AR038956A1 - Uso de un compuesto que regula la produccion o niveles de peptidos beta amiloides para la manufactura de un medicamento para tratar la enfermedad de alzheimer y/o para regular dichos niveles de peptidos amiloides beta en un sujeto - Google Patents
Uso de un compuesto que regula la produccion o niveles de peptidos beta amiloides para la manufactura de un medicamento para tratar la enfermedad de alzheimer y/o para regular dichos niveles de peptidos amiloides beta en un sujetoInfo
- Publication number
- AR038956A1 AR038956A1 ARP020101893A ARP020101893A AR038956A1 AR 038956 A1 AR038956 A1 AR 038956A1 AR P020101893 A ARP020101893 A AR P020101893A AR P020101893 A ARP020101893 A AR P020101893A AR 038956 A1 AR038956 A1 AR 038956A1
- Authority
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- Argentina
- Prior art keywords
- aryl
- group
- alkyl
- independently selected
- substituted
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 8
- 238000004519 manufacturing process Methods 0.000 title 2
- 102000004196 processed proteins & peptides Human genes 0.000 title 2
- 108090000765 processed proteins & peptides Proteins 0.000 title 2
- 208000024827 Alzheimer disease Diseases 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 230000001105 regulatory effect Effects 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 26
- 125000003118 aryl group Chemical group 0.000 abstract 21
- 229910052739 hydrogen Inorganic materials 0.000 abstract 15
- 239000001257 hydrogen Substances 0.000 abstract 15
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 11
- 150000002431 hydrogen Chemical class 0.000 abstract 9
- 229910052736 halogen Inorganic materials 0.000 abstract 8
- 125000002947 alkylene group Chemical group 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- 239000012453 solvate Substances 0.000 abstract 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000001072 heteroaryl group Chemical class 0.000 abstract 3
- 125000000592 heterocycloalkyl group Chemical class 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000004104 aryloxy group Chemical class 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000003003 spiro group Chemical group 0.000 abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical class [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000000051 benzyloxy group Chemical class [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
Classifications
-
- 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
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
-
- 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
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- 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
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Hospice & Palliative Care (AREA)
- Psychiatry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Uso de por lo menos un compuesto seleccionado del grupo de compuestos (a), (b), (c), (d), (e), (f), (g) y (h) representados por las formulas: compuestos (a) de la formula (1) o una sal farmacéuticamente aceptable del mismo o un solvato del mismo, donde en la fórmula (1), Ar1 y Ar2 están independientemente seleccionados del grupo que consiste en arilo y arilo R4-sustituido; Ar3 es arilo ó arilo R5-sustituido; X, Y y Z están independientemente seleccionados del grupo que consiste en -CH2-, -CH(alquilo inferior)- y -C(dialquilo inferior)-; R y R2 están independientemente seleccionados del grupo que consiste en -OR6, -O(CO)R6, -O(CO)OR9 y -O(CO)NR6R7; R1 y R3 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo inferior y arilo; q es 0 ó 1; r es 0 ó 1; m, n y p están independientemente seleccionados entre 0, 1, 2, 3 ó 