CR20210050A - Agente profiláctico o terapéutico para atrofia muscular espinal - Google Patents

Agente profiláctico o terapéutico para atrofia muscular espinal

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Publication number
CR20210050A
CR20210050A CR20210050A CR20210050A CR20210050A CR 20210050 A CR20210050 A CR 20210050A CR 20210050 A CR20210050 A CR 20210050A CR 20210050 A CR20210050 A CR 20210050A CR 20210050 A CR20210050 A CR 20210050A
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CR
Costa Rica
Prior art keywords
aliphatic heterocycle
optionally substituted
prophylactic
therapeutic agent
muscular atrophy
Prior art date
Application number
CR20210050A
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English (en)
Inventor
Koji Ono
Shunya Suzuki
Hiroki TAKAHAGI
Koji Fuji
Takeshi Yamasaki
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Reborna Biosciences Inc
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Application filed by Reborna Biosciences Inc filed Critical Reborna Biosciences Inc
Publication of CR20210050A publication Critical patent/CR20210050A/es

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    • C07D487/02Heterocyclic 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
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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
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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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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    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
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Abstract

Un agente profiláctico o terapéutico para atrofia muscular espinal de acuerdo con la presente invención incluye un compuesto representado por la fórmula (I) o una sal de este: Fórmula química 1 en donde: W1, W2 yW3 se seleccionan cada uno independientemente del grupo que consiste en C-R2, C-R3, C-Rc y C-Rd, y se definen mediante uno de los siguientes (i) a (iv): (i) cuando W3 es C-R2, entonces W1 es C-R3, W2 es C-Rc o N, y R1 es un átomo de hidrógeno; (ii) cuando W3 es C-R3, entonces W1 es C-R2, W2 es C-Rc o N, y R1 es un átomo de hidrógeno, alquilo C1–8 o alcoxi C1–8; (iii) cuando W1 es C-R2, entonces W2 es C-Rc o N, W3 es C-Rd, y R1 es un heterociclo alifático que contiene uno o más átomos de nitrógeno, donde el heterociclo alifático se sustituye opcionalmente con un sustituyente no aromático; y (iv) cuando W2 es C-R2, W1 es C-Rc, W3 es C-Rd, y R1 es un heterociclo alifático que contiene uno o más átomos de nitrógeno, donde el heterociclo alifático se sustituye opcionalmente con un sustituyente no aromático; R2 es un anillo aromático de 6 o más miembros opcionalmente sustituido con un sustituyente no aromático; R3 es un heterociclo alifático que contiene uno o más átomos de nitrógeno, donde el heterociclo alifático se sustituye opcionalmente con un sustituyente no aromático; Q1 se selecciona de C-Ra y N; Q2 se selecciona de C-Rb y N; y Ra, Rb, Rc y Rd se seleccionan cada uno independientemente del grupo que consiste en un átomo de hidrógeno, halógeno, alquilo C1–8, alcoxi C1–8 y un grupo ciano.
CR20210050A 2018-06-27 2019-06-27 Agente profiláctico o terapéutico para atrofia muscular espinal CR20210050A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2018122551 2018-06-27
PCT/JP2019/025732 WO2020004594A1 (ja) 2018-06-27 2019-06-27 脊髄性筋萎縮症の予防または治療剤

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CR20210050A true CR20210050A (es) 2021-06-10

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CR20210050A CR20210050A (es) 2018-06-27 2019-06-27 Agente profiláctico o terapéutico para atrofia muscular espinal

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US (1) US12012410B2 (es)
EP (1) EP3816160A4 (es)
JP (1) JP7427252B2 (es)
KR (1) KR102693282B1 (es)
CN (1) CN112469707B (es)
AU (2) AU2019293757B2 (es)
BR (1) BR112020026637A2 (es)
CA (1) CA3105174A1 (es)
CL (1) CL2020003386A1 (es)
CO (1) CO2021000808A2 (es)
CR (1) CR20210050A (es)
EA (1) EA202190116A1 (es)
IL (1) IL279786B2 (es)
JO (1) JOP20200338A1 (es)
MX (1) MX2020014116A (es)
MY (1) MY203060A (es)
PE (1) PE20211585A1 (es)
PH (1) PH12020552263A1 (es)
SG (1) SG11202013088YA (es)
UA (1) UA128696C2 (es)
WO (1) WO2020004594A1 (es)
ZA (1) ZA202100556B (es)

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TW202216710A (zh) 2020-07-02 2022-05-01 美商雷密克斯醫療公司 調節剪接之化合物及方法
CN117015536A (zh) * 2020-07-02 2023-11-07 雷密克斯医疗公司 作为核酸剪接和增殖性疾病治疗的调节剂的2-(吲唑-5-基)-6-(哌啶-4-基)-1,7-萘啶衍生物及相关化合物
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