AR038178A1 - Combinacion de inhibidores de ptm o inhibidores de la secrecion de apob con fibratos para la utilizacion como medicamentos - Google Patents
Combinacion de inhibidores de ptm o inhibidores de la secrecion de apob con fibratos para la utilizacion como medicamentosInfo
- Publication number
- AR038178A1 AR038178A1 ARP030100056A ARP030100056A AR038178A1 AR 038178 A1 AR038178 A1 AR 038178A1 AR P030100056 A ARP030100056 A AR P030100056A AR P030100056 A ARP030100056 A AR P030100056A AR 038178 A1 AR038178 A1 AR 038178A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- atom
- amino
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000003112 inhibitor Substances 0.000 title abstract 5
- 229940125753 fibrate Drugs 0.000 title abstract 3
- 102100040202 Apolipoprotein B-100 Human genes 0.000 title 1
- 101000889953 Homo sapiens Apolipoprotein B-100 Proteins 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 230000028327 secretion Effects 0.000 title 1
- -1 trifluoromethoxy, amino Chemical group 0.000 abstract 20
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 19
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 15
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 229910052760 oxygen Inorganic materials 0.000 abstract 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 13
- 125000001841 imino group Chemical group [H]N=* 0.000 abstract 12
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 11
- 125000004434 sulfur atom Chemical group 0.000 abstract 11
- 125000004429 atom Chemical group 0.000 abstract 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 7
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 6
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 abstract 5
- 125000006576 di-(C1-C3-alkyl)-aminocarbonyl group Chemical group 0.000 abstract 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 3
- 125000006842 cycloalkyleneimino group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 3
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 3
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 2
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 2
- 125000006164 6-membered heteroaryl group Chemical group 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 2
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 2
- 125000002619 bicyclic group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005549 heteroarylene group Chemical group 0.000 abstract 2
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 abstract 1
- 125000006545 (C1-C9) alkyl group Chemical group 0.000 abstract 1
- 102100031545 Microsomal triglyceride transfer protein large subunit Human genes 0.000 abstract 1
- BQOWUDKEXDCGQS-UHFFFAOYSA-N [CH]1CCCC1 Chemical compound [CH]1CCCC1 BQOWUDKEXDCGQS-UHFFFAOYSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 231100000304 hepatotoxicity Toxicity 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical group O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 230000007056 liver toxicity Effects 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 108010038232 microsomal triglyceride transfer protein Proteins 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
Classifications
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- 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
-
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
-
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/192—Carboxylic acids, e.g. valproic acid having aromatic groups, e.g. sulindac, 2-aryl-propionic acids, ethacrynic acid
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- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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- 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
