AR056891A1 - Derivados policiclicos de indazol que son inhibidores de erk - Google Patents
Derivados policiclicos de indazol que son inhibidores de erkInfo
- Publication number
- AR056891A1 AR056891A1 ARP060105474A ARP060105474A AR056891A1 AR 056891 A1 AR056891 A1 AR 056891A1 AR P060105474 A ARP060105474 A AR P060105474A AR P060105474 A ARP060105474 A AR P060105474A AR 056891 A1 AR056891 A1 AR 056891A1
- Authority
- AR
- Argentina
- Prior art keywords
- substituted
- alkyl
- group
- independently selected
- cycloalkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- C07D403/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur 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
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Se describen métodos para el tratamiento de cáncer donde se usan los compuestos de formula (1). Reivindicacion 1: Un compuesto de formula [1], o las sales farmacéuticamente aceptables de éste, donde Y1, Y2, e Y3 están cada uno independientemente seleccionado del grupo que consiste en: -CH=, -N= y -CR9=; z es 1 a 3; Q es un sustituyente seleccionado del grupo de formulas [2]; cada Q1 representa un anillo seleccionado independientemente del grupo que consiste en: cicloalquilo, cicloalquilo sustituido, heterocicloalquilo, heterocicloalquilo sustituido, arilo, arilo sustituido, heteroarilo, y heteroarilo sustituido, donde dichos anillos sustituidos están sustituidos con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste en los restos R10; con la condicion de que cuando Q1 es arilo, heteroarilo, arilo sustituido o heteroarilo sustituido entonces los átomos de carbono en la union del anillo no están sustituidos; Q2 representa un anillo seleccionado del grupo que consiste en cicloalquilo, cicloalquilo sustituido, heterocicloalquilo, y heterocicloalquilo sustituido, donde dichos anillos sustituidos están sustituidos con 1 a 3 sustituyentes independientemente seleccionados del grupo que consiste en restos R10; Z1 representa -(C(R24)2)w- donde cada R24 está independientemente seleccionado del grupo que consiste en: H, alquilo y F, y donde w es 1, 2 o 3; Z2 está seleccionado del grupo que consiste en: -N(R44)-, -O- y -C(R46)2-; m es 1 a 6; n es 1 a 6; p es 0 a 6; t es 0, 1 o 2; R1 está seleccionado del grupo que consiste en (1) -CN, (2) -NO2, (3) -OR10, (4) -SR10, (5) -N(R10)2, (6) R10, (7) -C(O)R10, (8) -(C(R30)2)n-NR32-C(O)-R10, (9) -(C(R30)2)n-NR32-S(O)t-R10, (10) -(C(R30)2)n-NR32-C(O)-N(R32)- R10, (11) un resto de formula [3], (12) -CF3, (13) -C(O)OR10, (14) -(C(R30)2)nR13 (por ejemplo, -(CH2)nR13), (15) alquenilo, (16) -NR32-C(O)-R14, (17) -N(R10)-C(:O)-N(R10)2, donde cada R10 está seleccionado independientemente, (18) -N(R10)-S(O)t- R10, donde cada R10 está seleccionado independientemente, (19) -C(=NH)-N(R32)-R15, (20) -C(O)-NR32-(C(R30)2)p-OR10, (21) -C(O)N(R10)2 donde cada R10 está seleccionado independientemente, (22) -C(O)-NR32-C(R18)3, (23) -C(O)-NR32-(C(R30)2)n-C(O)- N(R10)2, (24) heterocicloalquenilo, (25) un resto formula [4], y (26) arilalquenil-; R2 está seleccionado del grupo que consiste en (1) H, (2) -CN, (3) halo, (4) alquilo, (5) alquilo sustituido donde cada alquilo sustituido está sustituido con 1 a 3 sustituyentes seleccionados del grupo que consiste en: (a) -OH, (b) -O-alquilo (por ejemplo, -O-(alquilo C1-3), (c) -O-alquilo sustituido con 