AR080982A1 - Derivados de quinoxalina - Google Patents
Derivados de quinoxalinaInfo
- Publication number
- AR080982A1 AR080982A1 ARP110101476A AR080982A1 AR 080982 A1 AR080982 A1 AR 080982A1 AR P110101476 A ARP110101476 A AR P110101476A AR 080982 A1 AR080982 A1 AR 080982A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- substituted
- nr14r15
- alkoxy
- haloalkyl
- Prior art date
Links
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical class N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 80
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 29
- 125000000217 alkyl group Chemical group 0.000 abstract 26
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 13
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 7
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 7
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 7
- 229910052760 oxygen Inorganic materials 0.000 abstract 7
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- 229910052717 sulfur Inorganic materials 0.000 abstract 6
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000005842 heteroatom Chemical group 0.000 abstract 5
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 3
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 3
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- -1 R13 Chemical group 0.000 abstract 1
- 125000005157 alkyl carboxy group Chemical group 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052731 fluorine Chemical group 0.000 abstract 1
- 239000011737 fluorine Chemical group 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000005020 hydroxyalkenyl group Chemical group 0.000 abstract 1
- 125000005016 hydroxyalkynyl group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A—HUMAN NECESSITIES
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- 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
- A61K31/498—Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- 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
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- 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
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/08—Bridged systems
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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Abstract
Composiciones farmacéuticas que comprenden dichos compuestos, a procesos para la preparacion de dichos compuestos y al uso de dichos compuestos en el tratamiento de enfermedades, por ejemplo, cáncer. Reivindicacion 1: Un compuesto de la formula (1) incluyendo cualquier forma tautomérica o estereoquímicamente isomérica de ellos, en donde n representa un numero entero igual a 0, 1, 2, 3 o 4; R1 representa hidrogeno, alquilo C1-6, alquenilo C2-4, hidroxialquilo C1-6, haloalquilo C1-6, hidroxihaloalquilo C1-6, cianoalquilo C1-4, alcoxi C1-6-alquilo C1-6, en donde cada alquilo C1-6 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo, alquilo C1-6 sustituido con -NR4R5, alquilo C1-6 sustituido con -C(=O)-NR4R5, -S(=O)2-alquilo C1-6, -S(=O)2-haloalquilo C1-6, -S(=O)2-NR14R15, alquilo C1-6 sustituido con -S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-NR14R15, alquilo C1-6 sustituido con -NH-S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -NR12-S(=O)2-NR14R15, R6, alquilo C1-6 sustituido con R6, alquilo C1-6 sustituido con -C(=O)-R6, hidroxialquilo C1-6 sustituido con R6, alquilo C1-6 sustituido con -Si(CH3)3, alquilo C1-6 sustituido con -P(=O)(OH)2 o alquilo C1-6 sustituido con -P(=O)(Oalquilo C1-6)2; cada R1a está seleccionado, de modo independiente, de hidrogeno, alquilo C1-4, hidroxialquilo C1-4, alquilo C1-4 sustituido con amino o mono- o di(alquil C1-4)amino o -NH(cicloalquilo C3-8), cianoalquilo C1-4, alcoxi C1-4-alquilo C1-4 y alquilo C1-4 sustituido con uno o varios átomos de fluor; cada R2 está seleccionado, de modo independiente, de hidroxilo, halogeno, ciano, alquilo C1-4, alquenilo C2-4, alquinilo C2-4, alcoxi C1-4, hidroxialquilo C1-4, hidroxialcoxi C1-4, haloalquilo C1-4, haloalcoxi C1-4, hidroxihaloalquilo C1-4, hidroxihaloalcoxi C1-4, alcoxi C1-4-alquilo C1-4, haloalcoxi C1-4-alquilo C1-4, alcoxi C1-4-alquilo C1-4, en donde cada alquilo C1-4 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo, hidroxihaloalcoxi C1-4-alquilo C1-4, R13, alquilo C1-4 sustituido con R13, alquilo C1-4 sustituido con -C(=O)-R13, alcoxi C1-4 sustituido con R13, alcoxi C1-4 sustituido con -C(=O)-R13, -C(=O)-R13, alquilo C1-4 sustituido con -NR7R8, alquilo C1-4 sustituido con -C(=O)-NR7R8, alcoxi C1-4 sustituido con -NR7R8, alcoxi C1-4 sustituido con -C(=O)-NR7R8, -NR7R8 y -C(=O)-NR7R8, o cuando dos grupos R2 están unidos a átomos de carbono adyacentes, se pueden tomar juntos para formar un radical de la formula -O-(C(R17)2)p-O-; -X-CH=CH-; o -X-CH=N-; en donde R17 representa hidrogeno o fluor, p