AR041594A1 - Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1 - Google Patents
Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1Info
- Publication number
- AR041594A1 AR041594A1 ARP030103716A ARP030103716A AR041594A1 AR 041594 A1 AR041594 A1 AR 041594A1 AR P030103716 A ARP030103716 A AR P030103716A AR P030103716 A ARP030103716 A AR P030103716A AR 041594 A1 AR041594 A1 AR 041594A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heterocyclyl
- carbocyclyl
- carbamoyl
- amino
- Prior art date
Links
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 2
- 102000008645 11-beta-Hydroxysteroid Dehydrogenase Type 1 Human genes 0.000 title 1
- 108010088011 11-beta-Hydroxysteroid Dehydrogenase Type 1 Proteins 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 30
- -1 nitro, cyano, hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 abstract 28
- 125000000623 heterocyclic group Chemical group 0.000 abstract 14
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 9
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 5
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 125000004760 (C1-C4) alkylsulfonylamino group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 3
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 3
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 3
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 101100451537 Caenorhabditis elegans hsd-1 gene Proteins 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 2
- 239000003814 drug Substances 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 230000005764 inhibitory process Effects 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004169 (C1-C6) alkyl 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
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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
- C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/443—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- 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
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
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- A61P5/00—Drugs for disorders of the endocrine system
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61P9/00—Drugs for disorders of the cardiovascular system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
- C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
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- C—CHEMISTRY; METALLURGY
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- 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
- C07D405/06—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 carbon chain containing only aliphatic carbon atoms
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- C07D409/06—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 carbon chain containing only aliphatic carbon atoms
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- 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
- C07D417/06—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 carbon chain containing only aliphatic carbon atoms
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- C07D417/14—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 three or more hetero rings
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Se describe el uso de un compuesto en la fabricación de un medicamento para usar en la inhibición de 11 HSD1, también reivindica proceso y composiciones farmacéuticas y compuestos. Reivindicación 1: El uso de un compuesto caracterizado porque responde a la fórmula (1) donde: El anillo A se selecciona entre carbociclilo o heterociclilo; donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R9. R1 es un sustituyente sobre C y se selecciona entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N-(C1-4 alquil)carbamoilo, N,N-(C1-4alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z-; donde R1 puede estar sustituido opcionalmente sobre C con uno o más grupos seleccionados entre R3; y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R4; n es 0-5; donde los