ME02730B - Modulatori enzima koji modifikuju metil, njihove kompozicije i upotreba - Google Patents
Modulatori enzima koji modifikuju metil, njihove kompozicije i upotrebaInfo
- Publication number
- ME02730B ME02730B MEP-2017-141A MEP2017141A ME02730B ME 02730 B ME02730 B ME 02730B ME P2017141 A MEP2017141 A ME P2017141A ME 02730 B ME02730 B ME 02730B
- Authority
- ME
- Montenegro
- Prior art keywords
- methyl
- compound
- cancer
- piperidin
- pharmaceutically acceptable
- Prior art date
Links
- 102000004190 Enzymes Human genes 0.000 title 1
- 108090000790 Enzymes Proteins 0.000 title 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical class [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 title 1
- 239000000203 mixture Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 16
- 150000003839 salts Chemical class 0.000 claims 7
- -1 -OCHF2 Chemical group 0.000 claims 6
- 206010028980 Neoplasm Diseases 0.000 claims 4
- 201000011510 cancer Diseases 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- RQOXQFWLPWTPPB-QGZVFWFLSA-N 1-[(1r)-1-[1-(2,2-difluoroethyl)piperidin-4-yl]ethyl]-n-[(4-methoxy-6-methyl-2-oxo-1h-pyridin-3-yl)methyl]-2-methylindole-3-carboxamide Chemical compound C1=C(C)NC(=O)C(CNC(=O)C=2C3=CC=CC=C3N([C@H](C)C3CCN(CC(F)F)CC3)C=2C)=C1OC RQOXQFWLPWTPPB-QGZVFWFLSA-N 0.000 claims 1
- RQOXQFWLPWTPPB-UHFFFAOYSA-N 1-[1-[1-(2,2-difluoroethyl)piperidin-4-yl]ethyl]-n-[(4-methoxy-6-methyl-2-oxo-1h-pyridin-3-yl)methyl]-2-methylindole-3-carboxamide Chemical compound C1=C(C)NC(=O)C(CNC(=O)C=2C3=CC=CC=C3N(C(C)C3CCN(CC(F)F)CC3)C=2C)=C1OC RQOXQFWLPWTPPB-UHFFFAOYSA-N 0.000 claims 1
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 206010005003 Bladder cancer Diseases 0.000 claims 1
- 206010006187 Breast cancer Diseases 0.000 claims 1
- 208000026310 Breast neoplasm Diseases 0.000 claims 1
- 206010009944 Colon cancer Diseases 0.000 claims 1
- 201000010915 Glioblastoma multiforme Diseases 0.000 claims 1
- 206010025323 Lymphomas Diseases 0.000 claims 1
- 206010060862 Prostate cancer Diseases 0.000 claims 1
- 208000000236 Prostatic Neoplasms Diseases 0.000 claims 1
- 208000006265 Renal cell carcinoma Diseases 0.000 claims 1
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims 1
- 230000004663 cell proliferation Effects 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 208000029742 colonic neoplasm Diseases 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 208000035475 disorder Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 208000005017 glioblastoma Diseases 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 201000007270 liver cancer Diseases 0.000 claims 1
- 208000014018 liver neoplasm Diseases 0.000 claims 1
- 201000001441 melanoma Diseases 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- HPODOLXTMDHLLC-QGZVFWFLSA-N n-[(4-methoxy-6-methyl-2-oxo-1h-pyridin-3-yl)methyl]-2-methyl-1-[(1r)-1-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]ethyl]indole-3-carboxamide Chemical compound C1=C(C)NC(=O)C(CNC(=O)C=2C3=CC=CC=C3N([C@H](C)C3CCN(CC(F)(F)F)CC3)C=2C)=C1OC HPODOLXTMDHLLC-QGZVFWFLSA-N 0.000 claims 1
- HPODOLXTMDHLLC-UHFFFAOYSA-N n-[(4-methoxy-6-methyl-2-oxo-1h-pyridin-3-yl)methyl]-2-methyl-1-[1-[1-(2,2,2-trifluoroethyl)piperidin-4-yl]ethyl]indole-3-carboxamide Chemical compound C1=C(C)NC(=O)C(CNC(=O)C=2C3=CC=CC=C3N(C(C)C3CCN(CC(F)(F)F)CC3)C=2C)=C1OC HPODOLXTMDHLLC-UHFFFAOYSA-N 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 208000015347 renal cell adenocarcinoma Diseases 0.000 claims 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 1
- 201000005112 urinary bladder cancer Diseases 0.000 claims 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
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D401/02—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
- C07D401/12—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 chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Epidemiology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
Claims (12)
1. Jedinjenje koje ima strukturnu formulu (II): ili njegova farmaceutski prihvatljiva so, gde: A je CH ili N; R1a je izabran od -C1-C2 alkila i -O-(C1-C2 alkila), gde je R1a izborno supstituisan sa jednim ili više fluoro; R4a je izabran od 1-halo(C1-C3)alkil-piperidin-4-ila, C3-C6 cikloalkila izborno supstituisanog sa jednim ili više fluoro i tetrahidropiranila; i R13 je izabran od vodonika, halo, fenila, piridinila i -O-(C1-C4 alkila).
