AR073348A1 - Inhibidores ciclicos de 11 beta-hidroxiesteroide deshidrogenasa 1 - Google Patents
Inhibidores ciclicos de 11 beta-hidroxiesteroide deshidrogenasa 1Info
- Publication number
- AR073348A1 AR073348A1 ARP090102835A ARP090102835A AR073348A1 AR 073348 A1 AR073348 A1 AR 073348A1 AR P090102835 A ARP090102835 A AR P090102835A AR P090102835 A ARP090102835 A AR P090102835A AR 073348 A1 AR073348 A1 AR 073348A1
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- Prior art keywords
- alkyl
- alkoxy
- 2nhc
- nhs
- cycloalkyl
- Prior art date
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- 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
- C07D413/10—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 aromatic rings
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
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- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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Abstract
utiles para el tratamiento terapéutico de enfermedades asociadas con la modulacion o inhibicion de 11beta-HSD1 en mamíferos. También se refiere a composiciones farmacéuticas de los nuevos compuestos y métodos para su uso en la reduccion o control de la produccion de cortisol en una célula o la inhibicion de la conversion de cortisona en cortisol en una célula. Reivindicacion 1: Un compuesto representado por la formula estructural (1) en la que: R1 (a) está ausente o (b) se selecciona entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-3-alcoxi C1-3 o alcoxi C1-3-alquilo C1-3 y está opcionalmente sustituido hasta con cuatro grupos seleccionados independientemente entre fluor, ciano, oxo, R4, R4O-, (R4)2N-, R4O2C-, R4S, R4S(=O)-, R4S(=O)2-, R4C(=O)NR4-, (R4)2NC(=O)-, (R4)2NC(=O)O-, (R4)2NC(=O)NR4-, R4OC(=O)NR4-, (R4)2NC(=NCN)NR4-, (R4O)2P(=O)O-, (R4O)2P(=O)NR4-, R4OS(=O)NR4-, (R4)2NS(=O)2O-, (R4)2NS(=O)2NR4-, R4S(=O)2NR4-, R4S(=O)2NHC(=O)-, R4S(=O)2NHC(=O)O-, R4S(=O)2NHC(=O)NR4-, R4OS(=O)2NHC(=O)-, R4OS(=O)2NHC(=O)O-, R4OS(=O)2NHC(=O)NR4-, (R4)2NS(=O)2NHC(=O)-, (R4)2NS(=O)2NHC(=O)O-, (R4)2NS(=O)2NHC(=O)NR4-, R4C(=O)NHS(=O)2-, R4C(O)NHS(=O)2O-, R4C(=O)NHS(=O)2NR4-, R4OC(=O)NHS(=O)2-, R4OC(=O)NHS(=O)2O-, R4OC(=O)NHS(=O)2NR4-, (R4)2NC(=O)NHS(=O)2-, (R4)2NC(=O)NHS(=O)2O-, (R4)2NC(=O)NHS(=O)2NR4-, heterociclilo, heteroarilo, arilamino y heteroarilamino; n es 0,1, 2 o 3; G1 es alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, haloalcoxi C1-4, halogeno, ciano o nitro; G2a es cicloalquilo C3-4; el oxodihidropiridilo de la formula estructural (1) está opcionalmente sustituido en un átomo de carbono del anillo con fluor, cloro, ciano, hidroxi, amino, alquilo C1-4, cicloalquilo C3-4, cicloalquil C3-4-alquilo C1-2, haloalquilo C1-4, alcoxi C1-4, haloalcoxi C1-4, CONH2, alquilaminocarbonilo C1-4, dialquilaminocarbonilo C1-4 o alquilcarbonilamino C1-4; R2 es alquilo C1-6, arilo, heteroarilo, cicloalquilo o heterociclilo y opcionalmente sustituido hasta con 4 grupos seleccionados independientemente entre fluor, cloro, bromo, yodo, ciano, nitro, amino, hidroxi, carboxi, alquilo