valores de R1 pueden ser iguales o diferentes; X es un enlace simple, -C(O)-, -S(O)2, -C(O)NR11, -C(S)NR11, -C(O)O-, -C(=NR11)- o -CH2-; donde R11 se selecciona entre H, C1-4 alquilo, carbociclilo y heterociclilo; Y es H, C1-6 alquilo, C2-6 alquenilo, C2-6 alquinilo, carbociclilo o heterociclilo; donde Y puede estar sustituido opcionalmente sobre C con uno o más R2; donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R5; R2 es un sustituyente sobre C y se selecciona entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, trifluorometilo, trifluorometoxi, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4 alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N,(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, C1-4 alcoxicarbonilamino, C1-4 alcoxicarbonil-N-(C1-4 alquil)amino, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, aminotiocarboniltio, N-(C1-4 alquil)aminotiocarboniltio, N,N-(C1-4 alquil)2 aminotiocarboniltio, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z-; donde R2 puede estar sustituido opcionalmente sobre C con uno o más grupos seleccionados entre R6, y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R7; R3 y R6 se seleccionan en forma independiente entre halo, nitro, ciano, hidroxi, amino, carboxi, carbamoilo, mercapto, sulfamoilo, trifluorometilo, trifluorometoxi, C1-4 alquilo, C2-4 alquenilo, C2-4 alquinilo, C1-4 alcoxi, C1-4 alcanoilo, C1-4 alcanoiloxi, N-(C1-4 alquil)amino, N,N-(C1-4 alquil)2amino, C1-4 alcanoilamino, N-(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, C1-4 alquilS(O)a donde a es entre 0 y 2, C1-4 alcoxicarbonilo, C1-4 alcoxicarbonilamino, C1-4 alcoxicarbonil-N-(C1-4 alquil)amino, N-(C1-4 alquil)sulfamoilo, N,N-(C1-4 alquil)2sulfamoilo, C1-4 alquilsulfonilamino, carbociclilo, heterociclilo, carbociclil C0-4 alquilen-Z- y heterociclil C0-4 alquilen-Z- donde R3 y R6 pueden estar sustituidos opcionalmente en forma independiente sobre C con uno o más R8; y donde si dicho heterociclilo contiene una porción -NH- este N puede estar sustituido opcionalmente con un grupo seleccionado entre R13; R4, R5, R7, R9 y R13 se seleccionan en forma independiente entre C1-4 alquilo, C1-4 alcanoilo, C1-4 alquilsulfonilo, C1-4 alcoxicarbonilo, carbamoilo, N-(C1-4 alquil)carbamoilo, N,N-(C1-4 alquil)2carbamoilo, bencilo, benciloxicarbonilo, benzoilo y fenilsulfonilo; R8 se selecciona entre halo, nitro, ciano, hidroxi, trifluorometoxi, trifluorometilo, amino, carboxi, carbamoilo, mercapto, sulfamoilo, metilo, etilo, metoxi, etoxi, acetilo, acetoxi, metilamino, etilamino, dimetilamino, dietilamino, N-metil-N-etilamino, acetilamino, N-metilcarbamoilo, N-etilcarbamoilo, N,N-dimetilcarbamoilo, N,N-dietilcarbamoilo, N-metil-N-etilcarbamoilo, metilito, etiltio, metilsulfinilo, etilsulfinilo, mesilo, etilsulfonilo, metoxicarbonilo, etoxicarbonilo, N-metilsulfamoilo, N-etilsulfamoilo, N,N-dimetilsulfamoilo, N,N-dietilsulfamoilo o N-metil-N-etilsulfamoilo; Z es -S(O)a-, -O-, -NR10-, -C(O)-, -C(O)NR11-, -NR10C(O)-, -OC(O)NR10- o -SO2NR10-; donde a es entre 0 y 2; donde R10 se selecciona entre H y C1-4 alquilo; R12 es hidroxi, metilo, etilo o propilo; m es 0 o 1; q es 0 o 1; o una sal aceptable para uso farmacéutico del mismo, en la fabricación de un medicamento para usar en la inhibición de 11betaHSD1.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0223573A GB0223573D0 (en) | 2002-10-11 | 2002-10-11 | Chemical compounds |
| GB0310446A GB0310446D0 (en) | 2003-05-07 | 2003-05-07 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR041594A1 true AR041594A1 (es) | 2005-05-26 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030103716A AR041594A1 (es) | 2002-10-11 | 2003-10-10 | Derivados de 1,4 piperidina disustituida y su uso como inhibidores de 11-beta hidroxiesteroide dehidrogenasa tipo 1 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20050256159A1 (es) |
| EP (1) | EP1556349A1 (es) |
| JP (1) | JP2006506451A (es) |
| KR (1) | KR20050051691A (es) |
| AR (1) | AR041594A1 (es) |
| AU (1) | AU2003269242A1 (es) |
| BR (1) | BR0315166A (es) |
