AR073450A1 - Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de ppar - Google Patents
Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de pparInfo
- Publication number
- AR073450A1 AR073450A1 ARP090102006A ARP090102006A AR073450A1 AR 073450 A1 AR073450 A1 AR 073450A1 AR P090102006 A ARP090102006 A AR P090102006A AR P090102006 A ARP090102006 A AR P090102006A AR 073450 A1 AR073450 A1 AR 073450A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- nrx
- aryl
- alkyloxy
- optionally substituted
- Prior art date
Links
- 102100036869 Diacylglycerol O-acyltransferase 1 Human genes 0.000 title abstract 5
- 108050004099 Diacylglycerol O-acyltransferase 1 Proteins 0.000 title abstract 5
- 239000003112 inhibitor Substances 0.000 title abstract 5
- 239000000556 agonist Substances 0.000 title abstract 2
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 title 1
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 title 1
- 239000000890 drug combination Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 33
- 125000003545 alkoxy group Chemical group 0.000 abstract 24
- 125000003118 aryl group Chemical group 0.000 abstract 17
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 229910052739 hydrogen Inorganic materials 0.000 abstract 11
- 239000001257 hydrogen Substances 0.000 abstract 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 11
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 10
- 229910052717 sulfur Inorganic materials 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 8
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 7
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 7
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000005842 heteroatom Chemical group 0.000 abstract 6
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000000169 tricyclic heterocycle group Chemical group 0.000 abstract 4
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000004104 aryloxy group Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 239000003614 peroxisome proliferator Substances 0.000 abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 abstract 2
- 239000000651 prodrug Substances 0.000 abstract 2
- 229940002612 prodrug Drugs 0.000 abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000003830 C1- C4 alkylcarbonylamino group Chemical group 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000018 receptor agonist Substances 0.000 abstract 1
- 229940044601 receptor agonist Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Chemical group 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
-
- 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
- A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
-
- 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
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- 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
- A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
-
- 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
- A61P3/04—Anorexiants; Antiobesity agents
-
- 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
- A61P3/06—Antihyperlipidemics
-
- 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
-
- 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
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- 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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Urology & Nephrology (AREA)
- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Psychiatry (AREA)
- Gastroenterology & Hepatology (AREA)
- Ophthalmology & Optometry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