representa 1 o 2 y X representa O o S; R3 representa hidroxilo, alcoxi C1-6, hidroxialcoxi C1-6, alcoxi C1-6 sustituido con -NR10R11, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, haloalquilo C1-6 opcionalmente sustituido con -O-C(=O)-alquilo C1-6, hidroxialquilo C1-6 opcionalmente sustituido con -O-C(=O)-alquilo C1-6, hidroxialquenilo C2-6, hidroxialquinilo C2-6, hidroxihaloalquilo C1-6, cianoalquilo C1-6, alquilo C1-6 sustituido con carboxilo, alquilo C1-6 sustituido con -C(=O)-alquilo C1-6, alquilo C1-6 sustituido con -C(=O)-O-alquilo C1-6, alquilo C1-6 sustituido con alcoxi C1-6-alquil C1-6-O-C(=O)-, alquilo C1-6 sustituido con alcoxi C1-6-alquil C1-6-C(=O)-, alquilo C1-6 sustituido con -O-C(=O)-alquilo C1-6, alcoxi C1-6-alquilo C1-6, en donde cada alquilo C1-6 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo o con -O-C(=O)-alquilo C1-6, alquenilo C2-6 sustituido con alcoxi C1-6, alquinilo C2-6 sustituido con alcoxi C1-6, alquilo C1-6 sustituido con R9 y opcionalmente sustituido con -O-C(=O)-alquilo C1-6, alquilo C1-6 sustituido con -C(=O)-R9, alquilo C1-6 sustituido con hidroxilo y R9, alquenilo C2-6 sustituido con R9, alquinilo C2-6 sustituido con R9, alquilo C1-6 sustituido con -NR10R11, alquenilo C2-6 sustituido con -NR10R11, alquinilo C2-6 sustituido con -NR10R11, alquilo C1-6 sustituido con hidroxilo y -NR10R11, alquilo C1-6 sustituido con uno o dos halogenos y -NR10R11, -alquil C1-6-C(R12)=N-O-R12, alquilo C1-6 sustituido con -C(=O)-NR10R11, alquilo C1-6 sustituido con -O-C(=O)-NR10R11, -S(=O)2-alquilo C1-6, -S(=O)2-haloalquilo C1-6, -S(=O)2-NR14R15, alquilo C1-6 sustituido con -S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-NR14R15, alquilo C1-6 sustituido con -NR12-S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -NR12-S(=O)2-NR14R15, R13, alquilo C1-6 sustituido con -P(=O)(OH)2 o alquilo C1-6 sustituido con -P(=O)(Oalquilo C1-6)2; R4 y R5 representan cada uno, de modo independiente, hidrogeno, alquilo C1-6, hidroxialquilo C1-6, haloalquilo C1-6, hidroxihaloalquilo C1-6, alcoxi C1-6-alquilo en donde cada alquilo C1-6 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo, -S(=O)2-alquilo C1-6, -S(=O)2-haloalquilo C1-6, -S(=O)2-NR14R15, alquilo C1-6 sustituido con -S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-NR14R15, alquilo C1-6 sustituido con -NH-S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-NR14R15, R13 o alquilo C1-6 sustituido con R13; R6 representa cicloalquilo C3-8, cicloalquenilo C3-8, fenilo, heterociclilo monocíclico de 4 a 7 miembros que contiene al menos un heteroátomo seleccionado de N, O o S; dicho cicloalquilo C3-8, cicloalquenilo C3-8, fenilo, heterociclilo monocíclico de 4 a 7 miembros, opcionalmente y, de modo independiente, cada uno sustituido con 1, 2, 3, 4 o 5 sustituyentes, estando seleccionado cada sustituyente de modo independiente de ciano, alquilo C1-6, cianoalquilo C1-6, hidroxilo, carboxilo, hidroxialquilo C1-6, halogeno, haloalquilo C1-6, hidroxihaloalquilo C1-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-6, alquil C16-O-C(=O)-, -NR14R15, -C(=O)-NR14R15, alquilo C1-6 sustituido con -NR14R15, alquilo C1-6 sustituido con -C(=O)-NR14R15, -S(=O)2-alquilo C1-6, -S(=O)2- haloalquilo C1-6, -S(=O)2-NR14R15, alquilo C1-6 sustituido con -S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-haloalquilo C1-6, alquilo C 1-6 sustituido con -S(=O)2-NR4R15, alquilo C1-6 sustituido con -NH-S(=O)2- alquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-haloalquilo C1-6 o alquilo C1-6 sustituido con -NH-S(=O)2-NR14R15; R7 y R8 representan cada uno, de modo independiente, hidrogeno, alquilo C1-6, hidroxialquilo C1-6, haloalquilo C1-6, hidroxihaloalquilo C1-6 o alcoxi C1-6-alquilo C1-6; R9 representa cicloalquilo C3-8, cicloalquenilo C3-8, fenilo, naftilo o heterociclilo monocíclico o bicíclico de 3 a 12 miembros que contiene al menos un heteroátomo seleccionado de N, O o S, estando dicho cicloalquilo C3-8, cicloalquenilo C3-8, fenilo, naftilo o heterociclilo monocíclico o bicíclico de 3 a 12 miembros opcional e independientemente sustituido con 1, 2, 3, 4 o 5 sustituyentes, estando seleccionado cada sustituyente de modo independiente de =O, alquilo C1-4, hidroxilo, carboxilo, hidroxialquilo C1-4, ciano, cianoalquilo C1-4, alquil C1-4-O-C(=O)-, alquilo C1-4 sustituido con alquil C1-4-O-C(=O)-, alquil C1-4-C(=O)-, alcoxi C1-4-alquilo C1-4, en donde cada alquilo C1-4 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo, halogeno, haloalquilo C1-4, hidroxihaloalquilo C1-4, -NR14R15, -C(=O)-NR14R15, alquilo C1-4 sustituido con -NR14R15, alquilo C1-4 sustituido con -C(=O)-NR14R15, alcoxi C1-4, -S(=O)2-alquilo C1-4, -S(=O)2-haloalquilo C1-4, -S(=O)2-NR14R15, alquilo C1-4 sustituido con -S(=O)2-NR14R15, alquilo C1-4 sustituido con -NH-S(=O)2-alquilo C1-4, alquilo