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- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
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- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- Heart & Thoracic Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Gastroenterology & Hepatology (AREA)
- Urology & Nephrology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Utilización de fibratos para reducir la toxicidad hepática de inhibidores PTM, proteína de transferencia de triglicéridos microsomal, así como composiciones farmacéuticas que contienen un inhibidor de PTM y un fibrato. Reivindicación 3: Utilización según la reivindicación 1 ó 2, siendo el inhibidor de PTM un compuesto de la fórmula general (1), en la que: X1 significa el grupo CR1, X2 significa el grupo CR2, X3 significa el grupo CR3 y X4 significa el grupo CR4, o uno o dos de los grupos X1 a X4 significan en cada caso un átomo de N y los restantes grupos X1 a X4 significan tres o dos de los grupos CR1 a CR4, significando R1, R2, R3 y R4 en cada caso un átomo de H o significando uno o dos de los grupos R1 a R4, independientemente uno de otro, en cada caso un átomo de F, Cl, o Br, un grupo alquilo C1-3, un grupo trifluorometilo, hidroxi, alcoxi C1-3, trifluorometoxi, amino, alquil C1-3-amino o di-(alquil C1-3)-amino y significando los restantes grupos R1 a R4 en cada caso un átomo de H, pudiendo adoptar R4, adicionalmente, junto con R5 el significado de un puente -(CH2)n, en el que n representa el número 1, 2 ó 3 y Aa significa un enlace, un átomo de O ó S, un grupo -NH-, -N(alquilo C1-3)-, sulfinilo, sulfonilo o carbonilo, uno de los grupos -CH2-, -(CH2)2-, -CH=CH-, -CsC-, -OCH2-, -CH2O, -NH-CH2-, -CH2-NH-,-NH-CO-, -CO-NH-, -NH-SO2- o -SO2-NH-, en los que un átomo de H unido a un átomo de C y/o un átomo de H unido a un átomo de N puede estar en cada caso reemplazado por un grupo alquilo C1-3, y en donde un heteroátomo del grupo Aa no está enlazado con un átomo de N de un grupo heteroarilo de 5 miembros del grupo Ra, Ra significa un grupo fenilo, 1-naftilo o 2-naftilo, un grupo heteroarilo de 5 miembros unido a través de un átomo de C o N que contiene un grupo imino, eventualmente sustituido con un grupo alquilo C1-4, o alquil C1-4-carbonilo, un átomo de O ó S, un grupo imino, eventualmente sustituido con un grupo alquilo C1-4 o un átomo de O ó S y , adicionalmente, un átomo de N, o un grupo imino, eventualmente sustituido con un grupo alquilo C1-4 y dos átomos de N, o un átomo de O ó S y dos átomos de N, un grupo heteroarilo de 6 miembros que contiene uno o dos átomos de N, pudiendo estar condensado un anillo de fenilo a los grupos heteroarilo de 5 o 6 miembros precedentemente mencionados a través de dos átomos de C contiguos y pudiendo estar unidos los grupos heteroarilo bicíclicos, así formados, a través de la parte heteroatómica o carbocíclica y pudiendo estar monosustituido los grupos fenilo y naftilo, así como los radicales heteroarilo monocíclicos y bicíclicos precedentemente mencionados, en el esqueleto de carbonos, con un átomo de F, Cl, o Br, con un grupo alquilo C1-4 ,con un grupo cicloalquilo C3-7, trifluorometilo, fenilo, hidroxi, alcoxi C1-3, trifluorometoxi, amino, alquilo C1-3-amino, di-(alquil C1-3)-amino, acetilamino, N-(alquil C1-3)-acetil-amino, propionilamino, N-(alquil C1-3)-propionilamino, acetilo, propionilo, alcoxi C1-3-carbonilo, aminocarbonilo, alquil C1-3-amino-carbonilo, di-(alquil C1-3)-amino-carbonilo o ciano o con excepción de radicales heteroarilo de 5 miembros que contienen más de dos heteroátomos, pudiendo estar también di-sustituidos con los sustituyentes precedentemente mencionados, pudiendo ser los sustituyentes iguales o diferentes, un grupo cicloalquilo C3-7, pudiendo estar reemplazado en cada caso el grupo metileno en posición 4 de un