AR035759A1 - Compuestos acilurea antagonistas de la funcion mpc-1, un procedimiento para su preparacion, composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentos - Google Patents
Compuestos acilurea antagonistas de la funcion mpc-1, un procedimiento para su preparacion, composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentosInfo
- Publication number
- AR035759A1 AR035759A1 ARP020100728A ARP020100728A AR035759A1 AR 035759 A1 AR035759 A1 AR 035759A1 AR P020100728 A ARP020100728 A AR P020100728A AR P020100728 A ARP020100728 A AR P020100728A AR 035759 A1 AR035759 A1 AR 035759A1
- Authority
- AR
- Argentina
- Prior art keywords
- lower alkyl
- optionally substituted
- aryl
- cycloalkyl
- heteroaryl
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—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
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- 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
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- 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
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
- C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
- C07D241/40—Benzopyrazines
- C07D241/42—Benzopyrazines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/34—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings
- C07D265/36—1,4-Oxazines; Hydrogenated 1,4-oxazines condensed with carbocyclic rings condensed with one six-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
- C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
- C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
- C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Hematology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Quinoline Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Un compuesto acilurea de fórmula (1), (2) o (3) en la cual: n es un entero de 0 a 4 en fórmula (1), y es un entero de 0 a 2 en fórmula (2) y fórmula (3); X e Y están independientemente O, S, CH-R8, o N-R7 en fórmula (1) y Fórmula (2), y son independientemente N y C-R7 en la fórmula (3); Z es N o C-R8; con la condición de que por lo menos uno de X, Y y Z es un átomo de anillo que no es de carbono; cada R1 es independientemente, alquilo inferior opcionalmente sustituido, alquenilo, alquinilo, cicloalquilo, cicloalquil(alquilo inferior), heterocicloalquilo opcionalmente sustituido, arilo, opcionalmente sustituido, heteroarilo opcionalmente sustituido, arilo opcionalmente sustituido (alquilo inferior), halo (alquilo inferior), -CF3, halógeno, nitro, -CN, -OR9, -SR9, -NR9R10, -NR9 (carboxi(alquilo inferior)), -C(=O)R9, -C(=O)OR9, -C(=O)NR9R10, -OC(=O)R9, -SO2R9, -OSO2R9, -SO2NR9R10, -NR9SO2R10 o -NR9C(=O)R10, donde R9 y R10 son independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquilo inferior -N(alquilo C1-2)2, alquilo inferior (heterocicloalquilo opcionalmente sustituido), alquenilo, alquinilo, cicloalquilo opcionalmente sustituido, cicloalquilo (alquilo inferior), heterocicloalquilo (alquilo inferior) opcionalmente sustituido, arilo (alquilo inferior), arilo opcionalmente sustituido, heteroarilo, heteroarilo (alquilo inferior), o R9 y R10 conjuntamente son -(CH2)4-6- opcionalmente interrumpido con uno de O, S, NH, N-(arilo), N-(aril(alquilo inferior)), -N-(CH2)1-6C(=O)OR10 o un grupo N- (alquilo C1-2 opcionalmente sustituido), o en la fórmula (1), n=2 y los dos R1' conjuntamente