C1-4 sustituido con - NH-S(=O)2-haloalquilo C1-4, alquilo C1-4 sustituido con -NH-S(=O)2-NR14R15, R13, -C(=O)-R13, alquilo C1-4 sustituido con R13, fenilo opcionalmente sustituido con R16, fenilalquilo C1-6, en donde el fenilo está opcionalmente sustituido con R16, un heterociclilo monocíclico aromático de 5 o 6 miembros que contiene al menos un heteroátomo seleccionado de N, O o S en donde dicho heterociclilo está opcionalmente sustituido con R16; o cuando dos de los sustituyentes de R9 están unidos al mismo átomo, se pueden tomar juntos para formar un heterociclilo monocíclico saturado de 4 a 7 miembros que contiene al menos un heteroátomo seleccionado de N, O o S; R10 y R11 representan cada uno, de modo independiente, hidrogeno, carboxilo, alquilo C1-6, cianoalquilo C1-6, alquilo C1-6 sustituido con -NR14R15, alquilo C1-6 sustituido con -C(=O)-NR14R15, haloalquilo C1-6, hidroxialquilo C1-6, hidroxihaloalquilo C1-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-6, en donde cada alquilo C1-6 puede estar opcionalmente sustituido con uno o dos grupos hidroxilo, R6, alquilo C1-6 sustituido con R6, -C(=O)-R6, -C(=O)-alquilo C1-6, -C(=O)-hidroxialquilo C1-6, -C(=O)-haloalquilo C1-6,-C(=O)- hidroxihaloalquilo C1-6, alquilo C1-6 sustituido con -Si(CH3)3, -S(=O)2-alquilo C1-6, -S(=O)2-haloalquilo C1-6, -S(=O)2-NR14R15, alquilo C1-6 sustituido con -S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-haloalquilo C1-6, alquilo C1-6 sustituido con -S(=O)2-NR14R15, alquilo C1-6 sustituido con -NH-S(=O)2-alquilo C1-6, alquilo C1-6 sustituido con -NH-S(=O)2-haloalquilo C1-6 o alquilo C1-6 sustituido con -NH-S(=O)2-NR14R15; R12 representa hidrogeno o alquilo C1-4 opcionalmente sustituido con alcoxi C1-4; R13 representa cicloalquilo C3-8 o un heterociclilo monocíclico saturado de 4 a 6 miembros que contiene al menos un heteroátomo seleccionado de N, O o S, en donde dicho cicloalquilo C3-8 o heterociclilo monocíclico está opcionalmente sustituido con 1, 2 o 3 sustituyentes seleccionados cada uno, de modo independiente, de halogeno, hidroxilo, alquilo C1-6, -C(=O)-alquilo C1-6, alcoxi C1-6 o -NR14R15; R14 y R15 representan cada uno, de modo independiente, hidrogeno o haloalquilo C1-4 o alquilo C1-4 opcionalmente sustituido con un sustituy
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Country Status (41)
Families Citing this family (102)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI2118074T1 (sl) | 2007-02-01 | 2014-05-30 | Resverlogix Corp. | Spojine za preprečevanje in zdravljenje kardiovaskularnih bolezni |
| CN105859639A (zh) | 2009-03-18 | 2016-08-17 | 雷斯韦洛吉克斯公司 | 新的抗炎剂 |
| BRPI1014956B8 (pt) | 2009-04-22 | 2021-05-25 | Resverlogix Corp | agentes anti-inflamatórios |
| GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
| GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118654D0 (en) * | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
| GB201209613D0 (en) * | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| ES2984771T3 (es) | 2012-06-13 | 2024-10-31 | Incyte Holdings Corp | Compuestos tricíclicos sustituidos como inhibidores de FGFR |
| RU2019102203A (ru) | 2012-07-11 | 2019-03-05 | Блюпринт Медсинс Корпорейшн | Ингибиторы рецептора фактора роста фибробластов |
| WO2014026125A1 (en) | 2012-08-10 | 2014-02-13 | Incyte Corporation | Pyrazine derivatives as fgfr inhibitors |
| DK2906531T3 (en) * | 2012-10-15 | 2018-02-05 | Resverlogix Corp | APPLICABLE COMPOUNDS IN THE SYNTHESIS OF BENZAMIDE COMPOUNDS |
| WO2014071358A2 (en) | 2012-11-05 | 2014-05-08 | Foundation Medicine, Inc. | Novel ntrk1 fusion molecules and uses thereof |
| AU2013337264B2 (en) | 2012-11-05 | 2018-03-08 | Foundation Medicine, Inc. | Novel fusion molecules and uses thereof |
| US9719970B2 (en) | 2012-11-30 | 2017-08-01 | Waters Technologies Corporation | Methods and apparatus for the analysis of vitamin D metabolites |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| EP3939614A1 (en) | 2013-01-18 | 2022-01-19 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
| AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
| CN111793068A (zh) * | 2013-03-15 | 2020-10-20 | 西建卡尔有限责任公司 | 杂芳基化合物和其用途 |
| TWI647220B (zh) | 2013-03-15 | 2019-01-11 | 美商西建卡爾有限責任公司 | 雜芳基化合物及其用途 |
| KR102350704B1 (ko) | 2013-03-15 | 2022-01-13 | 셀젠 카르 엘엘씨 | 헤테로아릴 화합물 및 이의 용도 |
| EA035095B1 (ru) | 2013-04-19 | 2020-04-27 | Инсайт Холдингс Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
| GB201307577D0 (en) * | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
| CN104163794A (zh) * | 2013-10-17 | 2014-11-26 | 中国药科大学 | 2-氨基芳环类血管内皮生长因子受体(vegfr)抑制剂及其制备方法和用途 |
| PT3395814T (pt) | 2013-10-25 | 2022-07-27 | Blueprint Medicines Corp | Inibidores do recetor do fator de crescimento de fibroblastos |
