AR117978A1 - Inhibidores de 15-pgdh - Google Patents
Inhibidores de 15-pgdhInfo
- Publication number
- AR117978A1 AR117978A1 ARP200100274A ARP200100274A AR117978A1 AR 117978 A1 AR117978 A1 AR 117978A1 AR P200100274 A ARP200100274 A AR P200100274A AR P200100274 A ARP200100274 A AR P200100274A AR 117978 A1 AR117978 A1 AR 117978A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- optionally
- substituent selected
- alkyl
- alkoxy
- Prior art date
Links
- 108010051913 15-hydroxyprostaglandin dehydrogenase Proteins 0.000 title 1
- 102100030489 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Human genes 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 125000001424 substituent group Chemical group 0.000 abstract 71
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 23
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 13
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 10
- 229910052736 halogen Inorganic materials 0.000 abstract 9
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 9
- 229910052739 hydrogen Inorganic materials 0.000 abstract 9
- 239000001257 hydrogen Substances 0.000 abstract 9
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 9
- 125000006615 aromatic heterocyclic group Chemical group 0.000 abstract 7
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 6
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 6
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 abstract 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 4
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 3
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 3
- 150000002825 nitriles Chemical class 0.000 abstract 3
- 125000006636 (C3-C8) cycloalkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- -1 amino, carbonyl Chemical group 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052710 silicon Inorganic materials 0.000 abstract 1
- 125000003003 spiro group Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 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
- C07D401/10—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 aromatic rings
-
- 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
- C07D211/36—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 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
- C07D211/38—Halogen atoms or nitro radicals
-
- 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
- C07D211/80—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 two double bonds between ring members or between ring members and non-ring members
- C07D211/84—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 two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen directly attached to ring carbon atoms
- C07D211/86—Oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
- C07D217/22—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems 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 carbon atoms of the nitrogen-containing ring
- C07D217/24—Oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/26—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings condensed with carbocyclic rings or ring systems
- C07D237/30—Phthalazines
- C07D237/32—Phthalazines with oxygen atoms directly attached to carbon atoms of the nitrogen-containing ring
-
- 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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- 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
- C07D401/14—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 three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
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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
- C07D405/10—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 aromatic rings
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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
- C07D405/14—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 three or more hetero rings
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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
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D413/14—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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Reivindicación 1: Un compuesto que tiene la fórmula (1), fórmula (2), fórmula (3) y fórmula (4), o una sal farmacéuticamente aceptable de este, donde G¹ es un grupo fenilo que tiene opcionalmente al menos un sustituyente seleccionado del grupo A, un grupo heterocíclico aromático de 5 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo A, un grupo heterocíclico aromático de 6 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo A, un grupo bicíclico aromático que tiene de 8 a 10 átomos y que tiene opcionalmente al menos un sustituyente seleccionado del grupo A, un grupo heterocíclico fusionado que tiene 9 ó 10 átomos y que tiene opcionalmente al menos un sustituyente seleccionado del grupo A, un grupo cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A o un grupo heterocicloalquilo de 3 a 8 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo A; G² es -C(=O)-X, -C(=O)-CHR¹R², -CH(OH)-CHR¹R², -CH(NY₂)-CHR¹R², -S-CHR¹R², -S(=O)₂-X, -S(=O)-CHR¹R² o -SO₂-CHR¹R² donde X es -NR¹R²; Q¹ es -C(R³)=C(R⁴)-, -C(R⁵)=N-, -N=C(R⁵)-, -O- o -S-; Q² es -C(R⁶)= o -N=; Q³ -C(R⁷)=C(R⁸)-, -C(R⁹)=N-, -N=C(R⁹)-, -NY-, -O- o -S-; Q⁴ es -C(R¹⁰)= o -N=; cada uno de R¹ y R² se selecciona independientemente de hidrógeno, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; o R¹ y R² se toman juntos con el átomo de nitrógeno al cual R¹ y R² están unidos para formar un grupo heterocicloalquilo que contiene átomos de nitrógeno de 3 a 10 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo B o el átomo de carbono al cual R¹ y R² están unidos para formar