4; con la condición de que por lo menos uno de q y r es 1, y la suma de m, n, p, q y r es 1, 2, 3, 4, 5 ó 6; y con la condición de que cuando p es 0 y r es 1, la suma de m, q y n es 1, 2, 3, 4 ó 5; R4 representa 1-5 sustituyentes independientemente seleccionados del grupo que consiste en alquilo inferior, -OR6, -O(CO)R6, -O(CO)OR9, -O(CH2)1-5OR6, -O(CO)NR6R7, -NR6R7, -NR6(CO)R7, -NR6(CO)OR9, -NR7(CO)NR7R8, -NR6SO2R9, -COOR6, -CONR6R7, -COR6, -SO2NR6R7, S(O)0-2R9, -O(CH2)1-10-COOR6, -O(CH2)1-10-CONR6R7, -(alquileno inferior)COOR6, -CH=CH-COOR6, -CF3, -CN, -NO2 y halógeno; R5 representa 1-5 sustituyentes independientemente seleccionados del grupo que consiste en -OR6, -O(CO)R6, -O(CO)OR9, -O(CH2)1-5OR6, -O(CO)NR6R7, -NR6R7, -NR6(CO)R7, -NR6(CO)OR9, -NR6(CO)NR7R8, -NR6SO2R9, -COOR6, -CONR6R7, -COR6, -SO2NR6R7, S(O)0-2R9, -O(CH2)1-10-COOR6, -O(CH2)1-10CONR6R7, -(alquileno inferior)COOR6 y -CH=CH-COOR6; R6, R7 y R8 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo inferior, arilo y alquilo inferior arilo-sustituido; y R9 es alquilo inferior, arilo o alquilo inferior arilo-sustituido; compuesto (b) de la fórmula (2) o una sal o solvato del mismo; compuesto (c) de la fórmula (3) o una sal farmacéuticamente aceptable del mismo o un solvato del mismo, donde, en la fórmula (3): Ar1 es arilo R3-sustituido; Ar2 es arilo R4-sustituido; Ar3 es arilo R5-sustituido; Y y Z están independientemente seleccionados del grupo que consiste en -CH2-, -CH(alquilo inferior)- y -C(dialquilo inferior)-; A está seleccionado entre -O-, -S-, -S(O)- ó -S(O)2-; R1 está seleccionado del grupo que consiste en -OR6, -O(CO)R6, -O(CO)OR9 y -O(CO)NR6R7; R2 está seleccionado del grupo que consiste en hidrógeno, alquilo inferior y arilo; ó R1 y R2 conjuntamente son =O; q es 1, 2 ó 3; p es 0, 1, 2, 3 ó 4; R5 representa 1-3 sustituyentes independientemente seleccionados del grupo que consiste en -OR6, -O(CO)R6, -O(CO)OR9, -O(CH2)1-5OR9, -O(CO)NR6R7, -NR6R7, -NR6(CO)R7, -NR6(CO)OR9, -NR6(CO)NR7R8, -NR6SO2-alquilo inferior, -NR6SO2-arilo, -CONR6R7, -COR6, -SO2NR6R7, S(O)0-2-alquilo, S(O)0-2-arilo, -O(CH2)1-10-COOR6, -O(CH2)1-10CONR6R7, o-halógeno, m-halógeno, o-alquilo inferior, m-alquilo inferior, -(alquileno inferior)-COOR6, y -CH=CH-COOR6; R3 y R4 representan independientemente 1-3 sustituyentes independientemente seleccionados del grupo que consiste en R5, hidrógeno, p-alquilo inferior, arilo, -NO2, -CF3 y p-halógeno; R6, R7 y R8 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo inferior, arilo y alquilo inferior arilo-sustituido; y R9 es alquilo inferior, arilo ó alquilo inferior arilo-sustituido; compuesto (d) de la fórmula (4) o una sal farmacéuticamente aceptable del mismo o un solvato del mismo, donde, en la fórmula (4): A está seleccionado del grupo que consiste en heterocicloalquilo R2-sustituido, heteroarilo R2-sustituido, heterocicloalquilo benzofusionado R2-sustituido, y heteroarilo benzofusionado R2-sustituido; Ar1 es arilo ó arilo R3-sustituido; Ar2 es arilo ó arilo R4-sustituido; Q es un enlace o, con el carbono del anillo de la azetidinona en posición 3 forma el grupo espiro de la fórmula (5); y R1 está seleccionado del grupo que consiste en : -(CH2)q, donde q es 2-6, con la condición de que cuando Q forma un anillo espiro, q puede ser también cero ó 1; -(CH2)e-G-(CH2)r-, donde G es -O-, -C(O)-, fenileno, -NR8- ó -S(O)0-2, e es 0-5 y r es 0-5, con la condición de que la suma de e y r sea 1-6; -(alquenileno C2-6)-; y -(CH2)f-V-(CH2)g-, donde V es cicloalquileno C3-6, f es 1-5 y g es 0-5, con la condición de que la suma de f y g es 1-6; R6 está seleccionado de: >CH-, >C(alquilo C1-6)-, >CF-, >C(OH)-, >C(C6H4-R9)-, >N-, ó >N+O-; R6 y R7 están