2.Jedinjenje prema patentnom zahtevu 1, naznačeno time što R1a je izabran od -OCH3, -CH3, -OCHF2, i -CH2CH3.
3. Jedinjenje prema patentnom zahtevu 1 ili 2, naznačeno time što je R4a izabran od 4,4-difluorocikloheksila, ciklopropila, tetrahidropiran-4-il, 1-(2-fluoroetil)-piperidin-4-ila, 1-(2,2-difluoroetil)-piperidin-4-ila, 1-(2,2,2-trifluoroetil)-piperidin-4-ila.
4. Jedinjenje prema bilo kom od patentnih zahteva 1 do 3, naznačeno time što R13 je izabran od vodonika, hloro, fluoro, -OCH(CH3)2, fenila i piridin-2-ila.
5. Jedinjenje prema patentnom zahtevu 1, naznačeno tim što, jedinjenje je N-((4-metoksi-6-metil-2-okso-1,2-dihidropiridin-3-il)metil)-2-metil-1-(1-(1-(2,2,2-trifluoroetil)piperidin-4-il)etil)-1H-indol-3-karboksamid, ili njegova farmaceutski prihvatljiva so.
6. Jedinjenje prema patentnom zahtevu 5, naznačeno time što, jedinjenje je R-N-((4-metoksi-6-metil-2-okso-1,2-dihidropiridin-3-il)metil)-2-metil-1-(1-(1-(2,2,2-trifluoroetil)piperidin-4-il)etil)-1H-indol-3-karboksamid, ili njegova farmaceutski prihvatljiva so.
7. Jedinjenje prema patentnom zahtevu 1, naznačeno time što, jedinjenje je 1-(1-(1-(2,2-difluoroetil)piperidin-4-il)etil)-N-((4-metoksi-6-metil-2-okso-1,2-dihidropiridin-3-il)metil)-2-metil-1H-indol-3-karboksamid, ili njegova farmaceutski prihvatljiva so.
8.Jedinjenje prema patentnom zahtevu 7, naznačeno time što, jedinjenje je R-1-(1-(1-(2,2-difluoroetil)piperidin-4-il)etil)-N-((4-metoksi-6-metil-2-okso-1,2-dihidropiridin-3-il)metil)-2-metil-1H-indol-3-karboksamid, ili njegova farmaceutski prihvatljiva so.
9. Farmaceutska kompozicija koja sadrži jedinjenje prema bilo kom od patentnih zahteva 1 do 8, ili njegovu farmaceutski prihvatljivu so i farmaceutski prihvatljiv nosač.
10. Jedinjenje prema bilo kom od patentnih zahteva 1 do 8 ili njegova farmaceutski prihvatljiva so, za upotrebu u lečenju bolesti ili poremećaja povezanog sa ćelijskom proliferacijom.
