-09-17 CN CN201580062951.4A patent/CN107001331A/zh active Pending
- 2015-09-17 MA MA039484A patent/MA39484A/fr unknown
- 2015-09-17 BR BR112017005444A patent/BR112017005444A2/pt not_active IP Right Cessation
- 2015-09-17 AU AU2015316796A patent/AU2015316796A1/en not_active Abandoned
- 2015-09-17 CU CUP2017000029A patent/CU20170029A7/es unknown
- 2015-09-17 CR CR20170100A patent/CR20170100A/es unknown
- 2015-09-17 MX MX2017003664A patent/MX2017003664A/es unknown
- 2015-09-17 EP EP15763619.2A patent/EP3194379A1/en not_active Withdrawn
- 2015-09-17 AP AP2017009803A patent/AP2017009803A0/en unknown
- 2015-09-17 JP JP2017514825A patent/JP6664385B2/ja not_active Expired - Fee Related
- 2015-09-17 KR KR1020177010425A patent/KR20170049604A/ko not_active Withdrawn
- 2015-09-18 UY UY0001036311A patent/UY36311A/es not_active Application Discontinuation
- 2015-09-18 TW TW104131025A patent/TW201615636A/zh unknown
-
2017
- 2017-03-09 IL IL251071A patent/IL251071A0/en unknown
- 2017-03-16 PH PH12017500509A patent/PH12017500509A1/en unknown
- 2017-03-17 CL CL2017000654A patent/CL2017000654A1/es unknown
- 2017-03-17 DO DO2017000078A patent/DOP2017000078A/es unknown
- 2017-03-17 EC ECIEPI201716797A patent/ECSP17016797A/es unknown
- 2017-03-17 CO CONC2017/0002532A patent/CO2017002532A2/es unknown
- 2017-03-17 NI NI201700034A patent/NI201700034A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| PH12017500509A1 (en) | 2017-08-30 |
| CL2017000654A1 (es) | 2017-12-11 |
| BR112017005444A2 (pt) | 2018-04-24 |
| US10350206B2 (en) | 2019-07-16 |
| CR20170100A (es) | 2017-04-24 |
| MA39484A (fr) | 2016-03-24 |
| NI201700034A (es) | 2017-06-16 |
| JP2017530962A (ja) | 2017-10-19 |
| IL251071A0 (en) | 2017-04-30 |
| TN2017000092A1 (en) | 2018-07-04 |
| US20170273980A1 (en) | 2017-09-28 |
| EP3194379A1 (en) | 2017-07-26 |
| AU2015316796A1 (en) | 2017-03-30 |
| EA201790649A1 (ru) | 2017-09-29 |
| JP6664385B2 (ja) | 2020-03-13 |
| AP2017009803A0 (en) | 2017-03-31 |
| WO2016042084A1 (en) | 2016-03-24 |
| UY36311A (es) | 2016-04-29 |
| DOP2017000078A (es) | 2017-06-30 |
| TW201615636A (zh) | 2016-05-01 |
| MX2017003664A (es) | 2017-07-13 |
| CU20170029A7 (es) | 2017-08-08 |
| CO2017002532A2 (es) | 2017-07-11 |
| KR20170049604A (ko) | 2017-05-10 |
| EA032401B1 (ru) | 2019-05-31 |
| CN107001331A (zh) | 2017-08-01 |
| ECSP17016797A (es) | 2017-05-31 |
| CA2961589A1 (en) | 2016-03-24 |
| SG11201702082VA (en) | 2017-04-27 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PE20170697A1 (es) | Indazoles sustituidos con benzilo como inhibidores de bub1 | |
| MX2020005348A (es) | Formas cristalinas de la n-(4-(4-(ciclopropilmetil)piperazin-1-car bonil)fenil)quinolin-8-sulfonamida. | |
| CY1123443T1 (el) | Οξεα καρβαμοϋλοξυμεθυλ-τριαζολ-κυκλοεξυλιου ως ανταγωνιστες lpa | |
| MX384087B (es) | Piperidinas como inhibidores de menina. | |
| PE20180508A1 (es) | Amidas heterociclicas como inhibidores de quinasa | |
| MX2020011558A (es) | Imidazolonilquinolinas y el uso de las mismas como inhibidores de cinasa atm. | |
| MX2017004234A (es) | Inhibidor del egfr y preparacion y aplicacion del mismo. | |
| PE20190395A1 (es) | Pirimidin-2-ilamino-1h-pirazoles como inhibidores de lrrk2 para el uso en el tratamiento de trastornos neurodegenerativos | |
| ZA202101788B (en) | Aminopyrimidine/pyrazine derivatives as ctps1 inhibitors | |
| PE20181288A1 (es) | Derivados de dihidroimidazopirazinona usados en el tratamiento del cancer | |
| PE20170143A1 (es) | Benzimidazol-2-aminas como inhibidores de midh1 | |
| TN2018000276A1 (en) | Inhibitors of receptor-interacting protein kinase 1. | |
| MX2022000376A (es) | Aminopirimidinas como inhibidores de alk. | |
| EA201790715A1 (ru) | Новые соединения | |
| PE20170695A1 (es) | Compuestos de indol carboxamida utiles como inhibidores de cinasas | |
| EA201791305A1 (ru) | Конденсированные пиримидины для лечения вич | |
| PE20170939A1 (es) | Pirimidinonas como inhibidores del factor xia | |
| PH12020500343A1 (en) | Pyruvate kinase activators for use in treating blood disorders | |
| PE20170664A1 (es) | Agonistas del receptor de apelina(apj) y usos de los mismos | |
| NZ722624A (en) | Fused pyrimidines as inhibitors of p97 complex | |
| EA201790395A1 (ru) | Производные аминотриазина, подходящие для применения в качестве соединений-ингибиторов tank-связывающей киназы | |
| TN2018000020A1 (en) | Colony stimulating factor-1 receptor (csf-1r) inhibitors. | |
| PH12016501941A1 (en) | Use of heterocyclic compounds for controlling nematodes | |
| PE20161236A1 (es) | Compuesto de triazina y su uso para fines medicos | |
| EA201891768A1 (ru) | Кристаллическая форма a агониста tlr7, ее способ получения и использование |