AR126584A1 - Inhibidores de pgdh de pirrolo[2,3-b]piridina y métodos para hacerlos y usarlos - Google Patents

Inhibidores de pgdh de pirrolo[2,3-b]piridina y métodos para hacerlos y usarlos

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Publication number
AR126584A1
AR126584A1 ARP220101992A ARP220101992A AR126584A1 AR 126584 A1 AR126584 A1 AR 126584A1 AR P220101992 A ARP220101992 A AR P220101992A AR P220101992 A ARP220101992 A AR P220101992A AR 126584 A1 AR126584 A1 AR 126584A1
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Argentina
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substituted
unsubstituted
alkyl
nr8r9
cycloalkyl
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ARP220101992A
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English (en)
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Sundeep Fahr Bruce Rai Roopa Green Michael J Dugar
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Epirium Bio Inc
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Publication of AR126584A1 publication Critical patent/AR126584A1/es

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    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non 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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    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/553Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one oxygen as ring hetero atoms, e.g. loxapine, staurosporine
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    • C07DHETEROCYCLIC COMPOUNDS
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  • Health & Medical Sciences (AREA)
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  • Organic Chemistry (AREA)
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Abstract

En el presente documento, se divulgan compuestos inhibidores de 15-hidroxiprostaglandina deshidrogenasa. Tales compuestos pueden administrarse a sujetos para los que la modulación de las cantidades de prostaglandina puede resultar beneficiosa. Reivindicación 1: Un compuesto de fórmula (1), o una sal o solvato farmacéuticamente aceptable de este; caracterizado porque, el anillo Q es arilo C₆ o heteroarilo de 5 a 10 miembros; W es -CR⁶R⁶ -, -O-, -S-, -NR⁵ -, -S(O)₂- o -C(O)-; R¹ y R² son cada uno independientemente H, halógeno, -CN, -OR¹⁰, -C(O)R¹⁰, -C(O)OR¹⁰, -NR⁸R⁹, -C(O)NR⁸R⁹, alquilo C₁-C₆ sustituido o no sustituido, o sustituido o cicloalquilo C₃-C₈ no sustituido; cada R³ se selecciona independientemente de H, halógeno, -CN, -NR⁸R⁹, -OR¹⁰, CN, -C(O)R¹⁰, -C(O)OR¹⁰, -C(O)NR⁸R⁹, -SOR¹¹, -SO₂R¹¹, -SO₂NR⁸R⁹, -NR¹²C(O)R¹⁰, -NR¹²C(O)OR¹⁰, -NR¹²C(O)NR⁸R⁹, -OC(O)NR⁸R⁹, - NR¹²SO₂R¹⁰, -NR¹²SO₂NR⁸R⁹, alquilo C₁-C₆ sustituido o no sustituido, haloalquilo C₁-C₆ sustituido o no sustituido, cicloalquilo C₃-C₈ sustituido o no sustituido, heterocicloalquilo C₃-C₈ sustituido o no sustituido, arilo C₆ sustituido o no sustituido, o heteroarilo de 5 a 10 miembros sustituido o no sustituido; R⁵ es H, alquilo C₁-C₆ o -C(O)R¹⁰; cada R⁶ es independientemente H, halógeno, CN, -NR⁸R⁹, -OR¹⁰, -C(O)R¹⁰, - C(O)OR¹⁰, -C(O)NR⁸R⁹, -SOR¹¹, -SO₂R¹¹, alquilo C₁-C₆ sustituido o no sustituido; o dos R⁶ pueden juntarse con los átomos a los que se adjuntan para formar un anillo de cicloalquilo C₃-C₆ o heterocicloalquilo C₃-C₈; R⁷ es H, halógeno, -CN, -NR¹⁰R¹⁰, -OR¹⁰, -C(O)R¹⁰, -C(O)OR¹⁰, o alquilo C₁-C₆ sustituido o no sustituido; cada R⁸ y R⁹ se seleccionan independientemente en cada aparición de H, alquilo C₁-C₆, alquenilo C₂-C₆, alquinilo C₂-C₆, heteroalquilo C₁-C₆, haloalquilo C₁-C₆ y cicloalquilo C₃-C₁₀; cada R¹⁰ se selecciona independientemente de H, alquilo C₁-C₆, alquenilo C₂-C₆, heteroalquilo C₁-C₆, haloalquilo C₁-C₆, cicloalquilo C₃-C₈, arilo C₆-C₁₀ y heteroarilo de 5 a 10 miembros; cada R¹¹ se selecciona independientemente de alquilo C₁-C₆, alquenilo C₂-C₆, heteroalquilo C₁-C₆, haloalquilo C₁-C₆, cicloalquilo C₃-C₈, arilo C₆-C₁₀ y heteroarilo de 5 a 10 miembros; cada R¹² se selecciona independientemente de H, alquilo C₁-C₆, alquenilo C₂-C₆, haloalquilo C₁-C₆ y cicloalquilo C₃-C₈; n y m son cada uno independientemente 0, 1, 2 o 3; q es 0, 1, 2 o 3; y p es 1, 2, 3 o 4. Reivindicación 65: Una composición farmacéutica caracterizada porque comprende un compuesto de una cualquiera de las reivindicaciones 1 a 64, o una sal o solvato farmacéuticamente aceptable de este, y un excipiente farmacéuticamente aceptable.
ARP220101992A 2021-07-28 2022-07-27 Inhibidores de pgdh de pirrolo[2,3-b]piridina y métodos para hacerlos y usarlos AR126584A1 (es)

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US (1) US20240294519A1 (es)
EP (1) EP4376841A4 (es)
JP (1) JP2024529508A (es)
KR (1) KR20240102934A (es)
CN (1) CN118338902A (es)
AR (1) AR126584A1 (es)
AU (1) AU2022319753A1 (es)
CA (1) CA3227277A1 (es)
IL (1) IL310438A (es)
TW (1) TW202310836A (es)
WO (1) WO2023009642A1 (es)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12249948B2 (en) 2022-08-30 2025-03-11 Schweitzer Engineering Laboratories, Inc. Split-phase protection of generators
WO2024158931A1 (en) * 2023-01-25 2024-08-02 Epirium Bio Inc. Pgdh inhibitors and methods of making and using

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201711234D0 (en) * 2017-07-12 2017-08-23 Galapagos Nv Pyrrolopyrimidine and pyrrolopyridine derivatives
IL294881A (en) * 2020-01-23 2022-09-01 Myoforte Therapeutics Inc pgdh inhibitors and methods of preparation and use
EP4228650A4 (en) * 2020-10-15 2024-12-18 Myoforte Therapeutics Inc. INHALATED FORMULATIONS OF PGDH INHIBITORS AND METHODS OF USE THEREOF

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CA3227277A1 (en) 2023-02-02
EP4376841A1 (en) 2024-06-05
AU2022319753A1 (en) 2024-02-22
KR20240102934A (ko) 2024-07-03
US20240294519A1 (en) 2024-09-05
JP2024529508A (ja) 2024-08-06
IL310438A (en) 2024-03-01
EP4376841A4 (en) 2025-06-18
CN118338902A (zh) 2024-07-12
TW202310836A (zh) 2023-03-16
WO2023009642A1 (en) 2023-02-02

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