AR092108A1 - Piridazina 1,4 disustituida, analogos de la misma y metodos para tratar las enfermedades relacionadas con deficiencia del smn - Google Patents

Piridazina 1,4 disustituida, analogos de la misma y metodos para tratar las enfermedades relacionadas con deficiencia del smn

Info

Publication number
AR092108A1
AR092108A1 ARP130102863A ARP130102863A AR092108A1 AR 092108 A1 AR092108 A1 AR 092108A1 AR P130102863 A ARP130102863 A AR P130102863A AR P130102863 A ARP130102863 A AR P130102863A AR 092108 A1 AR092108 A1 AR 092108A1
Authority
AR
Argentina
Prior art keywords
alkyl
substituted
independently selected
alkoxy
mono
Prior art date
Application number
ARP130102863A
Other languages
English (en)
Inventor
Noel Chin Donovan
Dales Natalie
Fazal Aleem
Brian Hurley Timothy
Kerrigan John
Obrien Gary
Shu Lei
Sung Moo
Kim Cheung Atwood
Sun Robert
Original Assignee
Novartis Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49029227&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR092108(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of AR092108A1 publication Critical patent/AR092108A1/es

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic 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
    • A61K31/495—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
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic 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
    • A61K31/535—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
    • 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
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • 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
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/20—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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
    • C07D403/10—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 carbon chain containing aromatic 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
    • C07D403/14—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
    • 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
    • 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
    • C07D413/14—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
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/14—Ortho-condensed systems
    • 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
    • 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
    • C07D487/10—Spiro-condensed systems