constituyen =O; R2, R3 y R8 son independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo, alquinilo, cicloalquilo, cicloalquil (alquilo inferior), heterocicloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, heteroarilo opcionalmente sustituido, aril (alquilo inferior) opcionalmente sustituido, halo (alquilo inferior), -CF3, halógeno, nitro, -CN, -OR9, -SR9, -NR9R10, -NR9(CH2)1-6C(=O)OR10, -C(=O)R9, -C(=O)OR9, -C(=O)NR9R10, -OC(=O)R9, -SO2R9, -OSO2R9, -SO2NR9R10, -NR9SO2R10 o -NR9C(=O)R10, donde R9 y R10 son independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquilo inferior-N(alquilo C1-2)2, alquilo inferior (heterocicloalquilo opcionalmente sustituido), alquenilo, alquinilo, cicloalquilo opcionalmente sustituido, cicloalquil (alquilo inferior), heterocicloalquilo (alquilo inferior) opcionalmente sustituido, aril (alquilo inferior), arilo, opcionalmente sustituido, heteroarilo, heteroaril (alquilo inferior),o R9 y R10 conjuntamente son -(CH2)4-6- opcionalmente interrumpidos con uno de O, S, NH, N-(arilo), N-(aril (alquilo inferior)), N-(CH2)1-6C(=O)OR10 o un grupo N-(alquilo C1-2 opcionalmente sustituido); cada R7 es independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo, alquinilo, cicloalquil (alquilo inferior), arilo, arilo sustituido, aril (alquilo inferior), arilo (alquilo inferior) sustituido, halo (alquilo inferior), -C(=O)R9, -C(=O)OR9, -C(=O)NR9R10, -SO2OR9, -SO2NR9R10, donde R9 y R10 son independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquilo inferior -N(alquilo C1-2)2, alquilo inferior (heterocicloalquilo opcionalmente sustituido), alquenilo, alquinilo, cicloalquilo opcionalmente sustituido, cicloalquilo (alquilo inferior), heterocicloalquilo (alquilo inferior) opcionalmente sustituido, aril (alquilo inferior), arilo opcionalmente sustituido, heteroarilo, heteroarilo (alquilo inferior), o R9 y R10 conjuntamente son -(CH2)4-6- opcionalmente interrumpido con uno de O, S, NH, N-(arilo), N-(aril (alquilo inferior)), N-(CH2)1-6C(=O)OR10 o un grupo N-(alquilo C1-2 opcionalmente sustituido); R4 y R5 son independientemente, hidrógeno, alquilo inferior, alquilo inferior opcionalmente sustituido, arilo opcionalmente sustituido, o aril (alquilo inferior) opcionalmente sustituido, o, conjuntamente, son -(CH2)2-4-; R6 es hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo, alquinilo, cicloalquilo, cicloalquil (alquilo inferior), heterocicloalquilo opcionalmente sustituido, arilo opcionalmente sustituido, aril (alquilo inferior) opcionalmente sustituido, heteroarilo opcionalmente sustituido, heteroaril (alquilo inferior) opcionalmente sustituido, -C(=O)R11, -C(=O)OR11, -C(O)NR11R12, -SO2R11 o -SO2NR11R12, donde R11 y R12 son independientemente, hidrógeno, alquilo inferior opcionalmente sustituido, alquenilo, alquinilo, cicloalquilo, cicloalquilo (alquilo inferior), arilo, ariloxi opcionalmente sustituido, heteroarilo, heteroaril (alquilo inferior), o R11 y R12 conjuntamente son -(CH2)4-6; o una sal farmacéuticamente aceptable del mismos opcionalmente en forma de un estereoisómero único o una mezcla de estereoisómeros del mismo; un procedimiento para su preparación, composición farmacéutica y el uso de dichos compuestos para la preparación de medicamentos, en el cual el desorden o enfermedad alérgico, inflamatorio, o autoinmune está seleccionado del grupo que consiste en asma, arteriosclerosis, glomerulonefritis, pancreatitis, restenosis, artritis reumatoide, nefropatía diabética, fibrosis pulmonar, enfermedad inflamatoria del intestino, enfermedad de Crohn y rechazo a los trasplantes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27279201P | 2001-03-01 | 2001-03-01 |