C1-6, hidroxialquilo C1-6, cicloalquilo C3-6, hidroxicicloalquilo C3-6, cicloalquilalquilo C4-7, alquenilo C2-6, haloalquenilo C2-6, hidroxialquenilo C2-6, alquinilo C2-6, cicloalquil C3-6-alquinilo C2-4, haloalquilo C1-6, halocicloalquilo C3-6, halocicloalquilalquilo C4-7, alcoxi C1-6, cicloalcoxi C3-6, cicloalquilalcoxi C4-7, haloalcoxi C1-6, halocicloalcoxi C3-6, halocicloalquilalcoxi C4-7, alquiltio C1-6, cicloalquiltio C3-6, cicloalquilalquiltio C4-7, haloalquiltio C1-6, halocicloalquiltio C3-6, halocicloalquilalquiltio C4-7, alcanosulfinilo C1-6, cicloalcanosulfinilo C3-6, cicloalquilalcanosulfinilo C4-7, haloalcanosulfinilo C1-6, halocicloalcanosulfinilo C3-6, halocicloalquilalcanosulfinilo C4-7, alcanosulfonilo C1-6, cicloalcanosulfonilo C3-6, cicloalquilalcanosulfonilo C4-7, haloalcanosulfonilo C1-6, halocicloalcanosulfonilo C3-6, halocicloalquilalcanosulfonilo C4-7, alquilamino C1-6, dialquilamino C1-6, alcoxi C1-6-alcoxi C1-6, haloalcoxi C1-6-alcoxi C1-6, alcoxicarbonilo C1-6, H2NCO, H2NSO2, alquilaminocarbonilo C1-6, dialquilaminocarbonilo C1-6, alcoxi C1-3-alquilaminocarbonilo C1-3, heterociclilcarbonilo, alquilaminosulfonilo C1-6, dialquilaminosulfonilo C1-6, heterociclilsulfonilo, alquilcarbonilamino C1-6, alquilcarbonilamino C1-6-alquilo C1-6, alquilsulfonilamino C1-6, alquilsulfonilamino C1-6-alquilo C1-6, alcoxicarbonil C1-6-alcoxi C1-6, alcoxi C1-6-alquilo C1-6, haloalcoxi C1-6-alquilo C1-6, hidroxialcoxi C1-6, heteroarilo, oxo, aminoalquilo C1-6, alquilamino C1-6-alquilo C1-6, dialquilamino C1-6-alquilamino C1-6-alcoxi C2-6, alquilamino C1-6-alcoxi C2-6, dialquilamino C1-6-alcoxi C2-6, alquilcarbonilo C1-6, cicloalquilcarbonilo C3-6, cicloalquilaminocarbonilo C3-6, {cicloalquil C3-6}{alquil C1-6}aminocarboniIo, dicicloalquiIaminocarbonilo C3-6, cicloalquilaminosulfonilo C3-6, {cicloalquil C3-6}{alquil C1-6}aminosulfonilo, dicicloalquilaminosulfonilo C3-6, cianoalquilo C1-6, aminocarbonilalquilo C1-6, alquilaminocarboniI C1-6-alquilo C1-6, dialquilaminocarbonil C1-6-alquilo C1-6, cicloalquilaminocarbonil C3-6-alquilo C1-6, {cicloalquil C3-6}{alquil C1-6}aminocarbonilalquilo C1-6 y dicicloalquilaminocarbonil C3-6-alquilo C1-6; R3 se selecciona entre alquilo C1-6, alquenilo C2-6, alquinilo C2-6, cicloalquil C3-5-alquilo C1-4, alcoxi C1-3-alcoxi C1-3 o alcoxi C1-3-alquilo C1-3 y está opcionalmente sustituido hasta con cuatro grupos seleccionados independientemente entre fluor, ciano, oxo, R4, R4O-, (R4)2N-, R4O2C-, R4C(=O)O-, R4S, R4S(=O)-, R4S(=O)2-, R4C(=O)NR4-, (R4)2NC(=O)-, (R4)2NC(=O)O-, (R4)2NC(=O)NR4-, R4OC(=O)NR4-, (R4)2NC(=NCN)NR4-, (R4O)2P(=O)O-, (R4O)2P(=O)NR4-, R4OS(=O)NR4-, (R4)2NS(=O)2O-, (R4)2NS(=O)2NR4-, R4S(=O)2NR4-, R4S(=O)2NHC(=O)-, R4S(=O)2NHC(=O)O-, R4S(=O)2NHC(=O)NR4-, R4OS(=O)2NHC(=O)-, R4OS(=O)2NHC(=O)O-, R4OS(=O)2NHC(=O)NR4-, (R4)2NS(=O)2NHC(=O)-, (R4)2NS(=O)2NHC(=O)O-, (R4)2NS(=O)2NHC(=O)NR4-, R4C(=O)NHS(=O)2-, R4C(O)NHS(=O)2O-, R4C(=O)NHS(=O)2NR4-, R4OC(=O)NHS(=O)2-, R4OC(=O)NHS(=O)2O-, R4OC(=O)NHS(=O)2NR4-, (R4)2NC(=O)NHS(=O)2-, (R4)2NC(=O)NHS(=O)2O-, (R4)2NC(=O)NHS(=O)2NR4-, espirocicloalquilo, heterociclilo (opcionalmente sustituido con alquilo, haloalquilo, halogeno o oxo), heteroarilo (opcionalmente sustituido con alquilo, haloalquilo, alcoxi, alquiltio, alquilsulfonilo, halogeno, trifluorometilo, dialquilamino, nitro, ciano, CO2H, CONH2, amido N-monoalquil-sustituido, amido N,N-dialquil-sustituido u oxo), arilamino (opcionalmente sustituido con alquilo, alcoxi, alquiltio, alquilsulfonilo, halogeno, trifluorometilo, dialquilamino, nitro, ciano, CO2H, CONH2, amido N-monoalquil-sustituido y amido N,N-dialquil-sustituido) y heteroarilamino (opcionalmente sustituido con alquilo, haloalquilo, alcoxi, alquiltio, alquilsulfonilo, halogeno, trifluorometilo, dialquilamino, nitro, ciano, CO2H, CONH2, amido N-monoalquil-sustituido, amido N,N-dialquil-sustituido u oxo); y R4 se selecciona independientemente entre H, alquilo C1-6, haloalquilo C1-6, aminoalquilo C1-6, alquilamino C1-6-alquilo C1-6, dialquilamino C1-6-alquilo C1-6, hidroxialquilo C1-6 y alcoxi C1-6-alquilo C1-6; o una sal farmacéuticamente aceptable, enantiomero o diastereomero del mismo.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13714808P | 2008-07-25 | 2008-07-25 | |
PCT/US2008/009017 WO2009017664A1 (en) | 2007-07-26 | 2008-07-25 | CYCLIC INHIBITORS OF 11β-HYDROXYSTERIOD DEHYDROGENASE 1 |
US20678509P | 2009-02-04 | 2009-02-04 | |
PCT/US2009/002653 WO2009134400A1 (en) | 2008-05-01 | 2009-04-30 | Cyclic inhibitors of 11beta-hydroxysteroid dehydrogenase 1 |
Publications (1)
Publication Number | Publication Date |
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AR073348A1 true AR073348A1 (es) | 2010-11-03 |
Family
ID=41090311
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP090102835A AR073348A1 (es) | 2008-07-25 | 2009-07-24 | Inhibidores ciclicos de 11 beta-hidroxiesteroide deshidrogenasa 1 |
Country Status (24)
Country | Link |
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US (3) | US8114868B2 (es) |
EP (2) | EP2687525B1 (es) |
JP (2) | JP5379160B2 (es) |
KR (1) | KR20110050459A (es) |
CN (3) | CN104327062A (es) |
AR (1) | AR073348A1 (es) |
AU (1) | AU2009274567B2 (es) |
CA (1) | CA2730499A1 (es) |
CL (2) | CL2011000159A1 (es) |
CO (1) | CO6351743A2 (es) |
DK (1) | DK2324018T3 (es) |
EA (2) | EA201490304A1 (es) |
EC (1) | ECSP10010633A (es) |
ES (1) | ES2432150T3 (es) |
IL (1) | IL210452A (es) |
MA (1) | MA32596B1 (es) |
NZ (1) | NZ590495A (es) |
PE (1) | PE20110566A1 (es) |
PH (1) | PH12014501532A1 (es) |
PL (1) | PL2324018T3 (es) |
RU (1) | RU2539979C2 (es) |
TW (1) | TW201004946A (es) |
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- 2011-10-28 CL CL2011002697A patent/CL2011002697A1/es unknown
-
2012
- 2012-01-11 US US13/347,799 patent/US20120184549A1/en not_active Abandoned
- 2012-10-05 US US13/646,031 patent/US8754076B2/en active Active
-
2013
- 2013-09-26 JP JP2013199445A patent/JP5870073B2/ja active Active
-
2014
- 2014-07-02 PH PH12014501532A patent/PH12014501532A1/en unknown
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