Abstract

El presente proporciona una combinación de agentes farmacológicamente activos y una composición farmacéutica. Reivindicación 1: Un compuesto o sal del mismo según la fórmula (1), A es 2-hidroxi-fenilo que se sustituye por 0, 1, 2, ó 3 sustituyentes seleccionados independientemente a partir de alquilo C₁₋₄, en donde 2 grupos alquilo C₁₋₄ pueden combinarse con los átomos a los que están unidos para formar un anillo de 5 - 6 miembros y se sustituye por 0 ó 1 sustituyentes seleccionados a partir de oxo, oxima e hidroxilo, haloalquilo C₁₋₄, dihaloalquilo C₁₋₄, trihaloalquilo C₁₋₄, alcoxilo C₁₋₄, alcoxi C₁₋₄-cicloalquilo C₃₋₇, haloalcoxilo C₁₋₄, dihaloalcoxilo C₁₋₄, trihaloalcoxilo C₁₋₄, hidroxilo, ciano, halógeno, amino, mono- y di-alquil C₁₋₄amino, heteroarilo, alquilo C₁₋₄ sustituido por hidroxilo, alcoxilo C₁₋₄ sustituido por arilo, amino, -C(O)NH-alquilo C₁₋₄-heteroarilo, -NHC(O)-heteroarilo-alquilo C₁₋₄-, alquilo C₁₋₄C₍O₎NH₋ₕₑₜₑʳₒₐʳⁱₗₒ, ₐₗqᵘⁱₗₒ C₁₋₄NHC(O)-heteroarilo, cicloalquilo de 3 - 7 miembros, cicloalquenilo de 5 - 7 miembros o heterociclo de 5, 6 ó 9 miembros que contiene 1 ó 2 heteroátomos independientemente seleccionados a partir de S, O y N, en donde heteroarilo tiene 5, 6 ó 9 átomos de anillo, 1, 2 ó 3 heteroátomos de anillo seleccionados a partir de N, O y S y sustituido por 0, 1, ó 2 sustituyentes seleccionados independientemente a partir de oxo, hidroxilo, nitro, halógeno, alquilo C₁₋₄, alquenilo C₁₋₄, alcoxilo C₁₋₄, cicloalquilo C₃₋₇, alquil C₁₋₄-OH, trihaloalquilo C₁₋₄, mono- y di-alquil C₁₋₄amino, -C(O)NH₂, -NH₂, -NO₂, hidroxi-alquil C₁₋₄amino, hidroxialquilo C₁₋₄, heterocicloalquilo C₁₋₄ de 4 - 7 miembros, aminoalquilo C₁₋₄ y mono- y di-alquil C₁₋₄aminoalquilo C₁₋₄; o A es 2-naftilo opcionalmente sustituido en la posición 3 por hidroxilo y adicionalmente sustituido por 0, 1, ó 2 sustituyentes seleccionados a partir de hidroxilo, ciano, halógeno, alquilo C₁₋₄, alquenilo C₂₋₄, alcoxilo C₁₋₅, en donde el alcoxilo no es sustituido o se sustituye por hidroxilo, alcoxilo C₁₋₄, amino, N(H)C(O)alquilo C₁₋₄, N(H)C(O)₂alquilo C₁₋₄, alquileno heterociclo de 4 a 7 miembros, heterociclo de 4 a 7 miembros y mono- y di-alquil C₁₋₄amino; o A es heteroarilo de 6 miembros que tiene 1 - 3 átomos de nitrógeno de anillo, tal heteroarilo de 6 miembros es sustituido por fenilo o un heteroarilo que tiene 5 ó 6 átomos de anillo, 1 ó 2 heteroátomos de anillo seleccionados independientemente a partir de N, O y S y sustituido por 0, 1, ó 2 sustituyentes seleccionados independientemente a partir de alquilo C₁₋₄, mono- y di-alquil C₁₋₄amino, hidroxi-alquil C₁₋₄amino, hidroxialquilo C₁₋₄, aminoalquilo C₁₋₄ y mono- y di-alquil C₁₋₄amino-alquilo C₁₋₄; o A es heteroarilo bicíclico que tiene 9 a 10 átomos de anillo, y 1, 2, ó 3 heteroátomos de anillo seleccionados independientemente a partir de N, O ó S, tal heteroarilo bicíclico se sustituye por 0, 1, ó 2 sustituyentes seleccionados independientemente a partir de ciano, halógeno, hidroxilo, alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₄, alcoxilo C₁₋₄ y alcoxilo C₁₋₄ sustituido por hidroxilo, alcoxilo C₁₋₄, amino y mono- y di-alquil C₁₋₄amino; o A es heteroarilo tricíclico que tiene 12 ó 13 átomos de anillo, y 1, 2, ó 3 heteroátomos de anillo seleccionados independientemente a partir de N, O ó S, tal heteroarilo tricíclico se sustituye por 0, 1, ó 2 sustituyentes seleccionados independientemente a partir de ciano, halógeno, hidroxilo, alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₄, alcoxilo C₁₋₄, alcoxilo C₁₋₄ sustituido por hidroxilo, alcoxilo C₁₋₄, amino, mono- y di-alquil C₁₋₄amino y heteroarilo, en donde dicho heteroarilo tiene 5, 6 ó 9 átomos de anillo, 1, 2 ó 3 heteroátomos de anillo seleccionados a partir de N, O y S y sustituido por 0, 1, ó 2 sustituyentes seleccionados independientemente a partir de oxo, hidroxilo, nitro, halógeno, alquilo C₁₋₄, alquenilo C₁₋₄, alcoxilo C₁₋₄, cicloalquilo C₃₋₇, alquil C₁₋₄-OH, trihaloalquilo C₁₋₄, mono- y di-alquil C₁₋₄amino, -C(O)NH₂, -NH₂, -NO₂, hidroxi-alquil C₁₋₄amino, hidroxialquilo C₁₋₄, heterocicloalquilo C₁₋₄ de 4 - 7 miembros, aminoalquilo C₁₋₄ y mono- y di-alquil C₁₋₄aminoalquilo C₁₋₄; B es un grupo de la fórmula (2), en donde m, n y p son independientemente seleccionados a partir de 0 ó 1; R, R¹, R², R³, y R⁴ son independientemente seleccionados a partir del grupo que consta de hidrógeno, alquilo C₁₋₄, tal alquilo se sustituye opcionalmente por hidroxilo, amino o mono- y di-alquil C₁₋₄amino; R⁵ y R⁶ son independientemente seleccionados a partir de hidrógeno y flúor; o R y R³, tomados en combinación forman un anillo heterocíclico condensado de 5 ó 6 miembros que tiene 0 ó 1 heteroátomos adicionales de anillo seleccionados a partir de N, O ó S; R¹ y R³, tomados en combinación forman un grupo alquileno C₁₋₃; R¹ y R⁵, tomados en combinación forman un grupo alquileno C₁₋₃; R³ y R⁴, tomados en combinación con el átomo de carbono al que están unidos, forman un cicloalquilo C₃₋₆ espirocíclico; X es CRARB, O, NR⁷ o un enlace; R⁷ es hidrógeno, o alquilo C₁₋₄; RA y RB son independientemente seleccionados a partir de hidrógeno y alquilo C₁₋₄, o RA y RB, tomados en combinación, forman un grupo alquileno C₂₋₅ divalente; Z es CR⁸ o N; cuando Z es N, X es un enlace; R⁸ es hidrógeno o tomados en combinación con R⁶ forman un enlace doble; o B es un grupo de la fórmula (3), en donde p y q son independientemente seleccionados a partir del grupo que consta de 0, 1, y 2; R⁹ y R¹³ son independientemente seleccionados a partir de hidrógeno y alquilo C₁₋₄; R¹⁰ y R¹⁴ son independientemente seleccionados a partir de hidrógeno, amino, mono- y di-alquil C₁₋₄amino y alquilo C₁₋₄, tal alquilo se sustituye opcionalmente por hidroxilo, amino o mono- y di-alquil C₁₋₄amino; R¹¹ es hidrógeno, alquilo C₁₋₄, amino o mono- y di-alquil C₁₋₄amino; R¹² es hidrógeno o alquilo C₁₋₄; o R⁹ y R¹¹, tomados en combinación forman un azaciclo saturado que tiene 4 a 7 átomos de anillo, el cual es opcionalmente sustituido por 1 - 3 grupos alquilo C₁₋₄; o R¹¹ y R¹², tomados en combinación forman un azaciclo saturado que tiene 4 a 7 átomos de anillo, el cual es opcionalmente sustituido por 1 - 3 grupos alquilo C₁₋₄.
ARP130102863A 2012-08-13 2013-08-13 Piridazina 1,4 disustituida, analogos de la misma y metodos para tratar las enfermedades relacionadas con deficiencia del smn AR092108A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201261682448P 2012-08-13 2012-08-13

