AR085149A1 - Moduladores del receptor de glucagon - Google Patents
Moduladores del receptor de glucagonInfo
- Publication number
- AR085149A1 AR085149A1 ARP120100379A ARP120100379A AR085149A1 AR 085149 A1 AR085149 A1 AR 085149A1 AR P120100379 A ARP120100379 A AR P120100379A AR P120100379 A ARP120100379 A AR P120100379A AR 085149 A1 AR085149 A1 AR 085149A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- fluorine
- cycloalkyl
- independently
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non 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
- A61K31/505—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
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/16—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or 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
- C07D231/18—One oxygen or sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C07D233/61—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/68—Halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/70—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
- C07D249/06—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- C07D401/12—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
- C07D403/04—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
- C07D405/14—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
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Electrotherapy Devices (AREA)
- Peptides Or Proteins (AREA)
Abstract
Se ha encontrado que los compuestos de fórmula (1) actúan como antagonistas o agonistas inversos de glucagón. En consecuencia, los compuestos de fórmula (1) y las composiciones farmacéuticas del mismo son útiles para el tratamiento de enfermedades, trastornos o afecciones mediadas por glucagón.Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable del mismo; en la que R1 es un grupo heteroarilo de 5 miembros unido a través de bien un átomo de carbono o un átomo de nitrógeno y que está opcionalmente condensado con un cicloalquilo C4-7, un fenilo o un heteroarilo de 6 miembros; estando el heteroarilo de 5 miembros opcionalmente sustituido con uno a cuatro sustituyentes seleccionados cada uno independientemente de entre halo, -S(O)2-alquilo C1-3, -S-alquilo C1-3, hidroxilo, -C(O)NRaRb, cicloalquilo C3-5, ciano, fenilo que está opcionalmente sustituido con uno a tres halo, ciano, alquilo C1-3 o alcoxi C1-3, heteroarilo de 6 miembros que está opcionalmente sustituido con uno a tres halo, ciano, alquilo C1-3 o alcoxi C1-3, alquilo C1-6 opcionalmente sustituido con uno a tres flúor, o alcoxi C1-6 opcionalmente sustituido con uno a tres flúor; Ra y Rb son cada uno independientemente H o alquilo C1-3; R2 es H o metilo; R3 es tetrazolilo, -CH2-tetrazolilo, -(CH2)2SO3H o -(CH2)2CO2H, -CH2CHFCO2H o -CH2CHOHCO2H; A1, A2, A3 y A4 son cada uno independientemente CR4 o N, con la condición de que no más de dos de entre A1, A2, A3 y A4 sean N; R4 en cada aparición es independientemente H, halo, ciano, alquilo C1-3 opcionalmente sustituido con uno a tres flúor, o alcoxi C1-3 opcionalmente sustituido con uno a tres flúor; L es -X-CH(R5)- o -CH(R5)-X-; X es CH2, O o NH; R5 es alquilo C1-6 que está opcionalmente sustituido con uno a tres flúor, hidroxilo o metoxi; cicloalquilo C3-7 que está opcionalmente sustituido con uno a dos alquilo C1-3 que están opcionalmente sustituidos con uno a tres flúor y pudiendo estar reemplazados uno a dos carbonos del cicloalquilo C3-7 por un NH, N-alquilo C1-3, O ó S; o cicloalquil C3-7-alquilo C1-6, en el que el grupo cicloalquilo C3-7 de dicho cicloalquil C3-7-alquilo C1-6 está opcionalmente sustituido con uno a dos alquilo C1-3 que están opcionalmente sustituidos con uno a tres flúor; B1, B2, B3 y B4 son cada uno independientemente CR6 o N, con la condición de que no más de dos de B1, B2, B3 y B4 sean N; y R6 en cada aparición es independientemente H, halo, alquilo C1-3 opcionalmente sustituidos con uno a tres flúor, o alcoxi C1-3 opcionalmente sustituido con uno a tres flúor.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161440578P | 2011-02-08 | 2011-02-08 | |