| WO2015108992A1 (en) | 2014-01-15 | 2015-07-23 | Blueprint Medicines Corporation | Heterobicyclic compounds and their use as fgfr4 receptor inhibitors |
| HUE053653T2 (hu) * | 2014-03-26 | 2021-07-28 | Astex Therapeutics Ltd | FGFR inhibitor és IGF1R inhibitor kombinációi |
| ES3014202T3 (en) * | 2014-03-26 | 2025-04-21 | Astex Therapeutics Ltd | Cmet-inhibitors for use in delaying the emergence in resistance to fgfr inhibitors |
| JO3512B1 (ar) * | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
| CN105017227B (zh) * | 2014-07-08 | 2018-03-09 | 四川百利药业有限责任公司 | N‑(1h‑吡唑‑5‑基)喹唑啉‑4‑胺类化合物 |
| US9951047B2 (en) | 2014-08-18 | 2018-04-24 | Eisai R&D Management Co., Ltd. | Salt of monocyclic pyridine derivative and crystal thereof |
| SMT202200177T1 (it) * | 2014-09-26 | 2022-05-12 | Janssen Pharmaceutica Nv | Uso di gruppi di geni mutanti del fgfr nell'identificazione di pazienti affetti da cancro che saranno responsivi al trattamento con un inibitore del fgfr |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| TWI695837B (zh) | 2014-12-04 | 2020-06-11 | 比利時商健生藥品公司 | 作為激酶調節劑之三唑並嗒 |
| JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| EA038045B1 (ru) | 2015-02-20 | 2021-06-28 | Инсайт Корпорейшн | Бициклические гетероциклы в качестве ингибиторов fgfr |
| US9580423B2 (en) | 2015-02-20 | 2017-02-28 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| JO3789B1 (ar) | 2015-03-13 | 2021-01-31 | Resverlogix Corp | التراكيب والوسائل العلاجية المعتمدة لمعالجة الامراض المتعلقة بالمتممة |
| EP3275442B1 (en) | 2015-03-25 | 2021-07-28 | National Cancer Center | Therapeutic agent for bile duct cancer |
| TWI703984B (zh) * | 2015-04-03 | 2020-09-11 | 英商阿斯特克斯治療有限公司 | 用於癌症治療之fgfr/pd-1組合療法 |
| US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
| RU2747644C2 (ru) * | 2015-09-23 | 2021-05-11 | Янссен Фармацевтика Нв | Бигетероарил-замещенные 1,4-бензодиазепины и пути их применения для лечения рака |
| HRP20201157T1 (hr) * | 2015-09-23 | 2020-11-13 | Janssen Pharmaceutica N.V. | Triciklički heterocikli za liječenje raka |
| CN105596330B (zh) * | 2015-12-11 | 2018-10-16 | 深圳市坤健创新药物研究院 | 虚拟筛选化合物在制备激酶抑制剂中的应用和药物 |
| WO2017104739A1 (ja) | 2015-12-17 | 2017-06-22 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 乳がん治療剤 |
| CN107459519A (zh) | 2016-06-06 | 2017-12-12 | 上海艾力斯医药科技有限公司 | 稠合嘧啶哌啶环衍生物及其制备方法和应用 |
| US20190192522A1 (en) | 2016-09-08 | 2019-06-27 | Blueprint Medicines Corporation | Inhibitors of the fibroblast growth factor receptor 4 in combination with cyclin-dependent kinase inhibitors |
| BR112019007271A2 (pt) * | 2016-10-10 | 2019-09-17 | Dev Ct Biotechnology | compostos de quinoxalina como inibidores do receptor da tirosina quinase do tipo iii |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| JOP20190280A1 (ar) * | 2017-06-02 | 2019-12-02 | Janssen Pharmaceutica Nv | مثبطات fgfr2 لعلاج سرطان الأوعية الصفراوية |
| CN118638025A (zh) * | 2017-08-21 | 2024-09-13 | 细胞基因公司 | 制备(s)-4,5-二氨基-5-氧代戊酸叔丁酯的工艺 |
| US11661411B2 (en) | 2017-12-01 | 2023-05-30 | Board Of Regents Of The University Of Nebraska | Quinoxaline compounds and uses thereof |
| BR112020017922A2 (pt) | 2018-03-28 | 2020-12-22 | Eisai R&D Management Co., Ltd. | Agente terapêutico para carcinoma hepatocelular |
| JP7491510B2 (ja) * | 2018-04-26 | 2024-05-28 | メディシナル バイオコンバージェンス リサーチ センター | mTOR阻害剤としての新規化合物及びその用途 |
| US11174257B2 (en) | 2018-05-04 | 2021-11-16 | Incyte Corporation | Salts of an FGFR inhibitor |
| RS66310B1 (sr) | 2018-05-04 | 2025-01-31 | Incyte Corp | Čvrsti oblici inhibitora fgfr i procesi za njegovu pripremu |
| US12133851B2 (en) | 2018-09-21 | 2024-11-05 | Janssen Pharmaceutica Nv | Treatment of cholangiocarcinoma |
| WO2020131674A1 (en) * | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer |
| EP3898626A1 (en) | 2018-12-19 | 2021-10-27 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
| WO2020185532A1 (en) | 2019-03-08 | 2020-09-17 | Incyte Corporation | Methods of treating cancer with an fgfr inhibitor |
| WO2020205493A1 (en) | 2019-03-29 | 2020-10-08 | Janssen Pharmaceutica Nv | Fgfr tyrosine kinase inhibitors for the treatment of urothelial carcinoma |
| EP3946340A1 (en) | 2019-03-29 | 2022-02-09 | Janssen Pharmaceutica NV | Fgfr tyrosine kinase inhibitors for the treatment of urothelial carcinoma |
| WO2020208592A1 (en) * | 2019-04-12 | 2020-10-15 | Dr. Reddy’S Laboratories Limited | Process for preparation of erdafitinib, its purification and amorphous solid dispersion |
| CN111909044A (zh) * | 2019-05-09 | 2020-11-10 | 南京爱德程医药科技有限公司 | 2-(烷基氨基)乙基苯甲酸酯类化合物的合成方法 |
| WO2021007269A1 (en) | 2019-07-09 | 2021-01-14 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| TWI759829B (zh) * | 2019-08-23 | 2022-04-01 | 財團法人生物技術開發中心 | 作為第iii型受體酪胺酸激酶抑制劑之雜環吡唑衍生物 |
| AU2020352668A1 (en) | 2019-09-26 | 2022-03-31 | Janssen Pharmaceutica Nv | Use of FGFR inhibitors in FGFR-genetically altered cancers to enhance patient response to immune checkpoint inhibitors in sequential treatment settings |
| WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
| PH12022550892A1 (en) | 2019-10-14 | 2023-05-03 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| US11566028B2 (en) | 2019-10-16 | 2023-01-31 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN110790677B (zh) * | 2019-11-05 | 2022-04-29 | 浙江工业大学 | 一种金刚烷甲酰胺类化合物及其制备方法和应用 |
| MX2022006370A (es) | 2019-11-25 | 2022-09-07 | Amgen Inc | Compuestos heterocíclicos como inhibidores de delta-5 desaturasa y métodos de uso. |
| EP4069696A1 (en) | 2019-12-04 | 2022-10-12 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| AU2020395185A1 (en) | 2019-12-04 | 2022-06-02 | Incyte Corporation | Derivatives of an FGFR inhibitor |
| CN113024518A (zh) * | 2019-12-09 | 2021-06-25 | 武汉九州钰民医药科技有限公司 | 一种厄达替尼的制备方法 |
| CN113024517A (zh) * | 2019-12-09 | 2021-06-25 | 武汉九州钰民医药科技有限公司 | 一种制备厄达替尼的方法 |
| US12012409B2 (en) | 2020-01-15 | 2024-06-18 | Incyte Corporation | Bicyclic heterocycles as FGFR inhibitors |
| CN114945367A (zh) * | 2020-01-17 | 2022-08-26 | 贝达医药公司 | 作为fgfr激酶抑制剂的哒嗪和1,2,4-三嗪衍生物 |
| AU2021220285A1 (en) | 2020-02-12 | 2022-10-06 | Janssen Pharmaceutica Nv | FGFR tyrosine kinase inhibitors for the treatment of high-risk non-muscle invasive bladder cancer |
| IL295515A (en) | 2020-02-12 | 2022-10-01 | Janssen Pharmaceutica Nv | Fgfr tyrosine kinase inhibitors and anti-pd1 agents for the treatment of urothelial carcinoma |
| WO2022040111A2 (en) | 2020-08-17 | 2022-02-24 | Teva Pharmaceuticals International Gmbh | Solid state forms of erdafitinib salts and processes for preparation of erdafitinib |
| CN112920167B (zh) * | 2020-08-19 | 2022-08-26 | 四川大学华西医院 | 靶向fgfr和hdac的双靶点抑制剂及其制备方法和应用、药物组合物及药剂 |
| KR20230069958A (ko) | 2020-09-14 | 2023-05-19 | 얀센 파마슈티카 엔.브이. | Fgfr 억제제 조합 요법 |
| JP2024513575A (ja) | 2021-04-12 | 2024-03-26 | インサイト・コーポレイション | Fgfr阻害剤及びネクチン-4標的化剤を含む併用療法 |
| JP2024518612A (ja) | 2021-05-19 | 2024-05-01 | ヤンセン ファーマシューティカ エヌ.ベー. | 進行性固形腫瘍の治療のためのfgfrチロシンキナーゼ阻害剤 |
| WO2022261160A1 (en) | 2021-06-09 | 2022-12-15 | Incyte Corporation | Tricyclic heterocycles as fgfr inhibitors |
| TW202313610A (zh) | 2021-06-09 | 2023-04-01 | 美商英塞特公司 | 作為fgfr抑制劑之三環雜環 |
| US20240382483A1 (en) | 2021-06-22 | 2024-11-21 | Blueprint Medicines Corporation | Heterocyclic egfr inhibitors for use in the treatment of cancer |
| AU2022365014A1 (en) | 2021-10-12 | 2024-05-30 | Taris Biomedical Llc | Erdafitinib formulations and systems for intravesical administration |
| JP2024540411A (ja) | 2021-11-08 | 2024-10-31 | プロジェントス・セラピューティクス・インコーポレイテッド | 血小板由来成長因子受容体(pdgfr)アルファ阻害剤及びその使用 |
| EP4479055A1 (en) * | 2022-02-18 | 2024-12-25 | TARIS Biomedical LLC | Erdafitinib formulations and osmotic systems for intravesical administration |
| CN115108926B (zh) * | 2022-04-02 | 2023-06-20 | 上海工程技术大学 | 一种用于制备厄达替尼的中间体化合物及制备方法 |
| CN120813357A (zh) | 2023-02-13 | 2025-10-17 | 詹森药业有限公司 | 用于治疗高风险非肌层浸润性膀胱癌的fgfr酪氨酸激酶抑制剂 |
| CN120731076A (zh) | 2023-02-13 | 2025-09-30 | 塔里斯生物医药公司 | 膀胱内施用厄达替尼以用于治疗膀胱癌 |
| CN119101036A (zh) * | 2023-06-08 | 2024-12-10 | 广州六顺生物科技有限公司 | 喹喔啉类化合物及其应用 |
| WO2025059602A1 (en) | 2023-09-14 | 2025-03-20 | Taris Biomedical Llc | Methods of treating bladder cancer using intravesical administration of erdafitinib |
| CN119350298A (zh) * | 2024-10-09 | 2025-01-24 | 沈阳药科大学 | 一种厄达替尼的制备方法以及用于该方法的中间体化合物 |
Family Cites Families (128)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2940972A (en) | 1957-06-27 | 1960-06-14 | Thomae Gmbh Dr K | Tri-and tetra-substituted pteridine derivatives |
| US4666828A (en) | 1984-08-15 | 1987-05-19 | The General Hospital Corporation | Test for Huntington's disease |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4801531A (en) | 1985-04-17 | 1989-01-31 | Biotechnology Research Partners, Ltd. | Apo AI/CIII genomic polymorphisms predictive of atherosclerosis |
| US5272057A (en) | 1988-10-14 | 1993-12-21 | Georgetown University | Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase |
| US5192659A (en) | 1989-08-25 | 1993-03-09 | Genetype Ag | Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes |
| GB9125001D0 (en) | 1991-11-25 | 1992-01-22 | Ici Plc | Heterocyclic compounds |
| AU6909194A (en) | 1993-05-14 | 1994-12-12 | Board Of Regents, The University Of Texas System | Preparation of n-cyanodithioimino-carbonates and 3-mercapto-5-amino-1h-1,2,4-triazole |
| US5700823A (en) | 1994-01-07 | 1997-12-23 | Sugen, Inc. | Treatment of platelet derived growth factor related disorders such as cancers |
| US6331555B1 (en) | 1995-06-01 | 2001-12-18 | University Of California | Treatment of platelet derived growth factor related disorders such as cancers |
| US6218529B1 (en) | 1995-07-31 | 2001-04-17 | Urocor, Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate, breast and bladder cancer |