Publications (1)

Publication Number Publication Date
AR092108A1 true AR092108A1 (es) 2015-03-25

Family

ID=49029227

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP130102863A AR092108A1 (es) 2012-08-13 2013-08-13 Piridazina 1,4 disustituida, analogos de la misma y metodos para tratar las enfermedades relacionadas con deficiencia del smn

Country Status (41)

Country Link
US (6) US8729263B2 (es)
EP (3) EP4101849A1 (es)
JP (1) JP6190883B2 (es)
KR (3) KR20220029764A (es)
CN (1) CN104583196B (es)
AP (1) AP2015008242A0 (es)
AR (1) AR092108A1 (es)
BR (1) BR112015003004B1 (es)
CA (1) CA2880273A1 (es)
CL (1) CL2015000331A1 (es)
CR (1) CR20150078A (es)
CU (1) CU20150014A7 (es)
CY (1) CY1124882T1 (es)
DK (1) DK2885288T3 (es)
EA (1) EA032005B1 (es)
EC (1) ECSP15009862A (es)
ES (2) ES2950450T3 (es)
GT (1) GT201500030A (es)
HK (1) HK1207862A1 (es)
HR (1) HRP20211957T1 (es)
HU (1) HUE057007T2 (es)
IL (1) IL237067B (es)
JO (1) JO3530B1 (es)
LT (1) LT2885288T (es)
MA (1) MA37834A1 (es)
MX (2) MX2015001892A (es)
MY (2) MY174339A (es)
NZ (1) NZ704738A (es)
PE (2) PE20201165A1 (es)
PH (1) PH12015500236A1 (es)
PL (1) PL2885288T3 (es)
PT (1) PT2885288T (es)
RS (1) RS62692B1 (es)
SG (2) SG11201500507UA (es)
SI (1) SI2885288T1 (es)
TN (1) TN2015000038A1 (es)
TW (1) TWI635083B (es)
UA (1) UA114726C2 (es)
UY (1) UY34974A (es)
WO (1) WO2014028459A1 (es)
ZA (1) ZA201500531B (es)

