AR078326A1 - Quinazolinas como inhibidores de los canales ionicos de potasio y composiciones farmaceuticas que los contienen - Google Patents
Quinazolinas como inhibidores de los canales ionicos de potasio y composiciones farmaceuticas que los contienenInfo
- Publication number
- AR078326A1 AR078326A1 ARP100103247A ARP100103247A AR078326A1 AR 078326 A1 AR078326 A1 AR 078326A1 AR P100103247 A ARP100103247 A AR P100103247A AR P100103247 A ARP100103247 A AR P100103247A AR 078326 A1 AR078326 A1 AR 078326A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heterocyclyl
- heteroaryl
- cycloalkyl
- alkenyl
- Prior art date
Links
Classifications
-
- 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
- A61K31/495—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
- A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
-
- 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
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
- A61K31/54—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 sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/549—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 sulfur as the ring hetero atoms, e.g. sulthiame having two or more nitrogen atoms in the same ring, e.g. hydrochlorothiazide
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
-
- 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
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- 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
- C07D405/02—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 two hetero rings
- C07D405/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D417/02—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
-
- 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
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Oncology (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Emergency Medicine (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Catching Or Destruction (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Los compuestos son utiles como inhibidores de la funcion de los canales de potasio y en el tratamiento y prevencion de arritmia, trastornos asociados con IKur y otros trastornos mediados por la funcion de los canales ionicos. Reivindicacion 1: Un compuesto, caracterizado porque tiene la formula (1) o un enantiomero, diastereomero, tautomero o sales del mismo, en la que: X es H, -OH, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, alquenilo C2-12 alquinilo C2-12, cicloalquilo C3-10, un heteroarilo de 4 a 12 miembros, heterociclilo de 4 a 12 miembros, -CN, -NO2, -NR11SO2R12, -SO2NR11R12, -CONR11R12, -NR11CONR11R12, -NCOR11, -NR11SO2NR11R12, -OCONR11R12, -CO2R11 o -NR11R12; Y es H, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, alquenilo C2-12, alquinilo C2-12, cicloalquilo C3-10, un heteroarilo de 4 a 12 miembros, heterociclilo de 4 a 12 miembros, -CN, -NO2, -SO2NR11R12, -CONR11R12, -NR11CONR11R12, -NCOR11, -NR11SO2NR11R12, -OCONR11R12, -CO2R11 o -NR11R12; Z es H, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, alquenilo C2-12, alquinilo C2-12, cicloalquilo C3-10, un heteroarilo de 6 a 12 miembros, heterociclilo de 4 a 12 miembros, -NO2, -NR11SO2R12, -SO2NR11R12, -NR11CONR11R12, -NCOR11, -NR11SO2NR11R12, -OCONR11R12, -CO2R11 o -NR11R12; A es -(CH2)m-R2, -CH(R25)(R26), -CH(R26)CO2-R2a o -(CH2)n-1-NR25-CO2-R24; m es 0 a 4; n es 1 a 4; n-1 es 2 a 4; R1 es -OH, F, Cl, Br, I, alquilo C1-10, haloalquilo C1-10, alquenilo C2-12, cicloalquilo C3-10, -CN, -(CH2)n-SO2NR11R12, -(CH2)n-CO2R11 o -(CH2)n-NR11SO2R12, pudiendo estar el alquenilo y cicloalquilo opcionalmente sustituidos