Publications (1)
Publication Number | Publication Date |
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AR035759A1 true AR035759A1 (es) | 2004-07-07 |
Family
ID=23041292
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP020100728A AR035759A1 (es) | 2001-03-01 | 2002-02-28 | Compuestos acilurea antagonistas de la funcion mpc-1, un procedimiento para su preparacion, composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentos |
Country Status (15)
Country | Link |
---|---|
US (2) | US6809113B2 (es) |
EP (1) | EP1363897B1 (es) |
JP (1) | JP4291576B2 (es) |
KR (1) | KR20040018336A (es) |
CN (1) | CN1259315C (es) |
AR (1) | AR035759A1 (es) |
AT (1) | ATE313537T1 (es) |
BR (1) | BR0207750A (es) |
CA (1) | CA2439849A1 (es) |
DE (1) | DE60208159T2 (es) |
ES (1) | ES2254653T3 (es) |
HK (1) | HK1060728A1 (es) |
MX (1) | MXPA03007861A (es) |
TW (1) | TWI245761B (es) |
WO (1) | WO2002070509A2 (es) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE60144284D1 (de) | 2000-11-01 | 2011-05-05 | Millennium Pharm Inc | Stickstoffhaltige heterozyklische verbindungen und verfahren zu deren herstellung |
US7732162B2 (en) | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
WO2006029173A2 (en) * | 2004-09-08 | 2006-03-16 | Boys Town National Research Hospital | Treatment of glomerular basement membrane disease involving matrix metalloproteinase-12 |
MX2007012082A (es) | 2005-03-31 | 2007-11-20 | Pfizer Prod Inc | Derivados de ciclopentapiridina y tetrahidroquinolina. |
WO2007066496A1 (en) * | 2005-12-07 | 2007-06-14 | Sumitomo Chemical Company, Limited | Benzoylurea compound and use thereof |
US7601716B2 (en) * | 2006-05-01 | 2009-10-13 | Cephalon, Inc. | Pyridopyrazines and derivatives thereof as ALK and c-Met inhibitors |
CA2658719A1 (en) * | 2006-07-24 | 2008-01-31 | Yeda Research And Development Co. Ltd. | Pharmaceutical compositions comprising ccl2 and use of same for the treatment of inflammation |
US20080076120A1 (en) * | 2006-09-14 | 2008-03-27 | Millennium Pharmaceuticals, Inc. | Methods for the identification, evaluation and treatment of patients having CC-Chemokine receptor 2 (CCR-2) mediated disorders |
EP2089383B1 (en) | 2006-11-09 | 2015-09-16 | Probiodrug AG | 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one derivatives as inhibitors of glutaminyl cyclase for the treatment of ulcer, cancer and other diseases |
DK2091948T3 (da) | 2006-11-30 | 2012-07-23 | Probiodrug Ag | Nye inhibitorer af glutaminylcyclase |
CA2672229A1 (en) * | 2006-12-14 | 2008-06-19 | Actogenix N.V. | Delivery of binding molecules to induce immunomodulation |
CA2679446C (en) | 2007-03-01 | 2016-05-17 | Probiodrug Ag | New use of glutaminyl cyclase inhibitors |
US9656991B2 (en) | 2007-04-18 | 2017-05-23 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
US8356920B2 (en) * | 2007-12-12 | 2013-01-22 | Levine Jonathan E | Lighting device |
WO2010068881A1 (en) * | 2008-12-12 | 2010-06-17 | Forest Laboratories Holdings Limited | Novel benzodioxane and benzoxazine derivatives useful as cc chemokine receptor ligands |
