AR068051A1 - Compuestos moduladores de la pi3k quinasa,composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento del cancer. - Google Patents
Compuestos moduladores de la pi3k quinasa,composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento del cancer.Info
- Publication number
- AR068051A1 AR068051A1 ARP080103383A ARP080103383A AR068051A1 AR 068051 A1 AR068051 A1 AR 068051A1 AR P080103383 A ARP080103383 A AR P080103383A AR P080103383 A ARP080103383 A AR P080103383A AR 068051 A1 AR068051 A1 AR 068051A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkynyl
- alkenyl
- ring
- members
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 102000010400 1-phosphatidylinositol-3-kinase activity proteins Human genes 0.000 title 1
- 206010028980 Neoplasm Diseases 0.000 title 1
- 108091007960 PI3Ks Proteins 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 23
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 12
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 abstract 12
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 10
- 125000005842 heteroatom Chemical group 0.000 abstract 10
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 abstract 9
- 229920006395 saturated elastomer Polymers 0.000 abstract 9
- 125000002619 bicyclic group Chemical group 0.000 abstract 7
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 6
- 125000002950 monocyclic group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 5
- -1 C1-6-N-di-C1-8 alkyl Chemical group 0.000 abstract 5
- 125000005843 halogen group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000004122 cyclic group Chemical group 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
- C07D277/82—Nitrogen atoms
-
- 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
- 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
- C07D413/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D417/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Reivindicacion 1: Un compuesto de formula (1) o una de sus sales farmacéuticamente aceptables, donde A1 es CR3 o N; A2 es CR4 o N; A3 es CR5 o N; y A4 es CR6 o N; siempre que no más de dos de A1, A2, A3 y A4 sean N; X es O o S; R1 es H, alquilo C1-6, alquenilo C2-6, alquinilo C2-6 o cicloalquilo C3-6; R2 es alquilo C1-6-R7a, alquenilo C2-6-R7a, alquinilo C2-6-R7a, cicloalquilo C3-6-R7a, C(O)R7a, C(=O)NHR7a, cooR7a, S(O)2R7a o un anillo monocíclico parcial o totalmente saturado o totalmente insaturado de 5 o 6 miembros formado de átomos de carbono y que incluye 1 a 3 heteroátomos que se seleccionan de N, O y S, donde el alquilo C1-6-R7a, alquenilo C2-6-R7a, alquinilo C2-6-R7a y cicloalquilo C3-6-R7a están opcionalmente sustituidos con 1 a 5 sustituyentes de R9; R3 es H, halo, haloalquilo, OH, NH2, alquilo C1-8, -O-alquilo C1-8, -O-haloalquilo C1-8, - alquil C1-6-O-alquilo C1-6, -S-alquilo C1-8, -alquil C1-6-S-alquilo C1-6, -NH-alquilo C1-8, -N-dialquilo C1-8, -alquil C1-6-NH-alquilo C1-6, -alquilo C1-4-OH, alquil C1-6-NH,, alquil C1-6-N-di-alquilo C1-8, alquenilo C2-8, alquinilo C2-8 o cicloalquilo C3-6; R4 es H, halo, haloalquilo, OH, NH2, alquilo C1-6, -O-alquilo C1-6, -O-haloalquilo C1-6, -alquil C1-6-O-alquilo C1-6, -S-alquilo C1-6, -alquil C1-6-S-alquilo C1-6, -NH-alquilo C1-6, -N-dialquilo C1-6, -alquil C1-6-NH-alquilo C1-6, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6 