US201161441044P | 2011-02-09 | 2011-02-09 | |
US201261585834P | 2012-01-12 | 2012-01-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR085149A1 true AR085149A1 (es) | 2013-09-11 |
Family
ID=45607316
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP120100379A AR085149A1 (es) | 2011-02-08 | 2012-02-06 | Moduladores del receptor de glucagon |
Country Status (38)
Country | Link |
---|---|
US (5) | US8507533B2 (es) |
EP (1) | EP2673260B1 (es) |
JP (1) | JP5562495B2 (es) |
KR (2) | KR101585840B1 (es) |
CN (2) | CN103370306B (es) |
AP (1) | AP3338A (es) |
AR (1) | AR085149A1 (es) |
AU (1) | AU2012215114B2 (es) |
BR (1) | BR112013020035A2 (es) |
CA (1) | CA2825102C (es) |
CL (1) | CL2013002053A1 (es) |
CO (1) | CO6741217A2 (es) |
CR (1) | CR20130372A (es) |
CY (1) | CY1118039T1 (es) |
DK (1) | DK2673260T3 (es) |
DO (1) | DOP2013000181A (es) |
EA (1) | EA023517B1 (es) |
EC (1) | ECSP13012871A (es) |
ES (1) | ES2597972T3 (es) |
GE (1) | GEP20156351B (es) |
GT (1) | GT201300196A (es) |
HK (2) | HK1188992A1 (es) |
HR (1) | HRP20161177T1 (es) |
HU (1) | HUE030364T2 (es) |
IL (1) | IL227559A (es) |
LT (1) | LT2673260T (es) |
ME (1) | ME02502B (es) |
MX (1) | MX2013009140A (es) |
NI (1) | NI201300068A (es) |
PE (1) | PE20140253A1 (es) |
PT (1) | PT2673260T (es) |
RS (1) | RS55225B1 (es) |
SG (1) | SG192004A1 (es) |
SI (1) | SI2673260T1 (es) |
TW (3) | TW201540710A (es) |
UY (1) | UY33896A (es) |
WO (1) | WO2012107850A1 (es) |
ZA (1) | ZA201306310B (es) |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL227559A (en) * | 2011-02-08 | 2016-04-21 | Pfizer | Glucagon receptor modulator |
WO2012170931A2 (en) | 2011-06-10 | 2012-12-13 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
WO2013059677A1 (en) | 2011-10-19 | 2013-04-25 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
EP2832725A4 (en) | 2012-03-29 | 2015-11-25 | Takeda Pharmaceutical | AROMATIC RING CONNECTION |
US9580407B2 (en) | 2012-12-07 | 2017-02-28 | Merck Sharp & Dohme Corp. | Regioselective N-2 arylation of indazoles |
MX2015014407A (es) | 2013-04-15 | 2015-12-07 | Du Pont | Amidas fungicidas. |
CN107235960B (zh) * | 2016-03-29 | 2021-01-29 | 浙江海正药业股份有限公司 | 酰胺类衍生物、其制备方法及其在医药上的用途 |
DK3573611T3 (da) * | 2017-01-24 | 2022-04-11 | Alphala Co Ltd | Amidforbindelser og anvendelse deraf |
US10357493B2 (en) | 2017-03-10 | 2019-07-23 | Selenity Therapeutics (Bermuda), Ltd. | Metalloenzyme inhibitor compounds |
IL270068B (en) | 2017-04-24 | 2022-06-01 | Tesaro Inc | Manufacturing methods of Niraprib |
CA3089374A1 (en) * | 2018-02-28 | 2019-09-06 | Basf Se | Use of alkoxypyrazoles as nitrification inhibitors |
WO2019224139A1 (de) * | 2018-05-24 | 2019-11-28 | Bayer Aktiengesellschaft | Verfahren zur herstellung von halogenierten n-arylpyrazolen |
US11066404B2 (en) | 2018-10-11 | 2021-07-20 | Incyte Corporation | Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors |
WO2020168197A1 (en) | 2019-02-15 | 2020-08-20 | Incyte Corporation | Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors |
TW202100520A (zh) | 2019-03-05 | 2021-01-01 | 美商英塞特公司 | 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物 |
US11919904B2 (en) | 2019-03-29 | 2024-03-05 | Incyte Corporation | Sulfonylamide compounds as CDK2 inhibitors |
WO2020223558A1 (en) | 2019-05-01 | 2020-11-05 | Incyte Corporation | Tricyclic amine compounds as cdk2 inhibitors |
US11440914B2 (en) | 2019-05-01 | 2022-09-13 | Incyte Corporation | Tricyclic amine compounds as CDK2 inhibitors |
KR20220064369A (ko) | 2019-08-14 | 2022-05-18 | 인사이트 코포레이션 | Cdk2 저해제로서의 이미다졸릴 피리디미딘일아민 화합물 |
BR112022006977A2 (pt) | 2019-10-11 | 2022-09-20 | Incyte Corp | Aminas bicíclicas como inibidores de cdk2 |
MX2022011025A (es) * | 2020-03-06 | 2022-10-07 | Alphala Co Ltd | Procesos para producir compuestos de amida, y su forma cristalina y de sal. |
CN111793033A (zh) * | 2020-08-10 | 2020-10-20 | 成都正善达生物医药科技有限公司 | 一种普那布林中间体咪唑甲醛类化合物的制备方法 |
US11981671B2 (en) | 2021-06-21 | 2024-05-14 | Incyte Corporation | Bicyclic pyrazolyl amines as CDK2 inhibitors |
US11976073B2 (en) | 2021-12-10 | 2024-05-07 | Incyte Corporation | Bicyclic amines as CDK2 inhibitors |
Family Cites Families (111)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5320825A (en) | 1991-05-01 | 1994-06-14 | Trustees Of The University Of Pennsylvania | Serotonin reuptake inhibitors for S.P.E.C.T. imaging |
WO1994014427A2 (en) | 1992-12-23 | 1994-07-07 | Zymogenetics, Inc. | Use of skyrin and analogues for the treatment of diabetes mellitus and process for their preparation |
ATE189217T1 (de) | 1993-03-19 | 2000-02-15 | Merck & Co Inc | Phenoxyphenylessigsäurederivate |
GB9408185D0 (en) | 1994-04-25 | 1994-06-15 | Fujisawa Pharmaceutical Co | New benzamide derivatives, processes for the preparation thereof and pharmaceutical composition comprising the same |
DE4426346A1 (de) | 1994-07-25 | 1996-02-01 | Basf Ag | Herbizide Pyrazinderivate |
GB2292149A (en) | 1994-08-09 | 1996-02-14 | Ferring Res Ltd | Peptide inhibitors of pro-interleukin-1beta converting enzyme |
AU3642795A (en) | 1994-09-27 | 1996-04-19 | Merck & Co., Inc. | Endothelin receptor antagonists for the treatment of emesis |
US5837719A (en) | 1995-08-10 | 1998-11-17 | Merck & Co., Inc. | 2,5-substituted aryl pyrroles, compositions containing such compounds and methods of use |
EP0859771A4 (en) | 1995-10-31 | 2000-03-15 | Merck & Co Inc | SUBSTITUTED PYRIDYL PYRROLES, COMPOSITIONS CONTAINING SUCH COMPOUNDS AND METHOD OF USE |
AR008789A1 (es) | 1996-07-31 | 2000-02-23 | Bayer Corp | Piridinas y bifenilos substituidos |
US5776954A (en) | 1996-10-30 | 1998-07-07 | Merck & Co., Inc. | Substituted pyridyl pyrroles, compositions containing such compounds and methods of use |
CA2271893A1 (en) | 1996-11-20 | 1998-05-28 | Linda L. Chang | Triaryl substituted imidazoles as glucagon antagonists |
US5880139A (en) | 1996-11-20 | 1999-03-09 | Merck & Co., Inc. | Triaryl substituted imidazoles as glucagon antagonists |
IL130181A0 (en) | 1996-12-05 | 2000-06-01 | Amgen Inc | Substituted pyrimidone and pyridone compounds and methods of use |
JP2002514195A (ja) | 1996-12-05 | 2002-05-14 | アムジエン・インコーポレーテツド | 置換ピリミジン化合物およびそれの使用 |
PL334059A1 (en) | 1996-12-11 | 2000-01-31 | Basf Ag | Ketone benzamides useful as calpain inhibitors |
JPH10259176A (ja) | 1997-03-17 | 1998-09-29 | Japan Tobacco Inc | 血管新生阻害作用を有する新規アミド誘導体及びその用途 |
WO1999001423A1 (en) | 1997-07-01 | 1999-01-14 | Novo Nordisk A/S | Glucagon antagonists/inverse agonists |
US6022884A (en) | 1997-11-07 | 2000-02-08 | Amgen Inc. | Substituted pyridine compounds and methods of use |