MX2012002993A (es) | 2009-09-11 | 2012-04-19 | Probiodrug Ag | Derivados heterociclicos como inhibidores de ciclasa glutaminilo. |
WO2011107530A2 (en) | 2010-03-03 | 2011-09-09 | Probiodrug Ag | Novel inhibitors |
JP5688745B2 (ja) | 2010-03-10 | 2015-03-25 | プロビオドルグ エージー | グルタミニルシクラーゼ(qc、ec2.3.2.5)の複素環阻害剤 |
EP2560953B1 (en) | 2010-04-21 | 2016-01-06 | Probiodrug AG | Inhibitors of glutaminyl cyclase |
ES2570167T3 (es) | 2011-03-16 | 2016-05-17 | Probiodrug Ag | Derivados de benzimidazol como inhibidores de glutaminil ciclasa |
EP2522341A1 (en) * | 2011-05-13 | 2012-11-14 | Tragex Pharma | Pharmaceutical compositions comprising Neuropilin inhibitors, and their use for the prevention and/or treatment of angiogenic disorders and cancers |
RU2720237C2 (ru) | 2013-11-18 | 2020-04-28 | Форма Терапеутикс, Инк. | Композиции, содержащие бензопиперазин, в качестве ингибиторов бромодоменов вет |
ES2860695T3 (es) | 2013-11-18 | 2021-10-05 | Forma Therapeutics Inc | Composiciones de tetrahidroquinolina como inhibidores de bromodominio BET |
EP4252629A3 (en) | 2016-12-07 | 2023-12-27 | Biora Therapeutics, Inc. | Gastrointestinal tract detection methods, devices and systems |
EP3554541B1 (en) | 2016-12-14 | 2023-06-07 | Biora Therapeutics, Inc. | Treatment of a disease of the gastrointestinal tract with a chemokine/chemokine receptor inhibitor |
US11351227B2 (en) * | 2017-04-27 | 2022-06-07 | Washington University | Chemokine decoy receptors of rodent gammaherpesviruses and uses thereof |
ES2812698T3 (es) | 2017-09-29 | 2021-03-18 | Probiodrug Ag | Inhibidores de glutaminil ciclasa |
EP3643711A1 (en) | 2018-10-24 | 2020-04-29 | Bayer Animal Health GmbH | New anthelmintic compounds |
EP3883634A1 (en) | 2018-11-19 | 2021-09-29 | Progenity, Inc. | Methods and devices for treating a disease with biotherapeutics |
EP4309722A2 (en) | 2019-12-13 | 2024-01-24 | Biora Therapeutics, Inc. | Ingestible device for delivery of therapeutic agent to the gastrointestinal tract |
Family Cites Families (23)
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IE32700B1 (en) | 1968-02-03 | 1973-10-31 | Beecham Group Ltd | Penicillins |
GB1250611A (es) | 1968-02-03 | 1971-10-20 | ||
DE2131034A1 (de) | 1971-06-23 | 1973-01-11 | Hoechst Ag | Acylharnstoffe und verfahren zu ihrer herstellung |
DE2652004C3 (de) | 1976-11-15 | 1979-09-13 | Basf Ag, 6700 Ludwigshafen | l-Acyl-2-arylamino-2-imidazoline, Verfahren zu ihrer Herstellung und ihre Verwendung |
US4163784A (en) | 1978-03-09 | 1979-08-07 | Pfizer Inc. | Heterocyclylcarbonyl derivatives of urea, agents for dissolution of gallstones |
GB8528234D0 (en) | 1985-11-15 | 1985-12-18 | Wyeth John & Brother Ltd | Heterocyclic compounds |
JP2650055B2 (ja) | 1988-11-28 | 1997-09-03 | キヤノン株式会社 | 電子写真感光体 |
FR2672888B1 (fr) | 1991-02-14 | 1994-02-04 | Fabre Medicament Pierre | Nouvelles urees et thiourees, leur preparation et leur application en therapeutique. |
JP3964478B2 (ja) | 1995-06-30 | 2007-08-22 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | ヘテロ環含有カルボン酸誘導体及びそれを含有する医薬 |
WO1997024325A1 (en) | 1995-12-28 | 1997-07-10 | Takeda Chemical Industries, Ltd. | DIPHENYLMETHANE DERIVATIVES AS MIP-1α/RANTES RECEPTOR ANTAGONISTS |
JPH09255572A (ja) | 1996-03-26 | 1997-09-30 | Takeda Chem Ind Ltd | ケモカイン受容体拮抗剤 |
US6686353B1 (en) | 1996-05-20 | 2004-02-03 | Teijin Intellectual Property Center Limited | Diarylalkyl cyclic diamine derivatives as chemokine receptor antagonists |
