ES2746558T3 - Activadores de piruvato cinasa R para uso en terapia - Google Patents
Activadores de piruvato cinasa R para uso en terapia Download PDFInfo
- Publication number
- ES2746558T3 ES2746558T3 ES12721111T ES12721111T ES2746558T3 ES 2746558 T3 ES2746558 T3 ES 2746558T3 ES 12721111 T ES12721111 T ES 12721111T ES 12721111 T ES12721111 T ES 12721111T ES 2746558 T3 ES2746558 T3 ES 2746558T3
- Authority
- ES
- Spain
- Prior art keywords
- compound
- pharmaceutically acceptable
- phenyl
- nmr
- mhz
- 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.)
- Active
Links
- 0 CCC*C(C)(c1ccccc1)O Chemical compound CCC*C(C)(c1ccccc1)O 0.000 description 9
- CUWMMYFPUKXUKK-GZIVZEMBSA-N C=C/C=C(/CCCN(CC1)CCN1C(c(cc1)cc(OC(F)(F)F)c1NS(c1cccc2c1nccc2)(=O)=O)=O)\C=C Chemical compound C=C/C=C(/CCCN(CC1)CCN1C(c(cc1)cc(OC(F)(F)F)c1NS(c1cccc2c1nccc2)(=O)=O)=O)\C=C CUWMMYFPUKXUKK-GZIVZEMBSA-N 0.000 description 1
- WIWMGDGHUBIGQE-UHFFFAOYSA-N C=[I]c1cc(Cl)cc(CN(CC2)CCN2C(c(cc2OC(F)(F)F)ccc2NS(=O)=O)=O)c1 Chemical compound C=[I]c1cc(Cl)cc(CN(CC2)CCN2C(c(cc2OC(F)(F)F)ccc2NS(=O)=O)=O)c1 WIWMGDGHUBIGQE-UHFFFAOYSA-N 0.000 description 1
- FMLPQHJYUZTHQS-UHFFFAOYSA-N CC(C1)NCCN1C(OC(C)(C)C)=O Chemical compound CC(C1)NCCN1C(OC(C)(C)C)=O FMLPQHJYUZTHQS-UHFFFAOYSA-N 0.000 description 1
- NDUURDFTSPYVKW-UHFFFAOYSA-N CC(CN(CC1CCCC1)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O Chemical compound CC(CN(CC1CCCC1)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O NDUURDFTSPYVKW-UHFFFAOYSA-N 0.000 description 1
- NHYTWSQSLVYPOZ-UHFFFAOYSA-N CC(CN(CC1COCC1)CC1)N1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound CC(CN(CC1COCC1)CC1)N1C(c(cc1)ccc1NS(=O)=O)=O NHYTWSQSLVYPOZ-UHFFFAOYSA-N 0.000 description 1
- OLEZEIWUFBLCOI-UHFFFAOYSA-N CC(CN(CC1OCCCC1)CC1)N1C(c(cc1)ccc1NS(=O)=O)=C(C)C Chemical compound CC(CN(CC1OCCCC1)CC1)N1C(c(cc1)ccc1NS(=O)=O)=C(C)C OLEZEIWUFBLCOI-UHFFFAOYSA-N 0.000 description 1
- ZBSYMYROECDZJU-UHFFFAOYSA-N CC(CN(Cc(c(F)c1)cc(F)c1F)CC1)N1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound CC(CN(Cc(c(F)c1)cc(F)c1F)CC1)N1C(c(cc1)ccc1NS(=O)=O)=O ZBSYMYROECDZJU-UHFFFAOYSA-N 0.000 description 1
- HLRSCXPFFRCILA-UHFFFAOYSA-N CC(CN(Cc(c(F)cc(F)c1)c1F)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O Chemical compound CC(CN(Cc(c(F)cc(F)c1)c1F)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O HLRSCXPFFRCILA-UHFFFAOYSA-N 0.000 description 1
- AHKWNCXDRVTWQX-UHFFFAOYSA-N CC(CN(Cc(cc1)ccc1F)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O Chemical compound CC(CN(Cc(cc1)ccc1F)CC1)N1C(c(ccc(NS(=O)=O)c1)c1Cl)=O AHKWNCXDRVTWQX-UHFFFAOYSA-N 0.000 description 1
- NSYMPDFDSMYUIR-UHFFFAOYSA-N CC(CN(Cc(cc1F)cc(F)c1F)CC1C)N1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound CC(CN(Cc(cc1F)cc(F)c1F)CC1C)N1C(c(cc1)ccc1NS(=O)=O)=O NSYMPDFDSMYUIR-UHFFFAOYSA-N 0.000 description 1
- GNPXMCPJHGMZJK-UHFFFAOYSA-N CC(CN(Cc1cc(F)cc(F)c1F)CC1C)N1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound CC(CN(Cc1cc(F)cc(F)c1F)CC1C)N1C(c(cc1)ccc1NS(=O)=O)=O GNPXMCPJHGMZJK-UHFFFAOYSA-N 0.000 description 1