independientemente seleccionados del grupo que consiste en -CH2-, -CH(alquilo C1-6)-, -C(di-alquilo (C1-6)), -CH=CH- y -C(alquilo C1-6)=CH-; ó R5 conjuntamente con un R6 adyacente, ó R5 conjuntamente con un R7 adyacente, forman un -CH=CH- o un grupo -CH=C(alquilo C1-6)-; a y b son independientemente 0, 1, 2 ó 3, con la condición de que ambos no sean cero; con la condición de que cuando R6 es -CH=CH- ó -C(alquilo C1-6)=CH-, a sea 1; con la condición de que cuando R7 es -CH=CH- ó -C(alquilo C1-6)=CH-, b sea 1; con la condición de que cuando a es 2 ó 3, las R6 puedan ser iguales o diferentes; y con la condición de que cuando b es 2 ó 3, las R7 puedan ser iguales o diferentes; y cuando Q es un enlace, R1 puede estar también seleccionado entre los radicales del grupo de fórmulas (6) donde M es -O-, -S-, -S(O)- ó -S(O)2-; X, Y y Z están independientemente seleccionados del grupo que consiste en -CH2-, -CH(alquilo C1-6)- y -C(di-alquilo (C1-6)); R10 y R12 están independientemente seleccionados del grupo que consiste en -OR14, -O(CO)R14, -O(CO)OR16 y -O(CO)NR14R15; R11 y R13 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo (C1-6) y arilo; ó R10 y R11 conjuntamente son =O, ó R12 y R13 conjuntamente son =O; d es 1, 2 ó 3; h es 0, 1, 2, 3 ó 4; s es 0 ó 1; t es 0 ó 1; m, n y p son independientemente 0-4; con la condición de que por lo menos uno de s y t sea 1, y la suma de m, n, p, s y t es 1-6; con la condición de que cuando p es 0 y t es 1, la suma de m, s y n sea 1-5; y con la condición de que cuando p es 0 y s es 1, la suma de m, t y n es 1-5; v es 0 ó 1; j y k son independientemente 1-5, con la condición de que la suma de j, k y v sea 1-5; R2 representa 1-3 sustituyentes en los átomos de carbono del anillo seleccionados del grupo que consiste en hidrógeno, alquilo (C1-10), alquenilo (C2-10), alquinilo (C2-10), cicloalquilo (C3-6), cicloalquenilo (C3-6), arilo R17-sustituido, bencilo R17-sustituido, benciloxi R17-sustituido, ariloxi R17-sustituido, halógeno, -NR14R15, NR14R15(alquileno C1-6)-, NR14R15C(O)(alquileno C1-6)-, -NHC(O)R16, OH, alcoxi C1-6, -OC(O)R16, -COR14, hidroxialquilo (C1-6), alcoxi (C1-6)-alquilo (C1-6), NO2, -S(O)0-2R16, -SO2NR14R15 y -(alquileno C1-6)COOR14; cuando R2 es un sustituyente en un anillo heterocicloalquilo, R2 es tal como se ha definido, ó es =O o un grupo de la fórmula (7) y, cuando R2 es un sustituyente en un nitrógeno del anillo sustituible, es hidrógeno, alquilo (C1-6,), arilo, alcoxi (C1-6), ariloxi, alquilcarbonilo (C1-6), arilcarbonilo, hidroxi, -(CH2)1-6CONR18R18, un radical del grupo de fórmulas (8); donde J es -O-, -NH-, -NR18- ó -CH2-; R3 y R4 están independientemente seleccionados del grupo que consiste en 1-3 sustituyentes independientemente seleccionados del grupo que consiste en alquilo (C1-6), -OR14, -O(CO)R14, -O(CO)OR16, -O(CH2)1-5OR14, -O(CO)NR14R15, -NR14R15, -NR14(CO)R15, -NR14(CO)OR16, -NR14(CO)NR15R19, -NR14SO2R16, -COOR14, -CONR14R15, -COR14, -SO2NR14R15, S(O)0-2R16, -O(CH2)1-10-COOR14, -O(CH2)1-10CONR14R15, -(alquileno C1-6)-COOR14, -CH=CH-COOR14, -CF3, -CN, -NO2 y halógeno; R8 es hidrógeno, alquilo (C1-6), arilalquilo (C1-6), -C(O)R14 ó -COOR14; R9 y R17 representan independientemente 1-3 grupos que están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo (C1-6), alcoxi (C1-6), -COOH, -NO2, -NR14R15, -OH y halógeno; R14 y R15 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo (C1-6), arilo y alquilo (C1-6) arilo-sustituido; R16 es alquilo (C1-6), arilo ó arilo R17-sustituido; R18 es hidrógeno ó alquilo (C1-6); y R19 es hidrógeno, hidroxi ó alcoxi (C1-6), (e) compuestos de la fórmula (9) o una sal farmacéuticamente aceptable del mismo o un solvato del mismo, donde, en