La presente se refiere a combinaciones de un inhibidor de DGAT y un agonista del receptor activado por el proliferador de peroxisoma (PPAR) o una de sus prodrogas. Se refiere además a métodos para preparar dichas combinaciones, composiciones farmacéuticas que comprenden dichas combinaciones así como el uso de un medicamento de dichas combinaciones. La presente también se refiere a inhibidores de DGAT; se refiere además a métodos para preparar tales compuestos, composiciones farmacéuticas que comprenden dichos compuestos así como al uso de un medicamento de dichos compuestos. Reivindicacion 1: Una combinacion de un agonista de PPAR-a o una de sus prodrogas y un inhibidor de DGAT donde el inhibidor de DGAT se selecciona entre a) un compuesto que tiene la formula (1) incluyendo cualquiera de sus formas estereoquímicamente isoméricas, donde A representa CH o N; X representa O o NRx; la línea de puntos representa un enlace opcional en el caso en que A representa un átomo de carbono; Y representa un enlace directo; -NRx-C(=O)-; -C(=O)-NRx-; -NRx-C(=O)-Z-; -NRx-C(=O)-Z-NRy-; -NRx-C(=O)-Z-NRy-C(=O)-; -NRx-C(=O)-Z-NRy-C(=O)-O-; -NRx-C(=O)-Z-O; -NRx-C(=O)-Z-O-C(=O)-; -NRx-C(=O)-Z-C(=O)-; -NRx-C(=O)-Z-C(=O)-O-; -NRx-C(=O)-O-Z-C(=O)-; -NRx-C(=O)-O-Z-C(=O)-O-; -NRx-C(=O)-O-Z-O-C(=O)-; -NRx-C(=O)-Z-C(=O)-NRy-; -NRx-C(=O)-Z-NRy-C(=O)-NRy-; -C(=O)-Z-; -C(=O)-Z-O-; -C(=O)-NRx-Z-; -C(=O)-NRx-Z-O-; -C(=O)-NRx-Z-C(=O)-O-; -C(=O)-NRx-Z-O-C(=O)-; -C(=O)-NRx-O-Z-; -C(=O)-NRx-Z-NRy-; -C(=O)-NRx-Z-NRy-C(=O)-; -C(=O)-NRx-Z-NRy-C(=O)-O-; Z representa un radical bivalente seleccionado entre alcanodiilo C1-6, alquenodiilo C2-6 o alquinodiilo C2-6 donde cada uno de dichos alcanodiilo C1-6, alquenodiilo C2-6 o alquinodiilo C2-6 puede estar sustituido en forma opcional con alquiloxi C1-4, alquiltio C1-4, hidroxilo, ciano o arilo; y donde dos átomos de hidrogeno enlazados al mismo átomo de carbono en la definicion de Z pueden estar reemplazado en forma opcional por alcanodiilo C1-6; Rx representa hidrogeno o alquilo C1-4; Ry representa hidrogeno; alquilo C1-4 sustituido en forma opcional con cicloalquilo C3-6 o arilo o Het; alquenilo C2-4; o -S(=O)p-arilo; R1 representa alquilo C1-12 sustituido en forma opcional con ciano, alquiloxi C1-4, alquilo C1-4-oxialquiloxi C1-4, cicloalquilo C3-6 o arilo; alquenilo C2-6; alquinilo C2-6; cicloalquilo C3-6; arilo1; arilo1-alquilo C1-6, Het1 o Het1-alquilo C1-6; con la condicion de que cuando Y representa -NRx-C(=O)-Z-; -NRx-C(=O)-Z-NRy-; -NRx-C(=O)-Z-C(=O)-NRy-; -C(=O)-Z-; -NRx-C(=O)-Z-NRy-C(=O)-NRy-; -C(=O)-NRx-Z-; -C(=O)-NRx-O-Z-; o -C(=O)-NRx-Z-NRy-; entonces R1 pueda representar además hidrogeno; R2 y R3 representan cada uno de manera independiente hidrogeno; hidroxilo; carboxilo; halo; alquilo C1-6; polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; polihalo-alquiloxi C1-6; alquiloxicarbonilo C1-6; ciano; aminocarbonilo; mono- o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono- o di (alquil C1-4)amino; -S(=O)p-alquilo C1-4; R4 representa hidrogeno; hidroxilo; carboxilo; halo; alquilo C1-6; polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; poIihaIo-alquiloxi C1-6; alquiloxicarbonilo C1-6 donde alquilo C1-6 puede estar sustituido en forma opcional con arilo; ciano; alquilcarbonilo C1-6; nitro; amino; mono- o di(alquil C1-4)amino; alquilcarbonilamino C1-4; -S(=O)p-alquilo C1-4; R6R5N-C(=O)-; R6R5N-alquilo C1-6; cicloalquilo C3-6; arilo; ariloxi; arilalquilo C1-4; arilo-C(=O)-alquilo C1-4; arilo-C(=O)-; Het; Het-alquilo C1-4; Het-C(=O)-alquilo C1-4; Het-C(=O)-; Het-O-; R5 representa hidrogeno; alquilo C1-4 sustituido en forma opcional con hidroxilo o alquiloxi C1-4; R8R7N-alquilo C1-4; alquiloxi C1-4; Het; arilo; R8R7N-C(=O)-alquilo C1-4; R6 representa hidrogeno o alquilo C1-4; R7 representa hidrogeno; alquilo C1-4; alquilcarbonilo C1-4; R8 representa hidrogeno o alquilo C1-4; o R7 y R8 pueden tomarse junto con el nitrogeno al cual están unidos para formar un heterociclo monocíclico, saturado, de 5, 6 o 7 miembros que puede contener además uno o más heteroátomos seleccionados cada uno de manera independiente entre O, S, S(=O)p o N; y dicho heterociclo puede estar sustituido en forma opcional con alquilo C1-4; R9 representa hidrogeno, halo, alquilo C1-4; alquilo C1-4 sustituido con hidroxilo; arilo representa fenilo o fenilo sustituido con por lo menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, cada sustituyente seleccionado