- YWXAARJNHGLODT-UHFFFAOYSA-N CC(c(c(F)c(cc1)F)c1F)N(CC1)CC(C)N1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound CC(c(c(F)c(cc1)F)c1F)N(CC1)CC(C)N1C(c(cc1)ccc1NS(=O)=O)=O YWXAARJNHGLODT-UHFFFAOYSA-N 0.000 description 1
- DFQBOPCFSUDSQZ-OMZFTRSQSA-N CC/C=C(\C)/NS(c1cccc2c1N=CCCC=C2)(=O)=O Chemical compound CC/C=C(\C)/NS(c1cccc2c1N=CCCC=C2)(=O)=O DFQBOPCFSUDSQZ-OMZFTRSQSA-N 0.000 description 1
- ADAKKOMDBULNIN-UHFFFAOYSA-N CCC(COC)OC(N(CC1)CC(C)N1C(c(cc1)ccc1NS(=O)=O)=O)=O Chemical compound CCC(COC)OC(N(CC1)CC(C)N1C(c(cc1)ccc1NS(=O)=O)=O)=O ADAKKOMDBULNIN-UHFFFAOYSA-N 0.000 description 1
- XUUHHFSFLCXXBT-UHFFFAOYSA-N C[n]1cnc(CN(CC2)CCN2C(c(cc2OC(F)(F)F)ccc2NS(=O)=O)=O)c1 Chemical compound C[n]1cnc(CN(CC2)CCN2C(c(cc2OC(F)(F)F)ccc2NS(=O)=O)=O)c1 XUUHHFSFLCXXBT-UHFFFAOYSA-N 0.000 description 1
- WQKFFZGREJJXTG-UHFFFAOYSA-N Cc(nc1)cnc1C(N(CC1)CCN1C(c(cc1)ccc1NS(=O)=O)=O)=O Chemical compound Cc(nc1)cnc1C(N(CC1)CCN1C(c(cc1)ccc1NS(=O)=O)=O)=O WQKFFZGREJJXTG-UHFFFAOYSA-N 0.000 description 1
- ZNYJSUKJOWETKU-UHFFFAOYSA-N Cc1cc(F)cc(C(N(CC2)CCN2C(c(cc2)ccc2NS(=O)=O)=O)=O)c1 Chemical compound Cc1cc(F)cc(C(N(CC2)CCN2C(c(cc2)ccc2NS(=O)=O)=O)=O)c1 ZNYJSUKJOWETKU-UHFFFAOYSA-N 0.000 description 1
- SCGPOBHJJNYCTN-UHFFFAOYSA-N O=C(c(cc1)cnc1NS(=O)=O)N1CCN(CC2CC2)CC1 Chemical compound O=C(c(cc1)cnc1NS(=O)=O)N1CCN(CC2CC2)CC1 SCGPOBHJJNYCTN-UHFFFAOYSA-N 0.000 description 1
- NWFQKZXJXWGXKP-UHFFFAOYSA-N O=C(c(cc1C(F)(F)F)ccc1NS(=O)=O)N1CCN(Cc2ccncc2)CC1 Chemical compound O=C(c(cc1C(F)(F)F)ccc1NS(=O)=O)N1CCN(Cc2ccncc2)CC1 NWFQKZXJXWGXKP-UHFFFAOYSA-N 0.000 description 1
- MJGVGNMYEJRRNB-UHFFFAOYSA-N O=C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)N1CCN(CC2CCCC2)CC1 Chemical compound O=C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)N1CCN(CC2CCCC2)CC1 MJGVGNMYEJRRNB-UHFFFAOYSA-N 0.000 description 1
- GOCJGLZXRQGEMN-UHFFFAOYSA-N O=C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)N1CCN(CCc(ccnc2)c2F)CC1 Chemical compound O=C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)N1CCN(CCc(ccnc2)c2F)CC1 GOCJGLZXRQGEMN-UHFFFAOYSA-N 0.000 description 1
- KYOMBKBEBHHERB-UHFFFAOYSA-N O=C(c(ccc(NS(=O)=O)c1)c1Cl)N1CCN(Cc(c(F)c2)cc(F)c2F)CC1 Chemical compound O=C(c(ccc(NS(=O)=O)c1)c1Cl)N1CCN(Cc(c(F)c2)cc(F)c2F)CC1 KYOMBKBEBHHERB-UHFFFAOYSA-N 0.000 description 1
- LNRQAQVZIFYRBZ-UHFFFAOYSA-N O=C(c(nc1)cnc1NS(=O)=O)N1CCN(Cc(cc2)ccc2F)CC1 Chemical compound O=C(c(nc1)cnc1NS(=O)=O)N1CCN(Cc(cc2)ccc2F)CC1 LNRQAQVZIFYRBZ-UHFFFAOYSA-N 0.000 description 1
- MBTZFKWICAIMHN-UHFFFAOYSA-N O=C(c1c[s]cn1)N(CC1)CCN1C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)=O Chemical compound O=C(c1c[s]cn1)N(CC1)CCN1C(c(cc1OC(F)(F)F)ccc1NS(=O)=O)=O MBTZFKWICAIMHN-UHFFFAOYSA-N 0.000 description 1
- WETHWBWDEMTTMV-UHFFFAOYSA-N O=C(c1ncc[s]1)N(CC1)CCN1C(c(cc1)ccc1NS(=O)=O)=O Chemical compound O=C(c1ncc[s]1)N(CC1)CCN1C(c(cc1)ccc1NS(=O)=O)=O WETHWBWDEMTTMV-UHFFFAOYSA-N 0.000 description 1