EP1042293B9 (en) | 1997-12-19 | 2008-09-03 | Amgen Inc. | Substituted pyridine and pyridazine compounds and their pharmaceutical use |
DE60035682T2 (de) | 1999-04-28 | 2008-04-30 | Sanofi-Aventis Deutschland Gmbh | Di-aryl-säurederivate als ppar rezeptor liganden |
WO2000064876A1 (en) | 1999-04-28 | 2000-11-02 | Aventis Pharma Deutschland Gmbh | Tri-aryl acid derivatives as ppar receptor ligands |
ES2250128T3 (es) | 1999-05-17 | 2006-04-16 | Novo Nordisk A/S | Antagonistas/agonistas inversos de glucagon. |
CN1437581A (zh) | 2000-06-23 | 2003-08-20 | 诺沃挪第克公司 | 胰高血糖素拮抗剂/反向激动剂 |
EP1345891A1 (en) | 2000-11-17 | 2003-09-24 | Novo Nordisk A/S | Glucagon antagonist/inverse agonist |
US20030203946A1 (en) | 2000-11-17 | 2003-10-30 | Carsten Behrens | Glucagon antagonists/inverse agonists |
GEP20053710B (en) | 2001-02-28 | 2005-12-26 | Merck & Co Inc | Acylated Piperidine Derivatives as Melanocortin-4 Receptor Agonists |
DE10110749A1 (de) | 2001-03-07 | 2002-09-12 | Bayer Ag | Substituierte Aminodicarbonsäurederivate |
EP1463715A1 (en) | 2001-12-03 | 2004-10-06 | Novo Nordisk A/S | Novel glucagon antagonists |
WO2003047626A1 (en) | 2001-12-03 | 2003-06-12 | Novo Nordisk A/S | Use of a glucokinase activator in combination with a glucagon antagonist for treating type 2 diabetes |
WO2003051357A1 (en) | 2001-12-19 | 2003-06-26 | Novo Nordisk A/S | Glucagon receptor antagonists/inverse agonists |
WO2003053938A1 (en) | 2001-12-20 | 2003-07-03 | Novo Nordisk A/S | Benzimidazols and indols as glucagon receptor antagonists/inverse agonisten |
JP2005518391A (ja) | 2001-12-21 | 2005-06-23 | ノボ ノルディスク アクティーゼルスカブ | Gk活性化剤としてのアミド誘導体 |
KR20090083491A (ko) | 2002-02-01 | 2009-08-03 | 다이닛본 스미토모 세이야꾸 가부시끼가이샤 | 2-퓨란 카르복시산 하이드라지드 화합물 및 그것을 함유하는 의약 조성물 |
MXPA04009040A (es) | 2002-03-20 | 2005-01-25 | Metabolex Inc | Acidos fenilaceticos sustituidos. |
WO2003087044A2 (en) | 2002-04-09 | 2003-10-23 | 7Tm Pharma A/S | Novel carboxamide compounds for use in mch receptor related disorders |
AU2003233780A1 (en) | 2002-06-27 | 2004-01-19 | Novo Nordisk A/S | Novel glucagon antagonists/inverse agonists |
JP4881559B2 (ja) | 2002-06-27 | 2012-02-22 | ノボ・ノルデイスク・エー/エス | 治療薬としてのアリールカルボニル誘導体 |
AU2003268529B2 (en) | 2002-09-12 | 2007-08-09 | Merck & Co., Inc. | Method of treating diabetes and related conditions |
US7196106B2 (en) | 2002-11-05 | 2007-03-27 | Merck & Co., Inc | Cyanothiophene derivatives, compositions containing such compounds and methods of use |
US20040097557A1 (en) | 2002-11-13 | 2004-05-20 | Duffy Joseph L. | Cyanothiophene derivatives, compositions containing such compounds and methods of use |
CA2508581A1 (en) | 2002-12-04 | 2004-06-17 | Merck & Co., Inc. | Spirocyclic ureas, compositions containing such compounds and methods of use |
AU2003291959A1 (en) | 2002-12-20 | 2004-07-14 | Novo Nordisk A/S | Novel glucagon antagonists |
US20040209928A1 (en) | 2002-12-30 | 2004-10-21 | Ravi Kurukulasuriya | Glucagon receptor antagonists/inverse agonists |
DE10300398A1 (de) | 2003-01-09 | 2004-07-22 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Verwendung von substituierten 2-Phenylbenzimidazolen als Arzneimittel |
US7151114B2 (en) | 2003-01-09 | 2006-12-19 | Boehringer Ingelheim International Gmbh | Use of substituted 2-phenylbenzimidazoles as medicaments |
WO2004063147A1 (en) | 2003-01-10 | 2004-07-29 | Novo Nordisk A/S | Salts and solvates of glucagon antagonists |
ATE490244T1 (de) | 2003-01-27 | 2010-12-15 | Merck Sharp & Dohme | Substituierte pyrazole, zusammensetzungen,die solche verbindungen enthalten, und anwendungsverfahren |