1 a 3 átomos de F, y (d) -N(R40)2 donde cada R40 está independientemente seleccionado del grupo que consiste en: (i) H, (ii) C1-3 alquilo, (iii) -CF3, y (e) halo, (6) alquinilo, (7) alquenilo, (8) -(CH2)mR11, (9) -N(R26)2, (10) -OR23, (11) -N(R26)C(O)R42, (12) cicloalquilo, (13) cicloalquilalquilo, (14) un resto de formula [5], (15) -O-(alquilo sustituido) donde cada alquilo sustituido está sustituido con 1 a 3 átomos de F, (16) -S(O)talquilo, (17) -C(O)-alquilo, (18) -C(=N-O-H)-alquilo, (19) -C(=N-O-alquilo)alquilo, donde cada alquilo está seleccionado independientemente, (20) un resto de formula [6] donde cada alquilo está seleccionado independientemente, (21) un resto de formula [7] donde cada alquilo está seleccionado independientemente, (22) -N(R48)-C(O)-R48 donde cada R48 está independientemente seleccionado del grupo que consiste en H y alquilo, y (23) -C(O)-alquilo, tal como, por ejemplo, -C(O)-(alquilo C1-6), tal como, por ejemplo, -C(O)CH3; donde cada R3, R4, R5, R6 y R7 está independientemente seleccionado del grupo que consiste en (1) H, (2) alquenilo, (3) alquenilo sustituido, (4) alquilo, (5) alquilo sustituido, (6) cicloalquilo, (7) cicloalquilo sustituido, (8) cicloalquilalquil-, (9) cicloalquilalquil- sustituido, (10) heterocicloalquilo, (11) heterocicloalquilo sustituido, (12) heterocicloalquilalquil-, (13) heterocicloalquilalquil- sustituido, (14) -C(O)R10, (15) arilheteroaril-, (16) arilheteroaril- sustituido, (17) heteroarilaril-, (18) heteroarilaril- sustituido, (19) arilo, (20) arilo sustituido, (21) heteroarilo, (22) heteroarilo sustituido, (23) heteroarilheteroaril-, (24) heteroarilheteroaril- sustituido, (25) arilaminoheteroaril-, (26) arilaminoheteroaril- sustituido, (27) arilalquinil-, (28) arilalquinil- sustituido, (29) heteroarilalquinil-, (30) heteroarilalquinil- sustituido, donde dichos grupos R3, R4, R5, R6 y R7 sustituidos (7), (9), (11), (13), (16), (18), (20), (22), (24), (26), (28) y (30) están sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: -NH2, alquilo, alquenilo, halo, -C(O)-NH-R28, -C(O)OR28, y -C(O)R28, y donde dichos grupos R3, R4, R5, R6 y R7 sustituidos (3) y (5) están sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: - NH2, halo (por ejemplo, F, CI y Br, y en otro ejemplo F), -C(O)NH-R28 (por ejemplo, -C(O)-NH-CH3), -C(O)OR28 (por ejemplo, -C(O)OC2H5), y -C(O)R28 (por ejemplo, -C(O)CH3); R5A está seleccionado del grupo que consiste en: halo, -OH, y -O-alquilo; R8 está seleccionado del grupo que consiste en: H, -OH, -N(R10)2, -NR10C(O)R12, y alquilo; cada R9 está independientemente seleccionado del grupo que consiste en halogeno, -CN, -NO2, -OR10, -SR10, -N(R10)2, y R10, cada R10 está independientemente seleccionado del grupo que consiste en H, alquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, alquilheteroaril-, alquilaril-, alquilo sustituido, arilo sustituido, arilalquilo sustituido, heteroarilo sustituido, heteroarilalquilo sustituido, cicloalquilo sustituido, cicloalquilalquilo sustituido, heterocicloalquilo sustituido, heterocicloalquilalquilo sustituido, alquilheteroaril- sustituido, alquilaril- sustituido, heterocicloalquenilo, y heterocicloalquenilo sustituido, y donde dicho alquilo sustituido R10 está sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: -NH2, -NHR20, -NO2, -CN, -OR26, halo, -C(O)-NH-R26, -C(O)OR26, y -C(O)R26, y dicho arilo sustituido, arilalquilo sustituido, heteroarilo sustituido, heteroarilalquilo sustituido, cicloalquilo sustituido, cicloalquilalquilo sustituido, heterocicloalquilo sustituido, heterocicloalquilalquilo sustituido, alquilheteroarilsustituido y alquilaril- sustituido R10 están sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: (1) -NH2, (2) -NO2, (3) -CN, (4) -OH, (5) -OR20, (6) - OCF3, (7) alquilo sustituido con 1 a 3 átomos de halo seleccionados independientemente, (8) -C(O)R38, (9) alquilo, (10) alquenilo, (11) halo, (12) -C(O)-NH-R26, (13) -C(O)OR38, (14) -C(O)-NR32-(C(R30)2)n-N(R38)2, (15) -S(O)tR38, (16) -C(O)-NR32-R38, (17) -NR32-C(O)-R38, (18) -C(=N)-NR32R38, (19) -NHR20, y (20) cicloalquilo; R11 está seleccionado del grupo que consiste en: F, -OH, -CN, -OR10, -NHNR1R10, -SR10 y heteroarilo; R12 está seleccionado del grupo que consiste en: alquilo, arilo, heteroarilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo y heterocicloalquilalquilo; R14 está seleccionado del grupo que consiste en: alquilo, arilo, heteroarilo, cicloalquilo, cicloalquilalquil-, heterocicloalquilo, alquilheterocicloalquilo, heterocicloalquilalquil-, alquilheteroaril- y alquilaril-; R15 está seleccionado del grupo que consiste en: H, -OH, alquilo, arilo, heteroarilo, cicloalquilo, cicloalquilalquil-, heterocicloalquilo y heterocicloalquilalquil- , alquilheteroaril- y alquilaril-; R20 representa alquilo; R23 está seleccionado del grupo que consiste en H, alquilo, arilo, cicloalquilo, y cicloalquilalquil-; cada R26 está independientemente seleccionado del grupo que consiste en H y alquilo; R28 es alquilo; cada R30 está independientemente seleccionado del grupo que consiste en H, alquilo, y F; cada R32 está independientemente seleccionado del grupo que consiste en H y alquilo, y donde cada R32 es general H; cada R35 está independientemente seleccionado del grupo que consiste en H y alquilo C1-6; R36 está seleccionado del grupo que consiste en: H, alquilo, y -O-alquilo; cada R38 está independientemente seleccionado del grupo que consiste en H, alquilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, cicloalquilo, cicloalquilalquilo, heterocicloalquilo, heterocicloalquilalquilo, alquilheteroaril-, alquilaril, alquilo sustituido, arilo sustituido, arilalquilo sustituido, heteroarilo sustituido, heteroarilalquilo sustituido, cicloalquilo sustituido, cicloalquilalquilo sustituido, heterocicloalquilo sustituido, heterocicloalquilalquilo sustituido, alquilheteroaril- sustituido y alquilaril- sustituido, y donde dicho alquilo sustituido R38 está sustituido con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: -NH2, -NO2, -CN, -OR26, halo, -C(O)-NH-R28, -C(O)OR28, y -C(O)R28, y dichos arilo sustituido, arilalquilo sustituido, heteroarilo sustituido, heteroarilalquilo sustituido, cicloalquilo sustituido, cicloalquilalquilo sustituido, heterocicloalquilo sustituido, heterocicloalquilalquilo sustituido, alquilheteroarilsustituido y alquilaril- sustituido R38 están sustituidos con 1 a 3 sustituyentes seleccionados independientemente del grupo que consiste en: (1) -NH2, (2) -NO2, (3) -CN, (4) -OH, (5) -OR20, (6) -OCF3, (7) -CF3, (8) -C(O)R26, (9) alquilo, (10) alquenilo, (11) halo, (12) -C(O)-NH-R26, (13) -C(O)OR26, (14) -C(O)-NR32- (C(R30)2)n-N(R26)2, (15) -S(O)R26, (16) -C(O)N(R32)(R26), (17) -NR32C(O)R26, (18) -C(=N)-NR32R26, (19) -NHR20; R42 