de manera independiente entre hidroxilo; carboxilo; halo; alquilo C1-6 sustituido en forma opcional con alquiloxi C1-4, amino o mono- o di(alquil C1-4)amino; polihalo-alquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; polihalo-alquiloxi C1-6; alquiloxicarbonilo C1-6; ciano; aminocarbonilo; mono- o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono- o di(alquil C1-4)amino; S(O)p-alquilo C1-4; arilo1 representa fenilo; naftalenilo o fluorenilo; cada uno de dichos fenilo, naftalenilo o fluorenilo sustituido en forma opcional con por lo menos un sustituyente en particular uno, dos, tres, cuatro o cinco sustituyentes, cada sustituyente seleccionado de manera independiente entre hidroxilo; oxo; carboxilo; halo; alquilo C1-6 sustituido en forma opcional con carboxilo, alquiloxicarbonilo C1-4 o arilo-C(=O)-; hidroxialquilo C1-6 sustituido en forma opcional con arilo o arilo-C(=O)-; polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; polihalo-alquiloxi C1-6; alquiloxicarbonilo C1-6 donde alquilo C1-6 puede estar sustituido en forma opcional con arilo; ciano; aminocarbonilo; mono- o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; amino; mono- o di(alquil C1-6)amino; R6R5N-alquilo C1-6; cicloalquilo C3-6-NRx-; arilo-NRx-; Het-NRx-; cicloalquilo C3-6-alquilo C1-4-NRx-; arilalquilo C1-4-NRx-; Het-alquilo C1-4-NRx-; -S(=O)p-alquilo C1-4; cicloalquilo C3-6; cicloalquilo C3-6-alquilo C1-4; cicloalquilo C3-6-C(=O)-; arilo; ariloxi; arilalquilo C1-4; arilo-C(=O)-; arilo-C(=O)-alquilo C1-4; Het; Het-alquilo C1-4; Het-C(=O)-; Het-C(=O)-alquilo C1-4; Het-O-; Het representa un heterociclo monocíclico aromático o no aromático que contiene por lo menos un heteroátomo cada uno seleccionado de manera independiente entre O, S, S(=O)p o N; o un heterociclo bicíclico o tricíclico aromático o no aromático que contiene por lo menos un heteroátomo cada uno seleccionado de manera independiente entre O, S, S(=O)p o N; dicho heterociclo monocíclico o dicho heterociclo bi- o tricíclico sustituidos en forma opcional con por lo menos un sustituyente en particular uno, dos, tres, cuatro o cinco sustituyentes, cada sustituyente seleccionado de manera independiente entre hidroxilo; oxo; carboxilo; halo; alquilo C1-6 sustituido en forma opcional con alquiloxi C1-4, amino o mono- o di(alquil C1-4)amino, polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6; polihalo-alquiloxi C1-6; alquilo C1-6-oxicarbonilo; ciano; aminocarbonilo, mono- o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; nitro; amino; mono- o di(alquil C1-4)amino; -S(=O)p-alquilo C1-4; Het1 representa un heterociclo monocíclico aromático o no aromático que contiene por lo menos un heteroátomo cada uno seleccionado de manera independiente entre O, S, S(=O)p o N; o un heterociclo bicíclico o tricíclico aromático o no aromático que contiene por lo menos un heteroátomo cada uno seleccionado de manera independiente entre O S, S(=O)p o N; dicho heterociclo monocíclico o dicho heterociclo bi- o tricíclico sustituidos en forma opcional con por lo menos un sustituyente, en particular uno, dos, tres, cuatro o cinco sustituyentes, cada sustituyente seleccionado de manera independiente entre hidroxilo; oxo; carboxilo; halo; alquilo C1-6 sustituido en forma opcional con carboxilo, alquiloxicarbonilo C1-4 o arilo-C(=O)-; hidroxialquilo C1-6 sustituido en forma opcional con arilo o arilo-C(=O)-; polihaloalquilo C1-6; alquiloxi C1-6 sustituido en forma opcional con alquiloxi C1-4; alquiltio C1-6, polihalo-alquiloxi C1-6; alquiloxi C1-4-carbonilo donde alquilo C1-6 puede estar sustituido en forma opcional con arilo; ciano; aminocarbonilo; mono- o di(alquil C1-4)aminocarbonilo; alquilcarbonilo C1-6; amino; mono- o di(alquil C1-4)amino; R6R5N-alquilo C1-6; cicloalquilo C3-6-NRx-; arilo-NRx-; Het-NRx-; cicloalquilo C3-6-alquilo C1-4-NRx-; arilalquilo C1-4-NRx-; Het-alquilo C1-4-NRx-; -S(=O)p-alquilo C1-4; cicloalquilo C3-6; cicloalquilo C3-6-alquilo C1-4; cicloalquilo C3-6-C(=O)-; arilo; ariloxi; arilalquilo