ES2569712T3 - Activadores de PKM2 bicíclicos - Google Patents
Activadores de PKM2 bicíclicos Download PDFInfo
- Publication number
- ES2569712T3 ES2569712T3 ES11811257.2T ES11811257T ES2569712T3 ES 2569712 T3 ES2569712 T3 ES 2569712T3 ES 11811257 T ES11811257 T ES 11811257T ES 2569712 T3 ES2569712 T3 ES 2569712T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- independently selected
- heteroatoms
- heterocyclyl
- 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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- 125000002619 bicyclic group Chemical group 0.000 title claims abstract description 36
- 101001091538 Homo sapiens Pyruvate kinase PKM Proteins 0.000 title claims description 10
- 102100034911 Pyruvate kinase PKM Human genes 0.000 title claims description 10
- 239000012190 activator Substances 0.000 title description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 187
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 126
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 81
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 72
- 125000003118 aryl group Chemical group 0.000 claims abstract description 69
- 239000001257 hydrogen Substances 0.000 claims abstract description 64
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 64
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 60
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 49
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 49
- 125000005843 halogen group Chemical group 0.000 claims abstract description 45
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 43
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims abstract description 40
- 125000004429 atom Chemical group 0.000 claims abstract description 39
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 31
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 30
- 125000002950 monocyclic group Chemical group 0.000 claims abstract description 30
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 30
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 28
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 27
- 125000004475 heteroaralkyl group Chemical group 0.000 claims abstract description 25
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims abstract description 19
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 19
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 16
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 14
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract description 12
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 11
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 10
- POPYULZWDOOFIW-UHFFFAOYSA-N 2-chloro-n-(2-oxo-1,4-dihydro-3,1-benzoxazin-7-yl)-5-(propan-2-ylsulfamoyl)benzamide Chemical compound CC(C)NS(=O)(=O)C1=CC=C(Cl)C(C(=O)NC=2C=C3NC(=O)OCC3=CC=2)=C1 POPYULZWDOOFIW-UHFFFAOYSA-N 0.000 claims abstract description 4
- ZLZUPKKXWJNTRA-UHFFFAOYSA-N 2-chloro-n-(3-methyl-2-oxo-1,4-dihydroquinazolin-7-yl)-5-(propan-2-ylsulfamoyl)benzamide Chemical compound CC(C)NS(=O)(=O)C1=CC=C(Cl)C(C(=O)NC=2C=C3NC(=O)N(C)CC3=CC=2)=C1 ZLZUPKKXWJNTRA-UHFFFAOYSA-N 0.000 claims abstract description 4
- ALRNFEILCIQGFU-UHFFFAOYSA-N methyl 4-(2-oxo-7-phenylmethoxy-4h-1,3-benzoxazin-3-yl)benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1N1C(=O)OC2=CC(OCC=3C=CC=CC=3)=CC=C2C1 ALRNFEILCIQGFU-UHFFFAOYSA-N 0.000 claims abstract description 4
- JWXGGPLYOQRMMH-UHFFFAOYSA-N 2-chloro-n-(2-oxo-3,4-dihydro-1h-quinazolin-7-yl)-5-(propan-2-ylsulfamoyl)benzamide Chemical compound CC(C)NS(=O)(=O)C1=CC=C(Cl)C(C(=O)NC=2C=C3NC(=O)NCC3=CC=2)=C1 JWXGGPLYOQRMMH-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000000034 method Methods 0.000 claims description 66
