AR119047A1 - Esteroides neuroactivos como moduladores de gabaa y su uso en el tratamiento de trastornos del snc - Google Patents
Esteroides neuroactivos como moduladores de gabaa y su uso en el tratamiento de trastornos del sncInfo
- Publication number
- AR119047A1 AR119047A1 ARP200101529A ARP200101529A AR119047A1 AR 119047 A1 AR119047 A1 AR 119047A1 AR P200101529 A ARP200101529 A AR P200101529A AR P200101529 A ARP200101529 A AR P200101529A AR 119047 A1 AR119047 A1 AR 119047A1
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- Argentina
- Prior art keywords
- substituted
- unsubstituted
- rga
- group
- alkyl
- Prior art date
Links
- 150000003431 steroids Chemical class 0.000 title 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 11
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 8
- 125000001072 heteroaryl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000004452 carbocyclyl group Chemical group 0.000 abstract 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 6
- 150000002431 hydrogen Chemical group 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 101000743846 Diplobatis ommata Ras-related protein Rab-10 Proteins 0.000 abstract 4
- 102000016304 Origin Recognition Complex Human genes 0.000 abstract 4
- 108010067244 Origin Recognition Complex Proteins 0.000 abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 229910052757 nitrogen Inorganic materials 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 239000001301 oxygen Substances 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 101000974356 Homo sapiens Nuclear receptor coactivator 3 Proteins 0.000 abstract 3
- 101000829425 Homo sapiens Steroid receptor RNA activator 1 Proteins 0.000 abstract 3
- 101000711846 Homo sapiens Transcription factor SOX-9 Proteins 0.000 abstract 3
- 102100022883 Nuclear receptor coactivator 3 Human genes 0.000 abstract 3
- 102100023706 Steroid receptor RNA activator 1 Human genes 0.000 abstract 3
- 125000006706 (C3-C6) carbocyclyl group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 101150007570 nra-1 gene Proteins 0.000 abstract 2
- 125000006239 protecting group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 208000019022 Mood disease Diseases 0.000 abstract 1
- 201000009916 Postpartum depression Diseases 0.000 abstract 1
- -1 Steroid compounds Chemical class 0.000 abstract 1
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 208000035475 disorder Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07J—STEROIDS
- C07J1/00—Normal steroids containing carbon, hydrogen, halogen or oxygen, not substituted in position 17 beta by a carbon atom, e.g. estrane, androstane
- C07J1/0003—Androstane derivatives
- C07J1/0011—Androstane derivatives substituted in position 17 by a keto group
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
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- C07J1/0003—Androstane derivatives
- C07J1/0018—Androstane derivatives substituted in position 17 beta, not substituted in position 17 alfa
- C07J1/0022—Androstane derivatives substituted in position 17 beta, not substituted in position 17 alfa the substituent being an OH group free esterified or etherified
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- C07J41/0055—Normal steroids containing one or more nitrogen atoms not belonging to a hetero ring not covered by C07J41/0005 the 17-beta position being substituted by an uninterrupted chain of at least three carbon atoms which may or may not be branched, e.g. cholane or cholestane derivatives, optionally cyclised, e.g. 17-beta-phenyl or 17-beta-furyl derivatives
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- C07J5/0007—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond not substituted in position 17 alfa