con uno o más R13; o R1 se selecciona del grupo de formulas (2); o R1 es el resto de formula (3); R2 es alquilo C1-10, ciclopropilo opcionalmente sustituido con uno o más R13; cicloalquilo C4-10 opcionalmente sustituido con uno o más R13bb; cicloalquenilo C3-10 opcionalmente sustituido con uno o más R13b; o -NR14R14; con la condicion de que R2 no sea -NR14R14 cuando m sea 0, 1 o 3; o R2 es el resto de formula (4); o R2 se selecciona del grupo de formulas (5); R2a es alquilo C1-10, cicloalquilo C3-10, arilo C6-10, -NR14R14, un heteroarilo de 4 a 12 miembros o heterociclilo de 4 a 12 miembros, cualquiera de los cuales está opcionalmente sustituido con uno o más R13 y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R11 y R12, en cada aparicion, se seleccionan independientemente de H, alquilo C1-10, haloalquilo C1-10, cicloalquilo C3-10, arilo C6-10, un heteroarilo de 4 a 12 miembros y un heterociclilo de 4 a 12 miembros, pudiendo estar el alquilo, cicloalquilo, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R13 y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; o R11 y R12 se toman junto con el nitrogeno al que están unidos formando un heterociclilo de 4 a 12 miembros, pudiendo estar el heterociclilo opcionalmente sustituido con uno o más R13 y el heterociclilo está constituido por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13, en cada aparicion, es independientemente H, -OH, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; con la condicion de que cuando R13 sea alquilo sustituido con un R14a, R14a no sea -OH; R13a, en cada aparicion, es independientemente H, -OH, F, Cl, Br, I, alquilo C2-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13aa, en cada aparicion, es independientemente H, -OH, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13a-1, en cada aparicion, es independientemente H, -OH, F, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13a-2, en cada aparicion, es independientemente H, -OH, F, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13a-4, en cada aparicion, es independientemente H, -OH, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -CONR14R14, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13b, en cada aparicion, es independientemente H, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un heterociclilo de 4 a 12 miembros, un heteroaril de 4 a 12 miembros-alquilo C1-10, -CN, -NO2, -(CH2)m-SO2R14, -NR14SO2R14, =O, -(CH2)m-SO2NR14R14, -(CH2)m-NR14SO2R14, -(CH2)n-NR14SO2NR14R14, -NR14SO2NR14R14, -CO2NR14R14, -NR14CO2NR14R14, -NR14COR14, -SO2NR14COR14, -SO2NR14CONR14R14, -NR14CO2R14, -CO2R14, -NR14R14, -NR14CONR14R14, -C(=NOR14)NR14R14, -CONR14OR14 o -NCOR14, pudiendo estar el alquilo, cicloalquilo, alquenilo, alcoxi, arilo, heteroarilo y heterociclilo opcionalmente sustituidos con uno o más R14a y el heteroarilo y heterociclilo están constituidos por átomos de carbono y 1, 2, 3 o 4 heteroátomos seleccionados independientemente del grupo constituido por N, S u O; R13bb, en cada aparicion, es independientemente H, F, Cl, Br, I, alquilo C1-10, alcoxi C1-10, haloalquilo C1-10, cicloalquilo C3-10, alquenilo C2-12, alquinilo C2-12, arilo C6-10, un heteroarilo de 4 a 12 miembros, un
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23945209P | 2009-09-03 | 2009-09-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078326A1 true AR078326A1 (es) | 2011-11-02 |
Family
ID=42942118
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103247A AR078326A1 (es) | 2009-09-03 | 2010-09-03 | Quinazolinas como inhibidores de los canales ionicos de potasio y composiciones farmaceuticas que los contienen |