| US5882864A (en) | 1995-07-31 | 1999-03-16 | Urocor Inc. | Biomarkers and targets for diagnosis, prognosis and management of prostate disease |
| TW472045B (en) | 1996-09-25 | 2002-01-11 | Astra Ab | Protein kinase C inhibitor compounds, method for their preparation, pharmaceutical composition thereof and intermediate used for their preparation |
| EP1001945B1 (en) | 1997-05-28 | 2011-03-02 | Aventis Pharmaceuticals Inc. | QUINOLINE AND QUINOXALINE COMPOUNDS WHICH INHIBIT PLATELET-DERIVED GROWTH FACTOR AND/OR p56lck TYROSINE KINASES |
| US6235740B1 (en) | 1997-08-25 | 2001-05-22 | Bristol-Myers Squibb Co. | Imidazoquinoxaline protein tyrosine kinase inhibitors |
| UA71555C2 (en) | 1997-10-06 | 2004-12-15 | Zentaris Gmbh | Methods for modulating function of serine/threonine protein kinases by 5-azaquinoline derivatives |
| AU3033500A (en) | 1999-01-15 | 2000-08-01 | Agouron Pharmaceuticals, Inc. | Non-peptide glp-1 agonists |
| SK3542002A3 (en) | 1999-09-15 | 2003-04-01 | Warner Lambert Co | Pteridinones as kinase inhibitors |
| DE10013318A1 (de) | 2000-03-17 | 2001-09-20 | Merck Patent Gmbh | Formulierung enthaltend Chinoxalinderivate |
| WO2002076985A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| ES2295441T3 (es) | 2001-12-18 | 2008-04-16 | MERCK & CO., INC. | Moduladores de pirazol heteroaril sustituido de receptor 5 metabotropico de glutamato. |
| SI1463506T1 (sl) | 2001-12-24 | 2010-01-29 | Astrazeneca Ab | Substituirani kinazolinski derivati kot inhibitorji kinaz Aurora |
| JP2003213463A (ja) | 2002-01-17 | 2003-07-30 | Sumitomo Chem Co Ltd | 金属腐食防止剤および洗浄液 |
| WO2003086394A1 (en) | 2002-04-08 | 2003-10-23 | Merck & Co., Inc. | Inhibitors of akt activity |
| US7074534B2 (en) | 2002-07-10 | 2006-07-11 | E. I. Du Pont De Nemours And Company | Polymeric charge transport compositions and electronic devices made with such compositions |
| US7825132B2 (en) | 2002-08-23 | 2010-11-02 | Novartis Vaccines And Diagnostics, Inc. | Inhibition of FGFR3 and treatment of multiple myeloma |
| JP4560483B2 (ja) | 2002-10-03 | 2010-10-13 | ターゲジェン インコーポレーティッド | 血管静態化物質およびそれらの使用法 |
| AR043059A1 (es) | 2002-11-12 | 2005-07-13 | Bayer Pharmaceuticals Corp | Derivados de indolil pirazinona utiles para el tratamiento de trastornos hiper-proliferativos |
| US7098332B2 (en) | 2002-12-20 | 2006-08-29 | Hoffmann-La Roche Inc. | 5,8-Dihydro-6H-pyrido[2,3-d]pyrimidin-7-ones |
| JP2006516561A (ja) | 2003-01-17 | 2006-07-06 | ワーナー−ランバート・カンパニー、リミテッド、ライアビリティ、カンパニー | 細胞増殖の阻害剤としての2−アミノピリジン置換ヘテロ環類 |
| WO2004098494A2 (en) | 2003-04-30 | 2004-11-18 | Cytokinetics, Inc. | Compounds, compositions, and methods |
| CN102584813B (zh) | 2003-05-14 | 2016-07-06 | Ngc药物公司 | 化合物及其在调节淀粉样蛋白β中的用途 |
| DE10323345A1 (de) | 2003-05-23 | 2004-12-16 | Zentaris Gmbh | Neue Pyridopyrazine und deren Verwendung als Kinase-Inhibitoren |
| DK1636228T3 (da) | 2003-05-23 | 2009-02-23 | Aeterna Zentaris Gmbh | Nye pyridopyraziner og deres anvendelse som kinasemodulatorer |
| WO2005007099A2 (en) | 2003-07-10 | 2005-01-27 | Imclone Systems Incorporated | Pkb inhibitors as anti-tumor agents |
| AU2004259000A1 (en) | 2003-07-21 | 2005-02-03 | Bethesda Pharmaceuticals, Inc. | Design and synthesis of optimized ligands for PPAR |
| TW200517381A (en) | 2003-08-01 | 2005-06-01 | Genelabs Tech Inc | Bicyclic heteroaryl derivatives |
| AU2004283479A1 (en) | 2003-10-17 | 2005-05-06 | 4 Aza Bioscience Nv | Heterocycle-substituted pteridine derivatives and their use in therapy |
| EP2762475A1 (en) | 2003-11-07 | 2014-08-06 | Novartis Vaccines and Diagnostics, Inc. | Pharmaceutically acceptable salts of quinolinone compounds and their medical use |
| SG150533A1 (en) | 2003-11-20 | 2009-03-30 | Janssen Pharmaceutica Nv | 6-alkenyl and 6-phenylalkyl substituted 2-quinolinones and 2- quinoxalinones as poly(adp-ribose) polymerase inhibitors |
| KR100861515B1 (ko) | 2003-11-24 | 2008-10-02 | 에프. 호프만-라 로슈 아게 | 피라졸릴 및 이미다졸릴 피리미딘 |
| AU2004303602C1 (en) * | 2003-12-23 | 2009-05-28 | Astex Therapeutics Limited | Pyrazole derivatives as protein kinase modulators |
| US7098222B2 (en) | 2004-05-12 | 2006-08-29 | Abbott Laboratories | Bicyclic-substituted amines having cyclic-substituted monocyclic substituents |
| US7205316B2 (en) | 2004-05-12 | 2007-04-17 | Abbott Laboratories | Tri- and bi-cyclic heteroaryl histamine-3 receptor ligands |
| BRPI0514691A (pt) | 2004-08-31 | 2008-06-17 | Astrazeneca Ab | composto ou um sal farmaceuticamente aceitável do mesmo, processo para preparar o mesmo, composição farmacêutica, e, uso de um composto ou um sal farmaceuticamente aceitável do mesmo |
| KR100875408B1 (ko) | 2004-10-14 | 2008-12-23 | 에프. 호프만-라 로슈 아게 | Cdk1 항증식성 활성을 갖는 1,5-나프티리딘 아졸리디논 |
| MX2007004480A (es) | 2004-10-15 | 2007-05-08 | Astrazeneca Ab | Quinoxalinas como inhibidores b raf. |