Families Citing this family (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9403815B2 (en) 2010-06-24 2016-08-02 The Regents Of The University Of California Compounds and uses thereof in modulating levels of various amyloid beta peptide alloforms
MY174339A (en) * 2012-08-13 2020-04-09 Novartis Ag 1,4-disubstituted pyridazine analogs and methods for treating smn-deficiency-related conditions
US9938263B2 (en) 2013-03-12 2018-04-10 The General Hospital Corporation Gamma-secretase modulators
KR102318727B1 (ko) * 2013-07-31 2021-10-28 노파르티스 아게 1,4-이치환된 피리다진 유사체 및 smn-결핍-관련 상태를 치료하기 위한 그의 용도
GB201410693D0 (en) 2014-06-16 2014-07-30 Univ Southampton Splicing modulation
WO2016054615A2 (en) 2014-10-03 2016-04-07 Cold Spring Harbor Laboratory Targeted augmentation of nuclear gene output
AU2015338946B2 (en) * 2014-10-31 2020-06-11 The General Hospital Corporation Potent gamma-secretase modulators
WO2016128343A1 (en) * 2015-02-09 2016-08-18 F. Hoffmann-La Roche Ag Compounds for the treatment of cancer
EP3053577A1 (en) 2015-02-09 2016-08-10 F. Hoffmann-La Roche AG Compounds for the treatment of cancer
WO2017060731A1 (en) 2015-10-09 2017-04-13 University Of Southampton Modulation of gene expression and screening for deregulated protein expression
LT3386511T (lt) 2015-12-10 2021-08-25 Ptc Therapeutics, Inc. Hantingtono ligos gydymo būdai
EP3390636B1 (en) 2015-12-14 2021-05-19 Cold Spring Harbor Laboratory Antisense oligomers for treatment of dravet syndrome
US11096956B2 (en) 2015-12-14 2021-08-24 Stoke Therapeutics, Inc. Antisense oligomers and uses thereof
BR112018017077A2 (pt) * 2016-02-23 2018-12-26 Univ Indiana Res & Tech Corp terapias de combinação para tratamento de atrofia muscular espinhal
MX2019014514A (es) 2017-06-05 2020-07-20 Ptc Therapeutics Inc Compuestos para tratar la enfermedad de huntington.
EP3638318A4 (en) 2017-06-14 2021-03-17 PTC Therapeutics, Inc. METHOD OF MODULATION OF RNA SPLICING
CA3067591A1 (en) 2017-06-28 2019-01-03 Ptc Therapeutics, Inc. Methods for treating huntington's disease
EP3645121A4 (en) 2017-06-28 2021-03-17 PTC Therapeutics, Inc. HUNTINGTON'S DISEASE TREATMENT METHODS
WO2019028440A1 (en) 2017-08-04 2019-02-07 Skyhawk Therapeutics, Inc. METHODS AND COMPOSITIONS FOR MODULATING SPLICING
CA3073515A1 (en) 2017-08-25 2019-02-28 Stoke Therapeutics, Inc. Antisense oligomers for treatment of conditions and diseases
AU2018388404B2 (en) 2017-12-22 2023-11-02 HiberCell Inc. Aminopyridine derivatives as phosphatidylinositol phosphate kinase inhibitors
EA202092001A1 (ru) 2018-03-27 2021-01-29 ПиТиСи ТЕРАПЬЮТИКС, ИНК. Соединения для лечения болезни гентингтона
EP3781564B1 (en) * 2018-04-10 2023-08-23 Skyhawk Therapeutics, Inc. Pyridazine derivatives for the treatment of cancer
US11858941B2 (en) 2018-06-27 2024-01-02 Ptc Therapeutics, Inc. Heterocyclic and heteroaryl compounds for treating Huntington's disease
WO2020005882A1 (en) 2018-06-27 2020-01-02 Ptc Therapeutics, Inc. Heteroaryl compounds for treating huntington's disease
US20210179586A1 (en) 2018-09-07 2021-06-17 Teva Pharmaceuticals International Gmbh Solid state forms of branaplam and their preparation
BR112021011744A2 (pt) 2018-12-21 2021-08-31 Novartis Ag Formulações orais de branaplam
KR20210135240A (ko) * 2019-02-05 2021-11-12 스카이호크 테라퓨틱스, 인코포레이티드 스플라이싱을 조절하는 방법 및 조성물
WO2020163405A1 (en) * 2019-02-05 2020-08-13 Skyhawk Therapeutics, Inc. Methods and compositions for modulating splicing
JP2022520051A (ja) * 2019-02-05 2022-03-28 スカイホーク・セラピューティクス・インコーポレーテッド スプライシングを調節するための方法および組成物