Country Status (32)
| Country | Link |
|---|---|
| US (9) | US8575184B2 (es) |
| EP (3) | EP3575288B1 (es) |
| JP (2) | JP5643312B2 (es) |
| KR (1) | KR101698631B1 (es) |
| CN (1) | CN102753535B (es) |
| AR (1) | AR078326A1 (es) |
| AU (1) | AU2010289641B2 (es) |
| BR (1) | BR112012008330B1 (es) |
| CA (1) | CA2772642C (es) |
| CL (1) | CL2012000583A1 (es) |
| CO (1) | CO6511220A2 (es) |
| CY (2) | CY1118488T1 (es) |
| DK (2) | DK3575288T3 (es) |
| EA (1) | EA021113B1 (es) |
| ES (3) | ES2900504T3 (es) |
| HR (2) | HRP20211973T1 (es) |
| HU (2) | HUE057433T2 (es) |
| IL (1) | IL218169A (es) |
| LT (2) | LT3575288T (es) |
| MX (1) | MX2012002099A (es) |
| MY (1) | MY160243A (es) |
| NZ (1) | NZ598516A (es) |
| PE (1) | PE20121153A1 (es) |
| PL (2) | PL3575288T3 (es) |
| PT (2) | PT2473487T (es) |
| SG (1) | SG178592A1 (es) |
| SI (2) | SI3575288T1 (es) |
| SM (3) | SMT202100717T1 (es) |
| TN (1) | TN2012000063A1 (es) |
| TW (1) | TWI488851B (es) |
| WO (1) | WO2011028741A1 (es) |
| ZA (1) | ZA201202383B (es) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH068949B2 (ja) | 1985-09-20 | 1994-02-02 | 富士写真フイルム株式会社 | ハロゲン化銀カラ−写真感光材料 |
| LT3575288T (lt) * | 2009-09-03 | 2021-12-10 | Bristol-Myers Squibb Company | Chinazolinai kaip kalio jonų kanalų inhibitoriai |
| AR079814A1 (es) * | 2009-12-31 | 2012-02-22 | Otsuka Pharma Co Ltd | Compuestos heterociclicos, composiciones farmaceuticas que los contienen y sus usos |
| JP6121658B2 (ja) * | 2011-06-29 | 2017-04-26 | 大塚製薬株式会社 | 治療用化合物、及び関連する使用の方法 |
| SG195200A1 (en) * | 2011-06-29 | 2013-12-30 | Otsuka Pharma Co Ltd | Quinazolines as therapeutic compounds and related methods of use |
| WO2013143319A1 (zh) * | 2012-03-26 | 2013-10-03 | 中国科学院福建物质结构研究所 | 喹唑啉衍生物及其用途 |
| SI2858987T1 (en) * | 2012-06-11 | 2018-06-29 | Bristol-Myers Squibb Company | PREPARATION OF 5-PHENYL-4- (PYRIDIN-2-ILLETHYLAMINO) -CHUINAZOLIN-2-YL) -PIRIDIN-3-SULPHONAMIDE PHOSPHORAMIDIC ACID |
| CN105143187B (zh) | 2013-02-28 | 2018-04-03 | 武田药品工业株式会社 | 制备磺酰氯化合物的方法 |
| US9050345B2 (en) | 2013-03-11 | 2015-06-09 | Bristol-Myers Squibb Company | Pyrrolotriazines as potassium ion channel inhibitors |
| EP2970295B1 (en) | 2013-03-11 | 2016-12-28 | Bristol-Myers Squibb Company | Pyrrolopyridazines as potassium ion channel inhibitors |
| US9403834B2 (en) | 2013-03-11 | 2016-08-02 | Bristol-Myers Squibb Company | Pyrrolotriazines as potassium ion channel inhibitors |
| US9242966B2 (en) * | 2013-03-11 | 2016-01-26 | Bristol-Myers Squibb Company | Phthalazines as potassium ion channel inhibitors |
| WO2014143609A1 (en) | 2013-03-11 | 2014-09-18 | Bristol-Myers Squibb Company | Isoquinolines as potassium ion channel inhibitors |
| CN105636955B (zh) * | 2013-10-17 | 2018-01-12 | 住友化学株式会社 | 四唑啉酮化合物及其用途 |
| US10428046B2 (en) | 2014-06-10 | 2019-10-01 | Ube Industries, Ltd. | N-substituted sulfonamide compound and method for producing same |
| US10774072B2 (en) | 2014-06-10 | 2020-09-15 | Ube Industries, Ltd. | Crystal of N-substituted sulfonamide compound |
| KR102374969B1 (ko) | 2014-06-10 | 2022-03-16 | 우베 고산 가부시키가이샤 | 헤테로 방향족 술폰아미드 화합물의 제조 방법 |
| KR20170117023A (ko) * | 2014-12-05 | 2017-10-20 | 서브라마니암 아난탄 | 생체 아민 수송 조절인자로서 헤테로환상 화합물 |
| JP2018509378A (ja) | 2014-12-05 | 2018-04-05 | サウザーン リサーチ インスチチュート | 生体アミン輸送モジュレータとしての新規なキナゾリン類 |
| CA2988637A1 (en) * | 2015-06-10 | 2016-12-15 | Bayer Pharma Aktiengesellschaft | Aromatic sulfonamide derivatives |
| PT3458443T (pt) | 2016-05-03 | 2020-11-05 | Bayer Pharma AG | Derivados de sulfonamida aromática |
| CN106432067B (zh) * | 2016-09-18 | 2019-04-19 | 北京天弘天达医药科技有限公司 | 一种3-吡啶磺酰氯的绿色化学合成方法 |
