AR073700A1 - Heterociclos y composiciones farmaceuticas para usarse en el tratamiento de cancer, infecciones y enfermedades autoinmunitarias - Google Patents
Heterociclos y composiciones farmaceuticas para usarse en el tratamiento de cancer, infecciones y enfermedades autoinmunitariasInfo
- Publication number
- AR073700A1 AR073700A1 ARP090103730A ARP090103730A AR073700A1 AR 073700 A1 AR073700 A1 AR 073700A1 AR P090103730 A ARP090103730 A AR P090103730A AR P090103730 A ARP090103730 A AR P090103730A AR 073700 A1 AR073700 A1 AR 073700A1
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- AR
- Argentina
- Prior art keywords
- nrg
- nrgc
- nrgrg
- group
- org
- Prior art date
Links
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 206010028980 Neoplasm Diseases 0.000 title 1
- 230000005784 autoimmunity Effects 0.000 title 1
- 201000011510 cancer Diseases 0.000 title 1
- 208000015181 infectious disease Diseases 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 2
- 125000006555 (C3-C5) cycloalkyl group Chemical group 0.000 abstract 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- -1 C1- halogenoalkyl 6 Chemical group 0.000 abstract 1
- 230000002159 abnormal effect Effects 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 230000004663 cell proliferation Effects 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- 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
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- 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
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Transplantation (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Compuestos de la formula general (1) los cuales son adecuados para el tratamiento de enfermedades que se caracterizan por una proliferacion celular excesiva o anormal, así como su utilizacion en el caso de un tratamiento de este tipo. Reivindicacion 1: Compuestos caracterizados porque tienen la formula general (1) en donde R1 es un heteroarilo monocíclico de 5 o 6 eslabones sustituido eventualmente con una o varios Rb y/o Rc iguales o diferentes, o un heteroarilo bicíclico de 9 a 10 eslabones con la estructura parcial (2) en donde el anillo que se une inmediatamente a Q, es heteroaromático; R2 es un radical eventualmente sustituido con uno o varios Rb y/o Rc iguales o diferentes, seleccionado del grupo constituido por arilo C6-10 y heteroarilo de 5-12 eslabones; R3 se selecciona del grupo constituido por hidrogeno, -CN, -NO2, -NH2, -NH(alquiloC1-4), -N(alquiloC1-4)2, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, cicloalquiloC3-5 y halogeno; X1, X2 y X3 en cada caso independientemente entre sí, se eligen del grupo constituido por nitrogeno y CR4, en donde al menos uno o máximo dos de los átomos X1, X2 y X3 en el anillo A son átomos de nitrogeno y cada R4 en cada caso independientemente entre si se selecciona del grupo constituido por hidrogeno, -CN, -NO2, -NH2, -NH(alquiloC1-4), -N(alquiloC1-4)2, alquilo C1-4, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, cicloalquiloC3-5 y halogeno; Q se selecciona del grupo constituido por el grupo de formulas (3), en donde en los heteroarilos con cinco anillos anteriormente descritos uno hasta tres átomos de hidrogeno de los anillos, en cada caso independientemente entre sí, pueden