o un anillo monocíclico parcial o totalmente saturado de 5 miembros o parcial o totalmente saturado o insaturado de 6 miembros o un anillo bicíclico parcial o totalmente saturado o insaturado de 8 a 10 miembros, dicho anillo o anillos están formados de átomos de carbono y opcionalmente incluyen 1 a 3 heteroátomos por anillo que se seleccionan de N, O y S, donde cada uno de dicho alquilo C1-6, alquenilo C2-8, alquinilo C2-8 y anillo está opcionalmente sustituido, de manera independiente, con 1 a 5 sustituyentes de R7, R8 o R9; R5 es H, halo, haloalquilo, OH, NH2, alquilo C1-6, -O-alquilo C1-6, -O-haloalquilo C1-8, -alquil C1-6-O-alquilo C1-6, -S-alquilo C1-6, -alquil C1-6-S-alquilo C1-6, -NH-alquilo C1-6, -N-dialquilo C1-6, -alquil C1-6-NH-alquilo C1-6, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6 o un anillo monocíclico parcial o totalmente saturado de 5 miembros o parcial o totalmente saturado o insaturado de 6 miembros o un anillo bicíclico parcial o totalmente saturado o insaturado de 8 a 10 miembros, dicho anillo o anillos están formados de átomos de carbono, y opcionalmente incluyen 1 a 3 heteroátomos por anillo que se seleccionan de N, O y S, donde cada uno de dichos alquilo C1-6, alquenilo C2-8, alquinilo C2-8 y anillo está opcionalmente sustituido, de manera independiente, con 1 a 5 sustituyentes de R7, R8 o R9 siempre que ninguno de R4 y R5 sea, de manera independiente, un anillo monocíclico parcial o totalmente saturado de 5 miembros o parcial o totalmente saturado o insaturado de 6 miembros o un anillo bicíclico parcial o totalmente saturado o insaturado de 8 a 10 miembros formado de átomos de carbono, que opcionalmente incluye 1 a 3 heteroátomos; R6 es H, halo, haloalquilo, OH, NH2, alquilo C1-8, -O-alquilo C1-8, -O-haloalquilo C1-8, -alquil C1-6-O-alquilo C1-6, -S-alquilo C1-8, -alquil C1-6-S-alquilo C1-6, -NH-alquilo C1-8. -N-dialquilo C1-8, -alquil C1-6-NH-alquilo C1-6, -alquilo C1-4-OH, alquil C1-6-NH2, alquil C1-6-N-dialquilo C1-8, alquenilo C2-8, alquinilo C2-8 o cicloalquilo C3-6; cada R7, de manera independiente, es H, alquilo C1-8. alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6, cicloalquenilo C4-8, NR8R9, OR8, SR8, OR9, SR9, C(O)R8, OC(O)R9. COOR9, C(O)R9, C(O)NR8R9, C(O)NR9R9, S(O)2R8, S(O)2R9, S(O)2NR8R9, S(O)2NR9R9. NR9S(O)2NR9R9, NR9S(O)2R8 o NR9S(O)2R9, cada uno de alquilo C1-8, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6 y cicloalquenilo C4-8 está opcionalmente sustituido con uno o más sustituyentes de R8, R9, NR8R9, NR9R9, OR8, SR8, OR9, SR9, C(O)R8, OC(O)R9, cooR9, C(O)R9, C(O)NR9R9, NR9C(O)R9, C(O)NR9R9, NR9C(O)NR9R9, S(O)2R8, S(O)2R9, S(O)2NR9R9, NR9S(O)2NR9R9, NR9S(O)2R8 o NR9S(O)2R9; cada R7a, de manera independiente, es H, alquilo C1-8, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6, cicloalquenilo C4-8, NR8R9, NR9R9, OR8, SR8, OR9, SR9, C(O)R8, OC(O)R9, COOR9, C(O)R9, C(O)NR8R9, NR9C(O)R9, C(O)NR9R9, NR9C(O)NR9R9, S(O)2R8, S(O)2R9, S(O)2NR8R9, S(O)2NR9R9, NR9S(O)2NR9R9, NR9S(O)2R8 o NR9S(O)2R9, cada uno de alquilo C1-8, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6 y cicloalquenilo C4-8 está opcionalmente sustituido con uno o más sustituyentes de R8, R9, NR8R9, NR9R9, OR8, SR8, OR9, SR9, C(O)R8, OC(O)R9, COOR9, C(O)R9, C(O)NR9R9, NR9C(O)R9, C(O)NR9R9, NR9C(O)NR9R9, S(O)2R8, S(O)2R9, S(O)2NR9R9, NR9S(O)2NR9R9, NR9S(O)2R8 