C1-4; arilo-C(=O)-, arilo-C(=O)-alquilo C1-4; Het; Het-alquilo C1-4; Het-C(=O)-; Het-C(=O)-alquilo C1-4; Het-O-; p representa 1 o 2; uno de sus N-oxidos, una de sus sales aceptables para el uso farmacéutico o uno de sus solvatos; b) un compuesto que tiene la formula (2) incluyendo cualquiera de sus formas estereoquímicamente isoméricas, donde A representa CH o N; la línea de puntos representa un enlace opcional en el caso en que A representa un átomo de carbono; X representa -NRx-C(=O)-; -Z-C(=O)-; -Z-NRx-C(=O)-; -S(=O)p-; -C(=S)-; -NRx-C(=S)-; -Z-C(=S)-; -Z-NRx-C(=S)-; -O-C(=O)-; -C(=O)-C(=O)-; Z representa un radical bivalente seleccionado entre alcanodiilo C1-6, alquenodiilo C2-6 o alquinodiilo C2-6 donde cada uno de dichos alcanodiilo C1-6, alquenodiilo C2-6 o alquinodiilo C2-6 puede estar sustituido en forma opcional con hidroxilo o amino; y donde dos átomos de hidrogeno enlazados al mismo átomo de carbono en el alcanodiilo C1-6 pueden estar reemplazados en forma opcional por alcanodiilo C1-6; Rx representa hidrogeno o alquilo C1-4; R1 representa un heterociclo monocíclico de 5 miembros que contiene por lo menos 2 heteroátomos; un heterociclo mo
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/EP2008/056983 WO2008148840A1 (en) | 2007-06-08 | 2008-06-05 | Piperidine/piperazine derivatives |
| PCT/EP2008/057008 WO2008148849A2 (en) | 2007-06-08 | 2008-06-05 | Piperidine/piperazine derivatives |
| PCT/EP2008/057011 WO2008148851A1 (en) | 2007-06-08 | 2008-06-05 | Piperidine/piperazine derivatives |
| PCT/EP2008/057060 WO2008148868A1 (en) | 2007-06-08 | 2008-06-06 | Piperidine/piperazine derivatives |
| EP08170780 | 2008-12-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR073450A1 true AR073450A1 (es) | 2010-11-10 |
Family
ID=40640200
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090102006A AR073450A1 (es) | 2008-06-05 | 2009-06-04 | Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de ppar |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US9107946B2 (es) |
| EP (1) | EP2296659B1 (es) |
| JP (1) | JP5579170B2 (es) |
| AR (1) | AR073450A1 (es) |
| AU (1) | AU2009253892B2 (es) |
| CA (1) | CA2725933C (es) |
| ES (1) | ES2617619T3 (es) |
| PE (2) | PE20100083A1 (es) |
| TW (1) | TWI460175B (es) |
| UY (1) | UY31863A (es) |
| WO (1) | WO2009147170A2 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1356816B1 (en) | 2001-01-29 | 2009-12-23 | Shionogi & Co., Ltd. | Medicinal preparation containing 5-methyl-1-phenyl-2-(1h)-pyridone as active ingredient |
| AU2007245059B2 (en) | 2006-03-31 | 2011-07-28 | Novartis Ag | New compounds |
| AU2008258549B2 (en) | 2007-06-08 | 2013-11-14 | Janssen Pharmaceutica N.V. | Piperidine/piperazine derivatives |
| CN101678019B (zh) | 2007-06-08 | 2016-03-30 | 詹森药业有限公司 | 哌啶/哌嗪衍生物 |
| JO2972B1 (en) | 2007-06-08 | 2016-03-15 | جانسين فارماسوتيكا ان. في | Piperidine / piperazine derivatives |
| ES2483898T3 (es) | 2007-06-08 | 2014-08-08 | Janssen Pharmaceutica, N.V. | Derivados de piperidina/piperazina |
| AR066169A1 (es) | 2007-09-28 | 2009-07-29 | Novartis Ag | Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat |
| ES2617619T3 (es) | 2008-06-05 | 2017-06-19 | Janssen Pharmaceutica, N.V. | Combinaciones de fármacos que comprenden un inhibidor de DGAT y un agonista de PPAR |
| WO2011002067A1 (ja) * | 2009-07-02 | 2011-01-06 | 武田薬品工業株式会社 | 複素環化合物およびその用途 |
| WO2012158844A1 (en) | 2011-05-17 | 2012-11-22 | Shionogi & Co., Ltd. | Heterocyclic compounds |
| WO2013049621A1 (en) * | 2011-09-29 | 2013-04-04 | The Board Of Regents Of The University Of Oklahoma | Ophthalmic compositions comprising ppar-alpha agonists and methods of production and use thereof |
| AR091858A1 (es) * | 2012-07-25 | 2015-03-04 | Sova Pharmaceuticals Inc | INHIBIDORES DE CISTATIONIN-g-LIASA (CSE) |
| CA2937365C (en) | 2016-03-29 | 2018-09-18 | F. Hoffmann-La Roche Ag | Granulate formulation of 5-methyl-1-phenyl-2-(1h)-pyridone and method of making the same |