KR20210135507A (ko) 2019-02-06 2021-11-15 스카이호크 테라퓨틱스, 인코포레이티드 스플라이싱을 조절하는 방법 및 조성물
KR20210135511A (ko) * 2019-02-06 2021-11-15 스카이호크 테라퓨틱스, 인코포레이티드 스플라이싱을 조절하는 방법 및 조성물
WO2020190793A1 (en) * 2019-03-15 2020-09-24 Skyhawk Therapeutics, Inc. Compositions and methods for correction of aberrant splicing
JP2022533120A (ja) * 2019-05-13 2022-07-21 ピーティーシー セラピューティクス， インコーポレイテッド ハンチントン病を処置するための化合物
AR119731A1 (es) * 2019-05-17 2022-01-05 Novartis Ag Inhibidores del inflamasoma nlrp3
KR20220035937A (ko) 2019-07-25 2022-03-22 노파르티스 아게 조절 가능한 발현 시스템
CA3156848A1 (en) 2019-11-01 2021-05-06 Novartis Ag The use of a splicing modulator for a treatment slowing progression of huntington's disease
EP4110775A1 (en) 2020-02-28 2023-01-04 Remix Therapeutics Inc. Thiophenyl derivatives useful for modulating nucleic acid splicing
JP2023515621A (ja) 2020-02-28 2023-04-13 リミックス セラピューティクス インコーポレイテッド 複素環アミド及びスプライシングを調節するためのその使用
JP2023515618A (ja) 2020-02-28 2023-04-13 リミックス セラピューティクス インコーポレイテッド 核酸スプライシングを調節するためのピリダジン誘導体
AU2021228285A1 (en) 2020-02-28 2022-09-29 Remix Therapeutics Inc. Compounds and methods for modulating splicing
TW202208344A (zh) 2020-04-08 2022-03-01 美商雷密克斯醫療公司 調節剪接之化合物及方法
BR112022020418A2 (pt) 2020-04-08 2023-05-02 Remix Therapeutics Inc Compostos e métodos para modulação de splicing
JP2023522177A (ja) * 2020-04-09 2023-05-29 ピーティーシー セラピューティクス， インコーポレイテッド ハンチントン病を処置するための化合物
US20230287410A1 (en) 2020-05-11 2023-09-14 Stoke Therapeutics, Inc. Opa1 antisense oligomers for treatment of conditions and diseases
TW202208358A (zh) 2020-05-13 2022-03-01 美商Ｃｈｄｉ基金會股份有限公司 用於治療亨汀頓舞蹈症之htt調節劑
TW202216671A (zh) 2020-06-25 2022-05-01 瑞士商諾華公司 １，４—二取代的嗒𠯤化合物之製造方法
MX2023000167A (es) 2020-07-02 2023-05-03 Remix Therapeutics Inc Derivados de 5-[5-(piperidin-4-il)tieno[3,2-c]pirazol-2-il]indazol y compuestos relacionados como moduladores para el corte y empalme de ácidos nucleicos y para el tratamiento de enfermedades proliferativas.
KR20230051168A (ko) 2020-07-02 2023-04-17 레믹스 테라퓨틱스 인크. 2-(인다졸-5-일)-6-(피페리딘-4-일)-1,7-나프티리딘 유도체, 및 핵산 스플라이싱의 조절제로서의 및 증식성 질환의 치료를 위한 관련 화합물
TW202304446A (zh) 2021-03-29 2023-02-01 瑞士商諾華公司 剪接調節子用於減慢杭丁頓氏舞蹈症進展的治療之用途
WO2023034833A1 (en) 2021-08-30 2023-03-09 Remix Therapeutics Inc. Compounds and methods for modulating splicing
WO2023034836A1 (en) 2021-08-30 2023-03-09 Remix Therapeutics Inc. Compounds and methods for modulating splicing
TW202328135A (zh) 2021-08-30 2023-07-16 美商雷密克斯醫療公司 調節剪接之化合物及用途
WO2023034827A1 (en) 2021-08-30 2023-03-09 Remix Therapeutics Inc. Compounds and methods for modulating splicing
WO2023034812A1 (en) 2021-08-30 2023-03-09 Remix Therapeutics Inc. Compounds and methods for modulating splicing
WO2023064880A1 (en) 2021-10-13 2023-04-20 Remix Therapeutics Inc. Compounds and methods for modulating nucleic acid splicing
WO2023064879A1 (en) 2021-10-13 2023-04-20 Remix Therapeutics Inc. Compounds and methods for modulating nucleic acid splicing
WO2023092149A1 (en) * 2021-11-22 2023-05-25 Rgenta Therapeutics, Inc. Heterocyclic substituted 1,3,4-thiadiazole and pyridazine compounds and methods of using the same
TW202346305A (zh) 2022-01-05 2023-12-01 美商雷密克斯醫療公司 用於調節剪切之化合物及方法
WO2023133217A1 (en) 2022-01-05 2023-07-13 Remix Therapeutics Inc. 2-(indazol-5-yl)-6-(piperidin-4-yl)-1,7-naphthyridine derivatives and related compounds as modulators for splicing nucleic acids and for the treatment of proliferative diseases
WO2023133229A2 (en) 2022-01-05 2023-07-13 Remix Therapeutics Inc. Compounds and methods for modulating splicing
TWI778908B (zh) 2022-01-21 2022-09-21 大里興業股份有限公司 具有改良減振結構之氣動衝擊工具