o NR9S(O)2R9; R8 es un sistema de anillos parcial o totalmente saturado o insaturado monocíclico de 3 a 8 miembros o bicíclico de 6 a 12 miembros, dicho sistema de anillos está formado de átomos de carbono y opcionalmente incluye 1 a 3 heteroátomos si es monocíclico o 1 a 6 heteroátomos si es bicíclico, dichos heteroátomos se seleccionan de O, N o S, y donde cada anillo de dicho sistema de anillos está opcionalmente sustituido, de manera independiente, con 1 a 5 sustituyentes de R9; cada R9, de manera independiente, es H, F, CI, Br, I, haloalquilo, CN, OH, alquilo C1-6. -O-alquilo C1-6, -alquil C1-6-O-alquilo C1-6, -S-alquilo C1-6, -alquil C1-6-S-alquilo C1-6, -alquil C1-6-NH-alquilo C1-6, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-6, oxo, acetilo, bencilo o un sistema de anillos parcial o totalmente saturado o insaturado monocíclico de 5 a 8 miembros o bicíclico de 6 a 12 miembros, dicho sistema de anillos está formado de átomos de carbono y opcionalmente incluye 1 a 3 heteroátomos si es monocíclico o 1 a 6 heteroátomos si es bicíclico, dichos heteroátomos se seleccionan de O, N o S, donde cada uno de dichos alquilo C1-6. alquenilo C2-8, alquinilo C2-8 y anillo de dicho sistema de anillos está opcionalmente sustituido, de manera independiente, con 1 a 5 sustituyentes de halo, haloalquilo, CN, NH2, OH, metilo, metoxilo, etilo, etoxilo, propilo, propoxilo, isopropilo, ciclopropilo, butilo, isobutilo, ter-butilo, metilamino, dimetilamino, etilamino, dietilamino, isopropilamino, bencilo o fenilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US96326307P | 2007-08-02 | 2007-08-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR068051A1 true AR068051A1 (es) | 2009-11-04 |
Family
ID=39811462
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080103383A AR068051A1 (es) | 2007-08-02 | 2008-08-04 | Compuestos moduladores de la pi3k quinasa,composiciones farmaceuticas que los contienen y usos de los mismos en el tratamiento del cancer. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7928140B2 (es) |
| EP (1) | EP2183232B1 (es) |
| JP (1) | JP5561702B2 (es) |
| AR (1) | AR068051A1 (es) |
| AU (1) | AU2008282728B2 (es) |
| CA (1) | CA2694136C (es) |
| CL (1) | CL2008002294A1 (es) |
| ES (1) | ES2401557T3 (es) |
| PE (1) | PE20091008A1 (es) |
| TW (1) | TW200911798A (es) |
| WO (1) | WO2009017822A2 (es) |
Families Citing this family (89)
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|---|---|---|---|---|
| EP2211615A4 (en) * | 2007-10-22 | 2010-10-13 | Glaxosmithkline Llc | PYRIDOSULFONAMIDE DERIVATIVES AS PI3 KINASE INHIBITORS |
| US7820665B2 (en) | 2007-12-19 | 2010-10-26 | Amgen Inc. | Imidazopyridazine inhibitors of PI3 kinase for cancer treatment |
| NZ588700A (en) * | 2008-04-16 | 2012-07-27 | Vertex Pharma | Inhibitors of phosphatidylinositol 3-kinase (pi3k) |
| WO2009133127A1 (en) * | 2008-04-30 | 2009-11-05 | Merck Serono S.A. | Fused bicyclic compounds and use thereof as pi3k inhibitors |
| MX315904B (es) | 2008-05-30 | 2013-11-29 | Amgen Inc | Inhibidores de fosfoinosituro-3 cinasa. |
| EP2303886A2 (en) * | 2008-06-24 | 2011-04-06 | Takeda Pharmaceutical Company Limited | Pi3k/m tor inhibitors |
| CA2753560A1 (en) * | 2009-02-27 | 2010-11-25 | Vertex Pharmaceuticals Incorporated | Inhibitors of phosphatidylinositol 3-kinase |
