ES2637595T3 - Derivados de 7-(3,5-dimetil-4-isoxazolil)-8-(metiloxi)-1H-imidazo[4,5-c]quinolina - Google Patents
Derivados de 7-(3,5-dimetil-4-isoxazolil)-8-(metiloxi)-1H-imidazo[4,5-c]quinolina Download PDFInfo
- Publication number
- ES2637595T3 ES2637595T3 ES12716379.8T ES12716379T ES2637595T3 ES 2637595 T3 ES2637595 T3 ES 2637595T3 ES 12716379 T ES12716379 T ES 12716379T ES 2637595 T3 ES2637595 T3 ES 2637595T3
- Authority
- ES
- Spain
- Prior art keywords
- methyloxy
- imidazo
- dimethyl
- isoxazolyl
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- PXMPTQQLDBWGGR-UHFFFAOYSA-N 4-(8-methoxy-3h-imidazo[4,5-c]quinolin-7-yl)-3,5-dimethyl-1,2-oxazole Chemical class COC1=CC2=C3NC=NC3=CN=C2C=C1C=1C(C)=NOC=1C PXMPTQQLDBWGGR-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 185
- 150000003839 salts Chemical class 0.000 claims abstract description 91
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 41
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 10
- 229910052705 radium Inorganic materials 0.000 claims abstract description 10
- 229910052701 rubidium Inorganic materials 0.000 claims abstract description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 8
- 150000002367 halogens Chemical group 0.000 claims abstract description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 8
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims abstract description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims abstract description 5
- 229910003827 NRaRb Chemical group 0.000 claims abstract description 5
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims abstract description 5
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 4
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 4
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical group O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 7
- -1 3,5-dimethylisoxazol-4-yl Chemical group 0.000 claims description 83
- 238000011282 treatment Methods 0.000 claims description 29
- 239000008194 pharmaceutical composition Substances 0.000 claims description 28
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 10
- 239000003085 diluting agent Substances 0.000 claims description 8
- GORBSWFEJLHOHD-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-n-ethyl-8-methoxy-1-(1-methoxypropan-2-yl)imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(C(C)COC)C(NCC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C GORBSWFEJLHOHD-UHFFFAOYSA-N 0.000 claims description 6
- 206010028980 Neoplasm Diseases 0.000 claims description 6
- 125000002757 morpholinyl group Chemical group 0.000 claims description 5
- 238000002560 therapeutic procedure Methods 0.000 claims description 5
- UEUCJJAVDZDKPJ-GOSISDBHSA-N 4-[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-[(1r)-1-phenylethyl]imidazo[4,5-c]quinolin-2-yl]morpholine Chemical compound C1([C@@H](C)N2C3=C4C=C(C(=CC4=NC=C3N=C2N2CCOCC2)C2=C(ON=C2C)C)OC)=CC=CC=C1 UEUCJJAVDZDKPJ-GOSISDBHSA-N 0.000 claims description 4
- GPBXKDORLRYAFV-LJQANCHMSA-N 4-[8-methoxy-1-[(1r)-1-phenylethyl]-2-piperidin-1-ylimidazo[4,5-c]quinolin-7-yl]-3,5-dimethyl-1,2-oxazole Chemical compound C1([C@@H](C)N2C3=C4C=C(C(=CC4=NC=C3N=C2N2CCCCC2)C2=C(ON=C2C)C)OC)=CC=CC=C1 GPBXKDORLRYAFV-LJQANCHMSA-N 0.000 claims description 4
- IKTBLXAKAQPULU-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-n-ethyl-8-methoxy-1-[1-(1-methylpyrazol-4-yl)ethyl]imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(C(C)C4=CN(C)N=C4)C(NCC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C IKTBLXAKAQPULU-UHFFFAOYSA-N 0.000 claims description 4
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