Family Cites Families (58)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2427943C2 (de) 1974-06-10 1984-08-02 Dr. Karl Thomae Gmbh, 7950 Biberach Benzimidazole, Verfahren zu deren Herstellung und diese enthaltende Arzneimittel
DE2516040C2 (de) 1974-06-10 1984-12-20 Dr. Karl Thomae Gmbh, 7950 Biberach Benzimidazole, Verfahren zu deren Herstellung und diese enthaltende Arzneimittel
PT730590E (pt) 1993-11-24 2001-05-31 Du Pont Pharm Co Derivados de isoxazolina e isoxazole como antagonistas dos reciptores do fibrinogenio
CN1210274C (zh) 2000-02-11 2005-07-13 沃泰克斯药物股份有限公司 哌嗪和哌啶衍生物
EP1133993A1 (en) 2000-03-10 2001-09-19 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Substances for the treatment of spinal muscular atrophy
KR20030025235A (ko) 2000-06-07 2003-03-28 버텍스 파마슈티칼스 인코포레이티드 카스파제 억제제 및 이의 용도
US6376508B1 (en) 2000-12-13 2002-04-23 Academia Sinica Treatments for spinal muscular atrophy
US6982259B2 (en) 2002-04-30 2006-01-03 Schering Aktiengesellschaft N-heterocyclic derivatives as NOS inhibitors
RU2352568C9 (ru) 2002-08-09 2009-06-27 Астразенека Аб [1,2,4]оксадиазолы (варианты), способ их получения, фармацевтическая композиция и способ ингибирования активации метаботропных глютаматных рецепторов-5
EP1581525A2 (en) 2002-08-09 2005-10-05 AstraZeneca AB Compounds having an activity at metabotropic glutamate receptors
WO2004014370A2 (en) 2002-08-09 2004-02-19 Astrazeneca Ab Oxadiazoles as modulators of metabotropic glutamate receptor-5
AU2003280309A1 (en) * 2002-11-11 2004-06-03 Neurosearch A/S 1,4-diazabicyclo (3,2,2)nonane derivatives, preparation and therapeutical use thereof
CA2514733A1 (en) 2003-02-28 2004-09-16 Transform Pharmaceuticals, Inc. Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
WO2004110351A2 (en) 2003-05-14 2004-12-23 Anadys Pharmaceuticals, Inc. Heterocyclic compounds for treating hepatitis c virus
WO2005007644A1 (ja) 2003-06-27 2005-01-27 Banyu Pharmaceutical Co., Ltd ヘテロアリールオキシ含窒素飽和へテロ環誘導体
WO2005018547A2 (en) 2003-08-15 2005-03-03 Merck & Co., Inc. Mitotic kinesin inhibitors
US7399765B2 (en) * 2003-09-19 2008-07-15 Abbott Laboratories Substituted diazabicycloalkane derivatives
US7655657B2 (en) * 2003-12-22 2010-02-02 Abbott Laboratories Fused bicycloheterocycle substituted quinuclidine derivatives
WO2005077373A2 (en) 2004-02-03 2005-08-25 Astrazeneca Ab Treatment of gastro-esophageal reflux disease (gerd)
WO2005077368A2 (en) 2004-02-03 2005-08-25 Astrazeneca Ab Treatment of gastro-esophageal reflux disease (gerd)
FR2868780B1 (fr) 2004-04-13 2008-10-17 Sanofi Synthelabo Derives de la 1-amino-phthalazine, leur preparation et leur application en therapeutique
EP1753740A2 (en) 2004-05-21 2007-02-21 Merck & Co., Inc. Amino cyclopentyl heterocyclic and carbocyclic modulators of chemokine receptor activity
CA2571360C (en) 2004-06-18 2014-11-25 3M Innovative Properties Company Substituted imidazoquinolines, imidazopyridines, and imidazonaphthyridines useful in inducing cytokine biosynthesis in animals
AR051094A1 (es) 2004-09-20 2006-12-20 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa
DK1637141T3 (da) 2004-09-21 2012-02-27 Trobio Ab Stabiliseret proteasesammensætning omfattende en serinprotease, morpholinderivater og reversible inhibitorer af serinproteasen
US7354944B2 (en) 2004-10-18 2008-04-08 Amgen Inc. Thiadiazole compounds and methods of use
WO2006045716A1 (en) * 2004-10-20 2006-05-04 Neurosearch A/S Novel diazabicyclic aryl derivatives and their medical use