está seleccionado del grupo que consiste en: alquilo, arilo, heteroarilo, y cicloalquilo; R44 está seleccionado del grupo que consiste en: H, alquilo, cicloalquilo, y cicloalquilalquilo; y cada uno de R46 está independientemente seleccionado del grupo que consiste en: H, alquilo, cicloalquilo, y cicloalquilalquilo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US74985605P | 2005-12-13 | 2005-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR056891A1 true AR056891A1 (es) | 2007-10-31 |
Family
ID=37969564
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060105474A AR056891A1 (es) | 2005-12-13 | 2006-12-12 | Derivados policiclicos de indazol que son inhibidores de erk |
Country Status (29)
Country | Link |
---|---|
US (1) | US20070191604A1 (es) |
EP (1) | EP1966151B1 (es) |
JP (1) | JP4881957B2 (es) |
KR (1) | KR101417136B1 (es) |
CN (1) | CN101370784B (es) |
AR (1) | AR056891A1 (es) |
AT (1) | ATE527240T1 (es) |
AU (1) | AU2006326616B2 (es) |
BR (1) | BRPI0619823B8 (es) |
CA (1) | CA2633023C (es) |
CY (1) | CY1112760T1 (es) |
DK (1) | DK1966151T3 (es) |
EC (1) | ECSP088550A (es) |
ES (1) | ES2372976T3 (es) |
HK (1) | HK1114851A1 (es) |
HR (1) | HRP20110892T1 (es) |
IL (1) | IL192034A (es) |
MY (1) | MY149430A (es) |
NO (1) | NO341831B1 (es) |
NZ (1) | NZ569087A (es) |
PE (2) | PE20100562A1 (es) |
PL (1) | PL1966151T3 (es) |
PT (1) | PT1966151E (es) |
RS (1) | RS51981B (es) |
RU (1) | RU2442778C9 (es) |
SI (1) | SI1966151T1 (es) |
TW (1) | TWI344466B (es) |
WO (1) | WO2007070398A1 (es) |
ZA (1) | ZA200805525B (es) |
Families Citing this family (49)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8546404B2 (en) | 2005-12-13 | 2013-10-01 | Merck Sharp & Dohme | Compounds that are ERK inhibitors |
EP1984331B1 (en) * | 2006-02-16 | 2010-10-20 | Schering Corporation | Pyrrolidine derivatives as erk inhibitors |
EP2035416A1 (en) | 2006-06-30 | 2009-03-18 | Schering Corporation | Substituted piperidines that increase p53 activity and the uses thereof |
WO2008153858A1 (en) * | 2007-06-05 | 2008-12-18 | Schering Corporation | Polycyclic indazole derivatives and their use as erk inhibitors for the treatment of cancer |
CL2008001933A1 (es) * | 2007-06-29 | 2009-09-25 | Millennium Pharm Inc | Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros. |
EP2220503A1 (en) * | 2007-11-30 | 2010-08-25 | Schering Corporation | Braf biomarkers |
ES2556353T3 (es) * | 2008-02-21 | 2016-01-15 | Merck Sharp & Dohme Corp. | Compuestos que son inhibidores de las ERK |
AR072657A1 (es) | 2008-02-29 | 2010-09-15 | Genentech Inc | Compuestos inhibidores de raf y metodos para su uso |
US8637554B2 (en) * | 2008-05-07 | 2014-01-28 | The Trustees Of The University Of Pennsylvania | Methods for treating thyroid cancer |
US9229008B2 (en) | 2008-08-19 | 2016-01-05 | Merck Sharp & Dohme Corp. | IL-8 level as a determinant of responsivity of a cancer to treatment |
EP2316031B1 (en) * | 2008-08-19 | 2016-09-14 | Merck Sharp & Dohme Corp. | IL-8 biomarker for monitoring cancer treatment |
WO2011002887A1 (en) | 2009-07-02 | 2011-01-06 | Schering Corporation | FUSED TRICYCLIC COMPOUNDS AS NOVEL mTOR INHIBITORS |
WO2011041152A1 (en) | 2009-09-30 | 2011-04-07 | Schering Corporation | Novel compounds that are erk inhibitors |