| WO2006066361A1 (en) | 2004-12-24 | 2006-06-29 | The University Of Queensland | Method of treatment or prophylaxis |
| AU2006212726C1 (en) | 2005-02-14 | 2013-05-16 | Bionomics Limited | Novel tubulin polymerisation inhibitors |
| WO2006092430A1 (de) | 2005-03-03 | 2006-09-08 | Universität des Saarlandes | Selektive hemmstoffe humaner corticoidsynthasen |
| JP2008540535A (ja) | 2005-05-12 | 2008-11-20 | メルク エンド カムパニー インコーポレーテッド | チロシンキナーゼ阻害剤 |
| CA2608362A1 (en) | 2005-05-18 | 2006-11-23 | Wyeth | 4, 6-diamino-[1,7] naphthyridine-3-carbonitrile inhibitors of tpl2 kinase and methods of making and using the same |
| GB0513692D0 (en) | 2005-07-04 | 2005-08-10 | Karobio Ab | Novel pharmaceutical compositions |
| WO2007023186A1 (en) | 2005-08-26 | 2007-03-01 | Laboratoires Serono S.A. | Pyrazine derivatives and use as pi3k inhibitors |
| CA2628039A1 (en) | 2005-11-11 | 2007-05-18 | Aeterna Zentaris Gmbh | Novel pyridopyrazines and their use as modulators of kinases |
| EP1790342A1 (de) | 2005-11-11 | 2007-05-30 | Zentaris GmbH | Pyridopyrazin-Derivate und deren Verwendung als Modulatoren der Signaltransduktionswege |
| US8217042B2 (en) | 2005-11-11 | 2012-07-10 | Zentaris Gmbh | Pyridopyrazines and their use as modulators of kinases |
| DK1966214T3 (en) | 2005-12-21 | 2017-02-13 | Janssen Pharmaceutica Nv | TRIAZOLPYRIDAZINES AS TYROSINKINASA MODULATORS |
| US7998978B2 (en) | 2006-05-01 | 2011-08-16 | Pfizer Inc. | Substituted 2-amino-fused heterocyclic compounds |
| GB0609621D0 (en) | 2006-05-16 | 2006-06-21 | Astrazeneca Ab | Novel co-crystal |
| ATE549338T1 (de) | 2006-05-24 | 2012-03-15 | Boehringer Ingelheim Int | Substituierte pteridine, die mit einem viergliedrigen heterocyclus substituiert sind |
| TWI398252B (zh) | 2006-05-26 | 2013-06-11 | Novartis Ag | 吡咯并嘧啶化合物及其用途 |
| US20100016293A1 (en) | 2006-07-03 | 2010-01-21 | Rogier Adriaan Smits | Quinazolines and Related Heterocyclic Compounds, and Their Therapeutic Use |
| CN101600714B (zh) | 2006-11-10 | 2013-08-21 | 百时美施贵宝公司 | 吡咯并吡啶激酶抑制剂 |
| JP2008127446A (ja) | 2006-11-20 | 2008-06-05 | Canon Inc | 1,5−ナフチリジン化合物及び有機発光素子 |
| MX2009006466A (es) | 2006-12-13 | 2009-06-26 | Schering Corp | Metodos de tratamiento de cancer con inhibidores del receptor del factor 1 de crecimiento similar a la insulina. |
| RU2009122670A (ru) | 2006-12-21 | 2011-01-27 | Плекссикон, Инк. (Us) | Соединения и способы для модуляции киназ и показания к их применению |
| US20100216767A1 (en) | 2006-12-22 | 2010-08-26 | Mina Aikawa | Quinazolines for pdk1 inhibition |
| HRP20150642T1 (hr) * | 2006-12-22 | 2015-08-14 | Astex Therapeutics Limited | BICIKLIÄŚKE HETEROCIKLIÄŚKE TVARI KAO INHIBITORI FGFR-a |
| KR20080062876A (ko) | 2006-12-29 | 2008-07-03 | 주식회사 대웅제약 | 신규한 항진균성 트리아졸 유도체 |
| EP2150255A4 (en) * | 2007-05-10 | 2011-10-05 | Glaxosmithkline Llc | CHINOXALINE DERIVATIVES AS P13 KINASE INHIBITORS |
| EP1990342A1 (en) | 2007-05-10 | 2008-11-12 | AEterna Zentaris GmbH | Pyridopyrazine Derivatives, Process of Manufacturing and Uses thereof |
| WO2008150827A1 (en) | 2007-05-29 | 2008-12-11 | Smithkline Beecham Corporation | Naphthyridine, derivatives as p13 kinase inhibitors |
| AR066879A1 (es) | 2007-06-08 | 2009-09-16 | Novartis Ag | Derivados de quinoxalina como inhibidores de la actividad de cinasa de tirosina de las cinasas janus |
| BRPI0813105A2 (pt) | 2007-06-20 | 2015-08-04 | Mitsubishi Tanabe Pharma Corp | Derivado de sulfonamida de ácido malônico e uso faramacêutico do mesmo |
| WO2008155378A1 (en) | 2007-06-21 | 2008-12-24 | Janssen Pharmaceutica Nv | Polymorphic and hydrate forms, salts and process for preparing 6-{difluoro[6-(1-methyl-1h-pyrazol-4-yl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}quinoline |
| US20090263397A1 (en) | 2007-07-06 | 2009-10-22 | Buck Elizabeth A | Combination anti-cancer therapy |
| CN101827848B (zh) | 2007-08-08 | 2012-11-07 | 葛兰素史密丝克莱恩有限责任公司 | 作为IGF-1R抑制剂用于治疗癌症的2-[(2-{苯基氨基}-1H-吡咯并[2,3-d]嘧啶-4-基)氨基]苯甲酰胺衍生物 |
| WO2009021083A1 (en) | 2007-08-09 | 2009-02-12 | Smithkline Beecham Corporation | Quinoxaline derivatives as pi3 kinase inhibitors |
| WO2009019518A1 (en) | 2007-08-09 | 2009-02-12 | Astrazeneca Ab | Pyrimidine compounds having a fgfr inhibitory effect |
| US20090054304A1 (en) | 2007-08-23 | 2009-02-26 | Kalypsys, Inc. | Heterocyclic modulators of tgr5 for treatment of disease |
| WO2009064835A1 (en) * | 2007-11-16 | 2009-05-22 | Incyte Corporation | 4-pyrazolyl-n-arylpyrimidin-2-amines and 4-pyrazolyl-n-heteroarylpyrimidin-2-amines as janus kinase inhibitors |
| US20110129456A1 (en) | 2008-05-05 | 2011-06-02 | Yaolin Wang | Sequential Administration of Chemotherapeutic Agents for Treatment of Cancer |
| BRPI0913031A2 (pt) | 2008-05-23 | 2019-11-26 | Novartis Ag | derivados de quinolina e quinoxalinas como inibidores de proteína tirosina quinase, seus usos e processo de fabricação, bem como composições farmacêuticas e combinação que os compreende |