- 206010028980 Neoplasm Diseases 0.000 claims description 63
- 201000011510 cancer Diseases 0.000 claims description 41
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 40
- -1 (3,4-dihydro-4-methyl-3-oxo-2H-1,4-benzoxazin-6-yl) -2,4-dimethoxy-benzenesulfonamide Chemical compound 0.000 claims description 39
- 230000000694 effects Effects 0.000 claims description 35
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 32
- 239000008194 pharmaceutical composition Substances 0.000 claims description 24
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 239000003814 drug Substances 0.000 claims description 10
- 239000003937 drug carrier Substances 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 3
- 229940124530 sulfonamide Drugs 0.000 claims description 3
- INKFFVYXPKBVPP-UHFFFAOYSA-N 1,5-dimethyl-n-(4-methyl-3-oxo-1,4-benzoxazin-6-yl)pyrazole-4-sulfonamide Chemical compound C1=C2N(C)C(=O)COC2=CC=C1NS(=O)(=O)C=1C=NN(C)C=1C INKFFVYXPKBVPP-UHFFFAOYSA-N 0.000 claims description 2
- UQWDCSZVKTZFHO-UHFFFAOYSA-N 1-(difluoromethyl)-5-methyl-n-(4-methyl-3-oxo-1,4-benzoxazin-6-yl)pyrazole-4-sulfonamide Chemical compound C1=C2N(C)C(=O)COC2=CC=C1NS(=O)(=O)C=1C=NN(C(F)F)C=1C UQWDCSZVKTZFHO-UHFFFAOYSA-N 0.000 claims description 2
- NRHISPJBSLUXLJ-UHFFFAOYSA-N 2-fluoro-5-methyl-n-(4-methyl-3-oxo-1,4-benzoxazin-6-yl)benzenesulfonamide Chemical compound C1=C2N(C)C(=O)COC2=CC=C1NS(=O)(=O)C1=CC(C)=CC=C1F NRHISPJBSLUXLJ-UHFFFAOYSA-N 0.000 claims description 2
- HDOQHXLSUBVLBP-UHFFFAOYSA-N 3-[2-(4-bromophenyl)-2-oxoethyl]-6-methyl-3,4-dihydro-1,4-benzoxazin-2-one Chemical compound N1C2=CC(C)=CC=C2OC(=O)C1CC(=O)C1=CC=C(Br)C=C1 HDOQHXLSUBVLBP-UHFFFAOYSA-N 0.000 claims description 2
- QRULCCSIWIQXEP-UHFFFAOYSA-N 4-fluoro-3-methyl-n-(4-methyl-3-oxo-1,4-benzoxazin-6-yl)benzenesulfonamide Chemical compound C1=C2N(C)C(=O)COC2=CC=C1NS(=O)(=O)C1=CC=C(F)C(C)=C1 QRULCCSIWIQXEP-UHFFFAOYSA-N 0.000 claims description 2
- XUNNOAJNXXSASM-UHFFFAOYSA-N 6-chloro-n-(4-methyl-3-oxo-1,4-benzoxazin-6-yl)-2,3-dihydro-1,4-benzodioxine-7-sulfonamide Chemical compound O1CCOC(C=C2Cl)=C1C=C2S(=O)(=O)NC1=CC=C2OCC(=O)N(C)C2=C1 XUNNOAJNXXSASM-UHFFFAOYSA-N 0.000 claims description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 2
- PCIXUBNOXBNGJJ-UHFFFAOYSA-N methyl n-[2-[4,5-dimethoxy-2-[(4-methyl-3-oxo-1,4-benzoxazin-6-yl)sulfonylamino]phenyl]ethyl]carbamate Chemical compound COC(=O)NCCC1=CC(OC)=C(OC)C=C1NS(=O)(=O)C1=CC=C(OCC(=O)N2C)C2=C1 PCIXUBNOXBNGJJ-UHFFFAOYSA-N 0.000 claims description 2
- HIBQXWKGYXHFGE-UHFFFAOYSA-N n-(2,6-dimethylphenyl)-1,3-dimethyl-2-oxo-4h-quinazoline-6-sulfonamide Chemical compound C=1C=C2N(C)C(=O)N(C)CC2=CC=1S(=O)(=O)NC1=C(C)C=CC=C1C HIBQXWKGYXHFGE-UHFFFAOYSA-N 0.000 claims description 2
- IGYMDTWXXXVQOO-UHFFFAOYSA-N n-(3-fluoro-2-methylphenyl)-4-methyl-3-oxo-1,4-benzoxazine-6-sulfonamide Chemical compound C1=C2N(C)C(=O)COC2=CC=C1S(=O)(=O)NC1=CC=CC(F)=C1C IGYMDTWXXXVQOO-UHFFFAOYSA-N 0.000 claims description 2
- GMXCFYUIFRQIEC-INIZCTEOSA-N n-[2-[[[(2s)-1-cyclopentylpropan-2-yl]amino]methyl]phenyl]-2-oxo-1,4-dihydro-3,1-benzoxazine-6-sulfonamide Chemical compound C([C@H](C)NCC=1C(=CC=CC=1)NS(=O)(=O)C=1C=C2COC(=O)NC2=CC=1)C1CCCC1 GMXCFYUIFRQIEC-INIZCTEOSA-N 0.000 claims description 2
- 125000004494 ethyl ester group Chemical group 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 53
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 52
- 239000000203 mixture Substances 0.000 description 51
- 230000015572 biosynthetic process Effects 0.000 description 45
- 238000003786 synthesis reaction Methods 0.000 description 45
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 38
- 238000011282 treatment Methods 0.000 description 38
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- 239000000243 solution Substances 0.000 description 31