radical cicloalquilo de 6 o 7 miembros con un átomo de O ó S, con un grupo sulfinilo o sulfonilo o con un grupo imino, eventualmente sustituido con un grupo alquilo C1-5, fenilo, alquil C1-4-carbonilo, alcoxi C1-4-carbonilo, alquil C1-3-aminocarbonilo o di-(alquil C1-3)-amino-carbonilo, un grupo cicloalquilenimino de 4 a 7 miembros, en el que la parte de cicloalquileno puede estar condensada con un anillo de fenilo o uno o dos átomos de H pueden estar reemplazados en cada caso con un grupo alquilo C1-3 y/o en cada caso el grupo metileno en posición 4 de un grupo cicloalquilenimino de 6 o 7 miembros puede estar sustituido con un grupo hidroxicarbonilo, alcoxi C1-3-carbonilo, amino, alquil C1-3-amino, di-(alquil C1-3)-amino, aminocarbonilo, alquil C1-3-amino-carbonilo, di-(alquil C1-3)-aminocarbonilo o fenil-alquil C1-3-amino, o con un átomo de O ó S, con un grupo sulfinilo o sulfonilo o con un grupo imino eventualmente sustituido con un grupo alquilo C1-5, fenilo, alquil C1-4-carbonilo, alcoxi C1-4-carbonilo, alquil C1-3-aminocarbonilo o di-(alquil C1-3)-aminocarbonilo, o en un grupo cicloalquilenimino de 5, 6 o 7 miembros, un grupo -CH2 enlazado con el átomo de N de imino puede estar reemplazado por un grupo carbonilo o un grupo -(CH2)2- enlazado con el átomo de N de imino puede estar reemplazado por un grupo -CO-NR8, o un grupo -(CH2)3 enlazado con el átomo de N de imino puede estar reemplazado por un grupo -CO-NR8-CO, representando R8 un átomo de H o un grupo alquilo C1-3, R5 significa un átomo de H o un grupo alquilo C1-5, Het significa un grupo heteroarileno de 5 miembros unido a través de dos átomos de C o, si Het significa un grupo pirrol de doble enlace, unido también a través de un átomo de C y el átomo de N de imino, estando enlazado este último con el grupo carbonilo contiguo en la fórmula (1), el cual contiene un grupo imino sustituido con el grupo R9, un átomo de O ó S o un grupo imino sustituido con el grupo R9 o un átomo de O ó S y, adicionalmente, un átomo de N, significando R9 un átomo de H, un grupo alquilo C1-5, un grupo alquilo C2-3 sustituido en posición terminal con un grupo amino, alquil C1-3-amino, di-(alquil C1-3)-amino o alcoxi C1-5-carbonil-amino, un grupo carboxi-alquilo C1-3, alcoxi C1-3-carbonil-alquilo C1-3, fenilo, fenil-alquilo C1-3, alquil C1-5-carbonilo o fenilcarbonilo, o R9, junto con R6, representa un puente -(CH2)p, en el que p significa el número 2 ó 3, o un grupo imino eventualmente sustituido con un grupo alquilo C1-3 y dos átomos de N, o un átomo de O ó S y dos átomos de N, o significa un grupo heteroarileno de 6 miembros que contiene uno o dos átomos de N, estando los radicales heteroarileno precedentemente mencionados monosustituidos en el esqueleto de carbonos con un átomo de F, Cl, o Br, con un grupo alquilo C1-5, con un grupo cicloalquilo C3-7, trifluorometilo, hidroxi, alcoxi C1-3, trifluorometoxi, amino, alquil C1-3-amino, di-(alquil C1-3)-amino, acetilamino, N-(alquil C1-3)-acetilamino, propionilamino, N-(alquil C1-3)-propionilamino, acetilo, propionilo, benzoilo, alcoxi C1-3-carbonilo, aminocarbonilo, alquil C1-3amino-carbonilo, di-(alquil C1-3)-amino-carbonilo o ciano o, con excepción de radicales heteroarilo monocíclicos de 5 miembros que contienen más de un heteroátomo, pudiendo estar también disustituido con los sustituyentes precedentemente mencionados, pudiendo ser los sustituyentes iguales o diferentes, R6 significa un átomo de H o un grupo alquilo C1-6, R7 significa un grupo alquilo C1-9, un grupo alquenilo C3-9 o alquinilo C3-9 de cadena lineal o ramificada e insaturado una vez, dos veces o tres veces, estando aislados los enlaces múltiples del enlace N-C, un grupo alquilo C2-6 de cadena lineal que está sustituido en posición terminal con un grupo amino, alquil C1-3-amino