DE602004011511T2 (de) | 2003-04-14 | 2009-01-29 | The Institutes for Pharmaceutical Discovery, LLC, Branford | N-(((((1,3-thiazol-2-yl)amino)carbonyl)phenyl)sulphonyl)phenylalanin derivate und verwandte verbindungen zur behandlung von diabetes |
US7138529B2 (en) | 2003-04-16 | 2006-11-21 | Hoffmann-La Roche Inc. | Substituted 3-cyanothiophene acetamides as glucagon receptor antagonists |
AU2004236248A1 (en) | 2003-04-30 | 2004-11-18 | The Institutes For Pharmaceutical Discovery, Llc | Phenyl substituted carboxylic acids |
EP1626717A4 (en) | 2003-05-09 | 2009-09-09 | Merck & Co Inc | BENZIMIDAZOLE, COMPOSITIONS AND METHOD OF ADMINISTRATION CONTAINING SUCH COMPOUNDS |
US7355049B2 (en) | 2003-06-24 | 2008-04-08 | Hoffmann-La Roche Inc. | Biaryloxymethylarenecarboxylic acids as glycogen synthase activator |
JP4412098B2 (ja) | 2003-07-31 | 2010-02-10 | Jfeスチール株式会社 | 溶接熱影響部靭性に優れた低降伏比高強度鋼板及びその製造方法 |
US7501538B2 (en) | 2003-08-08 | 2009-03-10 | Transtech Pharma, Inc. | Aryl and heteroaryl compounds, compositions and methods of use |
WO2005058845A2 (en) | 2003-12-19 | 2005-06-30 | Novo Nordisk A/S | Novel glucagon antagonists/inverse agonists |
JP2007514794A (ja) | 2003-12-19 | 2007-06-07 | メルク エンド カムパニー インコーポレーテッド | 環式グアニジン、そのような化合物を含む組成、及び使用方法 |
UA84208C2 (en) | 2004-05-25 | 2008-09-25 | Пфайзер Продактс Инк. | Tetraazabenzo(e)azulene derivatives and analogs thereof |
US7989457B2 (en) * | 2004-05-28 | 2011-08-02 | Eli Lilly And Company | Glucagon receptor antagonists, preparation and therapeutic uses |
ES2306165T3 (es) | 2004-06-04 | 2008-11-01 | MERCK & CO., INC. | Derivados de pirazol, composiciones que contienen dichos compuestos y procedimientos de uso. |
PL1758853T3 (pl) | 2004-06-14 | 2010-06-30 | Lilly Co Eli | Antagoniści receptora glukagonu, wytwarzanie i zastosowania terapeutyczne |
WO2006017055A2 (en) | 2004-07-07 | 2006-02-16 | Merck & Co., Inc. | Pyrazole amide derivatives, compositions containing such compounds and methods of use |
CN1993124A (zh) | 2004-07-22 | 2007-07-04 | 默克公司 | 取代吡唑、含有这种化合物的组合物及其应用 |
DE102004051188A1 (de) | 2004-10-21 | 2006-04-27 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Cyanothiophene, deren Herstellung und deren Verwendung als Arzneimittel |
US7524870B2 (en) | 2004-12-03 | 2009-04-28 | Hoffmann-La Roche Inc. | Biaryloxymethylarenecarboxylic acids as glycogen synthase activators |
PA8660701A1 (es) | 2005-02-04 | 2006-09-22 | Pfizer Prod Inc | Agonistas de pyy y sus usos |
KR20070104409A (ko) | 2005-02-11 | 2007-10-25 | 일라이 릴리 앤드 캄파니 | 글루카곤 수용체 길항제로서의 치환된 티오펜 유도체, 제법및 치료 용도 |
CA2600159A1 (en) | 2005-03-21 | 2006-09-28 | Merck & Co., Inc. | Substituted aryl and heteroaryl derivatives, compositions containing such compounds and methods of use |
CA2600833A1 (en) | 2005-03-30 | 2006-10-05 | Merck & Co., Inc. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
CN101300232A (zh) | 2005-07-26 | 2008-11-05 | 默克公司 | 合成取代的吡唑的方法 |
US7754717B2 (en) | 2005-08-15 | 2010-07-13 | Amgen Inc. | Bis-aryl amide compounds and methods of use |
BRPI0616960B8 (pt) | 2005-10-06 | 2021-05-25 | Probi Ab | uso de lactobacilo para o tratamento de infecções virais |
TW200745031A (en) | 2005-10-13 | 2007-12-16 | Merck & Co Inc | Acyl indoles, compositions containing such compounds and methods of use |
AR056574A1 (es) | 2005-10-19 | 2007-10-10 | Merck & Co Inc | Derivados de pirazol, composiciones que contienen dichos compuestos y procedimientos de uso |
EP2298308B1 (en) | 2005-11-14 | 2013-01-16 | University Of Southern California | Integrin-binding small molecules |