| US8592448B2 (en) | 2008-11-20 | 2013-11-26 | OSI Pharmaceuticals, LLC | Substituted pyrrolo[2,3-b]-pyridines and -pyrazines |
| JP5662346B2 (ja) | 2009-01-21 | 2015-01-28 | バジリア ファルマスーチカ アーゲーBasilea Pharmaceutica AG | 新規二環式抗生物質 |
| CA2750051A1 (en) | 2009-02-02 | 2010-08-05 | Merck Sharp & Dohme Corp. | Inhibitors of akt activity |
| TW201041888A (en) | 2009-05-06 | 2010-12-01 | Plexxikon Inc | Compounds and methods for kinase modulation, and indications therefor |
| DK3517534T3 (da) | 2009-06-12 | 2024-05-27 | Abivax | Forbindelser, der er anvendelige til behandling af cancer |
| BR112012004533B1 (pt) | 2009-09-03 | 2021-11-09 | Bioenergenix | Composto, composição farmacêutica, e uso do composto |
| CA2772790C (en) | 2009-09-04 | 2017-06-27 | Benjamin Bader | Substituted aminoquinoxalines as tyrosine threonine kinase inhibitors |
| US20110123545A1 (en) | 2009-11-24 | 2011-05-26 | Bristol-Myers Squibb Company | Combination of vegfr2 and igf1r inhibitors for the treatment of proliferative diseases |
| EP2332939A1 (en) | 2009-11-26 | 2011-06-15 | Æterna Zentaris GmbH | Novel Naphthyridine derivatives and the use thereof as kinase inhibitors |
| CN110269856A (zh) | 2010-03-30 | 2019-09-24 | 维颂公司 | 多取代芳族化合物作为凝血酶的抑制剂 |
| GB201007286D0 (en) | 2010-04-30 | 2010-06-16 | Astex Therapeutics Ltd | New compounds |
| WO2011146591A1 (en) | 2010-05-19 | 2011-11-24 | Millennium Pharmaceuticals, Inc. | Substituted hydroxamic acids and uses thereof |
| WO2011149937A1 (en) | 2010-05-24 | 2011-12-01 | Intellikine, Inc. | Heterocyclic compounds and uses thereof |
| GB201020179D0 (en) | 2010-11-29 | 2011-01-12 | Astex Therapeutics Ltd | New compounds |
| CN102532141A (zh) | 2010-12-08 | 2012-07-04 | 中国科学院上海药物研究所 | [1,2,4]三唑并[4,3-b][1,2,4]三嗪类化合物、其制备方法和用途 |
| PT2670753T (pt) | 2011-01-31 | 2017-01-10 | Novartis Ag | Novos derivados heterocíclicos |
| WO2012106556A2 (en) | 2011-02-02 | 2012-08-09 | Amgen Inc. | Methods and compositons relating to inhibition of igf-1r |
| JP6130305B2 (ja) | 2011-02-23 | 2017-05-17 | インテリカイン, エルエルシー | キナーゼ阻害剤の組み合わせおよびそれらの使用 |
| WO2012118492A1 (en) | 2011-03-01 | 2012-09-07 | Array Biopharma Inc. | Heterocyclic sulfonamides as raf inhibitors |
| EP2702173A1 (en) | 2011-04-25 | 2014-03-05 | OSI Pharmaceuticals, LLC | Use of emt gene signatures in cancer drug discovery, diagnostics, and treatment |
| CA2846574C (en) | 2011-08-26 | 2020-07-07 | Neupharma, Inc. | Quinoxaline sulfonamide derivates for use as kinase inhibitors |
| CN115403531A (zh) | 2011-09-14 | 2022-11-29 | 润新生物公司 | 作为激酶抑制剂的化学实体、组合物及方法 |
| EP2757885B1 (en) | 2011-09-21 | 2017-03-15 | Neupharma, Inc. | Certain chemical entites, compositions, and methods |
| WO2013052699A2 (en) | 2011-10-04 | 2013-04-11 | Gilead Calistoga Llc | Novel quinoxaline inhibitors of pi3k |
| GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201118654D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| PT2771342T (pt) | 2011-10-28 | 2016-08-17 | Novartis Ag | Derivados de purina e o seu uso no tratamento de doença |
| GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
| JO3210B1 (ar) | 2011-10-28 | 2018-03-08 | Merck Sharp & Dohme | مثبط منصهر لبروتين نقل الكوليسترليستير اوكسازوليدينون ثمائي الحلقة |
| MX365214B (es) | 2012-03-08 | 2019-05-27 | Astellas Pharma Inc | Nuevo producto de fusion de fgfr3. |
| GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| US20150203589A1 (en) | 2012-07-24 | 2015-07-23 | The Trustees Of Columbia University In The City Of New York | Fusion proteins and methods thereof |
| EP3939614A1 (en) | 2013-01-18 | 2022-01-19 | Foundation Medicine, Inc. | Methods of treating cholangiocarcinoma |
| GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
| HK1226058A1 (zh) | 2013-08-02 | 2017-09-22 | 亚尼塔公司 | 单独地或与其它试剂联合地使用axl/cmet抑制剂治疗多种癌症的方法 |
| US9221804B2 (en) | 2013-10-15 | 2015-12-29 | Janssen Pharmaceutica Nv | Secondary alcohol quinolinyl modulators of RORγt |
| JO3512B1 (ar) * | 2014-03-26 | 2020-07-05 | Astex Therapeutics Ltd | مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز |
| HUE053653T2 (hu) | 2014-03-26 | 2021-07-28 | Astex Therapeutics Ltd | FGFR inhibitor és IGF1R inhibitor kombinációi |
| ES3014202T3 (en) | 2014-03-26 | 2025-04-21 | Astex Therapeutics Ltd | Cmet-inhibitors for use in delaying the emergence in resistance to fgfr inhibitors |
| JOP20200201A1 (ar) | 2015-02-10 | 2017-06-16 | Astex Therapeutics Ltd | تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين |
| US20160243228A1 (en) | 2015-02-19 | 2016-08-25 | Bioclin Therapeutics, Inc. | Methods, compositions, and kits for treatment of cancer |
| US10478494B2 (en) | 2015-04-03 | 2019-11-19 | Astex Therapeutics Ltd | FGFR/PD-1 combination therapy for the treatment of cancer |
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