| AU2018356430A1 (en) * | 2017-10-29 | 2020-04-30 | Bayer Aktiengesellschaft | Aromatic sulfonamide derivatives for the treatment of Ischemic Stroke |
| CN112135819A (zh) * | 2018-04-20 | 2020-12-25 | 拜耳公司 | 作为杀虫剂的杂芳基-三唑与杂芳基-四唑化合物 |
| WO2020234103A1 (en) | 2019-05-21 | 2020-11-26 | Bayer Aktiengesellschaft | Identification and use of kras inhibitors |
| CA3195519A1 (en) | 2020-09-18 | 2022-03-24 | Bayer Aktiengesellschaft | Pyrido[2,3-d]pyrimidin-4-amines as sos1 inhibitors |
| EP4074317A1 (en) | 2021-04-14 | 2022-10-19 | Bayer AG | Phosphorus derivatives as novel sos1 inhibitors |
| US20250289806A1 (en) * | 2022-04-28 | 2025-09-18 | University Of Miami | Compounds for proliferative disorders |
| EP4587439A1 (en) | 2022-09-16 | 2025-07-23 | Bayer Aktiengesellschaft | Sulfone-substituted pyrido[3,4-d]pyrimidine derivatives for the treatment of cancer |
| WO2024079252A1 (en) | 2022-10-13 | 2024-04-18 | Bayer Aktiengesellschaft | Sos1 inhibitors |
| WO2025202022A1 (en) | 2024-03-27 | 2025-10-02 | Bayer Aktiengesellschaft | Anticancer macrocyclic quinazoline-based inhibitors of the ineraction between ras and sos1 |
Family Cites Families (83)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3843791A (en) | 1973-01-11 | 1974-10-22 | Pfizer | Method of killing insects with quinazolinones and quinazoline-thiones |
| ES2104862T3 (es) | 1991-02-07 | 1997-10-16 | Roussel Uclaf | Derivados biciclicos nitrogenados, su procedimiento de preparacion, sus productos intermedios obtenidos, su aplicacion como medicamentos y composiciones farmaceuticas que los contienen. |
| US5710158A (en) | 1991-05-10 | 1998-01-20 | Rhone-Poulenc Rorer Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase |
| US6645969B1 (en) | 1991-05-10 | 2003-11-11 | Aventis Pharmaceuticals Inc. | Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase |
| GB9300059D0 (en) | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
| JP2657760B2 (ja) | 1992-07-15 | 1997-09-24 | 小野薬品工業株式会社 | 4−アミノキナゾリン誘導体およびそれを含有する医薬品 |
| GB9323290D0 (en) | 1992-12-10 | 1994-01-05 | Zeneca Ltd | Quinazoline derivatives |
| EP0655456B1 (en) | 1993-06-17 | 2000-09-06 | Otsuka Pharmaceutical Factory, Inc. | Phosphonic diester derivative |
| GB9314884D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Tricyclic derivatives |
| GB9314893D0 (en) | 1993-07-19 | 1993-09-01 | Zeneca Ltd | Quinazoline derivatives |
| IL112248A0 (en) | 1994-01-25 | 1995-03-30 | Warner Lambert Co | Tricyclic heteroaromatic compounds and pharmaceutical compositions containing them |
| IL112249A (en) | 1994-01-25 | 2001-11-25 | Warner Lambert Co | Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds |
| US5679683A (en) | 1994-01-25 | 1997-10-21 | Warner-Lambert Company | Tricyclic compounds capable of inhibiting tyrosine kinases of the epidermal growth factor receptor family |
| JPH083144A (ja) | 1994-06-21 | 1996-01-09 | Chugai Pharmaceut Co Ltd | キナゾリン及びキノリン誘導体 |
| TW414798B (en) | 1994-09-07 | 2000-12-11 | Thomae Gmbh Dr K | Pyrimido (5,4-d) pyrimidines, medicaments comprising these compounds, their use and processes for their preparation |
| GB9510757D0 (en) | 1994-09-19 | 1995-07-19 | Wellcome Found | Therapeuticaly active compounds |
| GB9424233D0 (en) | 1994-11-30 | 1995-01-18 | Zeneca Ltd | Quinazoline derivatives |
| GB9514265D0 (en) | 1995-07-13 | 1995-09-13 | Wellcome Found | Hetrocyclic compounds |
| AU7692996A (en) * | 1995-12-01 | 1997-06-27 | Ciba-Geigy Ag | Receptor antagonists |
| NZ325248A (en) * | 1995-12-23 | 1999-09-29 | Pfizer Res & Dev | Quinoline and quinazoline compounds useful in therapy |