un grupo cicloalquilo de 3 a 10 miembros tiene opcionalmente al menos un sustituyente seleccionado del grupo B, el grupo heterocicloalquilo que contiene átomos de nitrógeno de 3 a 10 miembros que tiene opcionalmente un enlace insaturado es un anillo monocíclico o un anillo fusionado, puenteado o espiro y el grupo heterocicloalquilo que contiene átomos de nitrógeno de 3 a 10 miembros contiene opcionalmente un átomo de silicio, un átomo de oxígeno o un átomo de azufre que sustituye un átomo de carbono; cada uno de R³ y R⁴ se selecciona independientemente de hidrógeno, halógeno, -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; R⁵ es hidrógeno, -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; R⁶ es hidrógeno, halógeno, -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; cada uno de R⁷ y R⁸ se selecciona independientemente de hidrógeno, halógeno, -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; R⁹ es hidrógeno o -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; R¹⁰ es hidrógeno, halógeno, -CN, -COOY, -NHC(O)Y, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; Y se selecciona independientemente de hidrógeno, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C o cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo C; el grupo A es halógeno, hidroxilo, carbonilo, nitrilo, carboxilo, formilo, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, alquilcarbonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, alcoxicarbonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, alquilsulfonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, alquilsulfonilamino C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, cicloalquilcarbonilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, cicloalcoxi C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, cicloalquilsulfonilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, cicloalquilsulfonilamino C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, heterocicloalquilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, heterocicloalquilcarbonilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, heterocicloalquilamino C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, heterocicloalquilaminocarbonilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, aminocarbonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, aminosulfonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, amino sustituido opcionalmente con uno o dos alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A1, fenilo que tiene opcionalmente al menos un sustituyente seleccionado del grupo B, un grupo heterocíclico aromático de 5 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo B, un grupo heterocíclico aromático de 6 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo B o un grupo heterocíclico que tiene opcionalmente al menos un sustituyente seleccionado del grupo B; el grupo A1 es halógeno, hidroxilo, amino, carbonilo, nitrilo, carboxilo, formilo, alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, alquilcarbonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, alcoxi C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, alcoxicarbonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, alquilsulfonilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, alquilsulfonilamino C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, cicloalquilo C₃₋₈ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, heterocicloalquilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, heterocicloalquilcarbonilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, heterocicloalquilamino C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, heterocicloalquilaminocarbonilo C₅₋₇ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, aminocarbonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, amino sustituido opcionalmente con uno o dos alquilo C₁₋₆ que tiene opcionalmente al menos un sustituyente seleccionado del grupo A2, un grupo heterocíclico aromático de 5 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo B, un grupo heterocíclico aromático de 6 miembros que tiene opcionalmente al menos un sustituyente seleccionado del grupo B o un grupo heterocíclico que tiene opcionalmente al menos un sustituyente seleccionado del grupo B; el grupo A2 es halógeno, hidroxilo, nitrilo, carboxilo, formilo, alquilo C₁₋₆, alquilcarbonilo C₁₋₆, alcoxi C₁₋₆, alcoxicarbonilo C₁₋₆, alquilsulfonilamino C₁₋₆, un grupo heterocíclico aromático de 5 miembros, un grupo heterocíclico aromático de 6 miembros, un grupo heterocíclico o un grupo heterocicloalquilo de 5 a 7 miembros; el grupo B es halógeno, hidroxilo, carbonilo, carboxilo, alquilo C₁₋₆, haloalquilo C₁₋₆, hidroxialquilo C₁₋₆, alquilcarbonilo C₁₋₆, alcoxi C₁₋₆, haloalcoxi C₁₋₆, alcoxicarbonilo C₁₋₆, alquilo C₁₋₆ sustituido con alcoxi C₁₋₆, alquilo C₁₋₆ sustituido con alcoxicarbonilo C₁₋₆, cicloalquilo C₃₋₈, cicloalquilcarbonilo C₃₋₈, cicloalcoxi C₃₋₈, aminocarbonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆, alquilsulfonilo C₁₋₆, aminosulfonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆, alquilsulfonilamino C₁₋₆, amino sustituido opcionalmente con uno o dos alquilo C₁₋₆ o un grupo heterocicloalquilo de 5 a 7 miembros; el grupo C es halógeno, hidroxilo, carboxilo, alquilcarbonilo C₁₋₆, alcoxi C₁₋₆, alcoxicarbonilo C₁₋₆, aminocarbonilo sustituido opcionalmente con uno o dos alquilo C₁₋₆, amino sustituido opcionalmente con uno o dos alquilo C₁₋₆ o un grupo heterocicloalquilo de 5 a 7 miembros; con la condición de que cuando Q³ es -N=C(R⁹)-, R⁹ es metilo, G¹ es un resto de fórmula (5), G² no es un resto de fórmula (6); y cuando Q³ es -N=C(R⁹)-, R⁹ es hidrógeno y G¹ es un resto de fórmula (7), G² no es un resto de fórmula (8).