- FIVLGTQJUXPVRU-UHFFFAOYSA-N 2-[[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-yl]amino]ethanol Chemical compound OCCNC1=NC2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N1CC1CCOCC1 FIVLGTQJUXPVRU-UHFFFAOYSA-N 0.000 claims description 3
- HCEZPGCCFZDDQO-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-n,n-dimethyl-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound CN(C)C1=NC2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N1CC1CCOCC1 HCEZPGCCFZDDQO-UHFFFAOYSA-N 0.000 claims description 3
- CUJZFENGTCXFNC-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-n-(2-methoxyethyl)-1-(pyridin-2-ylmethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(CC=4N=CC=CC=4)C(NCCOC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C CUJZFENGTCXFNC-UHFFFAOYSA-N 0.000 claims description 3
- 230000002757 inflammatory effect Effects 0.000 claims description 3
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- HHQIOVSKCYEFDZ-MRXNPFEDSA-N 2-[[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-[(1r)-1-phenylethyl]imidazo[4,5-c]quinolin-2-yl]amino]ethanol Chemical compound C1([C@@H](C)N2C3=C4C=C(C(=CC4=NC=C3N=C2NCCO)C2=C(ON=C2C)C)OC)=CC=CC=C1 HHQIOVSKCYEFDZ-MRXNPFEDSA-N 0.000 claims description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 2
- KBQLRXYOFJFCCX-UHFFFAOYSA-N 4-[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-yl]morpholine Chemical compound C1COCCN1C1=NC2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N1CC1CCOCC1 KBQLRXYOFJFCCX-UHFFFAOYSA-N 0.000 claims description 2
- NZVLCCBRSYNMIZ-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-(1-methoxypropan-2-yl)-n-(2-morpholin-4-ylethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound N=1C2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N(C(C)COC)C=1NCCN1CCOCC1 NZVLCCBRSYNMIZ-UHFFFAOYSA-N 0.000 claims description 2
- RWOFLHZRPGAHPW-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-n-(2-methoxyethyl)-1-(1-methoxypropan-2-yl)imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(C(C)COC)C(NCCOC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C RWOFLHZRPGAHPW-UHFFFAOYSA-N 0.000 claims description 2
- NDOYCNITPWYWHM-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-n-(2-methoxyethyl)-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(CC4CCOCC4)C(NCCOC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C NDOYCNITPWYWHM-UHFFFAOYSA-N 0.000 claims description 2
- XYYDBYHXTRBXDP-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-n-(2-morpholin-4-ylethyl)-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound C1COCCN1CCNC1=NC2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N1CC1CCOCC1 XYYDBYHXTRBXDP-UHFFFAOYSA-N 0.000 claims description 2
- OGTYKUGNAVOMRH-UHFFFAOYSA-N n'-[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-(1-methoxypropan-2-yl)imidazo[4,5-c]quinolin-2-yl]ethane-1,2-diamine Chemical compound COC1=CC2=C3N(C(C)COC)C(NCCN)=NC3=CN=C2C=C1C=1C(C)=NOC=1C OGTYKUGNAVOMRH-UHFFFAOYSA-N 0.000 claims description 2
- OSDROQOFDHWYKD-UHFFFAOYSA-N n'-[7-(3,5-dimethyl-1,2-oxazol-4-yl)-8-methoxy-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-yl]ethane-1,2-diamine Chemical compound NCCNC1=NC2=CN=C3C=C(C4=C(ON=C4C)C)C(OC)=CC3=C2N1CC1CCOCC1 OSDROQOFDHWYKD-UHFFFAOYSA-N 0.000 claims description 2
- VVNHPRQSIABGMX-UHFFFAOYSA-N 7-(3,5-dimethyl-1,2-oxazol-4-yl)-n-ethyl-8-methoxy-1-(oxan-4-ylmethyl)imidazo[4,5-c]quinolin-2-amine Chemical compound COC1=CC2=C3N(CC4CCOCC4)C(NCC)=NC3=CN=C2C=C1C=1C(C)=NOC=1C VVNHPRQSIABGMX-UHFFFAOYSA-N 0.000 claims 1
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- 239000011701 zinc Substances 0.000 description 1
- 229930195724 β-lactose Natural products 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