BR112012008849A2 (pt) | 2009-10-14 | 2015-09-22 | Schering Corp | composto, composição farmacêutica, e, uso de um composto |
WO2011123937A1 (en) * | 2010-04-06 | 2011-10-13 | University Health Network | Kinase inhibitors and method of treating cancer with same |
EP2584903B1 (en) | 2010-06-24 | 2018-10-24 | Merck Sharp & Dohme Corp. | Novel heterocyclic compounds as erk inhibitors |
WO2012015932A2 (en) * | 2010-07-27 | 2012-02-02 | Protexer, Inc. | Shoe cover removal apparatus |
US8883801B2 (en) | 2010-08-23 | 2014-11-11 | Merck Sharp & Dohme Corp. | Substituted pyrazolo[1,5-a]pyrimidines as mTOR inhibitors |
WO2012030685A2 (en) | 2010-09-01 | 2012-03-08 | Schering Corporation | Indazole derivatives useful as erk inhibitors |
CA2819373A1 (en) | 2010-12-09 | 2012-06-14 | Amgen Inc. | Bicyclic compounds as pim inhibitors |
WO2012087772A1 (en) | 2010-12-21 | 2012-06-28 | Schering Corporation | Indazole derivatives useful as erk inhibitors |
US9321756B2 (en) | 2011-03-22 | 2016-04-26 | Amgen Inc. | Azole compounds as PIM inhibitors |
IN2013MN02170A (es) | 2011-04-21 | 2015-06-12 | Piramal Entpr Ltd | |
US8901142B2 (en) | 2011-07-26 | 2014-12-02 | Merck Sharp & Dohme Corp. | Fused tricyclic compounds as mTOR inhibitors |
US8987274B2 (en) | 2011-10-28 | 2015-03-24 | Merck Sharp & Dohme Corp | Macrocycles that increase p53 activity and the uses thereof |
US9062071B2 (en) | 2011-12-21 | 2015-06-23 | Merck Sharp & Dohme Corp. | Substituted piperidines as HDM2 inhibitors |
WO2013109142A1 (en) | 2012-01-16 | 2013-07-25 | Stichting Het Nederlands Kanker Instituut | Combined pdk and mapk/erk pathway inhibition in neoplasia |
ITMI20120135A1 (it) * | 2012-02-02 | 2013-08-03 | Diab Int Ab | Procedimento per la produzione di schiume di pet e schiume di pet ottenute con questo procedimento |
US20150141470A1 (en) | 2012-05-08 | 2015-05-21 | The Broad Institute, Inc. | Diagnostic and treatment methods in patients having or at risk of developing resistance to cancer therapy |
CN103450163B (zh) * | 2012-05-29 | 2017-06-23 | 中国医学科学院药物研究所 | 吲唑类化合物、其制备方法及其药物用途 |
JP6186440B2 (ja) | 2012-09-19 | 2017-08-23 | ノバルティス アーゲー | キナーゼ阻害剤としてのジヒドロピロリジノピリミジン |
JP6280554B2 (ja) * | 2012-09-28 | 2018-02-14 | メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. | Erk阻害剤である新規化合物 |
WO2014100065A1 (en) | 2012-12-20 | 2014-06-26 | Merck Sharp & Dohme Corp. | Substituted imidazopyridines as hdm2 inhibitors |
US9629851B2 (en) | 2013-09-20 | 2017-04-25 | Stitching Het Nederlands Kanker Institut—Antoni Van Leeuwenhoek Ziekenhuis | ROCK in combination with MAPK pathway |
WO2015041534A1 (en) | 2013-09-20 | 2015-03-26 | Stichting Het Nederlands Kanker Instituut | P90rsk in combination with raf/erk/mek |
SI3063143T1 (sl) | 2013-11-01 | 2018-09-28 | Novartis Ag, | Aminoheteroaril benzamidi kot inhibitorji kinaze |
US20170027940A1 (en) | 2014-04-10 | 2017-02-02 | Stichting Het Nederlands Kanker Instituut | Method for treating cancer |
WO2015178770A1 (en) | 2014-05-19 | 2015-11-26 | Stichting Het Nederlands Kanker Instituut | Compositions for cancer treatment |
WO2016095089A1 (en) * | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
WO2016095088A1 (en) * | 2014-12-15 | 2016-06-23 | Merck Sharp & Dohme Corp. | Erk inhibitors |
EP3355923B1 (en) | 2015-10-01 | 2022-02-23 | Stichting Het Nederlands Kanker Instituut- Antoni van Leeuwenhoek Ziekenhuis | Histone deacetylase inhibitors for use in the treatment of drug resistant melanoma |