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Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11690847B2 (en) | 2016-11-30 | 2023-07-04 | Case Western Reserve University | Combinations of 15-PGDH inhibitors with corticosteroids and/or TNF inhibitors and uses thereof |
| AU2018215678A1 (en) | 2017-02-06 | 2019-08-22 | Board Of Regents Of The University Of Texas System | Compositions and methods of modulating short-chain dehydrogenase activity |
| MA55147A (fr) | 2018-11-21 | 2021-09-29 | Univ Texas | Compositions et procédés de modulation de l'activité de la déshydrogénase à chaîne courte |
| EP4377314A4 (en) * | 2021-07-28 | 2025-06-18 | Epirium Bio Inc. | BICYCLIC PGDH INHIBITORS AND METHODS OF PREPARATION AND USE |
| WO2023078461A1 (zh) * | 2021-11-08 | 2023-05-11 | 武汉人福创新药物研发中心有限公司 | 杂环类化合物及其制备方法和用途 |
| AU2022392348A1 (en) * | 2021-11-18 | 2024-07-04 | Wuhan Humanwell Innovative Drug Research and Development Center Limited Company | 15-pgdh inhibitor and use thereof |
| US20250154162A1 (en) * | 2022-01-28 | 2025-05-15 | Scinnohub Pharmaceutical Co., Ltd. | Compound for regulating and controlling 15-pgdh activity and preparation method therefor |
| US20250250283A1 (en) * | 2022-04-13 | 2025-08-07 | Scinnohub Pharmaceutical Co., Ltd. | Compound capable of regulating and controlling activity of 15-pgdh, and preparation method therefor |
| TW202404978A (zh) * | 2022-07-22 | 2024-02-01 | 大陸商賽諾哈勃藥業(成都)有限公司 | 一種調控15-pgdh活性的化合物、包含其的組合物及它們的用途 |
| TW202434211A (zh) * | 2023-02-17 | 2024-09-01 | 大陸商武漢人福創新藥物研發中心有限公司 | 亞碸類化合物及其用途 |
| WO2024230672A1 (zh) * | 2023-05-08 | 2024-11-14 | 武汉人福创新药物研发中心有限公司 | 杂环化合物的晶型、其盐、其盐的晶型及应用 |
| AU2024267728A1 (en) * | 2023-05-09 | 2025-11-06 | Amgen Inc. | 6,6-fused bicyclic amides and compositions for use as 15-prostaglandin dehydrogenase modulators |
| TW202446380A (zh) * | 2023-05-19 | 2024-12-01 | 大陸商成都倍特藥業股份有限公司 | 一種調控15-pgdh活性的化合物、包含其的藥物組合物及它們的用途 |
Family Cites Families (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2233197A (en) | 1996-03-11 | 1997-10-01 | Chugai Seiyaku Kabushiki Kaisha | Beta-anilinoethanethiol compounds, process for the preparation thereof, and process for preparing 3,4-dihydro-2h-1,4-benzothiazine compounds therefrom |
| US6245760B1 (en) | 1997-05-28 | 2001-06-12 | Aventis Pharmaceuticals Products, Inc | Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases |
| AU1457299A (en) * | 1997-11-12 | 1999-05-31 | Ariad Pharmaceuticals, Inc. | Novel signal transduction inhibitors, compositions containing them |
| US6303627B1 (en) * | 1998-06-19 | 2001-10-16 | Eli Lilly And Company | Inhibitors of serotonin reuptake |
| PE20010306A1 (es) | 1999-07-02 | 2001-03-29 | Agouron Pharma | Compuestos de indazol y composiciones farmaceuticas que los contienen utiles para la inhibicion de proteina kinasa |