- C07J5/0015—Normal steroids containing carbon, hydrogen, halogen or oxygen, substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane and substituted in position 21 by only one singly bound oxygen atom, i.e. only one oxygen bound to position 21 by a single bond not substituted in position 17 alfa not substituted in position 16
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- C07J7/001—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group
- C07J7/0015—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group not substituted in position 17 alfa
- C07J7/002—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by a keto group not substituted in position 17 alfa not substituted in position 16
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- C07J7/0065—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by an OH group free esterified or etherified
- C07J7/007—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of two carbon atoms not substituted in position 21 substituted in position 20 by an OH group free esterified or etherified not substituted in position 17 alfa
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- C07J9/005—Normal steroids containing carbon, hydrogen, halogen or oxygen substituted in position 17 beta by a chain of more than two carbon atoms, e.g. cholane, cholestane, coprostane containing a carboxylic function directly attached or attached by a chain containing only carbon atoms to the cyclopenta[a]hydrophenanthrene skeleton
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Abstract
Compuestos esteroides con actividad moduladora de GABAA, composiciones farmacéuticas que los comprenden y su uso para el tratamiento de trastornos del SNC, en particular un trastorno de humor tal como depresión y específicamente un trastorno de depresión severo y depresión posparto. Reivindicación 1: Un compuesto de la fórmula (1) o una sal farmacéuticamente aceptable de este; caracterizado porque: ⁻ ⁻ ⁻ ⁻ ⁻ ⁻ representa un enlace simple o doble, siempre que haya un enlace doble presente, entonces uno de R⁶ᵃ o R⁶ᵇ está ausente y R⁵ está ausente; RX se selecciona del grupo que consiste en halo, -CN, -OH, -ORQ¹ y alquilo sustituido o no sustituido, donde RQ¹ es alquilo sustituido o no sustituido; RY es halo o alquilo sustituido o no sustituido o RY y RX pueden unirse con los átomos que intervienen para formar un carbociclilo sustituido o no sustituido o un heterociclilo sustituido o no sustituido; R³ se selecciona del grupo que consiste en alquilo sustituido o no sustituido, alquenilo sustituido o no sustituido, alquinilo sustituido o no sustituido, carbociclilo sustituido o no sustituido, heterociclilo sustituido o no sustituido, arilo sustituido o no sustituido y heteroarilo sustituido o no sustituido; R⁵ es hidrógeno o metilo; cada instancia de R²² se selecciona de forma independiente del grupo que consiste en halógeno, -NO₂, -CN, -ORGA, -N(RGA)₂, -C(=O)RGA, -C(=O)ORGA, -OC(=O)RGA, -OC(=O)ORGA, -C(=O)N(RGA)₂, -N(RGA)C(=O)RGA, -OC(=O)N(RGA)₂, -N(RGA)C(=O)ORGA, -N(RGA)C(=O)N(RGA)₂, -SRGA, -S(=O)RGA, -S(=O)₂RGA, -S(=O)₂ORGA, -OS(=O)₂RGA, -S(=O)₂N(RGA)₂, -N(RGA)S(=O)₂RGA, alquilo sustituido o no sustituido, alquenilo sustituido o no sustituido, alquinilo sustituido o no sustituido, carbociclilo sustituido o no sustituido, heterociclilo sustituido o no sustituido, arilo sustituido o no sustituido y heteroarilo sustituido o no sustituido, donde cada instancia de RGA se selecciona de forma independiente del grupo que consiste en hidrógeno, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alquinilo C₂₋₆ sustituido o no sustituido, carbociclilo C₃₋₆ sustituido o no sustituido, heterociclilo de 3 a 6 miembros sustituido o no