11. Jedinjenje za upotrebu prema patentnom zahtevu 10, naznačeno time što, bolest je kancer.
12. Jedinjenje za upotrebu prema patentnom zahtevu 11, naznačeno time što je kancer izabran od kancera dojke, kancera prostate, kancera debelog creva, karcinoma renalnih ćelija, kancera glioblastoma multiforme, kancera bešike, melanoma, bronhijalnog kancera, limfoma i kancera jetre.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2013/025639 WO2013120104A2 (en) | 2012-02-10 | 2013-02-11 | Modulators of methyl modifying enzymes, compositions and uses thereof |
| EP14708987.4A EP2953941B1 (en) | 2013-02-11 | 2014-02-11 | Modulators of methyl modifying enzymes, compositions and uses thereof |
| PCT/US2014/015706 WO2014124418A1 (en) | 2013-02-11 | 2014-02-11 | Modulators of methyl modifying enzymes, compositions and uses thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ME02730B true ME02730B (me) | 2017-10-20 |
Family
ID=50239937
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MEP-2017-141A ME02730B (me) | 2013-02-11 | 2014-02-11 | Modulatori enzima koji modifikuju metil, njihove kompozicije i upotreba |
Country Status (16)
| Country | Link |
|---|---|
| EP (1) | EP2953941B1 (me) |
| KR (1) | KR102219441B1 (me) |
| CN (1) | CN105102446B (me) |
| CL (1) | CL2015002239A1 (me) |
| CR (1) | CR20150457A (me) |
| IL (1) | IL239985B (me) |
| MA (1) | MA38341B1 (me) |
| ME (1) | ME02730B (me) |
| PE (1) | PE20160044A1 (me) |
| PH (1) | PH12015501720B1 (me) |
| PL (1) | PL2953941T3 (me) |
| RS (1) | RS56207B1 (me) |
| SG (1) | SG11201506077XA (me) |
| SI (1) | SI2953941T1 (me) |
| TW (1) | TWI629273B (me) |
| WO (1) | WO2014124418A1 (me) |
Families Citing this family (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011160206A1 (en) | 2010-06-23 | 2011-12-29 | Morin Ryan D | Biomarkers for non-hodgkin lymphomas and uses thereof |
| EP2780013A4 (en) | 2011-11-18 | 2015-07-01 | Constellation Pharmaceuticals Inc | MODULATORS OF METHYL MODIFYING ENZYMES, COMPOSITIONS AND USES THEREOF |
| EP2812001B1 (en) | 2012-02-10 | 2017-06-14 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| AU2013331368A1 (en) | 2012-10-15 | 2015-04-30 | Epizyme, Inc. | Methods of treating cancer |
| EP3033334A1 (en) | 2013-08-15 | 2016-06-22 | Constellation Pharmaceuticals, Inc. | Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof |
| US10220036B2 (en) | 2014-12-23 | 2019-03-05 | Novartis Ag | Triazolopyrimidine compounds and uses thereof |
| WO2016130396A1 (en) * | 2015-02-13 | 2016-08-18 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| WO2017018975A1 (en) | 2015-07-24 | 2017-02-02 | Constellation Pharmaceuticals, Inc. | Combination therapies for modulation of histone methyl modifying enzymes |
| HK1256604A1 (zh) * | 2015-08-03 | 2019-09-27 | Constellation Pharmaceuticals, Inc. | Ezh2抑制剂和调节性t细胞功能的调制 |
| WO2017035234A1 (en) | 2015-08-24 | 2017-03-02 | Epizyme, Inc. | Method for treating cancer |
| TW201718598A (zh) | 2015-08-27 | 2017-06-01 | 美國禮來大藥廠 | Ｅｚｈ２抑制劑 |
| US10577350B2 (en) | 2015-08-28 | 2020-03-03 | Constellation Pharmaceuticals, Inc. | Crystalline forms of (R)-N-((4-methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide |
| EP4309738A3 (en) | 2015-10-06 | 2024-07-17 | Epizyme, Inc. | Method of treating medulloblastoma with an ezh2 inhibitor |
| EP3371601A1 (en) | 2015-11-05 | 2018-09-12 | Epizyme Inc | Flow cytometry for monitoring histone h3 methylation status |
| EP3407978A4 (en) | 2016-01-29 | 2020-01-15 | Epizyme Inc | POLYTHERAPY FOR THE TREATMENT OF CANCER |