| CA (1) | CA2501611A1 (es) |
| MX (1) | MXPA05003632A (es) |
| NO (1) | NO20051600L (es) |
| TW (1) | TW200413318A (es) |
| UY (1) | UY28014A1 (es) |
| WO (1) | WO2004033427A1 (es) |
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| EA029430B1 (ru) | 2013-06-21 | 2018-03-30 | Такеда Фармасьютикл Компани Лимитед | Производные 1-сульфонилпиперидина в качестве модуляторов рецепторов прокинетицина |
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| EP3573971A1 (en) | 2017-01-26 | 2019-12-04 | Araxes Pharma LLC | 1-(3-(6-(3-hydroxynaphthalen-1-yl)benzofuran-2-yl)azetidin-1yl)prop-2-en-1-one derivatives and similar compounds as kras g12c modulators for treating cancer |
| US11358959B2 (en) | 2017-01-26 | 2022-06-14 | Araxes Pharma Llc | Benzothiophene and benzothiazole compounds and methods of use thereof |
| JP7090099B2 (ja) | 2017-03-16 | 2022-06-23 | エフ.ホフマン-ラ ロシュ アーゲー | Atxインヒビターとしての新規二環式化合物 |
| MA50014A (fr) | 2017-04-20 | 2020-07-08 | Leidos Biomedical Res Inc | Modulateurs de k-ras |
| CN110831933A (zh) | 2017-05-25 | 2020-02-21 | 亚瑞克西斯制药公司 | 喹唑啉衍生物作为突变kras、hras或nras的调节剂 |
| US10745385B2 (en) | 2017-05-25 | 2020-08-18 | Araxes Pharma Llc | Covalent inhibitors of KRAS |
| US12134620B2 (en) | 2018-08-01 | 2024-11-05 | Araxes Pharma Llc | Heterocyclic spiro compounds and methods of use thereof for the treatment of cancer |
| CN115850241B (zh) * | 2021-09-24 | 2025-01-14 | 中国药科大学 | 一种含α-酮骨架的取代杂环类化合物及其用途 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8401092D0 (en) * | 1984-01-16 | 1984-02-15 | Fujisawa Pharmaceutical Co | Piperidine derivatives |
| JP2643168B2 (ja) * | 1987-08-24 | 1997-08-20 | エーザイ株式会社 | 不整脈治療・予防剤 |
| DE3854991T2 (de) * | 1987-11-27 | 1996-07-18 | Eisai Co Ltd | Cyclische Amine und pharmakologische Verbindungen |
| US4990511A (en) * | 1988-08-03 | 1991-02-05 | Takeda Chemical Industries, Ltd. | Amide compounds, their production and use |
| DE4407136A1 (de) * | 1994-03-04 | 1995-09-07 | Thomae Gmbh Dr K | Aroyl-1-azacycloalkane, deren Salze, diese Verbindungen enthaltende Arzneimittel und deren Verwendung sowie Verfahren zu ihrer Herstellung |
| JPH10287671A (ja) * | 1997-04-14 | 1998-10-27 | Nippon Soda Co Ltd | イミダゾリルメチルフェニルまたはピリジルメチルフェニル誘導体およびその製造方法 |
| JP2002515891A (ja) * | 1997-12-19 | 2002-05-28 | スミスクライン・ビーチャム・コーポレイション | 新規なピペリジン含有化合物 |
| GT199900167A (es) * | 1998-10-01 | 2001-03-21 | Nuevos bis-benzimidazoles. | |
| SE0001899D0 (sv) * | 2000-05-22 | 2000-05-22 | Pharmacia & Upjohn Ab | New compounds |
| DE10210779A1 (de) * | 2002-03-12 | 2003-10-09 | Merck Patent Gmbh | Cyclische Amide |
-
2003
- 2003-10-07 JP JP2005500993A patent/JP2006506451A/ja not_active Withdrawn
- 2003-10-07 EP EP03751021A patent/EP1556349A1/en not_active Withdrawn
- 2003-10-07 CA CA002501611A patent/CA2501611A1/en not_active Abandoned
- 2003-10-07 AU AU2003269242A patent/AU2003269242A1/en not_active Abandoned
- 2003-10-07 WO PCT/GB2003/004318 patent/WO2004033427A1/en not_active Ceased
- 2003-10-07 MX MXPA05003632A patent/MXPA05003632A/es not_active Application Discontinuation
- 2003-10-07 BR BR0315166-2A patent/BR0315166A/pt not_active Application Discontinuation
- 2003-10-07 US US10/529,951 patent/US20050256159A1/en not_active Abandoned
- 2003-10-07 KR KR1020057006250A patent/KR20050051691A/ko not_active Withdrawn
- 2003-10-08 TW TW092127964A patent/TW200413318A/zh unknown
- 2003-10-10 AR ARP030103716A patent/AR041594A1/es not_active Application Discontinuation
- 2003-10-10 UY UY28014A patent/UY28014A1/es unknown
-
2005
- 2005-03-30 NO NO20051600A patent/NO20051600L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2004033427A1 (en) | 2004-04-22 |
| US20050256159A1 (en) | 2005-11-17 |
| NO20051600L (no) | 2005-06-13 |
| MXPA05003632A (es) | 2005-06-03 |
| TW200413318A (en) | 2004-08-01 |
| JP2006506451A (ja) | 2006-02-23 |
| CA2501611A1 (en) | 2004-04-22 |
| UY28014A1 (es) | 2004-04-30 |
| EP1556349A1 (en) | 2005-07-27 |
| BR0315166A (pt) | 2005-08-16 |
| KR20050051691A (ko) | 2005-06-01 |
| AU2003269242A1 (en) | 2004-05-04 |
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