| EP0912559B1 (en) | 1996-07-13 | 2002-11-06 | Glaxo Group Limited | Fused heterocyclic compounds as protein tyrosine kinase inhibitors |
| WO1998029397A1 (en) | 1996-12-27 | 1998-07-09 | Yoshitomi Pharmaceutical Industries, Ltd. | Fused pyrimidine compounds and medicinal use thereof |
| WO1998038984A2 (en) | 1997-03-05 | 1998-09-11 | Sugen, Inc. | Formulations for hydrophobic pharmaceutical agents |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| IL148576A0 (en) | 1999-09-21 | 2002-09-12 | Astrazeneca Ab | Quinazoline derivatives and their use as pharmaceuticals |
| NZ517575A (en) * | 1999-09-30 | 2004-04-30 | Neurogen Corp | Certain alkylene diamine-substituted heterocycles |
| US6605615B2 (en) | 2000-03-01 | 2003-08-12 | Tularik Inc. | Hydrazones and analogs as cholesterol lowering agents |
| KR100774855B1 (ko) | 2000-04-27 | 2007-11-08 | 아스텔라스세이야쿠 가부시키가이샤 | 축합 헤테로아릴 유도체 |
| CN1474815A (zh) | 2000-09-20 | 2004-02-11 | Ĭ��ר���ɷ�����˾ | 4-氨基-喹唑啉 |
| EP1318985A2 (en) | 2000-09-20 | 2003-06-18 | MERCK PATENT GmbH | 4-amino-quinazolines |
| WO2002062767A1 (en) | 2001-02-07 | 2002-08-15 | Sumitomo Pharmaceuticals Company, Limited | Novel quinazoline derivatives |
| WO2002092579A1 (en) | 2001-05-14 | 2002-11-21 | Astrazeneca Ab | 4-anilinoquinazoline derivatives |
| US7829566B2 (en) | 2001-09-17 | 2010-11-09 | Werner Mederski | 4-amino-quinazolines |
| US7645878B2 (en) | 2002-03-22 | 2010-01-12 | Bayer Healthcare Llc | Process for preparing quinazoline Rho-kinase inhibitors and intermediates thereof |
| WO2004017950A2 (en) | 2002-08-22 | 2004-03-04 | Piramed Limited | Phosphadidylinositol 3,5-biphosphate inhibitors as anti-viral agents |
| WO2004030672A1 (en) | 2002-10-02 | 2004-04-15 | Merck Patent Gmbh | Use of 4 amino-quinazolines as anti cancer agents |
| AU2003258662A1 (en) | 2002-10-02 | 2004-04-23 | Merck Patent Gmbh | Use of 4-amino-quinazolines as anti cancer agents |
| AU2003290279A1 (en) | 2002-12-23 | 2004-07-14 | Astrazeneca Ab | Quinazoline derivatives |
| AU2003292435A1 (en) | 2002-12-23 | 2004-07-14 | Astrazeneca Ab | 4- (pyridin-4-ylamino) -quinazoline derivatives as anti-tumor agents |
| WO2004069145A2 (en) | 2003-02-07 | 2004-08-19 | Dr. Reddy's Laboratories Ltd. | Anticancer compounds, process for their preparation and pharmaceutical compositions containing them |
| CL2004000409A1 (es) * | 2003-03-03 | 2005-01-07 | Vertex Pharma | Compuestos derivados de 2-(cilo sustituido)-1-(amino u oxi sustituido)-quinazolina, inhibidores de canales ionicos de sodio y calcio dependientes de voltaje; composicion farmaceutica; y uso del compuesto en el tratamiento de dolor agudo, cronico, neu |
| CN1784391B (zh) * | 2003-03-03 | 2010-06-09 | 沃泰克斯药物股份有限公司 | 可用作离子通道调控剂的喹唑啉 |
| US7713983B2 (en) | 2003-03-03 | 2010-05-11 | Vertex Pharmaceuticals Incorporated | Quinazolines useful as modulators of ion channels |
| CN100475793C (zh) | 2003-03-31 | 2009-04-08 | 大正制药株式会社 | 喹唑啉衍生物及其制备药物的用途 |
| CA2528848C (en) | 2003-06-11 | 2012-09-04 | Xention Discovery Limited | Thienopyrimidine derivatives as potassium channel inhibitors |
| US7410975B2 (en) | 2003-06-20 | 2008-08-12 | Coley Pharmaceutical Group, Inc. | Small molecule toll-like receptor (TLR) antagonists |
| KR101218213B1 (ko) | 2003-07-03 | 2013-01-04 | 시토비아 인크. | 카스파제의 활성인자 및 세포자멸사의 유도인자로서의4-아릴아미노-퀴나졸린 |
| WO2005030217A1 (en) * | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Quinazoline potassium channel inhibitors |
| CA2543710A1 (en) | 2003-11-03 | 2005-05-12 | Warner-Lambert Company Llc | Novel norepinephrine reuptake inhibitors for the treatment of central nervous system disorders |