CA2259927A1 (en) | 1996-07-12 | 1998-01-22 | Leukosite, Inc. | Chemokine receptor antagonists and methods of use therefor |
EP0916668A4 (en) | 1996-07-29 | 2000-08-16 | Banyu Pharma Co Ltd | CHEMOKINE RECEPTOR ANTAGONISTS |
US6184235B1 (en) | 1996-08-14 | 2001-02-06 | Warner-Lambert Company | 2-phenyl benzimidazole derivatives as MCP-1 antagonists |
WO1998027815A1 (en) | 1996-12-20 | 1998-07-02 | Merck & Co., Inc. | Substituted aminoquinolines as modulators of chemokine receptor activity |
GB9716656D0 (en) | 1997-08-07 | 1997-10-15 | Zeneca Ltd | Chemical compounds |
JP2002502844A (ja) | 1998-02-03 | 2002-01-29 | ベーリンガー インゲルハイム ファルマ コマンディトゲゼルシャフト | 5員複素環縮合ベンゾ誘導体、その調製及び医薬品としてのそれらの使用 |
KR20010072080A (ko) | 1998-07-31 | 2001-07-31 | 쓰끼하시 다미까따 | 페닐아졸 화합물, 그의 제조 방법 및 고지혈증용 약제 |
US6316449B1 (en) | 1999-07-08 | 2001-11-13 | Millennium Pharmaceuticals, Inc. | Chemokine receptor antagonists |
US6777413B2 (en) | 2000-02-01 | 2004-08-17 | Millennium Pharmaceuticals, Inc. | 2-[1H]-quinolone and 2-[1H]-quinoxalone inhibitors of factor Xa |
AU2001236606A1 (en) | 2000-02-01 | 2001-08-14 | Cor Therapeutics, Inc. | 3,4-dihydro-2h-benzo(1,4)oxazine inhibitors of factor xa |
AU2001230537A1 (en) | 2000-02-01 | 2001-08-14 | Daiichi Pharmaceutical Co., Ltd. | Pyridoxazine derivatives |
-
2002
- 2002-02-25 TW TW091103254A patent/TWI245761B/zh not_active IP Right Cessation
- 2002-02-27 US US10/087,208 patent/US6809113B2/en not_active Expired - Fee Related
- 2002-02-28 CN CNB028057929A patent/CN1259315C/zh not_active Expired - Fee Related
- 2002-02-28 AT AT02709746T patent/ATE313537T1/de not_active IP Right Cessation
- 2002-02-28 CA CA002439849A patent/CA2439849A1/en not_active Abandoned
- 2002-02-28 ES ES02709746T patent/ES2254653T3/es not_active Expired - Lifetime
- 2002-02-28 AR ARP020100728A patent/AR035759A1/es unknown
- 2002-02-28 EP EP02709746A patent/EP1363897B1/en not_active Expired - Lifetime
- 2002-02-28 KR KR10-2003-7011481A patent/KR20040018336A/ko active IP Right Grant
- 2002-02-28 DE DE60208159T patent/DE60208159T2/de not_active Expired - Fee Related
- 2002-02-28 JP JP2002569829A patent/JP4291576B2/ja not_active Expired - Fee Related
- 2002-02-28 BR BR0207750-7A patent/BR0207750A/pt not_active IP Right Cessation
- 2002-02-28 WO PCT/US2002/006256 patent/WO2002070509A2/en active IP Right Grant
- 2002-02-28 MX MXPA03007861A patent/MXPA03007861A/es active IP Right Grant
-
2004
- 2004-05-11 HK HK04103275A patent/HK1060728A1/xx not_active IP Right Cessation
- 2004-10-19 US US10/969,440 patent/US7297696B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
DE60208159D1 (de) | 2006-01-26 |
MXPA03007861A (es) | 2004-10-15 |
US6809113B2 (en) | 2004-10-26 |
WO2002070509A8 (en) | 2003-11-06 |
US20050054668A1 (en) | 2005-03-10 |
CN1494539A (zh) | 2004-05-05 |
ATE313537T1 (de) | 2006-01-15 |
US20030105085A1 (en) | 2003-06-05 |
US7297696B2 (en) | 2007-11-20 |
JP4291576B2 (ja) | 2009-07-08 |
EP1363897A2 (en) | 2003-11-26 |
CN1259315C (zh) | 2006-06-14 |
JP2004527503A (ja) | 2004-09-09 |
DE60208159T2 (de) | 2006-08-17 |
WO2002070509A3 (en) | 2003-05-30 |
ES2254653T3 (es) | 2006-06-16 |
KR20040018336A (ko) | 2004-03-03 |
CA2439849A1 (en) | 2002-09-12 |
TWI245761B (en) | 2005-12-21 |
EP1363897B1 (en) | 2005-12-21 |
HK1060728A1 (en) | 2004-08-20 |
BR0207750A (pt) | 2004-03-23 |
WO2002070509A2 (en) | 2002-09-12 |
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