la fórmula (9): Ar1 es arilo, arilo R10-sustituido ó heteroarilo; Ar2 es arilo ó arilo R4-sustituido; Ar3 es arilo ó arilo R5-sustituido; X e Y están independientemente seleccionados del grupo que consiste en -CH2-, -CH(alquilo inferior)- y -C(dialquilo inferior)-; R es -OR6, -O(CO)R6, -O(CO)OR9, u -O(CO)NR6R7; R1 es hidrógeno, alquilo inferior ó arilo; ó R y R1 conjuntamente son =O, q es 0 ó 1; r es 0, 1 ó 2; m y n independientemente son 0, 1, 2, 3, 4 ó 5; con la condición de que la suma de m, n y q sea 1, 2, 3, 4 ó 5; R4 representa 1-5 sustituyentes independientemente seleccionados del grupo que consiste en alquilo inferior, -OR6, -O(CO)R6, -O(CO)OR9, -O(CH2)1-5OR6, -O(CO)NR6R7, -NR6R7, -NR6(CO)R7, -NR6(CO)OR9, -NR6(CO)NR7R8, -NR6SO2R9, -COOR6, -CONR6R7, -COR6, -SO2NR6R7, S(O)0-2R9, -O(CH2)1-10-COOR6, -O(CH2)1-10CONR6R7, -(alquileno inferior)COOR6 y -CH=CH-COOR6; R5 representa 1-5 sustituyentes independientemente seleccionados del grupo que consiste en -OR6, -O(CO)R, -O(CO)OR9, -O(CH2)1-5OR6, -O(CO)NR6R7, -NR6R7, -NR6(CO)R7, -NR6(CO)OR9, -NR6(CO)NR7R8, -NR6SO2R9, -COOR6, -CONR6R7, -COR6, -SO2NR6R7, S(O)0-2R9, -O(CH2)1-10-COOR6, -O(CH2)1-10CONR6R7, -CF3, -CN, -NO2, halógeno, -(alquileno inferior)COOR6 y -CH=CH-COOR6; R6, R7 y R8 están independientemente seleccionados del grupo que consiste en hidrógeno, alquilo inferior, arilo y alquilo inferior arilo-sustituido; R9 es alquilo inferior, arilo ó alquilo inferior arilo-sustituido; y R10 representa 1-5 sustituyentes independientemente seleccionados del grupo que consiste en alquilo inferior, -OR6, -O(CO)R6, -O(CO)OR9, -O(CH2)1-5OR6, -O(CO)N
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US29365101P | 2001-05-25 | 2001-05-25 | |
| US32391101P | 2001-09-21 | 2001-09-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR038956A1 true AR038956A1 (es) | 2005-02-02 |
Family
ID=26968071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020101893A AR038956A1 (es) | 2001-05-25 | 2002-05-22 | Uso de un compuesto que regula la produccion o niveles de peptidos beta amiloides para la manufactura de un medicamento para tratar la enfermedad de alzheimer y/o para regular dichos niveles de peptidos amiloides beta en un sujeto |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20030013699A1 (es) |
| EP (1) | EP1392287B8 (es) |
| JP (1) | JP2004532868A (es) |
| AR (1) | AR038956A1 (es) |
| AT (1) | ATE345792T1 (es) |
| AU (1) | AU2002308778A1 (es) |
| CA (1) | CA2447884A1 (es) |
| CY (1) | CY1105922T1 (es) |
| DE (1) | DE60216275T2 (es) |
| DK (1) | DK1392287T3 (es) |
| ES (1) | ES2275007T3 (es) |
| MX (1) | MXPA03010843A (es) |
| PT (1) | PT1392287E (es) |
| WO (1) | WO2002096415A2 (es) |
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| RS20100015A (sr) * | 2001-01-26 | 2010-12-31 | Schering Corporation | Kombinacija aktivatora receptora aktiviranog peroksizom- proliferatorom (ppar) fenofibrata sa inhibitorom apsorpcije sterola ezetimibom za vaskularne indikacije |
| CA2460340C (en) * | 2001-09-21 | 2011-02-15 | Schering Corporation | Methods and therapeutic combinations for the treatment of xanthoma using sterol absorption inhibitors |
| US7053080B2 (en) * | 2001-09-21 | 2006-05-30 | Schering Corporation | Methods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors |
| EP1485077A4 (en) * | 2002-03-12 | 2007-07-18 | Merck & Co Inc | DRUGS COMBINATION THERAPY |
| GB0215579D0 (en) | 2002-07-05 | 2002-08-14 | Astrazeneca Ab | Chemical compounds |
| EP2283838A3 (en) * | 2002-09-27 | 2011-04-20 | Martek Biosciences Corporation | Docosahexaenoic acid for treating subclinical inflammation |
| MXPA05004811A (es) | 2002-11-06 | 2005-07-22 | Schering Corp | Inhibidores de absorcion de colesterol para el tratamiento de trastornos autoinmunes. |