| JPWO2005080377A1 (ja) | 2004-02-20 | 2007-10-25 | キリンホールディングス株式会社 | TGFβ阻害活性を有する化合物およびそれを含んでなる医薬組成物 |
| WO2005087742A1 (en) | 2004-03-08 | 2005-09-22 | Exelixis, Inc. | Metabolic kinase modulators and methods of use as pesticides |
| CA2560098A1 (en) | 2004-03-15 | 2005-09-22 | Kyowa Hakko Kogyo Co., Ltd. | 2-aminoquinazoline derivative |
| CA2568304A1 (en) | 2004-06-10 | 2005-12-22 | Xention Discovery Limited | Furanopyrimidine compounds effective as potassium channel inhibitors |
| US20060014705A1 (en) | 2004-06-30 | 2006-01-19 | Howitz Konrad T | Compositions and methods for selectively activating human sirtuins |
| JP2008505907A (ja) | 2004-07-06 | 2008-02-28 | アンジオン バイオメディカ コーポレイション | 癌治療を目的として肝細胞増殖因子およびc−met活性を調整するキナゾリンモジュレーター |
| EP1879899B1 (en) | 2004-12-09 | 2010-08-04 | Xention Limited | Thienopyridine derivatives as potassium channel inhibitors |
| WO2006071095A1 (en) | 2004-12-31 | 2006-07-06 | Sk Chemicals Co., Ltd. | Quinazoline derivatives for the treatment and prevention of diabetes and obesity |
| EP1853302A2 (en) | 2005-02-18 | 2007-11-14 | Novartis Vaccines and Diagnostics, Inc. | Antiangiogenic agents with aldesleukin |
| AU2006224605B2 (en) | 2005-03-14 | 2012-03-01 | Aniona Aps | Potassium channel modulating agents and their medical use |
| BRPI0609719B8 (pt) | 2005-03-23 | 2021-05-25 | Hoffmann La Roche | derivados de acetilenil-pirazol-pirimidina como antagonistas de mgbur2 |
| WO2006105063A1 (en) | 2005-03-25 | 2006-10-05 | Scios Inc. | Heterobicylic inhibitors of tgfbeta |
| DK1869037T3 (da) | 2005-03-25 | 2011-10-24 | Tibotec Pharm Ltd | Heterobicykliske inhibitorer af HVC |
| WO2006118256A1 (ja) | 2005-04-28 | 2006-11-09 | Kyowa Hakko Kogyo Co., Ltd. | 2-アミノキナゾリン誘導体 |
| EP1901744A2 (en) | 2005-06-28 | 2008-03-26 | Bausch & Lomb Incorporated | Preparations comprising arylazine substituted with a carbonylic moiety to increase the activity of gelatinase a in ocular cells |
| GB0525164D0 (en) | 2005-12-09 | 2006-01-18 | Xention Discovery Ltd | Compounds |
| US20090306102A1 (en) | 2005-12-20 | 2009-12-10 | Eriksen Birgitte L | 2-pyridin-2-yl-quinazoline derivatives as potassium channel modulating agents for the treatment of respiratory diseases |
| JP2009520700A (ja) | 2005-12-21 | 2009-05-28 | ペインセプター ファーマ コーポレーション | 依存性イオンチャネルを調節するための組成物および方法 |
| DE102006012251A1 (de) | 2006-03-15 | 2007-11-08 | Grünenthal GmbH | Substituierte 4-Amino-chinazolin-Derivate und ihre Verwendung zur Herstellung von Arzneimitteln |
| WO2008003702A2 (en) | 2006-07-03 | 2008-01-10 | Vereniging Voor Christelijk Hoger Onderwijs, Wetenschappelijk Onderzoek En Patientenzorg | Fused bicyclic compounds interacting with the histamine h4 receptor |
| EP2061764B1 (en) | 2006-08-22 | 2014-07-02 | Technion Research & Development Foundation LTD. | Heterocyclic derivatives binding to the peripheral-type benzodiazepine receptor (pbr) |
| WO2008030120A1 (en) | 2006-09-07 | 2008-03-13 | Auckland Uniservices Limited | A method for the fluorescent detection of nitroreductase activity using nitro-substituted aromatic compounds |
| WO2008045529A1 (en) | 2006-10-12 | 2008-04-17 | Serenex, Inc. | Purine and pyrimidine derivatives for treatment of cancer and inflammatory diseases |
| US8039505B2 (en) | 2007-04-11 | 2011-10-18 | University Of Utah Research Foundation | Compounds for modulating T-cells |
| PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
| JP2010529031A (ja) | 2007-05-29 | 2010-08-26 | グラクソスミスクライン・リミテッド・ライアビリティ・カンパニー | Pi3キナーゼ阻害剤としてのナフチリジン誘導体 |
| US9603848B2 (en) | 2007-06-08 | 2017-03-28 | Senomyx, Inc. | Modulation of chemosensory receptors and ligands associated therewith |