US8501739B2 (en) * 2005-07-04 2013-08-06 High Point Pharmaceuticals, Llc Medicaments
AU2006323986A1 (en) * 2005-12-06 2007-06-14 Neurosearch A/S Novel diazabicyclic aryl derivatives and their medical use
TW200813051A (en) 2006-05-08 2008-03-16 Neurogen Corp Substituted azaspiro derivatives
US20080247964A1 (en) 2006-05-08 2008-10-09 Yuelian Xu Substituted azaspiro derivatives
JP5420398B2 (ja) 2006-05-19 2014-02-19 アッヴィ・バハマズ・リミテッド Ｃｎｓ活性縮合ビシクロ複素環置換アザ二環式アルカン誘導体
WO2008058064A1 (en) 2006-11-07 2008-05-15 Lexicon Pharmaceuticals, Inc. Amine-linked multicyclic compounds as inhibitors of the proline transporter
GB0704394D0 (en) 2007-03-07 2007-04-11 Senexis Ltd Compounds
EP2014656A3 (en) 2007-06-11 2011-08-24 High Point Pharmaceuticals, LLC New heteocyclic h3 antagonists
NZ585298A (en) 2007-11-16 2012-08-31 Rigel Pharmaceuticals Inc Carboxamide, sulfonamide and amine compounds for metabolic disorders
CN106432213A (zh) 2008-02-28 2017-02-22 沃泰克斯药物股份有限公司 作为cftr调节剂的杂芳基衍生物
WO2009137503A1 (en) 2008-05-05 2009-11-12 Envivo Pharmaceuticals, Inc. Hdac inhibitors and uses thereof
EP2288609A2 (en) 2008-06-10 2011-03-02 NeuroSearch A/S Indolyl-pyridazinyl-diazabicyclononane derivatives in labelled and unlabelled form and their use in diagnostic methods
GB0810902D0 (en) 2008-06-13 2008-07-23 Astex Therapeutics Ltd New compounds
EP2303859A4 (en) 2008-06-20 2012-08-22 Metabolex Inc ARYL GPR119 AGONISTS AND USES THEREOF
CA2735593C (en) 2008-09-03 2017-08-15 Repligen Corporation Compositions including 6-aminohexanoic acid derivatives as hdac inhibitors
JP2012505899A (ja) 2008-10-16 2012-03-08 シェーリング コーポレイション アジン誘導体およびそれの使用方法
EP2440559B1 (en) 2009-05-05 2018-01-10 Dana-Farber Cancer Institute, Inc. Egfr inhibitors and methods of treating disorders
CA2773182A1 (en) 2009-09-10 2011-03-17 F. Hoffmann-La Roche Ag Inhibitors of jak
TWI558398B (zh) 2009-09-22 2016-11-21 諾華公司 菸鹼乙醯膽鹼受體α７活化劑之用途
CN105906631A (zh) 2009-11-18 2016-08-31 普莱希科公司 用于激酶调节的化合物和方法及其适应症
WO2011078143A1 (ja) 2009-12-22 2011-06-30 塩野義製薬株式会社 ピリミジン誘導体およびそれらを含有する医薬組成物
EP2542549B1 (en) 2010-03-03 2016-05-11 Probiodrug AG Inhibitors of glutaminyl cyclase
WO2011130515A1 (en) * 2010-04-14 2011-10-20 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Arylthiazolyl piperidines and related compounds as modulators of survival motor neuron (smn) protein production
AR081626A1 (es) 2010-04-23 2012-10-10 Cytokinetics Inc Compuestos amino-piridazinicos, composiciones farmaceuticas que los contienen y uso de los mismos para tratar trastornos musculares cardiacos y esqueleticos
WO2012022467A2 (en) 2010-08-16 2012-02-23 Santhera Pharmaceuticals (Schweiz) Ag Novel benzoquinone derivatives and use thereof as modulators of mitochondrial function
BR112013023813A2 (pt) 2011-03-18 2016-12-13 Novartis Ag combinações de ativadores do receptor acetilcolina nicotínico alfa 7 e antagonistas de mglur5 para uso em dopamina induzida por discinesia na doença de parkinson
UA113223C2 (xx) 2012-08-13 2016-12-26 Арилетинілпіримідини
MY174339A (en) 2012-08-13 2020-04-09 Novartis Ag 1,4-disubstituted pyridazine analogs and methods for treating smn-deficiency-related conditions
AU2013353542B2 (en) 2012-11-27 2018-04-05 Thomas Helledays Stiftelse For Medicinsk Forskning Pyrimidine-2,4-diamine derivatives for treatment of cancer
US9040712B2 (en) * 2013-01-23 2015-05-26 Novartis Ag Thiadiazole analogs thereof and methods for treating SMN-deficiency-related-conditions
KR102318727B1 (ko) 2013-07-31 2021-10-28 노파르티스 아게 1,4-이치환된 피리다진 유사체 및 smn-결핍-관련 상태를 치료하기 위한 그의 용도