-
- 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
- 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
- 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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Transplantation (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1106799.8A GB201106799D0 (en) | 2011-04-21 | 2011-04-21 | Novel compounds |
| GB201106799 | 2011-04-21 | ||
| PCT/EP2012/057114 WO2012143416A2 (en) | 2011-04-21 | 2012-04-19 | Novel compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2637595T3 true ES2637595T3 (es) | 2017-10-13 |
Family
ID=44147382
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12716379.8T Active ES2637595T3 (es) | 2011-04-21 | 2012-04-19 | Derivados de 7-(3,5-dimetil-4-isoxazolil)-8-(metiloxi)-1H-imidazo[4,5-c]quinolina |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US8846709B2 (enExample) |
| EP (1) | EP2699573B1 (enExample) |
| JP (1) | JP5856673B2 (enExample) |
| ES (1) | ES2637595T3 (enExample) |
| GB (1) | GB201106799D0 (enExample) |
| WO (1) | WO2012143416A2 (enExample) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB201114103D0 (en) * | 2011-08-17 | 2011-09-28 | Glaxosmithkline Llc | Novel compounds |
| US9073878B2 (en) | 2012-11-21 | 2015-07-07 | Zenith Epigenetics Corp. | Cyclic amines as bromodomain inhibitors |
| US9765039B2 (en) | 2012-11-21 | 2017-09-19 | Zenith Epigenetics Ltd. | Biaryl derivatives as bromodomain inhibitors |
| AU2013365926B9 (en) | 2012-12-21 | 2019-01-17 | Zenith Epigenetics Ltd. | Novel heterocyclic compounds as bromodomain inhibitors |
| AU2014249034A1 (en) | 2013-03-11 | 2015-09-24 | Abbvie Inc. | Fused tetracyclic bromodomain inhibitors |
| AU2014249025A1 (en) | 2013-03-11 | 2015-09-17 | Abbvie Inc. | Bromodomain inhibitors |
| BR112015022417A2 (pt) | 2013-03-14 | 2017-07-18 | Convergene Llc | métodos e composições para inibição de proteínas contendo bromodomínio |
| SG11201506924YA (en) | 2013-03-15 | 2015-09-29 | Incyte Corp | Tricyclic heterocycles as bet protein inhibitors |
| TWI527811B (zh) * | 2013-05-09 | 2016-04-01 | 吉李德科學股份有限公司 | 作爲溴結構域抑制劑的苯並咪唑衍生物 |
| SI3010503T1 (sl) | 2013-06-21 | 2020-07-31 | Zenith Epigenetics Ltd. | Novi biciklični inhibitorji bromodomene |
| CN105492439B (zh) | 2013-06-21 | 2019-11-22 | 齐尼思表观遗传学有限公司 | 作为溴结构域抑制剂的取代的双环化合物 |
| AR096837A1 (es) | 2013-07-08 | 2016-02-03 | Incyte Corp | Heterociclos tricíclicos como inhibidores de proteínas bet |
| EP3024327B1 (en) * | 2013-07-25 | 2019-09-04 | Dana-Farber Cancer Institute, Inc. | Inhibitors of transcription factors and uses thereof |
| WO2015015318A2 (en) | 2013-07-31 | 2015-02-05 | Zenith Epigenetics Corp. | Novel quinazolinones as bromodomain inhibitors |
| WO2015049629A1 (en) * | 2013-10-01 | 2015-04-09 | Piramal Enterprises Limited | Imidazoquinoline compounds as bromodomain inhibitors |
| AU2013406206B2 (en) * | 2013-11-26 | 2017-07-20 | Gilead Sciences, Inc. | Quinoline derivatives as bromodomain inhibitors |
| WO2015081189A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
| WO2015081203A1 (en) | 2013-11-26 | 2015-06-04 | Incyte Corporation | Bicyclic heterocycles as bet protein inhibitors |
| WO2015095492A1 (en) | 2013-12-19 | 2015-06-25 | Incyte Corporation | Tricyclic heterocycles as bet protein inhibitors |
| UA119870C2 (uk) | 2014-04-23 | 2019-08-27 | Інсайт Корпорейшн | 1H-ПІРОЛО[2,3-c]ПІРИДИН-7(6H)-ОНИ ТА ПІРАЗОЛО[3,4-c]ПІРИДИН-7(6H)-ОНИ ЯК ІНГІБІТОРИ БІЛКІВ BET |
| US9527864B2 (en) | 2014-09-15 | 2016-12-27 | Incyte Corporation | Tricyclic heterocycles as BET protein inhibitors |
| EP3227281A4 (en) | 2014-12-01 | 2018-05-30 | Zenith Epigenetics Ltd. | Substituted pyridinones as bromodomain inhibitors |