o di-(alquil C1-3)-amino, un grupo alquilo C1-6 sustituido con un radical cicloalquilo C3-7, pudiendo estar reemplazado un átomo de H en posición 3 del radical ciclopentilo y en posición 4 de un radical cicloalquilo de 6 o 7 miembros, en cada caso con un grupo hidroxi, hidroxi-alquilo C1-3, alcoxi C1-5, alcoxi C1-5-alquilo C1-3, fenil-alcoxi C1-3-alquilo C1-3, amino, alquil C1-5-amino, di-(alquil C1-5)-amino, fenil-alquil C1-3-amino, alquil C1-5-carbonilamino, benzoil-amino, amino-alquilo C1-3, alquil C1-3-amino-alquilo C1-3, di-(alquil C1-3)-amino-alquilo C1-3, fenil-alquil C1-3-amino-alquilo C1-3, alquil C1-3-carbonilamino-alquilo C1-3, benzoilamino C1-3, fenilamino-carbonilo, fenil-alquil C1-3-amino-carbonilo, carboxi o alcoxi C1-3-carbonilo o pudiendo estar reemplazado en cada caso el grupo metileno en posición 4 de un radical cicloalquilo de 6 o 7 miembros con un átomo de, O ó S o con un grupo imino eventualmente sustituido con un grupo alquilo C1-6, fenilo, alquil C1-6-carbonilo, benzoílo, fenil-(alquil C1-3)-carbonilo, alquil C1-6-aminocarbonilo, di-(alquil C1-5)-aminocarbonilo, fenilamino-carbonilo, N-(alquil C1-3)-fenilcarbonilo, fenil-alquil C1-3-aminocarbonilo o N-(alquil C1-3)-fenil-alquilo C1-3-amino-carbonilo o pudiendo estar condensados en un radical cicloalquilo de 5 o 6 miembros uno o dos enlaces simples separados por al menos un enlace entre sí y separados de la posición 1, en cada caso con un radical fenilo, en donde en un sistema de anillo bicíclico o tricíclico así formado, el átomo de H unido al átomo de C saturado en la posición 1 puede estar reemplazado por un grupo alquil C1-5-amino-carbonilo, di-(alquil C1-5)-amino-carbonilo, fenil-alquil C1-3-amino-carbonilo o alcoxi C1-5-carbonilo, en los que grupos metilo terminales pueden estar fluorados en cada caso total o parcialmente, significa un grupo alquilo C1-6 eventualmente sustituido con un grupo cicloalquilo C3-7, que está sustituido con un grupo carboxi o alcoxi C1-3-carbonilo, con un grupo fenilo, 1-naftilo o 2-naftilo, con un grupo heteroarilo de 5 miembros unido a través de un átomo de C o N, que contiene un grupo imino eventualmente sustituido con un grupo alquilo C1-3, trifluorometilo, fenilo, fenil-alquilo C1-3, alquil C1-3-carbonilo, fenilcarbonilo o fenil-alquil C1-3-carbonilo, un átomo de O ó S, un grupo imino eventualmente sustituido con un grupo alquilo C1-3 o un átomo de O ó S y, adicionalmente, un átomo de N, o grupo imino eventualmente sustituido con un grupo alquilo C1-3 y dos átomos de N o un átomo de O ó S y dos átomos de N, con un grupo heteroarilo de 6 miembros que contiene uno dos átomos de N, pudiendo estar condensado un anillo de fenilo a los grupos heteroarilo de 5 o 6 miembros precedentemente mencionados a través
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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DE2002100633 DE10200633A1 (de) | 2002-01-10 | 2002-01-10 | Kombination von MTP Inhibitoren oder apoB-Sekretions-Inhibitoren mit Fibraten zur Verwendung als Arzneimittel |
DE10256184A DE10256184A1 (de) | 2002-12-02 | 2002-12-02 | Kombination von MTP Inhibitoren oder apoB-Sekretions-Inhibitoren mit Fibraten zur Verwendung als Arzneimittel |
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AR038178A1 true AR038178A1 (es) | 2005-01-05 |
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ARP030100056A Withdrawn AR038178A1 (es) | 2002-01-10 | 2003-01-10 | Combinacion de inhibidores de ptm o inhibidores de la secrecion de apob con fibratos para la utilizacion como medicamentos |
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EP (1) | EP1465613A2 (es) |
JP (1) | JP2005525309A (es) |
AR (1) | AR038178A1 (es) |
AU (1) | AU2003205570A1 (es) |
CA (1) | CA2471566A1 (es) |
PE (1) | PE20030924A1 (es) |