| CN105669647B (zh) * | 2016-02-22 | 2018-05-04 | 上海皓元生物医药科技有限公司 | 一种组蛋白甲基化酶ezh2抑制剂中间体的合成方法 |
| MA45406A (fr) | 2016-06-17 | 2019-04-24 | Epizyme Inc | Inhibiteurs d'ezh2 pour traiter le cancer |
| JP2019524872A (ja) * | 2016-06-20 | 2019-09-05 | ノバルティス アーゲー | 癌の治療に有用なイミダゾピリミジン化合物 |
| JP2019522049A (ja) | 2016-06-20 | 2019-08-08 | ノバルティス アーゲー | トリアゾロピリジン化合物及びその使用 |
| CA3027246A1 (en) | 2016-06-20 | 2017-12-28 | Novartis Ag | Crystalline forms of triazolopyrimidine compound |
| WO2018075598A1 (en) | 2016-10-19 | 2018-04-26 | Constellation Pharmaceuticals, Inc. | Synthesis of inhibitors of ezh2 |
| AU2017367768A1 (en) | 2016-12-02 | 2019-07-18 | Epizyme, Inc. | Combination therapy for treating cancer |
| AU2018210099A1 (en) | 2017-01-19 | 2019-08-15 | Daiichi Sankyo Company, Limited | Pharmaceutical composition used for treatment of HTLV-1-associated myelopathy |
| US10266542B2 (en) | 2017-03-15 | 2019-04-23 | Mirati Therapeutics, Inc. | EZH2 inhibitors |
| US11642346B2 (en) | 2017-03-31 | 2023-05-09 | Epizyme, Inc. | Combination therapy for treating cancer |
| WO2018231973A1 (en) | 2017-06-13 | 2018-12-20 | Epizyme, Inc. | Inhibitors of ezh2 and methods of use thereof |
| WO2019014191A1 (en) | 2017-07-10 | 2019-01-17 | Constellation Pharmaceuticals, Inc. | GENE EXPRESSION INDUCED BY EZH2 INHIBITOR |
| WO2019094552A1 (en) * | 2017-11-09 | 2019-05-16 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| US11529344B2 (en) | 2017-11-14 | 2022-12-20 | Pfizer Inc. | EZH2 inhibitor combination therapies |
| CN109879790B (zh) * | 2017-12-06 | 2022-09-20 | 华东师范大学 | 以吲哚或吲哚类似物为母核结构的酰胺类小分子有机化合物、用途及其制备方法 |
| WO2019133674A1 (en) | 2017-12-28 | 2019-07-04 | Constellation Pharmaceuticals, Inc. | Pharmacokinetic enhancement of ezh2 inhibitors through combination therapies |
| PT3746446T (pt) | 2018-01-31 | 2022-07-18 | Mirati Therapeutics Inc | Inibidores de prc2 |
| CN110229151B (zh) * | 2018-03-06 | 2021-09-10 | 上海海和药物研究开发股份有限公司 | 吲嗪类化合物、其制备方法及用途 |
| CN110229157B (zh) * | 2018-03-06 | 2022-06-21 | 上海海和药物研究开发股份有限公司 | 嘧啶并五元芳香杂环类化合物、其制备方法及用途 |
| EP3765458B1 (en) | 2018-03-14 | 2023-01-11 | Biogen MA Inc. | O-glycoprotein-2-acetamido-2-deoxy-3-d-glycopyranosidase inhibitors |
| CA3100977A1 (en) | 2018-05-21 | 2019-11-28 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
| EP3823671B1 (en) | 2018-07-09 | 2024-02-07 | Fondation Asile Des Aveugles | Inhibition of prc2 subunits to treat eye disorders |
| AU2019344922B2 (en) | 2018-09-19 | 2025-02-06 | Biogen Ma Inc. | O-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors |
| AR117252A1 (es) | 2018-12-05 | 2021-07-21 | Biogen Ma Inc | Inhibidores de o-glucoproteína-2-acetamido-2-desoxi-3-d-glucopiranosidasa de morfolinilo, piperazinilo, oxazepanilo y diazepanilo |
| WO2020139339A1 (en) | 2018-12-27 | 2020-07-02 | Constellation Pharmaceuticals, Inc. | Ezh2 and androgen receptor signaling inhibitors as tools for targeting prostate cancer |
| JP7504898B2 (ja) | 2019-02-04 | 2024-06-24 | バイオジェン・エムエイ・インコーポレイテッド | 二環式エーテルｏ－糖タンパク質－２－アセトアミド－２－デオキシ－３－ｄ－グルコピラノシダーゼ阻害剤 |
| US12421224B2 (en) | 2019-03-08 | 2025-09-23 | Biogen Ma Inc. | Azetidinyl O-glycoprotein-2-acetamido-2-deoxy-3-D-glucopyranosidase inhibitors |
| EP3959214A1 (en) | 2019-04-22 | 2022-03-02 | Mirati Therapeutics, Inc. | Naphthyridine derivatives as prc2 inhibitors |
| EP3980422A1 (en) | 2019-06-05 | 2022-04-13 | Mirati Therapeutics, Inc. | Imidazo[1,2-c]pyrimidine derivatives as prc2 inhibitors for treating cancer |