| HK1246273B (en) | 2014-12-01 | 2019-12-06 | 恒翼生物医药(上海)股份有限公司 | Substituted pyridines as bromodomain inhibitors |
| US10292968B2 (en) | 2014-12-11 | 2019-05-21 | Zenith Epigenetics Ltd. | Substituted heterocycles as bromodomain inhibitors |
| CA2966450A1 (en) | 2014-12-17 | 2016-06-23 | Olesya KHARENKO | Inhibitors of bromodomains |
| EP3253756B1 (en) * | 2015-02-03 | 2021-09-22 | Trillium Therapeutics Inc. | Fluorinated imidazo[4,5-c]quinoline derivatives as inhibitors of bromodomain containing proteins |
| GB201504694D0 (en) | 2015-03-19 | 2015-05-06 | Glaxosmithkline Ip Dev Ltd | Covalent conjugates |
| WO2016186453A1 (en) * | 2015-05-20 | 2016-11-24 | Kainos Medicine, Inc. | Quinoline derivatives as bromodomain inhibitors |
| AU2016276963C1 (en) | 2015-06-12 | 2021-08-05 | Dana-Farber Cancer Institute, Inc. | Combination therapy of transcription inhibitors and kinase inhibitors |
| WO2016203335A1 (en) | 2015-06-18 | 2016-12-22 | Pfizer Inc. | Novel pyrido[2,3-b]pyrazinones as bet-family bromodomain inhibitors |
| CA2996977A1 (en) | 2015-09-11 | 2017-03-16 | Dana-Farber Cancer Institute, Inc. | Acetamide thienotriazolodiazepines and uses thereof |
| BR112018004618A2 (pt) | 2015-09-11 | 2018-09-25 | Dana-Farber Cancer Institute, Inc. | ciano tienotriazoldiazepinas e usos das mesmas |
| TW201722966A (zh) | 2015-10-29 | 2017-07-01 | 英塞特公司 | Bet蛋白質抑制劑之非晶固體形式 |
| US10913752B2 (en) | 2015-11-25 | 2021-02-09 | Dana-Farber Cancer Institute, Inc. | Bivalent bromodomain inhibitors and uses thereof |
| EP4050005B1 (en) | 2015-11-25 | 2024-12-25 | Convergene Llc | Bicyclic bet bromodomain inhibitors and uses thereof |
| IL263824B2 (en) | 2016-06-20 | 2023-10-01 | Incyte Corp | Crystals in solid form in the presence of an inhibitor |
| WO2018196662A1 (zh) * | 2017-04-28 | 2018-11-01 | 四川科伦博泰生物医药股份有限公司 | 包含苯并二氮䓬类化合物的注射用组合物及其制备方法 |
| US12497395B2 (en) | 2019-04-24 | 2025-12-16 | Convergene, Llc | Small molecule bromodomain inhibitors and uses therof |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9004781D0 (en) | 1990-03-02 | 1990-04-25 | Glaxo Group Ltd | Device |
| EP1590348A1 (en) * | 2002-12-20 | 2005-11-02 | 3M Innovative Properties Company | Aryl / hetaryl substituted imidazoquinolines |
| JP4641526B2 (ja) | 2003-11-03 | 2011-03-02 | グラクソ グループ リミテッド | 流体分配デバイス |
| MX2008007864A (es) * | 2005-12-16 | 2009-03-04 | Coley Pharm Group Inc | Imidazoquinolinas, imidazonaftiridinas, e imidazopiridinas sustituidas, composiciones y metodos. |
| JP2008156311A (ja) | 2006-12-26 | 2008-07-10 | Institute Of Physical & Chemical Research | Ｂｒｄ２ブロモドメイン結合剤 |
| EP2239264A4 (en) | 2007-12-28 | 2012-01-11 | Mitsubishi Tanabe Pharma Corp | ANTITUMORAL MEDIUM |
-
2011
- 2011-04-21 GB GBGB1106799.8A patent/GB201106799D0/en not_active Ceased
-
2012
- 2012-04-19 JP JP2014505613A patent/JP5856673B2/ja not_active Expired - Fee Related
- 2012-04-19 WO PCT/EP2012/057114 patent/WO2012143416A2/en not_active Ceased
- 2012-04-19 US US14/111,783 patent/US8846709B2/en not_active Expired - Fee Related
- 2012-04-19 ES ES12716379.8T patent/ES2637595T3/es active Active
- 2012-04-19 EP EP12716379.8A patent/EP2699573B1/en not_active Not-in-force
Also Published As
| Publication number | Publication date |
|---|---|
| JP2014511893A (ja) | 2014-05-19 |
| WO2012143416A3 (en) | 2013-01-31 |
| GB201106799D0 (en) | 2011-06-01 |
| US8846709B2 (en) | 2014-09-30 |
| JP5856673B2 (ja) | 2016-02-10 |
| US20140045834A1 (en) | 2014-02-13 |
| WO2012143416A2 (en) | 2012-10-26 |
| EP2699573A2 (en) | 2014-02-26 |
| EP2699573B1 (en) | 2017-05-31 |
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