- GDUHYJFJTXACNF-UHFFFAOYSA-N OC1(C(c2cccc3c2nccc3)OC1)Cl Chemical compound OC1(C(c2cccc3c2nccc3)OC1)Cl GDUHYJFJTXACNF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
- C12N5/06—Animal cells or tissues; Human cells or tissues
- C12N5/0602—Vertebrate cells
- C12N5/0634—Cells from the blood or the immune system
- C12N5/0641—Erythrocytes
-
- 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
- A61K31/4965—Non-condensed pyrazines
-
- 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
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- 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
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/36—Sulfur atoms
-
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—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
- C07D417/02—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 two hetero rings
- C07D417/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Biomedical Technology (AREA)
- Hematology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Zoology (AREA)
- Genetics & Genomics (AREA)
- Diabetes (AREA)
- Microbiology (AREA)
- Cell Biology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- Immunology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161482166P | 2011-05-03 | 2011-05-03 | |
| PCT/US2012/036413 WO2012151452A1 (en) | 2011-05-03 | 2012-05-03 | Pyruvate kinase activators for use in therapy |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2746558T3 true ES2746558T3 (es) | 2020-03-06 |
Family
ID=46085224
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES12721111T Active ES2746558T3 (es) | 2011-05-03 | 2012-05-03 | Activadores de piruvato cinasa R para uso en terapia |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US9404081B2 (enExample) |
| EP (1) | EP2704720B1 (enExample) |
| JP (2) | JP6267112B2 (enExample) |
| CN (1) | CN103608016A (enExample) |
| AU (1) | AU2012250690B2 (enExample) |
| CA (1) | CA2834692A1 (enExample) |
| ES (1) | ES2746558T3 (enExample) |
| WO (1) | WO2012151452A1 (enExample) |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2406389B1 (en) | 2009-03-13 | 2019-05-08 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| CA2758071C (en) | 2009-04-06 | 2018-01-09 | Agios Pharmaceuticals, Inc. | Pyruvate kinase m2 modulators, therapeutic compositions and related methods of use |
| TWI691493B (zh) | 2009-06-29 | 2020-04-21 | 美商阿吉歐斯製藥公司 | 治療化合物及組成物 |
| WO2011050210A1 (en) | 2009-10-21 | 2011-04-28 | Agios Pharmaceuticals, Inc. | Methods and compositions for cell-proliferation-related disorders |
| WO2012088314A1 (en) | 2010-12-21 | 2012-06-28 | Agios Pharmaceuticals, Inc. | Bicyclic pkm2 activators |
| TWI549947B (zh) * | 2010-12-29 | 2016-09-21 | 阿吉歐斯製藥公司 | 治療化合物及組成物 |
| SMT202400081T1 (it) | 2011-05-03 | 2024-03-13 | Agios Pharmaceuticals Inc | Attivatori della piruvato chinasi per uso in terapia |
| ES2746558T3 (es) | 2011-05-03 | 2020-03-06 | Agios Pharmaceuticals Inc | Activadores de piruvato cinasa R para uso en terapia |