| CA2517571C (en) | 2003-03-07 | 2011-07-05 | Schering Corporation | Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof |
| US7459442B2 (en) * | 2003-03-07 | 2008-12-02 | Schering Corporation | Substituted azetidinone compounds, processes for preparing the same, formulations and uses thereof |
| MXPA05009502A (es) | 2003-03-07 | 2005-10-18 | Schering Corp | Compuestos de azetidinona sustituidos, formulaciones y usos de los mismos para el tratamiento de hipercolesterolemia. |
| MXPA05009501A (es) * | 2003-03-07 | 2005-10-18 | Schering Corp | Compuestos de azetidinona sustituidos, formulaciones y usos de los mismos para el tratamiento de hipercolesterolemia. |
| CN102584813B (zh) * | 2003-05-14 | 2016-07-06 | Ngc药物公司 | 化合物及其在调节淀粉样蛋白β中的用途 |
| ES2334029T3 (es) * | 2003-05-15 | 2010-03-04 | Roskamp Research Llc | Procedimiento para producir medicamentos para reducir la deposicion de amiloide, la neurotoxicidad de amiloide y la microgliosis. |
| US20050187278A1 (en) * | 2003-08-28 | 2005-08-25 | Pharmacia Corporation | Treatment or prevention of vascular disorders with Cox-2 inhibitors in combination with cyclic AMP-specific phosphodiesterase inhibitors |
| US20080260717A1 (en) * | 2003-10-31 | 2008-10-23 | Trustees Of Columbia University In The City Of New York | Methods for Reducing Seizure-Induced Neuronal Damage |
| WO2005061452A1 (en) | 2003-12-23 | 2005-07-07 | Astrazeneca Ab | Diphenylazetidinone derivates possessing cholesterol absorption inhibitory activity |
| US7803838B2 (en) * | 2004-06-04 | 2010-09-28 | Forest Laboratories Holdings Limited | Compositions comprising nebivolol |
| US7838552B2 (en) | 2004-06-04 | 2010-11-23 | Forest Laboratories Holdings Limited | Compositions comprising nebivolol |
| GB0419124D0 (en) | 2004-08-27 | 2004-09-29 | Proteome Sciences Plc | Methods and compositions relating to Alzheimer's disease |
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-
2002
- 2002-05-22 MX MXPA03010843A patent/MXPA03010843A/es active IP Right Grant
- 2002-05-22 AR ARP020101893A patent/AR038956A1/es unknown
- 2002-05-22 PT PT02774113T patent/PT1392287E/pt unknown
- 2002-05-22 JP JP2002592925A patent/JP2004532868A/ja active Pending
- 2002-05-22 AT AT02774113T patent/ATE345792T1/de not_active IP Right Cessation
- 2002-05-22 DK DK02774113T patent/DK1392287T3/da active
- 2002-05-22 ES ES02774113T patent/ES2275007T3/es not_active Expired - Lifetime
- 2002-05-22 DE DE60216275T patent/DE60216275T2/de not_active Expired - Fee Related
- 2002-05-22 CA CA002447884A patent/CA2447884A1/en not_active Abandoned
- 2002-05-22 US US10/154,106 patent/US20030013699A1/en not_active Abandoned
- 2002-05-22 AU AU2002308778A patent/AU2002308778A1/en not_active Abandoned
- 2002-05-22 EP EP02774113A patent/EP1392287B8/en not_active Expired - Lifetime
- 2002-05-22 WO PCT/US2002/016306 patent/WO2002096415A2/en not_active Ceased
-
2007
- 2007-01-15 CY CY20071100048T patent/CY1105922T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA03010843A (es) | 2004-02-17 |
| DE60216275D1 (de) | 2007-01-04 |
| DE60216275T2 (de) | 2007-06-21 |
| AU2002308778A1 (en) | 2002-12-09 |
| CY1105922T1 (el) | 2011-04-06 |
| ATE345792T1 (de) | 2006-12-15 |
| US20030013699A1 (en) | 2003-01-16 |
| EP1392287B1 (en) | 2006-11-22 |
| PT1392287E (pt) | 2007-02-28 |
| WO2002096415A2 (en) | 2002-12-05 |
| EP1392287B8 (en) | 2007-01-10 |
| CA2447884A1 (en) | 2002-12-05 |
| EP1392287A2 (en) | 2004-03-03 |
| ES2275007T3 (es) | 2007-06-01 |
| WO2002096415A3 (en) | 2003-01-16 |
| DK1392287T3 (da) | 2007-03-19 |
| JP2004532868A (ja) | 2004-10-28 |
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