sustituido, arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, un grupo protector de oxígeno cuando se une a oxígeno y un grupo protector de nitrógeno cuando se une a nitrógeno, o se toman dos grupos RGA con los átomos que intervienen para formar un anillo heterocíclico o heteroarilo sustituido o no sustituido; R¹ᵃ, R¹ᵇ, R²ᵃ, R²ᵇ, R⁴ᵃ, R⁴ᵇ, R⁷ᵃ, R⁷ᵇ, R¹¹ᵃ, R¹¹ᵇ, R¹²ᵃ y R¹²ᵇ se seleccionan cada uno de forma independiente del grupo que consiste en hidrógeno, halógeno, ciano, -NO₂, alquilo sustituido o no sustituido, alquenilo sustituido o no sustituido, alquinilo sustituido o no sustituido, carbociclilo sustituido o no sustituido, heterociclilo sustituido o no sustituido, arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, -ORA¹, -N(RA¹)₂, -SRA¹, -C(=O)RA¹, -C(=O)ORA¹, -C(=O)SRA¹, -C(=O)N(RA¹)₂, -OC(=O)RA¹, -OC(=O)ORA¹, -OC(=O)N(RA¹)₂, -OC(=O)SRA¹, -OS(=O)₂RA¹, -OS(=O)₂ORA¹, -OS(=O)₂N(RA¹)₂, -N(RA¹)C(=O)RA¹, -N(RA¹)C(=NRA¹)RA¹, -N(RA¹)C(=O)ORA¹, -N(RA¹)C(=O)N(RA¹)₂, -N(RA¹)C(=NRA¹) N(RA¹)₂, -N(RA¹)S(=O)₂RA¹, -N(RA¹)S(=O)₂ORA¹, -N(RA¹)S(=O)₂N(RA¹)₂, -SC(=O)RA¹, -SC(=O)ORA¹, -SC(=O)SRA¹, -SC(=O)N(RA¹)₂, -S(=O)₂RA¹, -S(=O)₂ORA¹ o -S(=O)₂N(RA¹)₂, donde cada instancia de RA¹ se selecciona de forma independiente del grupo que consiste en hidrógeno, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alquinilo C₂₋₆sustituido o no sustituido, carbociclilo C₃₋₆ sustituido o no sustituido, o heterociclilo de 3 a 6 miembros sustituido o no sustituido, arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, un grupo protector de oxígeno cuando se une a oxígeno, un grupo protector de nitrógeno cuando se une a nitrógeno y un grupo protector de azufre cuando se une a azufre, o se toman dos grupos RA¹ con los átomos que intervienen para formar un anillo heterocíclico sustituido o no sustituido; R⁶ᵃ y R⁶ᵇ se seleccionan cada uno de forma independiente del grupo que consiste en hidrógeno, halógeno, ciano, -NO₂, -OH, alquilo sustituido o no sustituido, alquenilo sustituido o no sustituido y alquinilo sustituido o no sustituido; o R⁶ᵃ y R⁶ᵇ se unen para formar un grupo oxo (=O); R¹⁵ᵃ, R¹⁵ᵇ, R¹⁶ᵃ y R¹⁶ᵇ se seleccionan cada uno de forma independiente del grupo que consiste en hidrógeno, halógeno, -CN, -NO₂, alquilo sustituido o no sustituido, alquenilo sustituido o no sustituido, alquinilo sustituido o no sustituido, carbociclilo sustituido o no sustituido, heterociclilo sustituido o no sustituido, arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, -ORC³, -N(RC³)₂, -SRC³, -C(=O)RC³, -C(=O)ORC³, -C(=O)SRC³, -C(=O)N(RC³)₂, -OC(=O)RC³, -OC(=O)ORC³, -OC(=O)N(RC³)₂, -OC(=O)SRC³, -OS(=O)₂RC³, -OS(=O)₂ORC³, -OS(=O)₂N(RC³)₂, -N(RC³)C(=O)RC³, -N(RC³)C(=NRC³)RC³, -N(RC³)C(=O)ORC³, -N(RC³)C(=O)N(RC³)₂, -N(RC³)C(=NRC³)N(RC³)₂, -N(RC³)S(=O)₂RC³, -N(RC³)S(=O)₂ORC³, -N(RC³)S(=O)₂N(RC³)₂, -SC(=O)RC³, -SC(=O)ORC³, -SC(=O)SRC³, -SC(=O)N(RC³)₂, -S(=O)₂RC³, -S(=O)₂ORC³ o -S(=O)₂N(RC³)₂, donde cada instancia de RC³ se selecciona de forma independiente del grupo que consiste en hidrógeno, alquilo C₁₋₆ sustituido o no sustituido, alquenilo C₂₋₆ sustituido o no sustituido, alquinilo C₂₋₆ sustituido o no sustituido, arilo sustituido o no sustituido, heteroarilo sustituido o no sustituido, carbociclilo sustituido o no sustituido o heterociclilo sustituido o no sustituido, un grupo protector de oxígeno cuando se une a oxígeno, un grupo protector de nitrógeno cuando se une a nitrógeno y un grupo protector de azufre cuando se une a azufre, o se toman dos grupos RC³ con los átomos que intervienen para formar un anillo heterocíclico sustituido o no sustituido; R¹⁹ es hidrógeno o alquilo sustituido o no sustituido y n se selecciona del grupo que consiste en 0, 1, 2 y 3.
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