| BR112022001161A2 (pt) * | 2019-07-24 | 2022-06-07 | Constellation Pharmaceuticals Inc | Formas cristalinas de 7-cloro-2-(4-(3-metoxiazetidin-1-il)ciclo-hexil)-2,4-dimetil-n-((6-metil-4-(metiltio)-2-óxo-1,2-di-hidropiridin-3-il)metil)benzo[d][1,3]dioxol-5-carboxamida |
| WO2021016409A1 (en) | 2019-07-24 | 2021-01-28 | Constellation Pharmaceuticals, Inc. | Ezh2 inhibition in combination therapies for the treatment of cancers |
| WO2021086966A1 (en) | 2019-10-29 | 2021-05-06 | Biogen Ma Inc. | Spirocyclic o-glycoprotein-2-acetamido-2-deoxy-3-d-glucopyranosidase inhibitors |
| UY39366A (es) | 2020-08-03 | 2022-02-25 | Biogen Ma Inc | Formas cristalinas de un inhibidor de la o-glucoproteína-2-acetamido-2-desoxi-3-d-glucopiranosidasa |
| CN112679505B (zh) * | 2020-12-25 | 2022-04-22 | 杭州澳赛诺生物科技有限公司 | 一种4-甲基-7H-吡咯并[2,3-d]嘧啶的合成方法 |
| WO2022150962A1 (en) | 2021-01-12 | 2022-07-21 | Westlake Pharmaceutical (Hangzhou) Co., Ltd. | Protease inhibitors, preparation, and uses thereof |
| WO2023111810A1 (en) | 2021-12-14 | 2023-06-22 | Pfizer Inc. | Combination therapies and uses for treating cancer |
| EP4514391A1 (en) | 2022-04-27 | 2025-03-05 | Daiichi Sankyo Company, Limited | Combination of antibody-drug conjugate with ezh1 and/or ezh2 inhibitor |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PT2566327T (pt) * | 2010-05-07 | 2017-05-26 | Glaxosmithkline Llc | Indoles |
| EP3323820B1 (en) * | 2011-02-28 | 2023-05-10 | Epizyme, Inc. | Substituted 6,5-fused bicyclic heteroaryl compounds |
| JO3438B1 (ar) * | 2011-04-13 | 2019-10-20 | Epizyme Inc | مركبات بنزين مستبدلة بأريل أو أريل غير متجانس |
| EP2812001B1 (en) * | 2012-02-10 | 2017-06-14 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
-
2014
- 2014-02-11 PE PE2015001728A patent/PE20160044A1/es active IP Right Grant
- 2014-02-11 MA MA38341A patent/MA38341B1/fr unknown
- 2014-02-11 KR KR1020157024901A patent/KR102219441B1/ko active Active
- 2014-02-11 PL PL14708987T patent/PL2953941T3/pl unknown
- 2014-02-11 CN CN201480019417.0A patent/CN105102446B/zh active Active
- 2014-02-11 WO PCT/US2014/015706 patent/WO2014124418A1/en not_active Ceased
- 2014-02-11 EP EP14708987.4A patent/EP2953941B1/en active Active
- 2014-02-11 SG SG11201506077XA patent/SG11201506077XA/en unknown
- 2014-02-11 SI SI201430274T patent/SI2953941T1/sl unknown
- 2014-02-11 RS RS20170680A patent/RS56207B1/sr unknown
- 2014-02-11 ME MEP-2017-141A patent/ME02730B/me unknown
- 2014-02-11 TW TW103104340A patent/TWI629273B/zh active
-
2015
- 2015-07-16 IL IL239985A patent/IL239985B/en active IP Right Grant
- 2015-08-05 PH PH12015501720A patent/PH12015501720B1/en unknown
- 2015-08-11 CL CL2015002239A patent/CL2015002239A1/es unknown
- 2015-09-02 CR CR20150457A patent/CR20150457A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN105102446A (zh) | 2015-11-25 |
| TW201443038A (zh) | 2014-11-16 |
| EP2953941A1 (en) | 2015-12-16 |
| MA38341B1 (fr) | 2018-11-30 |
| PH12015501720A1 (en) | 2015-11-09 |
| HK1218648A1 (en) | 2017-03-03 |
| KR20150119201A (ko) | 2015-10-23 |
| IL239985B (en) | 2018-11-29 |
| IL239985A0 (en) | 2015-09-24 |
| TWI629273B (zh) | 2018-07-11 |
| CL2015002239A1 (es) | 2016-02-05 |
| EP2953941B1 (en) | 2017-04-05 |
| WO2014124418A1 (en) | 2014-08-14 |
| RS56207B1 (sr) | 2017-11-30 |
| SG11201506077XA (en) | 2015-08-28 |
| CR20150457A (es) | 2015-10-20 |
| MA38341A1 (fr) | 2018-01-31 |
| CN105102446B (zh) | 2018-01-23 |
| KR102219441B1 (ko) | 2021-02-23 |
| PE20160044A1 (es) | 2016-02-11 |
| PH12015501720B1 (en) | 2015-11-09 |
| PL2953941T3 (pl) | 2017-11-30 |
| SI2953941T1 (sl) | 2017-08-31 |
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