JP5198280B2 (ja) * | 2005-11-17 | 2013-05-15 | イーライ リリー アンド カンパニー | グルカゴン受容体アンタゴニスト、並びにその調製及び治療への使用 |
ES2391109T3 (es) | 2005-11-17 | 2012-11-21 | Eli Lilly And Company | Antagonistas del receptor de glucagón, preparación y usos terapéuticos |
AU2006341392B2 (en) * | 2005-11-18 | 2012-05-17 | Eli Lilly And Company | Glucagon receptor antagonists, preparation and therapeutic uses |
BRPI0618140A2 (pt) * | 2005-11-22 | 2011-08-16 | Lilly Co Eli | composto ou sal farmaceuticamente aceitável do mesmo, composição farmacêutica, e, uso de um composto ou um sal do mesmo |
CA2629311C (en) | 2005-11-23 | 2014-05-06 | Eli Lilly And Company | Glucagon receptor antagonists, preparation and therapeutic uses |
AU2006327892B2 (en) | 2005-12-19 | 2011-12-22 | Methylgene Inc. | Histone deacetylase inhibitors for enhancing activity of antifungal agents |
TW200806611A (en) | 2006-02-09 | 2008-02-01 | Daiichi Seiyaku Co | Novel amidopropionic acid derivatives and medicine containing the same |
EP2001472A2 (en) | 2006-03-23 | 2008-12-17 | Merck and Co., Inc. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
WO2007136577A2 (en) | 2006-05-16 | 2007-11-29 | Merck & Co., Inc. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
TW200821284A (en) | 2006-10-03 | 2008-05-16 | Merck & Co Inc | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
KR101538810B1 (ko) | 2007-02-09 | 2015-07-22 | 메타베이시스 테라퓨틱스, 인크. | 글루카곤 수용체의 길항제 |
JP2009040702A (ja) | 2007-08-07 | 2009-02-26 | Daiichi Sankyo Co Ltd | 新規アミドプロピオン酸誘導体を含有する医薬組成物 |
US8232413B2 (en) | 2007-09-12 | 2012-07-31 | Merck Sharp & Dohme Corp. | Process for the production of a crystalline glucagon receptor antagonist compound |
JP5450083B2 (ja) | 2007-11-01 | 2014-03-26 | 武田薬品工業株式会社 | 複素環化合物 |
ES2382579T3 (es) | 2007-12-11 | 2012-06-11 | Cadila Healthcare Limited | Peptidomiméticos con actividad antagonista de glucagón y agonista de GLP-1 |
MY158982A (en) | 2008-03-05 | 2016-11-30 | Takeda Pharmaceuticals Co | Heterocyclic compound |
EA018225B1 (ru) | 2008-03-07 | 2013-06-28 | Транстек Фарма, Инк. | Соединения оксадиазоантрацена для лечения диабета |
CA2724294A1 (en) | 2008-05-16 | 2009-11-19 | Schering Corporation | Glucagon receptor antagonists, compositions, and methods for their use |
CA2770298C (en) | 2008-08-13 | 2017-06-20 | Metabasis Therapeutics, Inc. | Glucagon antagonists |
WO2010019828A1 (en) | 2008-08-13 | 2010-02-18 | Metabasis Therapeutics, Inc. | Glucagon receptor antagonists |
EP2346830B1 (en) | 2008-09-15 | 2015-05-13 | Merck Sharp & Dohme Corp. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
WO2010039789A1 (en) | 2008-10-03 | 2010-04-08 | Schering Corporation | Spiro-imidazolone derivatives as glucagon receptor antagonists |
WO2010071750A1 (en) | 2008-12-19 | 2010-06-24 | Merck Sharp & Dohme Corp. | Glucagon receptor antagonist compounds |
US8697740B2 (en) | 2009-01-12 | 2014-04-15 | Merck Sharp & Dohme Corp. | Crystalline polymorphic forms of an antidiabetic compound |
US20110281795A1 (en) | 2009-01-28 | 2011-11-17 | Songnian Lin | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
US8809579B2 (en) | 2009-02-13 | 2014-08-19 | Merck Sharp & Dohme Corp. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
US8318667B2 (en) | 2009-02-25 | 2012-11-27 | Merck Sharp & Dohme Corp. | Glucagon receptor antagonist compounds, compositions containing such compounds and methods of use |
CN102459215B (zh) | 2009-05-14 | 2016-03-02 | 大日本住友制药株式会社 | 3-(4-氨基苯基)-2-呋喃甲酸衍生物及其药学上可接受的盐 |
WO2010144664A1 (en) | 2009-06-12 | 2010-12-16 | Schering Corporation | Thiophenes as glucagon receptor antagonists, compositions, and methods for their use |