EP3365334B1 (en) | 2015-10-21 | 2024-07-17 | Otsuka Pharmaceutical Co., Ltd. | Benzolactam compounds as protein kinase inhibitors |
WO2017099591A1 (en) | 2015-12-07 | 2017-06-15 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Treatment of inhibitor resistant braf-mutant cancers |
PL3426637T3 (pl) | 2016-03-11 | 2022-05-30 | Angel Pharmaceutical Co., Ltd. | Związki i sposoby modulowania kinazy tyrozynowej brutona |
WO2017204626A1 (en) | 2016-05-24 | 2017-11-30 | Stichting Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis | Combination therapy - combined map2k4/map3k1 and mek/erk inhibition |
CN109890827A (zh) * | 2016-10-05 | 2019-06-14 | 芝诺罗耶尔蒂里程碑有限责任公司 | 螺环化合物 |
GB201706327D0 (en) | 2017-04-20 | 2017-06-07 | Otsuka Pharma Co Ltd | A pharmaceutical compound |
US10508113B2 (en) | 2018-03-12 | 2019-12-17 | Abbvie Inc. | Inhibitors of tyrosine kinase 2 mediated signaling |
CN114605329B (zh) * | 2022-03-28 | 2024-01-26 | 河南中医药大学 | 取代的吲唑甲酰胺或取代的氮杂吲唑甲酰胺类flt3抑制剂及其用途 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9213077D0 (en) | 1992-06-19 | 1992-08-05 | Erba Carlo Spa | Polymerbound taxol derivatives |
NZ514583A (en) * | 2000-02-05 | 2004-05-28 | Vertex Pharma | Pyrazole compositions useful as inhibitors of ERK |
US6897231B2 (en) * | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
MY130778A (en) * | 2001-02-09 | 2007-07-31 | Vertex Pharma | Heterocyclic inhibitiors of erk2 and uses thereof |
PL374946A1 (en) * | 2002-09-05 | 2005-11-14 | Aventis Pharma S.A. | Novel aminoindazole derivatives as medicines and pharmaceutical compositions containing same |
-
2006
- 2006-12-11 PL PL06845064T patent/PL1966151T3/pl unknown
- 2006-12-11 CN CN2006800527776A patent/CN101370784B/zh active Active
- 2006-12-11 ES ES06845064T patent/ES2372976T3/es active Active
- 2006-12-11 SI SI200631221T patent/SI1966151T1/sl unknown
- 2006-12-11 MY MYPI20082076A patent/MY149430A/en unknown
- 2006-12-11 AT AT06845064T patent/ATE527240T1/de active
- 2006-12-11 JP JP2008545685A patent/JP4881957B2/ja not_active Expired - Fee Related
- 2006-12-11 BR BRPI0619823A patent/BRPI0619823B8/pt not_active IP Right Cessation
- 2006-12-11 WO PCT/US2006/046959 patent/WO2007070398A1/en active Application Filing
- 2006-12-11 US US11/636,954 patent/US20070191604A1/en not_active Abandoned
- 2006-12-11 CA CA2633023A patent/CA2633023C/en active Active
- 2006-12-11 RU RU2008128119/04A patent/RU2442778C9/ru active
- 2006-12-11 PT PT06845064T patent/PT1966151E/pt unknown
- 2006-12-11 RS RS20110516A patent/RS51981B/en unknown
- 2006-12-11 DK DK06845064.2T patent/DK1966151T3/da active
- 2006-12-11 KR KR1020087016729A patent/KR101417136B1/ko active IP Right Grant
- 2006-12-11 EP EP06845064A patent/EP1966151B1/en active Active
- 2006-12-11 AU AU2006326616A patent/AU2006326616B2/en not_active Ceased
- 2006-12-11 NZ NZ569087A patent/NZ569087A/en not_active IP Right Cessation
- 2006-12-12 PE PE2010000279A patent/PE20100562A1/es not_active Application Discontinuation
- 2006-12-12 TW TW095146375A patent/TWI344466B/zh not_active IP Right Cessation
- 2006-12-12 AR ARP060105474A patent/AR056891A1/es active IP Right Grant
- 2006-12-12 PE PE2006001592A patent/PE20071095A1/es active IP Right Grant
-
2008
- 2008-06-10 IL IL192034A patent/IL192034A/en active IP Right Grant