- 239000000047 product Substances 0.000 description 26
- 230000002829 reductive effect Effects 0.000 description 23
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 22
- 125000001424 substituent group Chemical group 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 239000007832 Na2SO4 Substances 0.000 description 21
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 21
- 239000012074 organic phase Substances 0.000 description 21
- 229910052938 sodium sulfate Inorganic materials 0.000 description 21
- 235000011152 sodium sulphate Nutrition 0.000 description 21
- 235000019439 ethyl acetate Nutrition 0.000 description 20
- 238000005160 1H NMR spectroscopy Methods 0.000 description 18
- 150000001412 amines Chemical class 0.000 description 18
- 102000013009 Pyruvate Kinase Human genes 0.000 description 17
- 108020005115 Pyruvate Kinase Proteins 0.000 description 17
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 17
- 239000001301 oxygen Substances 0.000 description 17
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- XPYBSIWDXQFNMH-UHFFFAOYSA-N D-fructose 1,6-bisphosphate Natural products OP(=O)(O)OCC(O)C(O)C(O)C(=O)COP(O)(O)=O XPYBSIWDXQFNMH-UHFFFAOYSA-N 0.000 description 11
- RNBGYGVWRKECFJ-ZXXMMSQZSA-N alpha-D-fructofuranose 1,6-bisphosphate Chemical compound O[C@H]1[C@H](O)[C@](O)(COP(O)(O)=O)O[C@@H]1COP(O)(O)=O RNBGYGVWRKECFJ-ZXXMMSQZSA-N 0.000 description 11
- 239000002585 base Substances 0.000 description 11
- RNBGYGVWRKECFJ-UHFFFAOYSA-N fructose-1,6-phosphate Natural products OC1C(O)C(O)(COP(O)(O)=O)OC1COP(O)(O)=O RNBGYGVWRKECFJ-UHFFFAOYSA-N 0.000 description 11
- 239000007858 starting material Substances 0.000 description 11
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
- 206010039491 Sarcoma Diseases 0.000 description 10
- 230000004913 activation Effects 0.000 description 10
- 150000001721 carbon Chemical group 0.000 description 10
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 10
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 10
- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 9
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 description 9
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- 239000003871 white petrolatum Substances 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229960000641 zorubicin Drugs 0.000 description 1
- FBTUMDXHSRTGRV-ALTNURHMSA-N zorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(\C)=N\NC(=O)C=1C=CC=CC=1)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 FBTUMDXHSRTGRV-ALTNURHMSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/12—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
- C07D265/14—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D265/18—1,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
- C07D265/36—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings condensed with one six-membered ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201061425557P | 2010-12-21 | 2010-12-21 | |
| US201061425513P | 2010-12-21 | 2010-12-21 | |
| US201061425499P | 2010-12-21 | 2010-12-21 | |
| US201061425528P | 2010-12-21 | 2010-12-21 | |
| US201061425513P | 2010-12-21 | ||
| US201061425557P | 2010-12-21 | ||
| US201061425499P | 2010-12-21 | ||
| US201061425528P | 2010-12-21 | ||
| PCT/US2011/066595 WO2012088314A1 (en) | 2010-12-21 | 2011-12-21 | Bicyclic pkm2 activators |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2569712T3 true ES2569712T3 (es) | 2016-05-12 |
Family
ID=45509688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES11811257.2T Active ES2569712T3 (es) | 2010-12-21 | 2011-12-21 | Activadores de PKM2 bicíclicos |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US9328077B2 (enExample) |