JP2012188352A (ja) | 2009-07-13 | 2012-10-04 | Dainippon Sumitomo Pharma Co Ltd | 3−(4−置換アルキル−フェニル)−2−フランカルボン酸誘導体およびその薬学的に許容される塩 |
WO2011027849A1 (ja) | 2009-09-04 | 2011-03-10 | 武田薬品工業株式会社 | 複素環化合物 |
US8735604B2 (en) | 2009-09-22 | 2014-05-27 | Merck Sharp & Dohme Corp. | Pyrrolidines as glucagon receptor antagonists, compositions, and methods for their use |
CA2794003A1 (en) | 2010-03-25 | 2011-09-29 | Merck Sharp & Dohme Corp. | Novel spiro imidazolones as glucagon receptor antagonists, compositions, and methods for their use |
AU2011232657A1 (en) | 2010-03-26 | 2012-09-27 | Merck Sharp & Dohme Corp. | Novel spiro imidazolone derivatives as glucagon receptor antagonists, compositions, and methods for their use |
CN102206172B (zh) | 2010-03-30 | 2015-02-25 | 中国医学科学院医药生物技术研究所 | 一组取代双芳基化合物及其制备方法和抗病毒应用 |
IL227559A (en) * | 2011-02-08 | 2016-04-21 | Pfizer | Glucagon receptor modulator |
-
2012
- 2012-01-25 IL IL227559A patent/IL227559A/en not_active IP Right Cessation
- 2012-01-25 CN CN201280008064.5A patent/CN103370306B/zh not_active Expired - Fee Related
- 2012-01-25 AP AP2013007012A patent/AP3338A/xx active
- 2012-01-25 GE GEAP201213184A patent/GEP20156351B/en unknown
- 2012-01-25 ME MEP-2016-180A patent/ME02502B/me unknown
- 2012-01-25 KR KR1020157007040A patent/KR101585840B1/ko not_active IP Right Cessation
- 2012-01-25 HU HUE12704132A patent/HUE030364T2/hu unknown
- 2012-01-25 JP JP2013552293A patent/JP5562495B2/ja not_active Expired - Fee Related
- 2012-01-25 ES ES12704132.5T patent/ES2597972T3/es active Active
- 2012-01-25 DK DK12704132.5T patent/DK2673260T3/en active
- 2012-01-25 BR BR112013020035A patent/BR112013020035A2/pt not_active Application Discontinuation
- 2012-01-25 PT PT127041325T patent/PT2673260T/pt unknown
- 2012-01-25 AU AU2012215114A patent/AU2012215114B2/en not_active Ceased
- 2012-01-25 MX MX2013009140A patent/MX2013009140A/es active IP Right Grant
- 2012-01-25 LT LTEP12704132.5T patent/LT2673260T/lt unknown
- 2012-01-25 SI SI201230703A patent/SI2673260T1/sl unknown
- 2012-01-25 KR KR1020137023535A patent/KR101638671B1/ko active IP Right Grant
- 2012-01-25 WO PCT/IB2012/050349 patent/WO2012107850A1/en active Application Filing
- 2012-01-25 EA EA201390969A patent/EA023517B1/ru not_active IP Right Cessation
- 2012-01-25 CN CN201510053906.4A patent/CN104744370A/zh active Pending
- 2012-01-25 PE PE2013001827A patent/PE20140253A1/es not_active Application Discontinuation
- 2012-01-25 SG SG2013054614A patent/SG192004A1/en unknown
- 2012-01-25 CA CA2825102A patent/CA2825102C/en not_active Expired - Fee Related
- 2012-01-25 EP EP12704132.5A patent/EP2673260B1/en active Active
- 2012-01-25 RS RS20160846A patent/RS55225B1/sr unknown
- 2012-02-06 TW TW104122773A patent/TW201540710A/zh unknown
- 2012-02-06 AR ARP120100379A patent/AR085149A1/es unknown
- 2012-02-06 TW TW101103776A patent/TWI490202B/zh not_active IP Right Cessation
- 2012-02-06 TW TW103114218A patent/TW201429947A/zh unknown
- 2012-02-07 UY UY0001033896A patent/UY33896A/es not_active Application Discontinuation
- 2012-02-07 US US13/367,459 patent/US8507533B2/en active Active
-
2013
- 2013-07-03 US US13/934,322 patent/US8859591B2/en not_active Expired - Fee Related
- 2013-07-15 CL CL2013002053A patent/CL2013002053A1/es unknown
- 2013-07-31 CR CR20130372A patent/CR20130372A/es unknown
- 2013-08-07 GT GT201300196A patent/GT201300196A/es unknown
- 2013-08-07 NI NI201300068A patent/NI201300068A/es unknown
- 2013-08-08 DO DO2013000181A patent/DOP2013000181A/es unknown