Also Published As

Publication number Publication date
KR20150041655A (ko) 2015-04-16
UA114726C2 (uk) 2017-07-25
CL2015000331A1 (es) 2015-08-28
US11229648B2 (en) 2022-01-25
GT201500030A (es) 2017-09-28
JP2015524842A (ja) 2015-08-27
EP3564233A1 (en) 2019-11-06
CA2880273A1 (en) 2014-02-20
NZ704738A (en) 2016-02-26
US20190358226A1 (en) 2019-11-28
US9545404B2 (en) 2017-01-17
CR20150078A (es) 2015-05-29
PH12015500236B1 (en) 2015-03-30
US8729263B2 (en) 2014-05-20
CN104583196B (zh) 2016-10-12
HK1207862A1 (en) 2016-02-12
LT2885288T (lt) 2021-12-27
MA37834A1 (fr) 2018-09-28
EP4101849A1 (en) 2022-12-14
KR102368439B1 (ko) 2022-02-28
MX2020010151A (es) 2021-01-15
DK2885288T3 (da) 2022-01-10
PE20151890A1 (es) 2016-01-13
CY1124882T1 (el) 2022-11-25
CU20150014A7 (es) 2015-07-30
IL237067B (en) 2019-03-31
ES2902198T3 (es) 2022-03-25
BR112015003004A2 (pt) 2017-07-04
JO3530B1 (ar) 2020-07-05
AU2013302859A1 (en) 2015-02-19
US20140213570A1 (en) 2014-07-31
EP2885288A1 (en) 2015-06-24
PH12015500236A1 (en) 2015-03-30
EA201590371A1 (ru) 2015-06-30
SI2885288T1 (sl) 2022-01-31
US10758533B2 (en) 2020-09-01
EP2885288B1 (en) 2021-10-06
TN2015000038A1 (en) 2016-06-29
UY34974A (es) 2014-03-31
MX2015001892A (es) 2015-05-07
US20220387428A1 (en) 2022-12-08
HUE057007T2 (hu) 2022-04-28
ES2950450T3 (es) 2023-10-10
KR20220029764A (ko) 2022-03-08
EP3564233B1 (en) 2023-05-03
SG11201500507UA (en) 2015-03-30
PT2885288T (pt) 2022-01-06
US20170290828A1 (en) 2017-10-12
PE20201165A1 (es) 2020-10-28
AU2013302859B2 (en) 2016-07-14
ZA201500531B (en) 2018-11-28
SG10201701123QA (en) 2017-04-27
BR112015003004B1 (pt) 2020-09-24
KR20200126016A (ko) 2020-11-05
JP6190883B2 (ja) 2017-08-30
RS62692B1 (sr) 2022-01-31
US10195196B2 (en) 2019-02-05
WO2014028459A1 (en) 2014-02-20
ECSP15009862A (es) 2019-03-29
EA032005B1 (ru) 2019-03-29
TW201412721A (zh) 2014-04-01
CN104583196A (zh) 2015-04-29
TWI635083B (zh) 2018-09-11
AP2015008242A0 (en) 2015-01-31
PL2885288T3 (pl) 2022-02-07
KR102172911B1 (ko) 2020-11-03
MY174339A (en) 2020-04-09
US20140051672A1 (en) 2014-02-20
HRP20211957T1 (hr) 2022-03-18
US20200345732A1 (en) 2020-11-05
MY176488A (en) 2020-08-12

Similar Documents

Publication Publication Date Title
AR092108A1 (es) Piridazina 1,4 disustituida, analogos de la misma y metodos para tratar las enfermedades relacionadas con deficiencia del smn
AR094557A1 (es) Tiadiazol, análogos del mismo, y métodos para el tratamiento de condiciones relacionadas con deficiencia de smn
AR116993A2 (es) Compuestos heterociclos bicíclicos y sus usos en terapia
AR087760A1 (es) Heterociclilaminas como inhibidores de pi3k
AR096979A1 (es) Derivados de pirrol, su procedimiento de preparación y las composiciones farmacéuticas que los contienen
AR108388A2 (es) Compuestos de oxazol sustituidos con indazol como inhibidores de pi3-quinasas
AR110139A1 (es) COMPUESTOS MONO Y ESPIROCÍCLICOS QUE CONTIENEN CICLOBUTANO Y AZETIDINA COMO INHIBIDORES DE LA INTEGRINA aV
AR104025A1 (es) Carbamatos de piperazina como moduladores de magl y/o abhd6, procesos para su preparación y composiciones farmacéuticas
AR090548A1 (es) Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
AR106595A1 (es) COMPUESTOS HETEROCÍCLICOS COMO INHIBIDORES DE PI3K-g
AR086357A1 (es) Derivados de indazol sustituidos activos como inhibidores de quinasas
AR090945A1 (es) Moduladores de la via del complemento y usos de los mismos
AR093364A1 (es) Imidazo[1,2-a]piridincarboxamidas aminosustituidas y su uso
AR089143A1 (es) Triazolopiridinas sustituidas con actividad inhibidora de ttk
AR089774A1 (es) Derivados de indolizina, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen
AR098853A1 (es) Pirazoles sustituidos y usos de los mismos
AR091193A1 (es) HETEROCICLOS DE 5 MIEMBROS QUE CONTIENEN NITROGENO SUSTITUIDO POR CARBOXAMIDA O SULFONAMIDA COMO MODULADORES PARA EL RECEPTOR NUCLEAR HUERFANO RORg
AR097008A1 (es) Derivados fosfatos, su procedimiento de preparación y las composiciones farmacéuticas que los contienen
AR095430A1 (es) Compuestos de pirimidina y piridina y su uso como inhibidores de la actividad de fgfr
AR100810A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR088829A1 (es) DERIVADOS DE CICLOHEXILAMINA QUE TIENEN ACTIVIDAD COMO AGONISTAS ADRENERGICOS b2 Y COMO ANTAGONISTAS MUSCARINICOS M3
AR100418A1 (es) Compuestos y composiciones para inducir condrogénesis
AR100806A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR089776A1 (es) 5,8-dihidro-6h-pirazolo[3,4-h]quinazolinas como inhibidores de igf-1r/ir
AR099913A1 (es) Derivados de indolizina, su procedimiento de preparación y las composiciones farmacéuticas que los contienen

Legal Events

Date Code Title Description
FG Grant, registration