| FR3050112B1 (fr) | 2016-04-15 | 2020-09-04 | Soc Civ Immobiliere Gecinq | Utilisation de l'acide fenofibrique dans le traitement des maladies hepatiques |
| EP3464262B1 (en) * | 2016-05-27 | 2020-02-26 | Bristol-Myers Squibb Company | Triazolones and tetrazolones as inhibitors of rock |
| US11046683B2 (en) | 2016-12-15 | 2021-06-29 | Ono Pharmaceutical Co., Ltd. | Activator of TREK (TWIK RElated K+ channels) channels |
| BR112019015394A2 (pt) | 2017-01-27 | 2020-03-10 | Genfit | Moduladores de rorgama e usos dos mesmos |
| CN106957280B (zh) * | 2017-03-13 | 2019-02-15 | 洛阳师范学院 | 醚类芳基哌嗪衍生物及其盐、制备方法以及在制备治疗抗肿瘤药物中的用途 |
| BR112020013672A2 (pt) | 2018-01-05 | 2020-12-01 | Cybrexa 1, Inc. | compostos, composições, e métodos para tratamento de doenças que envolvem tecidos afetados por ácidos ou hipoxia |
| JP7675060B2 (ja) | 2019-07-10 | 2025-05-12 | サイブレクサ 3,インコーポレイテッド | 治療薬としての微小管標的化剤のペプチドコンジュゲート |
| CA3146560A1 (en) | 2019-07-10 | 2021-01-14 | Cybrexa 2, Inc. | Peptide conjugates of cytotoxins as therapeutics |
Family Cites Families (83)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1383906A (en) | 1971-02-22 | 1974-02-12 | Bdh Pharmaceuticals Ltd | Pyridazinones |
| JPS5692887A (en) | 1979-12-05 | 1981-07-27 | Sumitomo Chem Co Ltd | N-substituted imidazole derivative |
| DE3338846A1 (de) * | 1982-10-29 | 1984-05-03 | Toyama Chemical Co. Ltd., Tokyo | Neue 4-oxo-1,4-dihydronicotinsaeurederivate und salze derselben, verfahren zu ihrer herstellung und antibakterielle mittel mit einem gehalt derselben |
| GB8729083D0 (en) | 1987-12-12 | 1988-01-27 | Pfizer Ltd | Triazole antifungal agents |
| JP2969359B2 (ja) | 1989-01-13 | 1999-11-02 | 武田薬品工業株式会社 | 環状アミン化合物 |
| DE4317093A1 (de) * | 1993-05-21 | 1994-11-24 | Basf Ag | Niedermolekulare und polymere flüssigkristalline Benztriazole und deren Verwendung |
| TW286317B (es) * | 1993-12-13 | 1996-09-21 | Hoffmann La Roche | |
| US5639754A (en) | 1994-07-12 | 1997-06-17 | Janssen Pharmaceutica N.V. | Urea and thiourea derivatives of azolones |
| FR2722788B1 (fr) * | 1994-07-20 | 1996-10-04 | Pf Medicament | Nouvelles piperazides derivees d'aryl piperazine, leurs procedes de preparation, leur utilisation a titre de medicament et les compositions pharmaceutiques les comprenant |
| DE19581346C2 (de) | 1994-09-30 | 1998-04-16 | Hitachi Ltd | Magnetische Aufzeichnungs/Wiedergabevorrichtung |
| SK282252B6 (sk) | 1995-01-11 | 2001-12-03 | Samjin Pharmaceutical Co., Ltd. | Piperazínové deriváty a farmaceutický prostriedok s ich obsahom |
| CA2228136A1 (en) | 1995-08-10 | 1997-02-20 | Merck & Co., Inc. | 2-substituted aryl pyrroles, compositions containing such compounds and methods of use |
| JPH11510511A (ja) | 1995-08-10 | 1999-09-14 | メルク エンド カンパニー インコーポレーテッド | 2,5−置換アリールピロール、この化合物を含有する組成物及び使用方法 |
| GB9702213D0 (en) | 1996-02-24 | 1997-03-26 | Zeneca Ltd | Chemical compounds |
| HN1997000027A (es) | 1996-12-06 | 1997-06-05 | Pfizer Prod Inc | Derivados de 6-fenil piridil - 2 amina |
| JPH11139969A (ja) | 1997-08-07 | 1999-05-25 | Tanabe Seiyaku Co Ltd | 医薬組成物 |
| DE19743435A1 (de) * | 1997-10-01 | 1999-04-08 | Merck Patent Gmbh | Benzamidinderivate |
| PL345283A1 (en) | 1998-07-20 | 2001-12-03 | Merck Patent Gmbh | Biphenyl derivatives |
| GB9826412D0 (en) | 1998-12-03 | 1999-01-27 | Glaxo Group Ltd | Chemical compounds |
| AUPP999799A0 (en) * | 1999-04-27 | 1999-05-20 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
| TR200103351T2 (tr) | 1999-05-21 | 2002-06-21 | Pfizer Products Inc. | Nos inhibitörleri için yeni farmasötik kombinasyonlar. |
| AU777961B2 (en) * | 1999-06-22 | 2004-11-04 | Neurosearch A/S | Novel benzimidazole derivatives and pharmaceutical compositions comprising these compounds |
| WO2001058885A1 (en) | 2000-02-10 | 2001-08-16 | Pharmacia & Upjohn Company | Oxazolidinone thioamides with piperazine amide substituents |
| GB0013378D0 (en) | 2000-06-01 | 2000-07-26 | Glaxo Group Ltd | Use of therapeutic benzamide derivatives |
| WO2001095856A2 (en) * | 2000-06-15 | 2001-12-20 | Chaconne Nsi Co., Ltd. | Urea derivative useful as an anti-cancer agent and process for preparing same |