TW (1) | TW200402292A (es) |
UY (1) | UY27610A1 (es) |
WO (1) | WO2003057205A2 (es) |
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GB0215293D0 (en) | 2002-07-03 | 2002-08-14 | Rega Foundation | Viral inhibitors |
MXPA05006744A (es) * | 2002-12-20 | 2005-09-08 | Pfizer Prod Inc | Inhibidores de la proteina microsomal de transferencia de trigliceridos. |
JP2007008816A (ja) * | 2003-10-15 | 2007-01-18 | Ube Ind Ltd | 新規イソキノリン誘導体 |
US7648998B2 (en) | 2003-12-22 | 2010-01-19 | K.U. Leuven Research & Development | Imidazo 4,5-c pyridine compounds and methods of antiviral treatment |
AU2005319167B2 (en) | 2004-12-21 | 2011-09-29 | Gilead Sciences, Inc. | Imidazo[4,5-C]pyridine compound and method of antiviral treatment |
US20060241073A1 (en) * | 2005-04-20 | 2006-10-26 | Wanders Ronaldus J A | Means and methods for counteracting fatty acid accumulation |
KR20080031038A (ko) * | 2005-07-29 | 2008-04-07 | 4에스체 악티엔게젤샤프트 | 신규의 헤테로환 NF-κB 억제제 |
WO2008005519A2 (en) | 2006-07-07 | 2008-01-10 | Gilead Sciences, Inc. | Novel pyridazine compound and use thereof |
JP5642922B2 (ja) * | 2007-04-24 | 2014-12-17 | サントリーホールディングス株式会社 | 複数の肝障害マーカーを指標とする肝障害の評価方法 |
CL2008001933A1 (es) | 2007-06-29 | 2009-09-25 | Millennium Pharm Inc | Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros. |
UA99466C2 (en) | 2007-07-06 | 2012-08-27 | Гилиад Сайенсиз, Инк. | Crystalline pyridazine compound |
EP2438059A1 (en) | 2009-06-05 | 2012-04-11 | Link Medicine Corporation | Aminopyrrolidinone derivatives and uses thereof |
JOP20200001A1 (ar) | 2017-07-11 | 2022-10-30 | Vertex Pharma | كاربوكسأميدات بوصفها معدلات لقنوات الصوديوم |
SI3762368T1 (sl) | 2018-03-08 | 2022-06-30 | Incyte Corporation | Aminopirazin diolne spojine kot zaviralci PI3K-y |
US11046658B2 (en) | 2018-07-02 | 2021-06-29 | Incyte Corporation | Aminopyrazine derivatives as PI3K-γ inhibitors |
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US5883109A (en) * | 1996-07-24 | 1999-03-16 | Bristol-Myers Squibb Company | Method for lowering serum lipid levels employing an MTP inhibitor in combination with another cholesterol lowering drug |
CA2325358C (en) * | 1999-11-10 | 2005-08-02 | Pfizer Products Inc. | 7-¬(4'-trifluoromethyl-biphenyl-2-carbonyl)amino|-quinoline-3-carboxylic acid amides, and methods of inhibiting the secretion of apolipoprotein b |
DE10033337A1 (de) * | 2000-07-08 | 2002-01-17 | Boehringer Ingelheim Pharma | Biphenylcarbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel |
DE10132686A1 (de) * | 2001-07-05 | 2003-01-16 | Boehringer Ingelheim Pharma | Heteroarylcarbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel |
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2003
- 2003-01-07 AU AU2003205570A patent/AU2003205570A1/en not_active Abandoned
- 2003-01-07 UY UY27610A patent/UY27610A1/es not_active Application Discontinuation
- 2003-01-07 EP EP03702391A patent/EP1465613A2/de not_active Ceased
- 2003-01-07 CA CA002471566A patent/CA2471566A1/en not_active Abandoned
- 2003-01-07 WO PCT/EP2003/000057 patent/WO2003057205A2/de active Application Filing
- 2003-01-07 JP JP2003557563A patent/JP2005525309A/ja active Pending
- 2003-01-08 TW TW092100321A patent/TW200402292A/zh unknown
- 2003-01-09 PE PE2003000036A patent/PE20030924A1/es not_active Application Discontinuation
- 2003-01-10 AR ARP030100056A patent/AR038178A1/es not_active Withdrawn
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WO2003057205A2 (de) | 2003-07-17 |
UY27610A1 (es) | 2003-08-29 |
PE20030924A1 (es) | 2003-12-17 |
AU2003205570A1 (en) | 2003-07-24 |
AU2003205570A8 (en) | 2003-07-24 |
WO2003057205A3 (de) | 2004-04-01 |
JP2005525309A (ja) | 2005-08-25 |
CA2471566A1 (en) | 2003-07-17 |
EP1465613A2 (de) | 2004-10-13 |
TW200402292A (en) | 2004-02-16 |
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