- 2013-08-08 CO CO13188635A patent/CO6741217A2/es unknown
- 2013-08-21 ZA ZA2013/06310A patent/ZA201306310B/en unknown
- 2013-09-09 EC ECSP13012871 patent/ECSP13012871A/es unknown
-
2014
- 2014-02-28 HK HK14101989.5A patent/HK1188992A1/zh not_active IP Right Cessation
- 2014-02-28 HK HK15108486.7A patent/HK1207858A1/xx unknown
- 2014-08-28 US US14/471,576 patent/US9073871B2/en not_active Expired - Fee Related
-
2015
- 2015-06-04 US US14/730,562 patent/US9452999B2/en not_active Expired - Fee Related
-
2016
- 2016-08-26 US US15/248,296 patent/US20160362392A1/en not_active Abandoned
- 2016-09-14 HR HRP20161177TT patent/HRP20161177T1/hr unknown
- 2016-09-21 CY CY20161100935T patent/CY1118039T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR085149A1 (es) | Moduladores del receptor de glucagon | |
AR081390A1 (es) | Compuestos de morfolina, composiciones farmaceuticas que los comprenden y su uso en el tratamiento de enfermedades mediadas por el antagonismo del receptor mineralocorticoide (mra) | |
AR086983A1 (es) | Derivados de azetidinil fenil, piridil o pirazinil carboxamida como inhibidores de jak | |
PE20190710A1 (es) | Compuestos de indol carboxamida utiles como inhibidores de cinasas | |
PE20141598A1 (es) | Derivados de dihidro-benzo-oxazina y dihidro-pirido-oxazina | |
PE20140245A1 (es) | Compuesto de furo[3,2-d]pirimidina | |
EA201591429A1 (ru) | 2,3-дизамещенные производные 1-ацил-4-амино-1,2,3,4-тетрагидрохинолинов и их применение в качестве ингибиторов бромодомена | |
PE20091100A1 (es) | Nuevos compuestos 010 | |
AR080878A1 (es) | Derivados heterociclicos de ariletinilo, composiciones farmaceuticas que los contienen, metodo para prepararlos y uso de los mismos en el tratamiento de la esquizofrenia y trastornos cognitivos. | |
AR085615A1 (es) | Derivados de fluoropiridinona utiles como agentes antibacterianos y composiciones farmaceuticas que los contienen | |
AR072952A1 (es) | Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso | |
ES2569539T3 (es) | Derivados de piperidin-4-il azetidina como inhibidores de JAK1 | |
AR066043A1 (es) | Derivados de benzamida sustituida como inhibidores de la 11-beta-hidroxi esteroide deshidrogenasa tipo 1(11betahsd1) | |
AR078976A1 (es) | Inhibidores heterociclicos de la proteina ns5a codificada por el virus de la hepatitis c(vhc), composiciones farmaceuticas que los comprenden y uso de los mismos para tratar infecciones por vhc | |
AR078944A1 (es) | Inhibidores de n1-pirazoloespirocetona acetil-coa carboxilasa | |
PE20142081A1 (es) | Inhibidores de quinurenina-3-monooxigenasa, composiciones farmaceuticas y metodo de uso de los mismos | |
AR086036A1 (es) | DERIVADOS DE ETINILO COMO MODULADORES ALOSTERICOS POSITIVOS DE (mGluR5) | |
AR084579A1 (es) | Moduladores del receptor de glucagon | |
MY170822A (en) | Ethynyl derivatives as mglur5 allosteric modulators | |
MY161403A (en) | 5- (phenyl/pyridinyl-ethinyl) -2-pyridine/ 2-pyrimidine-carborxamides as mglur5 modulators | |
AR077819A1 (es) | Compuestos heterociclicos antagonistas de esfingosina -1-fosfato (sip) | |
CO6801735A2 (es) | Derivados de pirazolidin-3-ona | |
AR084916A1 (es) | Derivados de pirazol y heterociclos, composiciones farmaceuticas que los contienen y uso de los mismos para prevenir y/o tratar enfermedades inflamatorias y alergicas | |
AR075032A1 (es) | Pirazinonas sustituidas | |
MX2019000361A (es) | Moduladores heteroaromaticos del receptor huerfano relacionado con retinoide gamma. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FB | Suspension of granting procedure |