| WO2009006141A2 (en) | 2007-07-05 | 2009-01-08 | Bausch & Lomb Incorporated | Authority to read as follows: compositions and methods for treating or controlling infections of the eye a sequelae thereof |
| US7829574B2 (en) | 2008-05-09 | 2010-11-09 | Hutchison Medipharma Enterprises Limited | Substituted quinazoline compounds and their use in treating angiogenesis-related diseases |
| CN101575333B (zh) | 2008-05-09 | 2011-06-22 | 和记黄埔医药(上海)有限公司 | 一种喹唑啉衍生物及其医药用途 |
| EP2279174A2 (en) | 2008-05-21 | 2011-02-02 | Genentech, Inc. | Arylsulfonamide compounds, compositions and methods of use |
| LT3575288T (lt) * | 2009-09-03 | 2021-12-10 | Bristol-Myers Squibb Company | Chinazolinai kaip kalio jonų kanalų inhibitoriai |
| EP2473054B1 (en) | 2009-09-04 | 2017-06-14 | The Regents of the University of Michigan | Compositions and methods for treatment of leukemia |
| AR079814A1 (es) | 2009-12-31 | 2012-02-22 | Otsuka Pharma Co Ltd | Compuestos heterociclicos, composiciones farmaceuticas que los contienen y sus usos |
-
2010
- 2010-09-01 LT LTEP19186129.3T patent/LT3575288T/lt unknown
- 2010-09-01 EP EP19186129.3A patent/EP3575288B1/en active Active
- 2010-09-01 CA CA2772642A patent/CA2772642C/en active Active
- 2010-09-01 CN CN201080049632.7A patent/CN102753535B/zh active Active
- 2010-09-01 EP EP16180810.0A patent/EP3124475B1/en active Active
- 2010-09-01 EP EP10754824.0A patent/EP2473487B1/en active Active
- 2010-09-01 MX MX2012002099A patent/MX2012002099A/es active IP Right Grant
- 2010-09-01 MY MYPI2012000987A patent/MY160243A/en unknown
- 2010-09-01 DK DK19186129.3T patent/DK3575288T3/da active
- 2010-09-01 HR HRP20211973TT patent/HRP20211973T1/hr unknown
- 2010-09-01 US US13/393,328 patent/US8575184B2/en active Active
- 2010-09-01 SM SM20210717T patent/SMT202100717T1/it unknown
- 2010-09-01 SI SI201032099T patent/SI3575288T1/sl unknown
- 2010-09-01 EA EA201270378A patent/EA021113B1/ru not_active IP Right Cessation
- 2010-09-01 HU HUE19186129A patent/HUE057433T2/hu unknown
- 2010-09-01 WO PCT/US2010/047430 patent/WO2011028741A1/en not_active Ceased
- 2010-09-01 ES ES19186129T patent/ES2900504T3/es active Active
- 2010-09-01 PT PT107548240T patent/PT2473487T/pt unknown
- 2010-09-01 KR KR1020127008470A patent/KR101698631B1/ko active Active
- 2010-09-01 TW TW099129546A patent/TWI488851B/zh active
- 2010-09-01 PL PL19186129T patent/PL3575288T3/pl unknown
- 2010-09-01 SG SG2012013918A patent/SG178592A1/en unknown
- 2010-09-01 SI SI201031326T patent/SI2473487T1/sl unknown
- 2010-09-01 PE PE2012000290A patent/PE20121153A1/es active IP Right Grant
- 2010-09-01 ES ES16180810T patent/ES2750598T3/es active Active
- 2010-09-01 PT PT191861293T patent/PT3575288T/pt unknown
- 2010-09-01 DK DK10754824.0T patent/DK2473487T3/en active
- 2010-09-01 AU AU2010289641A patent/AU2010289641B2/en active Active
- 2010-09-01 LT LTEP10754824.0T patent/LT2473487T/lt unknown
- 2010-09-01 NZ NZ598516A patent/NZ598516A/xx unknown
- 2010-09-01 BR BR112012008330-9A patent/BR112012008330B1/pt active IP Right Grant
- 2010-09-01 SM SM20170026T patent/SMT201700026T1/it unknown
- 2010-09-01 HR HRP20161669TT patent/HRP20161669T1/hr unknown
- 2010-09-01 ES ES10754824.0T patent/ES2609335T3/es active Active
- 2010-09-01 HU HUE10754824A patent/HUE032983T2/en unknown
- 2010-09-01 JP JP2012527985A patent/JP5643312B2/ja active Active
- 2010-09-01 PL PL10754824T patent/PL2473487T3/pl unknown
- 2010-09-03 AR ARP100103247A patent/AR078326A1/es active IP Right Grant
-
2012
- 2012-02-10 TN TNP2012000063A patent/TN2012000063A1/en unknown
- 2012-02-16 IL IL218169A patent/IL218169A/en active IP Right Grant