| EP1311272B1 (en) | 2000-03-03 | 2006-11-22 | Eisai Co., Ltd. | Novel methods using cholinesterase inhibitors |
| CZ303808B6 (cs) | 2001-05-24 | 2013-05-09 | Eli Lilly And Company | Nové pyrazolové deriváty jako farmaceutická cinidla |
| GB0115109D0 (en) | 2001-06-21 | 2001-08-15 | Aventis Pharma Ltd | Chemical compounds |
| US6787558B2 (en) * | 2001-09-28 | 2004-09-07 | Hoffmann-La Roche Inc. | Quinoline derivatives |
| IL161581A0 (en) | 2001-10-23 | 2004-09-27 | Applied Research Systems | Pyrazolidinone derivatives and their use |
| US7320967B2 (en) | 2002-04-23 | 2008-01-22 | L'oreal | Cosmetic composition, method of cosmetic treatment and preparation of a composition for promoting the growth and/or preventing or delaying the loss of hair |
| AU2003298514A1 (en) | 2002-05-17 | 2004-05-04 | Eisai Co., Ltd. | Methods and compositions using cholinesterase inhibitors |
| EP1594438B1 (fr) | 2003-02-12 | 2013-07-17 | L'Oréal | Utilisation d'un inhibiteur de 15-hydroxy prostaglandine déshydrogénase pour favoriser la pigmentation de la peau ou des phanères |
| WO2004089416A2 (en) * | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | Combination of an 11beta-hydroxysteroid dehydrogenase type 1 inhibitor and an antihypertensive agent |
| GB0320320D0 (en) * | 2003-08-29 | 2003-10-01 | Glaxo Group Ltd | Novel compounds |
| FR2869224B1 (fr) | 2004-04-22 | 2006-06-09 | Oreal | Compose 2-oxy-acetamide, ses utilisations et compositions pour stimuler ou induire la pousse des fibres keratiniques et/ou freiner leur chute |
| AR051780A1 (es) | 2004-11-29 | 2007-02-07 | Japan Tobacco Inc | Compuestos en anillo fusionados que contienen nitrogeno y utilizacion de los mismos |
| EP1851203A2 (en) | 2005-02-08 | 2007-11-07 | Merck & Co., Inc. | Inhibitors of checkpoint kinases |
| JP2008531542A (ja) | 2005-02-24 | 2008-08-14 | ファイザー・プロダクツ・インク | 抗癌剤として有用な二環式複素芳香族誘導体 |
| EP1896461A2 (en) | 2005-06-30 | 2008-03-12 | Amgen Inc. | Bis-aryl kinase inhibitors and their use in the treatment of inflammation, angiogenesis and cancer |
| US20070077215A1 (en) | 2005-10-05 | 2007-04-05 | L'oreal | Administration of phenylfurymethylthiazolidine-2,4-dione or phenylthienymethylthiazolidine-2,4-dione compounds for promoting and/or inducing and/or stimulating the pigmentation of keratinous substances and/or limiting their depigmentation and/or their whitening |
| JP2007161608A (ja) | 2005-12-09 | 2007-06-28 | Fujifilm Finechemicals Co Ltd | N−(ヘテロ)アリール置換含窒素ヘテロアリール化合物の製造方法 |
| BRPI0707764A2 (pt) | 2006-02-13 | 2011-05-10 | Hofemann La Roche Ag F | compostos, processo para a sua manufatura, composiÇÕes farmacÊuticas que contÊm, mÉtodo para o tratamento terapÊutico e / ou profilÁtico de enfermidades que sço moduladas por inibidores de l-cpt1 e usos dos compostos |
| US20080305169A1 (en) | 2006-05-26 | 2008-12-11 | Japan Tobacco Inc. | Pharmaceutical Compositions Comprising Nitrogen-Containing Fused Ring Coumpounds |