| CN102827170A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| CN102827073A (zh) | 2011-06-17 | 2012-12-19 | 安吉奥斯医药品有限公司 | 治疗活性组合物和它们的使用方法 |
| US9474779B2 (en) | 2012-01-19 | 2016-10-25 | Agios Pharmaceuticals, Inc. | Therapeutically active compositions and their methods of use |
| PT2968316T (pt) | 2013-03-13 | 2019-10-29 | Forma Therapeutics Inc | Derivados de 2-hidroxi-1-{4-[(4-fenilfenil)carbonil]piperazin-1-il}etano-1-ona e compostos relacionados como inibidores da sintase de ácidos gordos (fasn) para o tratamento do cancro |
| WO2014139144A1 (en) * | 2013-03-15 | 2014-09-18 | Agios Pharmaceuticals, Inc. | Therapeutic compounds and compositions |
| WO2015003355A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| US10376510B2 (en) | 2013-07-11 | 2019-08-13 | Agios Pharmaceuticals, Inc. | 2,4- or 4,6-diaminopyrimidine compounds as IDH2 mutants inhibitors for the treatment of cancer |
| WO2015003360A2 (en) | 2013-07-11 | 2015-01-15 | Agios Pharmaceuticals, Inc. | Therapeutically active compounds and their methods of use |
| US9579324B2 (en) | 2013-07-11 | 2017-02-28 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| US20150031627A1 (en) | 2013-07-25 | 2015-01-29 | Agios Pharmaceuticals, Inc | Therapeutically active compounds and their methods of use |
| UA121211C2 (uk) | 2014-03-14 | 2020-04-27 | Аджіос Фармасьютикалз, Інк. | Фармацевтична композиція, що містить тверду дисперсію, та спосіб лікування гострої мієлогенної/мієлоїдної лейкемії (гмл) |
| FR3030516B1 (fr) * | 2014-12-19 | 2019-12-27 | Galderma Research & Development | Derives sulfonamides bicycles en tant qu'agonistes inverses du recepteur gamma orphelin associe aux retinoides ror gamma (t) |
| PL3307271T3 (pl) * | 2015-06-11 | 2024-02-05 | Agios Pharmaceuticals, Inc. | Sposoby stosowania aktywatorów kinazy pirogronianowej |
| MX386735B (es) | 2015-10-15 | 2025-03-19 | Servier Lab | Terapia de combinacion para tratar tumores malignos. |
| ES2981538T3 (es) | 2015-10-15 | 2024-10-09 | Servier Lab | Terapia de combinación que comprende ivosidenib, citarabina y daunorrubicina o idarrubicina para el tratamiento de leucemia mielógena aguda |
| SMT201900517T1 (it) | 2017-03-20 | 2019-11-13 | Forma Therapeutics Inc | Composizioni di pirrolopirrolo come attivatori di piruvato chinasi (pkr) |
| RS64221B1 (sr) | 2017-08-15 | 2023-06-30 | Agios Pharmaceuticals Inc | Modulatori piruvat kinaze i njihova upotreba |
| US10980788B2 (en) | 2018-06-08 | 2021-04-20 | Agios Pharmaceuticals, Inc. | Therapy for treating malignancies |
| US11001588B2 (en) | 2018-09-19 | 2021-05-11 | Forma Therapeutics, Inc. | Activating pyruvate kinase R and mutants thereof |
| 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 |
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| AU2012250690B2 (en) | 2017-06-08 |
| JP6267112B2 (ja) | 2018-01-24 |
| JP6267299B2 (ja) | 2018-01-24 |
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