estar sustituidos con alquilo C1-6; L1 se selecciona del grupo constituido por (R2)-C(O)NH- y (R2)-NHC(O)-; cada Rb es un sustituyente adecuado, seleccionada en cada caso independientemente entre sí del grupo constituido por -ORc, -SRc, -NRcRc, -ONRcRc, -N(ORc)Rc, -NRgNRcRc, halogeno, -CN, -NO2, -N3, -C(O)Rc, -C(O)ORc, -C(O)NRcRc, -C(O)NRgNRcRc, -C(O)NRgORc, -C(NRg)Rc, -N=CRcRc, -C(NRg)ORc, -C(NRg)NRcRc, -C(NRg)NRgNRcRc, -C(NORg)Rc, -C(NORg)NRcRc, -C(NNRgRg)Rc, -OS(O)Rc, -OS(O)ORc, -OS(O)NRcRc, -OS(O)2Rc, -OS(O)2ORc, -OS(O)2NRcRc, -OC(O)Rc, -OC(O)ORc, -OC(O)NRcRc, -OC(NRg)Rc, -OC(NRg)NRcRc, -ONRgC(O)Rc, -S(O)Rc, -S(O)ORc, -S(O)NRcRc, -S(O)2Rc, -S(O)2ORc, -S(O)2NRcRc, -NRgC(O)Rc, -NRgC(O)ORc, -NRgC(O)NRcRc, -NRgC(O)NRgNRcRc, -NRgC(NRg)Rc, -N=CRcNRcRc, -NRgC(NRg)ORc, -NRgC(NRg)NRcRc, NRgC(NORg)Rc, -NRgS(O)Rc, -NRgS(O)ORc, -NRgS(O)2Rc, -NRgS(O)2ORc, -NRgS(O)2NRcRc, -NRgNRgC(O)Rc, -NRgNRgC(O)NRcRc, -NRgNRgC(NRg)Rc y -N(ORg)C(O)Rc, así como por los sustituyentes bivalentes =O, =S, =NRg, =NORg, y =NNRgRg y =NNRgC(O)NRgRg, en donde estos sustituyentes bivalentes solo pueden ser sustituyentes en sistemas anulares no aromáticos; cada Rc es, en cada caso de manera independiente entre si, hidrogeno o un radical eventualmente sustituido con uno o varios Rd y/o Re iguales o diferentes, seleccionado del grupo constituido por alquilo C1-6, heteroalquilo de 2-6 eslabones, halogenoalquilo C1-6, cicloalquilo C3-10, arilo C6-10, heteroarilo de 5-12 eslabones y heterocicloalquilo de 3-14 eslabones: cada Rd es un sustituyente adecuado seleccionado independientemente entre si del grupo constituido por -ORe, -SRe, -NReRe, -ONReRe, -N(ORe)Re, -NRgNReRe, halogeno, -CN, -NO2, -N3, -C(O)Re, -C(O)ORe, -C(O)NReRe, -C(O)NRgNReRe, -C(O)NRgORe, -C(NRg)Re, -N=CReRe, -C(NRg)ORe, -C(NRg)NReRe, -C(NRg)NRgNReRe, -C(NORg)Re, -C(NORg)NReRe, -C(NNRgRg)Re, -OS(O)Re, -OS(O)ORe, -OS(O)NReRe, -OS(O)2Re, -OS(O)2ORe, -OS(O)2NReRe, -OC(O)Re, -OC(O)ORe, -OC(O)NReRe, -OC(NRg)Re, -OC(NRg)NReRe, -ONRgC(O)Re, -S(O)Re, -S(O)ORe, -S(O)NReRe, -S(O)2Re, -S(O)2ORe, -S(O)2NReRe, -NRgC(O)Re, -NRgC(O)ORe, -NRgC(O)NReRe, -NRgC(O)NRgNReRe, -NRgC(NRg)Re, -N=CReNReRe, -NRgC(NRg)ORe, -NRgC(NRg)NReRe, -NRgC(NRg)SRe, -NRgC(NORg)Re, -NRgS(O)Re, -NRgS(O)ORe, -NRgS(O)2Re, -NRgS(O)2ORe, -NRgS(O)2NReRe, -NRgNRgC(O)Re, -NRgNRgC(O)NReRe, -NRgNRgC(NRg)Re y -N(ORg)C(O)Re, así como por los sustituyentes bivalentes =O, =S, =NRg, =NORg, y =NNRgRg y =NNRgC(O)NRgRg, en donde estos sustituyentes bivalentes solo pueden ser sustituyentes en sistemas anulares no aromáticos; cada Re es, en cada caso independientemente entre si, hidrogeno o un radical eventualmente sustituido con uno o varios Rf y/o Rg iguales o diferentes, seleccionado del grupo constituido por alquilo C1-6, heteroalquilo de 2-6 eslabones, halogenoalquilo C1-6, cicloalquilo C3-10, arilo C6-10, heteroarilo de 5-12 eslabones y heterocicloalquilo de 3-14 eslabones; cada Rf es un sustituyente adecuado seleccionado independientemente entre si del grupo constituido por -ORg, -SRg, -NRgRg, -ONRgRg, -N(ORg)Rg, -N(Rh)NRgRg, halogeno, -CN, -NO2, -N3, -C(O)Rg, -C(O)ORg, -C(O)NRgRg, -C(O)NRhNRgRg, -C(O)NRhORg, -C(NRh)Rg, -N=CRgRg, -C(NRh)ORg, -C(NRh)NRgRg, -C(NRh)NRhNRgRg, -C(NORh)Rg, -C(NORh)NRgRg, -C(NNRhRh)Rg, -OS(O)Rg, -OS(O)ORg, -OS(O)NRgRg, -OS(O)2Rg, -OS(O)2ORg, -OS(O)2NRgRg, -OC(O)Rg, -OC(O)ORg, -OC(O)NRgRg, -OC(NRh)Rg, -OC(NRh)NRgRg, -ONRhC(O)Rg, -S(O)Rg, -S(O)ORg, -S(O)NRgRg, -S(O)2Rg, -S(O)2ORg, -S(O)2NRgRg, -NRhC(O)Rg, -NRhC(O)ORg, -NRhC(O)NRgRg, -NRhC(O)NRhNRgRg, -NRhC(NRh)Rg, -N=CRgNRgRg, -NRhC(NRh)ORg, -NRhC(NRh)NRgRg, -NRhC(NORh)Rg, -NRhS(O)Rg, -NRhS(O)ORg, -NRhS(O)2Rg, -NRhS(O)2ORg, -NRhS(O)2NRgRg, -NRhNRhC(O)Rg, -NRhNRhC(O)NRgRg, -NRhNRhC(NRh)Rg y -N(ORh)C(O)Rg, así como por los sustituyentes bivalentes =O, =S, =NRh, =NORh, y =NNRhRh y =NNRhC(O)NRhRh, en donde estos sustituyentes bivalentes solo pueden ser sustituyentes en sistemas anulares no aromáticos; cada R9 es, en cada caso independientemente entre sí, hidrogeno o un radical eventualmente sustituido con uno o varios Rh iguales o diferentes, seleccionado del grupo constituido por alquilo C1-6, heteroalquilo de 2-6 eslabones, halogenoalquilo C1-6, cicloalquilo C3-10, arilo C6-10, heteroarilo de 5-12 eslabones y heterocicloalquilo de 3-14 eslabones; cada Rh, en cada caso independientemente entre sí, se selecciona del grupo constituido por hidrogeno, alquilo C1-6, heteroalquilo de 2-6 eslabones, halogenoalquilo C1-6, cicloalquilo C3-10, arilo C6-10, heteroarilo de 5-12 eslabones y heterocicloalquilo de 3-14 eslabones en donde los compuestos (1) también se presentan eventualmente en forma de sus tautomeros, sus racematos, sus enantiomeros, sus diastereomeros y sus mezclas o también en forma de sales correspondientes farmacologicamente inocuas de todas las formas antes mencionadas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08165437 | 2008-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR073700A1 true AR073700A1 (es) | 2010-11-24 |
Family
ID=40019293
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090103730A AR073700A1 (es) | 2008-09-29 | 2009-09-28 | Heterociclos y composiciones farmaceuticas para usarse en el tratamiento de cancer, infecciones y enfermedades autoinmunitarias |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US8778929B2 (es) |
| EP (1) | EP2350052B1 (es) |
| JP (1) | JP5603869B2 (es) |
| KR (1) | KR20110063574A (es) |
| CN (1) | CN102227421A (es) |
| AR (1) | AR073700A1 (es) |
| AU (1) | AU2009295855A1 (es) |
| BR (1) | BRPI0920608A2 (es) |
| CA (1) | CA2738448A1 (es) |
| CL (1) | CL2011000691A1 (es) |
| CO (1) | CO6351739A2 (es) |
| EA (1) | EA201100564A1 (es) |
| EC (1) | ECSP11010930A (es) |
| IL (1) | IL211744A0 (es) |
| MA (1) | MA32656B1 (es) |
| MX (1) | MX2011003292A (es) |
| PE (1) | PE20110294A1 (es) |
| TW (1) | TW201018670A (es) |
| UY (1) | UY32146A (es) |
| WO (1) | WO2010034838A2 (es) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CL2008001943A1 (es) * | 2007-07-02 | 2009-09-11 | Boehringer Ingelheim Int | Compuestos derivados de fenil-triazol, inhibidores de enzimas de señales especificas que participan del control de la proliferacion celular; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar cancer, infecciones, enfermedades inflamatorias y autoinmunes. |
| TW201014860A (en) | 2008-09-08 | 2010-04-16 | Boehringer Ingelheim Int | New chemical compounds |
| PE20110294A1 (es) | 2008-09-29 | 2011-05-26 | Boehringer Ingelheim Int | Compuestos heterociclicos como inhibidores de enzimas de senal especifica |