| WO2010100144A1 (en) * | 2009-03-04 | 2010-09-10 | Merck Serono S.A. | Fused bicyclic compounds as inhibitors for pi3 kinase |
| EP2408773A2 (en) | 2009-03-20 | 2012-01-25 | Amgen, Inc | Inhibitors of pi3 kinase |
| JPWO2010125799A1 (ja) | 2009-04-27 | 2012-10-25 | 塩野義製薬株式会社 | Pi3k阻害活性を有するウレア誘導体 |
| CA2760791C (en) * | 2009-05-07 | 2017-06-20 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
| SI2429995T1 (sl) | 2009-05-15 | 2014-05-30 | Novartis Ag | Arilpiridini kot inhibitorji aldosteron sintaze |
| EP2440058A4 (en) * | 2009-06-12 | 2012-11-21 | Dana Farber Cancer Inst Inc | MELTED HETEROCYCLIC COMPOUNDS AND APPLICATIONS THEREOF |
| PE20170003A1 (es) * | 2009-08-17 | 2017-03-15 | Intellikine Llc | Compuestos heterociclicos y usos de los mismos |
| ES2551002T3 (es) * | 2009-11-17 | 2015-11-13 | Novartis Ag | Derivados de aril-piridina como inhibidores de la aldosterona sintasa |
| EP2937345B1 (en) | 2009-12-29 | 2018-03-21 | Dana-Farber Cancer Institute, Inc. | Type ii raf kinase inhibitors |
| CN103153062B (zh) * | 2010-05-24 | 2015-07-15 | 因特利凯有限责任公司 | 杂环化合物及其用途 |
| CA2800664C (en) | 2010-06-01 | 2019-09-24 | Angion Biomedica Corp. | Benzothiazole cytochrome p450 inhibitors and therapeutic uses thereof |
| US10414760B2 (en) | 2016-11-29 | 2019-09-17 | Angion Biomedica Corp. | Cytochrome P450 inhibitors and uses thereof |
| JO2998B1 (ar) | 2010-06-04 | 2016-09-05 | Amgen Inc | مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان |
| DE102010033690A1 (de) * | 2010-08-06 | 2012-02-09 | Saltigo Gmbh | Verfahren zur Herstellung vom Aminoarylalkylverbindungen |
| TWI410425B (zh) * | 2010-12-03 | 2013-10-01 | Lilly Co Eli | 唑并[5,4-b]吡啶-5-基化合物 |
| EP2678018A4 (en) * | 2011-02-23 | 2015-09-30 | Intellikine Llc | COMBINATION OF CHINESE HEMMER AND USES THEREOF |
| WO2012116237A2 (en) | 2011-02-23 | 2012-08-30 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
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| SI2782570T1 (sl) * | 2011-11-21 | 2020-02-28 | Calithera Biosciences Inc. | Heterociklični inhibitorji glutaminaze |
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| EP2909194A1 (en) | 2012-10-18 | 2015-08-26 | Dana-Farber Cancer Institute, Inc. | Inhibitors of cyclin-dependent kinase 7 (cdk7) |
| USRE48175E1 (en) | 2012-10-19 | 2020-08-25 | Dana-Farber Cancer Institute, Inc. | Hydrophobically tagged small molecules as inducers of protein degradation |
| WO2014063054A1 (en) | 2012-10-19 | 2014-04-24 | Dana-Farber Cancer Institute, Inc. | Bone marrow on x chromosome kinase (bmx) inhibitors and uses thereof |
| US20160002185A1 (en) | 2013-02-19 | 2016-01-07 | Amgen Inc. | Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer |
| MX374513B (es) | 2013-03-14 | 2025-03-06 | Amgen Inc | Compuestos de morfolinona de ácido heteroarilo como inhibidores mdm2 para el tratamiento de cáncer. |
| WO2014177915A1 (en) | 2013-05-01 | 2014-11-06 | Piramal Enterprises Limited | Cancer combination therapy using imidazo[4,5-c]quinoline derivatives |
| CN104177346A (zh) * | 2013-05-21 | 2014-12-03 | 苏州科捷生物医药有限公司 | 喹唑啉类化合物及其用途 |
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| ES2676734T3 (es) | 2013-10-18 | 2018-07-24 | Syros Pharmaceuticals, Inc. | Compuestos heteroatómicos útiles para el tratamiento de enfermedades proliferativas |
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