- 2008-06-13 EC EC2008008550A patent/ECSP088550A/es unknown
- 2008-06-24 ZA ZA200805525A patent/ZA200805525B/xx unknown
- 2008-07-11 NO NO20083114A patent/NO341831B1/no not_active IP Right Cessation
- 2008-09-12 HK HK08110160.5A patent/HK1114851A1/xx not_active IP Right Cessation
-
2011
- 2011-11-30 HR HR20110892T patent/HRP20110892T1/hr unknown
-
2012
- 2012-01-04 CY CY20121100006T patent/CY1112760T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR056891A1 (es) | Derivados policiclicos de indazol que son inhibidores de erk | |
AR068046A1 (es) | Derivados policiclicos de indazol y su uso como inhibidores de erk para el tratamiento del cancer | |
AR059493A1 (es) | Compuestos inhibidores de erk | |
CO5680430A2 (es) | Derivados de 1-benzol-piperazina como inhibidores de la captacion de glicina para el ratamiento de psicosis | |
AR034390A1 (es) | Derivados de 1-sulfonil-tetrahidro quinolinas sustituidas, composiciones farmaceuticas y el uso de las mismas para la elaboracion de medicamentos como inhibidores de la gama secretasa | |
CO6190525A2 (es) | Fosfoindoles enantiomericamente puros como inhibidores de vih | |
AR051342A1 (es) | Derivados de purina, purinona, deazapurina y deazapurinona como inhibidores de la actividad de la protein quinasa; metodos para su preparacion, composiciones farmaceuticas que los contienen y su uso en la elaboracion de un medicamento para el tratamiento de enfermedades mediadas por la protein quina | |
AR047969A1 (es) | Pirazolotriazinas como inhibidores de quinasa | |
AR055878A1 (es) | Derivados de ciclopropanocarboxamida | |
AR109424A2 (es) | Pirimidil ciclopentanos hidroxilados y metoxilados como inhibidores de la proteína quinasa akt | |
AR050181A1 (es) | Derivados de urea ciclicos sustituidos, su preparacion y su uso farmaceutico como inhibidores de quinasa | |
TW200800949A (en) | Macrocylic inhibitors of hepatitis C virus | |
AR083339A1 (es) | Compuestos de quinazolina como bloqueadores de los canales de sodio | |
ES2531315T3 (es) | Compuestos de fosfinato antivíricos | |
ATE463483T1 (de) | 6-substituierte isochinolinderivate als rock-1- inhibitoren | |
AR048315A1 (es) | Compuestos heterociclicos inhibidores de la produccion de citocinas; composiciones farmaceuticas que los contienen y su uso en el tratamiento de enfermedades inflamatorias y oncologicas. | |
AR049170A1 (es) | Derivados de pirimidina para el tratamiento del crecimiento celular anormal | |
AR062785A1 (es) | Compuestos de 4-metilpiridopirimidinona, composiciones farmaceuticas que los contienen y usos en estados patologicos asociados al crecimiento anormal celular,tal como cancer. | |
AR068106A1 (es) | Derivados de indol 2-carboxi sustituidos y una composicion farmaceutica | |
RU2008152087A (ru) | Макроциклические оксимильные ингибиторы протеазы гепатита | |
AR066153A1 (es) | Derivados de piperidina / piperazina | |
AR095430A1 (es) | Compuestos de pirimidina y piridina y su uso como inhibidores de la actividad de fgfr | |
AR054088A1 (es) | Triazoles como inhibidores de proteinquinasas. composiciones farmaceuticas | |
AR069804A1 (es) | Agonistas del receptor glucocorticoide c20- c21 sustituido | |
CO5580747A2 (es) | Derivados e intermediarios de n-adamantilmetilo como composiciones farmaceuticas y procesos para su preparacion |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant, registration |