| CA2752265A1 (en) | 2009-02-17 | 2010-08-26 | Boehringer Ingelheim International Gmbh | Pyrimido [5,4-d] pyrimidine derivatives for the inhibition of tyrosine kinases |
| JP2011057661A (ja) * | 2009-08-14 | 2011-03-24 | Bayer Cropscience Ag | 殺虫性カルボキサミド類 |
| AR077975A1 (es) | 2009-08-28 | 2011-10-05 | Irm Llc | Derivados de pirazol pirimidina y composiciones como inhibidores de cinasa de proteina |
| US8865703B2 (en) | 2010-03-26 | 2014-10-21 | Boehringer Ingelheim International Gmbh | Pyridyltriazoles |
| EP2552905B1 (en) | 2010-03-26 | 2016-10-05 | Boehringer Ingelheim International GmbH | B-Raf kinase inhibitors |
| US8710055B2 (en) | 2010-12-21 | 2014-04-29 | Boehringer Ingelheim International Gmbh | Triazolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| US8889684B2 (en) | 2011-02-02 | 2014-11-18 | Boehringer Ingelheim International Gmbh | Azaindolylphenyl sulfonamides as serine/threonine kinase inhibitors |
| US9056867B2 (en) | 2011-09-16 | 2015-06-16 | Novartis Ag | N-substituted heterocyclyl carboxamides |
| MX354725B (es) | 2011-11-11 | 2018-03-16 | Novartis Ag | Metodo de tratamiento de una enfermedad proliferativa. |
| SG11201401260QA (en) | 2011-11-23 | 2014-07-30 | Novartis Ag | Pharmaceutical formulations |
| CA2769821C (en) | 2012-02-28 | 2020-08-11 | Michael Hatzinikolas | Self-releasing structural assembly |
| WO2013171641A1 (en) | 2012-05-15 | 2013-11-21 | Novartis Ag | Compounds and compositions for inhibiting the activity of abl1, abl2 and bcr-abl1 |
| ES2665539T3 (es) | 2012-05-15 | 2018-04-26 | Novartis Ag | Derivados de benzamida para inhibir la actividad de ABL1, ABL2 y BCR-ABL1 |
| AP3613A (en) | 2012-05-15 | 2016-02-29 | Novartis Ag | Benzamide derivatives for inhibiting the activity of abl1, abl2 and bcr-abl1 abl1abl2 bcr-abl1 |
| JP6078640B2 (ja) | 2012-05-15 | 2017-02-08 | ノバルティス アーゲー | Abl1、abl2およびbcr−abl1の活性を阻害するためのベンズアミド誘導体 |
| WO2017007755A1 (en) | 2015-07-06 | 2017-01-12 | Rodin Therapeutics, Inc. | Heterobicyclic n-aminophenyl-amides as inhibitors of histone deacetylase |
| JP6936796B2 (ja) | 2015-07-06 | 2021-09-22 | ロダン・セラピューティクス,インコーポレーテッド | ヒストンデアセチラーゼのヘテロハロ阻害剤 |
| WO2017069226A1 (ja) * | 2015-10-23 | 2017-04-27 | 田辺三菱製薬株式会社 | 新規含窒素芳香族複素環化合物 |
| CN106316864A (zh) * | 2016-08-22 | 2017-01-11 | 苏州天马精细化学品股份有限公司 | 4‑甲基‑3‑三氟甲基苯胺的制备方法 |
| AU2018207402B2 (en) | 2017-01-11 | 2023-09-28 | Alkermes, Inc. | Bicyclic inhibitors of histone deacetylase |
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| WO2010034838A2 (en) | 2010-04-01 |
| JP5603869B2 (ja) | 2014-10-08 |
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| MX2011003292A (es) | 2011-04-21 |
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| US8778929B2 (en) | 2014-07-15 |
| EP2350052A2 (en) | 2011-08-03 |
| CA2738448A1 (en) | 2010-04-01 |
| AU2009295855A1 (en) | 2010-04-01 |
| TW201018670A (en) | 2010-05-16 |
| CL2011000691A1 (es) | 2011-07-29 |
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| EP2350052B1 (en) | 2014-08-13 |
| UY32146A (es) | 2010-04-30 |
| ECSP11010930A (es) | 2011-04-29 |
| KR20110063574A (ko) | 2011-06-10 |
| US20110312939A1 (en) | 2011-12-22 |
| JP2012504114A (ja) | 2012-02-16 |
| BRPI0920608A2 (pt) | 2019-09-24 |
| PE20110294A1 (es) | 2011-05-26 |
| IL211744A0 (en) | 2011-06-30 |
| CN102227421A (zh) | 2011-10-26 |
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