| GB2363792A (en) | 2000-06-21 | 2002-01-09 | Portela & Ca Sa | Nitrocatechols |
| US20030060472A1 (en) * | 2000-06-21 | 2003-03-27 | Learmonth David Alexander | Novel substituted nitrocatechols, their use in the treatment of some central and peripheral nervous system disorders and pharmaceutical compositions containing them |
| JO2654B1 (en) | 2000-09-04 | 2012-06-17 | شركة جانسين فارماسوتيكا ان. في | Multiple aryl caroxa amides are useful as lipid - lowering agents |
| US7186683B2 (en) | 2000-09-18 | 2007-03-06 | Sanos Bioscience A/S | Use of GLP for the treatment, prevention, diagnosis, and prognosis of bone-related and nutrition-related disorders |
| AUPR201600A0 (en) | 2000-12-11 | 2001-01-11 | Fujisawa Pharmaceutical Co., Ltd. | Quinazolinone derivative |
| DE10063008A1 (de) * | 2000-12-16 | 2002-06-20 | Merck Patent Gmbh | Carbonsäureamidderivate |
| MXPA03006250A (es) | 2001-01-16 | 2003-09-22 | Astrazeneca Ab | Compuestos heterociclicos terapeuticos. |
| JO2390B1 (en) | 2001-04-06 | 2007-06-17 | شركة جانسين فارماسوتيكا ان. في | Diphenylcarboxamides act as lipid-lowering agents |
| DE10204116A1 (de) | 2002-02-01 | 2003-08-07 | Bayer Cropscience Ag | DELTA·1·-Pyrroline |
| ATE521592T1 (de) | 2002-03-13 | 2011-09-15 | Janssen Pharmaceutica Nv | Histone-deacetylase-inhibitoren |
| KR20040090978A (ko) | 2002-03-13 | 2004-10-27 | 얀센 파마슈티카 엔.브이. | 히스톤 디아세틸라제의 신규한 저해제로서의 설포닐-유도체 |
| EA200401289A1 (ru) | 2002-04-01 | 2005-04-28 | Кадила Хелзкэр Лимитед | Новые противоинфекционные соединения, способы их получения и фармацевтические композиции, содержащие эти соединения |
| TWI319387B (en) | 2002-04-05 | 2010-01-11 | Astrazeneca Ab | Benzamide derivatives |
| US7842693B2 (en) * | 2002-06-12 | 2010-11-30 | Chemocentryx, Inc. | Substituted piperazines |
| US7217726B2 (en) | 2002-08-22 | 2007-05-15 | Orchid Chemicals & Pharmaceuticals Limited | Antibacterial agents |
| AU2003293006A1 (en) | 2002-11-22 | 2004-06-18 | Japan Tobacco Inc. | Fused bicyclic nitrogen-containing heterocycles |
| TW200505450A (en) | 2003-02-03 | 2005-02-16 | Janssen Pharmaceutica Nv | Quinoline-derived amide modulators of vanilloid VR1 receptor |
| US7223788B2 (en) * | 2003-02-14 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Substituted N-aryl heterocycles, process for their preparation and their use as medicaments |
| DE10306250A1 (de) * | 2003-02-14 | 2004-09-09 | Aventis Pharma Deutschland Gmbh | Substituierte N-Arylheterozyklen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| AR044152A1 (es) | 2003-05-09 | 2005-08-24 | Bayer Corp | Derivados de alquilarilo, metodo de preparacion y uso para el tratamiento de la obesidad |
| US20070099884A1 (en) | 2003-06-06 | 2007-05-03 | Erondu Ngozi E | Combination therapy for the treatment of diabetes |
| US7132426B2 (en) * | 2003-07-14 | 2006-11-07 | Arena Pharmaceuticals, Inc. | Fused-aryl and heteroaryl derivatives as modulators of metabolism and the prophylaxis and treatment of disorders related thereto |
| DK1656361T3 (da) * | 2003-08-11 | 2008-05-05 | Hoffmann La Roche | Piperazin med OR-substitueret phenylgruppe og anvendelse deraf som GLYT1-inhibitorer |
| JP2005206492A (ja) | 2004-01-21 | 2005-08-04 | Sankyo Co Ltd | スルホンアミド化合物 |
| AU2005209115A1 (en) * | 2004-01-30 | 2005-08-11 | Japan Tobacco Inc. | Anorectic compounds |
| JP4787529B2 (ja) | 2004-04-09 | 2011-10-05 | 大塚製薬株式会社 | 医薬組成物 |
| WO2006004200A1 (ja) | 2004-07-02 | 2006-01-12 | Sankyo Company, Limited | ウレア誘導体 |
| AU2005271737A1 (en) * | 2004-08-03 | 2006-02-16 | Wyeth | Indazoles useful in treating cardiovascular diseases |
| CN100360525C (zh) | 2004-09-16 | 2008-01-09 | 中国科学院上海药物研究所 | 一类新的噁唑烷酮衍生物、其制备方法和用途 |
| WO2006034441A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
| GB0421908D0 (en) | 2004-10-01 | 2004-11-03 | Angeletti P Ist Richerche Bio | New uses |
| MX2007004217A (es) | 2004-10-15 | 2007-06-11 | Bayer Pharmaceuticals Corp | Preparacion y uso de derivados de acido bifenil-4-il-carbonilamino para el tratamiento de obesidad. |