| US20080064871A1 (en) | 2006-05-26 | 2008-03-13 | Japan Tobacco Inc. | Production Method of Nitrogen-Containing Fused Ring Compounds |
| ES2365258T3 (es) | 2006-06-26 | 2011-09-27 | Ucb Pharma S.A. | Derivados de tiazol condensados como inhibidores de quinasa. |
| JP2008037850A (ja) * | 2006-08-10 | 2008-02-21 | Mitsubishi Tanabe Pharma Corp | 新規置換ピペリジン誘導体 |
| SI2069324T1 (sl) | 2007-03-20 | 2013-10-30 | Curis, Inc. | Kondenzirani aminopiridini kot HSP90-inhibitorji |
| WO2009017838A2 (en) | 2007-08-01 | 2009-02-05 | Exelixis, Inc. | Combinations of jak-2 inhibitors and other agents |
| US7960376B2 (en) | 2007-09-14 | 2011-06-14 | Cara Therapeutics, Inc. | Benzo-fused heterocycles |
| RU2464269C2 (ru) | 2007-10-16 | 2012-10-20 | Дайити Санкио Компани, Лимитед | Пиримидилиндолиновое соединение |
| WO2009098458A2 (en) | 2008-02-05 | 2009-08-13 | Asterand Uk Limited | Biaryl amides |
| TWI386204B (zh) | 2008-04-10 | 2013-02-21 | Mitsubishi Tanabe Pharma Corp | 高半胱胺酸合成酶抑制劑 |
| JPWO2010027002A1 (ja) | 2008-09-05 | 2012-02-02 | 塩野義製薬株式会社 | Pi3k阻害活性を有する縮環モルホリン誘導体 |
| EP2210891A1 (en) | 2009-01-26 | 2010-07-28 | Domain Therapeutics | New adenosine receptor ligands and uses thereof |
| AR076381A1 (es) * | 2009-04-22 | 2011-06-08 | Janssen Pharmaceutica Nv | Azetidinil diamidas como inhibidores de monoacilglicerol lipasa |
| TWI495637B (zh) | 2009-04-22 | 2015-08-11 | Janssen Pharmaceutica Nv | 用作單醯基甘油脂肪酶抑制劑之雜芳族及芳族六氫吡基吖丁啶基醯胺(一) |
| US8367676B2 (en) * | 2009-06-30 | 2013-02-05 | Astrazeneca Ab | 2-carboxamide-7-piperazinyl-benzofuran derivatives 774 |
| EP2322176A1 (en) | 2009-11-11 | 2011-05-18 | Almirall, S.A. | New 7-phenyl-[1,2,4]triazolo[4,3-a]pyridin-3(2H)-one derivatives |
| EP2661431B1 (en) | 2011-01-05 | 2018-07-11 | Bioenergenix | Heterocyclic compounds for the inhibition of pask |
| US9249087B2 (en) | 2011-02-01 | 2016-02-02 | The Board Of Trustees Of The University Of Illinois | HDAC inhibitors and therapeutic methods using the same |
| JP2014518267A (ja) | 2011-06-27 | 2014-07-28 | 杏林製薬株式会社 | 細菌感染症の治療のための架橋二環式化合物 |
| WO2016144958A1 (en) | 2015-03-08 | 2016-09-15 | Case Western Reserve University | Inhibitors of short-chain dehydrogenase activity for treating fibrosis |
| JP6203820B2 (ja) | 2012-04-16 | 2017-09-27 | ケース ウエスタン リザーブ ユニバーシティ | 15−pgdh活性を調節する組成物および方法 |
| JP6157455B2 (ja) | 2012-04-25 | 2017-07-05 | 武田薬品工業株式会社 | 含窒素複素環化合物 |
| KR20150022789A (ko) | 2012-06-04 | 2015-03-04 | 키에시 파르마슈티시 엣스. 피. 에이. | 포스포디에스테라제 억제제로서 1-페닐-2-피리디닐 알킬 알코올의 유도체 |
| FR2992316A1 (fr) | 2012-06-22 | 2013-12-27 | Sanofi Sa | Derives de pyrimidinones, leur preparation et leur application en therapeutique |
| EP3057973B1 (en) | 2013-10-15 | 2019-09-04 | Case Western Reserve University | Compositions comprising a 15-pgdh inhibitor for the healing of wounds |
| US10016439B2 (en) | 2014-01-31 | 2018-07-10 | Ono Pharmaceutical Co., Ltd. | Fused imidazole compounds |