- 2012-03-02 CL CL2012000583A patent/CL2012000583A1/es unknown
- 2012-03-07 CO CO12040232A patent/CO6511220A2/es active IP Right Grant
- 2012-04-02 ZA ZA2012/02383A patent/ZA201202383B/en unknown
-
2013
- 2013-09-27 US US14/038,814 patent/US9458114B2/en active Active
-
2014
- 2014-10-30 JP JP2014221908A patent/JP5950978B2/ja active Active
-
2016
- 2016-08-29 US US15/249,710 patent/US9822096B2/en active Active
-
2017
- 2017-01-16 SM SM201700026T patent/SMT201700026B/it unknown
- 2017-01-23 CY CY20171100095T patent/CY1118488T1/el unknown
- 2017-10-04 US US15/724,566 patent/US10214511B2/en active Active
-
2019
- 2019-01-09 US US16/243,400 patent/US10676460B2/en active Active
-
2020
- 2020-05-01 US US16/864,825 patent/US11008306B2/en active Active
-
2021
- 2021-04-15 US US17/231,088 patent/US20220324836A1/en not_active Abandoned
- 2021-12-16 CY CY20211101107T patent/CY1125021T1/el unknown
-
2023
- 2023-03-24 US US18/125,826 patent/US20230322726A1/en not_active Abandoned
-
2025
- 2025-04-07 US US19/171,423 patent/US20250230144A1/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR078326A1 (es) | Quinazolinas como inhibidores de los canales ionicos de potasio y composiciones farmaceuticas que los contienen | |
| PE20151951A1 (es) | Heteroarildihidropirimidinas unidas por puentes en 6 para el tratamiento y la profilaxis de infeccion por el virus de la hepatitis b | |
| PH12014502866A1 (en) | Fungicidal heterocyclic carboxamides | |
| BR112015021027A2 (pt) | compostos terapêuticos | |
| AR077818A1 (es) | Composiciones pesticidas | |
| EA201690019A1 (ru) | Производное аминотриазина и содержащая его фармацевтическая композиция | |
| ES2770058T3 (es) | Compuestos y composiciones destinados a modular las actividades de quinasa de EGFR mutante | |
| PE20160608A1 (es) | Compuestos de quinolina selectivamente sustituida | |
| AR083367A1 (es) | Compuestos de tipo quinazolinona como antagonistas de crth | |
| AR103222A1 (es) | Procedimiento para la preparación de análogos de 4-fenil-5-alcoxicarbonil-2-tiazol-2-il-1,4-dihidropirimidina | |
| AR090539A1 (es) | COMPUESTOS INHIBIDORES DE b LACTAMASA | |
| EA201690760A1 (ru) | Производные карбоксамида и их применение в качестве медикаментов для лечения гепатита b | |
| EA201591775A1 (ru) | Замещенные ароматические соединения и связанный с ними способ лечения фиброза | |
| ES2539722T3 (es) | Compuesto de tetrahidrobenzotiofeno | |
| AR082889A1 (es) | Compuestos y composiciones para la inhibicion de nampt | |
| JP2016540742A5 (es) | ||
| AR093184A1 (es) | Compuesto de pirimidina sustituida como inhibidor de quinurenina-3-monooxigenasa y composicion farmaceutica que lo comprenden | |
| BR112016012123A8 (pt) | composto de triazolo-piridina | |
| PE20181039A1 (es) | Metodo para preparar derivados de acido 3-(2-anilino-1-ciclohexil-1h-bencimidazol-5-il)propanoico sustituido | |
| PH12017501652A1 (en) | Kv1.3 inhibitors and their medical application | |
| PE20141201A1 (es) | Compuestos de benzofurano para el tratamiento de infecciones por el virus de hepatitis c (hcv) | |
| MY182353A (en) | Novel sulfonimidoylpurinone compounds and derivatives for the treatment and prophylaxis of virus infection | |
| EA201600241A1 (ru) | Замещенные (2r,3r,5r)-3-гидрокси-(5-пиримидин-1-ил)тетрагидрофуран-2-илметил арил фосфорамидаты | |
| EA202090040A1 (ru) | Композиция для инъекции | |
| EA201891770A1 (ru) | Малеатная соль агониста tlr7, ее кристаллические формы c, d и e, способы получения и применение малеатной соли и кристаллических форм |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant, registration |