| ES2611604T3 (es) | 2004-10-22 | 2017-05-09 | Janssen Pharmaceutica Nv | Inhibidores de la c fms quinasa |
| WO2006064189A1 (en) * | 2004-12-14 | 2006-06-22 | Astrazeneca Ab | Oxadiazole derivatives as dgat inhibitors |
| EP1831393A1 (en) | 2004-12-22 | 2007-09-12 | Janssen Pharmaceutica N.V. | Diacylglycerol acyltransferase assay |
| GT200600046A (es) | 2005-02-09 | 2006-09-25 | Terapia de combinacion | |
| GB0505084D0 (en) | 2005-03-11 | 2005-04-20 | Glaxo Group Ltd | Compounds |
| JP5140577B2 (ja) | 2005-03-31 | 2013-02-06 | タケダ カリフォルニア インコーポレイテッド | ヒドロキシステロイドデヒドロゲナーゼ阻害剤 |
| BRPI0608659A2 (pt) | 2005-04-06 | 2010-11-30 | Astrazeneca Ab | composto, métodos para limitar a proliferação celular, de tratamento de um ser humano ou animal sofrendo de uma doença, e de tratamento de profilaxia do cáncer, para tratar cáncer, de tratamento de infecções associadas com cáncer, e de profilaxia de infecções associadas com cáncer, composição farmacêutica, uso de um composto ou um sal farmaceuticamente aceitável do mesmo, métodos para inibir chk1 cinase, e um pak cinase, e para limitar a tumorigênese em um ser humano ou animal, e, processo para a preparação de um composto ou um sal farmaceuticamente aceitável do mesmo |
| JP2008536947A (ja) | 2005-04-19 | 2008-09-11 | バイエル・フアーマシユーチカルズ・コーポレーシヨン | アリールアルキル酸誘導体およびそれらの使用 |
| MX2007015759A (es) * | 2005-06-11 | 2008-02-21 | Astrazeneca Ab | Derivados de oxadiazol como inhibidores de diacilglicerol aciltransferasa (dgat). |
| EP1904525A4 (en) | 2005-06-30 | 2009-10-21 | Ipsen Pharma | GLP-1 PHARMACEUTICAL COMPOSITIONS |
| JP2007131584A (ja) | 2005-11-11 | 2007-05-31 | Sankyo Co Ltd | 新規ベンゾオキサゾール誘導体 |
| CA2632936A1 (en) * | 2005-12-20 | 2007-06-28 | Merck Frosst Canada Ltd. | Heteroaromatic compounds as inhibitors of stearoyl-coenzyme a delta-9 desaturase |
| EP1966221A1 (en) | 2005-12-22 | 2008-09-10 | AstraZeneca AB | Pyrimido- [4, 5-]-oxazines for use as dgat inhibitors |
| EP1810974A1 (en) | 2006-01-18 | 2007-07-25 | Ludwig-Maximilians-Universität München | Preparation and use of magnesium amides |
| TW200804364A (en) | 2006-02-22 | 2008-01-16 | Boehringer Ingelheim Int | New compounds |
| US7728031B2 (en) | 2006-02-24 | 2010-06-01 | Abbott Laboratories | Octahydro-pyrrolo[3,4-b]pyrrole derivatives |
| US20090069304A1 (en) | 2006-03-03 | 2009-03-12 | Shionogi & Co., Ltd. | Mmp-13 selective inhibitor |
| CA2654670A1 (en) | 2006-07-06 | 2008-01-10 | Boehringer Ingelheim International Gmbh | New compounds |
| EP1918285A1 (en) * | 2006-11-03 | 2008-05-07 | Merck Sante | Diazepane-acetamide derivatives as selective 11beta-HSD1 inhibitors |
| GB0706793D0 (en) * | 2007-04-05 | 2007-05-16 | Evotec Ag | Compounds |
| EP2155687A1 (en) * | 2007-05-22 | 2010-02-24 | Via Pharmaceuticals, Inc. | Diacylglycerol acyltransferase inhibitors |
| CN101678019B (zh) * | 2007-06-08 | 2016-03-30 | 詹森药业有限公司 | 哌啶/哌嗪衍生物 |
| JO2972B1 (en) * | 2007-06-08 | 2016-03-15 | جانسين فارماسوتيكا ان. في | Piperidine / piperazine derivatives |
| AU2008258549B2 (en) * | 2007-06-08 | 2013-11-14 | Janssen Pharmaceutica N.V. | Piperidine/piperazine derivatives |
| ES2483898T3 (es) * | 2007-06-08 | 2014-08-08 | Janssen Pharmaceutica, N.V. | Derivados de piperidina/piperazina |
| ES2617619T3 (es) | 2008-06-05 | 2017-06-19 | Janssen Pharmaceutica, N.V. | Combinaciones de fármacos que comprenden un inhibidor de DGAT y un agonista de PPAR |
-
2009
- 2009-06-03 ES ES09757551.8T patent/ES2617619T3/es active Active
- 2009-06-03 EP EP09757551.8A patent/EP2296659B1/en active Active
- 2009-06-03 PE PE2009000769A patent/PE20100083A1/es not_active Application Discontinuation
- 2009-06-03 UY UY0001031863A patent/UY31863A/es unknown
- 2009-06-03 CA CA2725933A patent/CA2725933C/en active Active
- 2009-06-03 WO PCT/EP2009/056800 patent/WO2009147170A2/en not_active Ceased
- 2009-06-03 JP JP2011512112A patent/JP5579170B2/ja active Active
- 2009-06-03 AU AU2009253892A patent/AU2009253892B2/en not_active Ceased