| KR101551313B1 (ko) | 2014-07-28 | 2015-09-09 | 충남대학교산학협력단 | 신규한 인덴 유도체, 이의 제조방법 및 이를 유효성분으로 함유하는 망막 질환의 예방 또는 치료용 약학적 조성물 |
| CA2971413A1 (en) | 2014-12-16 | 2016-06-23 | Axovant Sciences Gmbh | Geminal substituted quinuclidine amide compounds as agonists of alpha-7 nicotinic acetylcholine receptors |
| CA2977345A1 (en) | 2015-02-24 | 2016-09-01 | Pitney Pharmaceuticals Pty Limited | Anticancer agent comprising aminoacetonitrile compound as active ingredient |
| KR101663277B1 (ko) * | 2015-03-30 | 2016-10-06 | 주식회사 녹십자 | TNIK, IKKε 및 TBK1 억제제로서의 피라졸계 유도체 및 이를 포함하는 약학적 조성물 |
| CA2982784A1 (en) | 2015-04-14 | 2016-10-20 | Case Western Reserve University | Compositions and methods of modulating short-chain dehydrogenase activity |
| EP3372601B1 (en) | 2015-10-22 | 2022-09-21 | Mitsubishi Tanabe Pharma Corporation | Novel bicyclic heterocyclic compound |
| AU2016343687A1 (en) | 2015-10-29 | 2018-06-07 | Effector Therapeutics, Inc. | Isoindoline, azaisoindoline, dihydroindenone and dihydroazaindenone inhibitors of Mnk1 and Mnk2 |
| WO2017147328A1 (en) * | 2016-02-23 | 2017-08-31 | Portola Pharmaceuticals, Inc. | Compounds for binding proprotein convertase subtilisin/kexin type 9 (pcsk9) |
| EP3484473A4 (en) | 2016-07-18 | 2020-03-18 | Case Western Reserve University | INHIBITORS OF SHORT-CHAIN DEHYDROGENASE ACTIVITY TO PROMOTE NEUROGENESIS AND INHIBIT NERVOUS DEATH |
| AU2018215678A1 (en) | 2017-02-06 | 2019-08-22 | Board Of Regents Of The University Of Texas System | Compositions and methods of modulating short-chain dehydrogenase activity |
| MX2020009782A (es) * | 2018-03-21 | 2021-01-20 | Relay Therapeutics Inc | Inhibidores de la fosfatasa shp2 y métodos para su uso. |
| US12138263B2 (en) * | 2018-03-21 | 2024-11-12 | Relay Therapeutics, Inc. | Pyrazolo[3,4-b]pyrazine SHP2 phosphatase inhibitors and methods of use thereof |
| CA3118752A1 (en) | 2018-11-09 | 2020-05-14 | Vivace Therapeutics, Inc. | Bicyclic compounds |
| KR20220146458A (ko) | 2020-01-23 | 2022-11-01 | 마이오포르테 테라퓨틱스 인코포레이티드 | Pgdh 억제제 및 그의 제조 및 사용 방법 |
-
2020
- 2020-01-29 EP EP20708859.2A patent/EP3917911A1/en active Pending
- 2020-01-29 US US17/310,268 patent/US12304897B2/en active Active
- 2020-01-29 JP JP2021544505A patent/JP7532385B2/ja active Active
- 2020-01-29 WO PCT/US2020/015683 patent/WO2020160151A1/en not_active Ceased
- 2020-01-30 TW TW109102863A patent/TW202214567A/zh unknown
- 2020-01-31 AR ARP200100274A patent/AR117978A1/es unknown
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| TW202214567A (zh) | 2022-04-16 |
| JP7532385B2 (ja) | 2024-08-13 |
| JP2022524290A (ja) | 2022-05-02 |
| WO2020160151A1 (en) | 2020-08-06 |
| US12304897B2 (en) | 2025-05-20 |
| EP3917911A1 (en) | 2021-12-08 |
| US20220073494A1 (en) | 2022-03-10 |
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