| EP (1) | EP2655350B1 (enExample) |
| JP (2) | JP6092118B2 (enExample) |
| CA (1) | CA2822432C (enExample) |
| ES (1) | ES2569712T3 (enExample) |
| MX (1) | MX336022B (enExample) |
| WO (1) | WO2012088314A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
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| BRPI1011587B1 (pt) | 2009-06-29 | 2020-03-24 | Agios Pharmaceuticals, Inc. | Compostos de quinolina sulfonamida com atividade moduladora de pmk2 e uso dos mesmos |
| CA2822432C (en) * | 2010-12-21 | 2019-09-24 | Agios Pharmaceuticals, Inc. | Bicyclic pkm2 activators |
| ES2644758T3 (es) | 2012-10-16 | 2017-11-30 | Tolero Pharmaceuticals, Inc. | Moduladores de PKM2 y métodos para su uso |
| CN105272904B (zh) * | 2014-07-18 | 2019-04-09 | 中国科学院广州生物医药与健康研究院 | N-苯基酰胺类化合物及其应用 |
| DE102017005091A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substituierte 3,4-Dihydropyrido[2,3-b]pyrazin-2(1H)-one |
| DE102017005089A1 (de) | 2016-05-30 | 2017-11-30 | Bayer Pharma Aktiengesellschaft | Substitulerte 3,4-Dihydrochinoxalin-2(1H)-one |
| HUE045261T2 (hu) | 2017-03-20 | 2019-12-30 | Forma Therapeutics Inc | Pirrolopirrol kompozíciók piruvát kináz (PKR) aktivátorokként |
| WO2019075367A1 (en) | 2017-10-13 | 2019-04-18 | Tolero Pharmaceuticals, Inc. | PKM2 ACTIVATORS IN COMBINATION WITH OXYGEN REACTIVE SPECIES FOR THE TREATMENT OF CANCER |
| JP2020537669A (ja) | 2017-10-19 | 2020-12-24 | 江▲蘇▼豪森▲薬▼▲業▼集▲団▼有限公司 | ピラゾリル基を含む三環式誘導体、その製造方法及び用途 |
| US12122778B2 (en) | 2018-09-19 | 2024-10-22 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
| CN113166060B (zh) | 2018-09-19 | 2024-01-09 | 诺沃挪第克健康护理股份公司 | 用丙酮酸激酶激活化合物治疗镰状细胞病 |
| JP7547360B2 (ja) | 2019-03-22 | 2024-09-09 | スミトモ ファーマ オンコロジー， インコーポレイテッド | Ｐｋｍ２モジュレーターを含む組成物およびそれを使用する処置の方法 |
| ES3042390T3 (en) | 2019-09-19 | 2025-11-20 | Novo Nordisk Healthcare Ag | Pyruvate kinase r (pkr) activating compositions |
| US11566030B2 (en) | 2021-02-08 | 2023-01-31 | Global Blood Therapeutics, Inc. | Substituted 2,6-dihydropyrrolo[3,4-c]pyrazoles as pyruvate kinase activators |
| US12128035B2 (en) | 2021-03-19 | 2024-10-29 | Novo Nordisk Health Care Ag | Activating pyruvate kinase R |
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2011
- 2011-12-21 CA CA2822432A patent/CA2822432C/en not_active Expired - Fee Related
- 2011-12-21 EP EP11811257.2A patent/EP2655350B1/en not_active Not-in-force
- 2011-12-21 ES ES11811257.2T patent/ES2569712T3/es active Active
- 2011-12-21 US US13/996,286 patent/US9328077B2/en not_active Expired - Fee Related
- 2011-12-21 WO PCT/US2011/066595 patent/WO2012088314A1/en not_active Ceased
- 2011-12-21 JP JP2013546384A patent/JP6092118B2/ja not_active Expired - Fee Related
- 2011-12-21 MX MX2013007268A patent/MX336022B/es unknown
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2016
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- 2016-03-29 JP JP2016066131A patent/JP2016153418A/ja not_active Withdrawn
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2017
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Also Published As
| Publication number | Publication date |
|---|---|
| HK1190406A1 (zh) | 2014-07-04 |
| CA2822432C (en) | 2019-09-24 |
| JP2016153418A (ja) | 2016-08-25 |
| EP2655350B1 (en) | 2016-03-09 |
| JP2014500330A (ja) | 2014-01-09 |
| US20160280697A1 (en) | 2016-09-29 |
| US9328077B2 (en) | 2016-05-03 |
| CA2822432A1 (en) | 2012-06-28 |
| MX336022B (es) | 2016-01-06 |
| US20140011804A1 (en) | 2014-01-09 |
| EP2655350A1 (en) | 2013-10-30 |
| WO2012088314A1 (en) | 2012-06-28 |
| JP6092118B2 (ja) | 2017-03-08 |
| US10087169B2 (en) | 2018-10-02 |
| US20170369481A1 (en) | 2017-12-28 |
| MX2013007268A (es) | 2013-12-06 |
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