- 2009-06-03 PE PE2013002163A patent/PE20140572A1/es not_active Application Discontinuation
- 2009-06-03 US US12/993,491 patent/US9107946B2/en active Active
- 2009-06-04 TW TW098118476A patent/TWI460175B/zh not_active IP Right Cessation
- 2009-06-04 AR ARP090102006A patent/AR073450A1/es unknown
-
2015
- 2015-07-08 US US14/793,896 patent/US9724418B2/en not_active Expired - Fee Related
-
2017
- 2017-06-20 US US15/627,475 patent/US20180028660A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP2296659B1 (en) | 2016-12-21 |
| ES2617619T3 (es) | 2017-06-19 |
| US9724418B2 (en) | 2017-08-08 |
| US20150320741A1 (en) | 2015-11-12 |
| EP2296659A2 (en) | 2011-03-23 |
| AU2009253892B2 (en) | 2015-07-30 |
| JP5579170B2 (ja) | 2014-08-27 |
| US20180028660A1 (en) | 2018-02-01 |
| TWI460175B (zh) | 2014-11-11 |
| US9107946B2 (en) | 2015-08-18 |
| WO2009147170A3 (en) | 2010-06-10 |
| AU2009253892A1 (en) | 2009-12-10 |
| US20110112111A1 (en) | 2011-05-12 |
| WO2009147170A2 (en) | 2009-12-10 |
| TW201014846A (en) | 2010-04-16 |
| PE20100083A1 (es) | 2010-02-17 |
| PE20140572A1 (es) | 2014-05-16 |
| CA2725933C (en) | 2018-01-16 |
| JP2011522000A (ja) | 2011-07-28 |
| UY31863A (es) | 2010-01-05 |
| CA2725933A1 (en) | 2009-12-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR073450A1 (es) | Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de ppar | |
| AR066911A1 (es) | Derivados de piperidina / piperazina | |
| AR066153A1 (es) | Derivados de piperidina / piperazina | |
| AR066154A1 (es) | Derivados de piperidina / piperazina | |
| AR067327A1 (es) | Derivados de piperidina / piperazina | |
| AR101106A1 (es) | Inhibidores de tirosina quinasa de bruton | |
| CO6260076A2 (es) | Derivados de uracilo o timina para el tratamiento de la hepatitis c | |
| AR077440A1 (es) | Bencenosulfonamidas como bloqueadores de canales de calcio y composiciones farmaceuticas | |
| AR076922A1 (es) | Benzodiazepinas como inhibidores de pi3k/mtor, una composicion farmaceutica que las comprende, metodos para su fabricacion y su uso en el tratamiento del cancer. | |
| AR082562A1 (es) | Derivados de isoxazolina como agentes antiparasitarios | |
| AR072952A1 (es) | Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso | |
| AR083367A1 (es) | Compuestos de tipo quinazolinona como antagonistas de crth | |
| AR082889A1 (es) | Compuestos y composiciones para la inhibicion de nampt | |
| AR076435A1 (es) | Compuestos de indazoles sustituidos, composiciones farmaceuticas que los contienen y procesos de obtencion de los mismos | |
| AR069435A1 (es) | Derivados de aminotiazol, proceso para la obtencion de los mismos, composiciones farmaceuticas y su uso como inhibidores de la fbpasa | |
| UY32490A (es) | Inhibidores de beta-secretasa | |
| AR075050A1 (es) | Dicianopiridinas alquilamino-sustituidas | |
| CL2011000032A1 (es) | Compuestos derivados macrocíclicos de indol[2,1-a]benzacepina sustituidos; composición farmacéutica que los comprende; y su uso para inhibir la replicación del virus de la hepatitis e (hcv). | |
| AR093184A1 (es) | Compuesto de pirimidina sustituida como inhibidor de quinurenina-3-monooxigenasa y composicion farmaceutica que lo comprenden | |
| PE20142081A1 (es) | Inhibidores de quinurenina-3-monooxigenasa, composiciones farmaceuticas y metodo de uso de los mismos | |
| CO6020016A1 (es) | Derivados de 1,2,4,5 tetrahidro-3h-benzapezinas su procedimiento de preparacion y las composiciones farmaceuticas que las contienen | |
| NI201000011A (es) | Derivados de pirimidina 934. | |
| AR082004A1 (es) | Compuestos de fusion de piridina | |
| AR054481A1 (es) | Derivados de 2-azetidinonas como inhibidores de la absorcion de colesterol | |
| AR049711A1 (es) | Compuestos heterociclicos condensados como inhibidores de la aldosterona sintasa; composiciones farmaceuticas que los contienen y su uso en la preparacion de un medicamento para el tratamiento o prevencion de enfermedades relacionadas con el hiperaldosterismo y por una liberacion excesiva de cortiso |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |