AR080792A1 - Compuesto de 1-acetil-indol, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para la inhibicion de la actividad de perk y para tratar o reducir la gravedad del cancer y otras dolencias. - Google Patents

Compuesto de 1-acetil-indol, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para la inhibicion de la actividad de perk y para tratar o reducir la gravedad del cancer y otras dolencias.

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Publication number
AR080792A1
AR080792A1 ARP110100955A ARP110100955A AR080792A1 AR 080792 A1 AR080792 A1 AR 080792A1 AR P110100955 A ARP110100955 A AR P110100955A AR P110100955 A ARP110100955 A AR P110100955A AR 080792 A1 AR080792 A1 AR 080792A1
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Argentina
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alkyl
fluoro
substituents independently
independently selected
iodo
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ARP110100955A
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English (en)
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Glaxosmithkline Llc
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    • 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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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
    • A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
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    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • 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
    • C07D403/04—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 directly linked by a ring-member-to-ring-member bond
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Compuesto de 1-acetil-indol, inhibidores de PERK, de la Formula 1: en la que R1 se selecciona de: bicicloheteroarilo, y bicicloheteroarilo sustituido con 1 a 5 sustituyentes independientemente seleccionados de: halogeno, alquilo C1-6, alquiloxi C1-4, -OH, hidroxialquilo C1-4, -COOH, -CONH2, tetrazol, -CF3, -alquil(C1-4)-O-alquilo(C1-4), -CH2CH2N(H)C(O)OCH2arilo, di(alquil C1-4)-aminoalquilo(C1-4), aminoalquilo(C1-4), -NO2, -NH2, -CN, arilo, arilo sustituido con 1 a 3 sustituyentes independientemente seleccionados de: alquilo C1-4, di-(alquil C1-4)-amino-(alquilo C1-4), fluoro, cloro, bromo, yodo y -CF3, heterocicloalquilo, heterocicloalquilo sustituido con 1 a 3 sustituyentes independientemente seleccionados de: alquilo C1-4, di-(alquil C1-4)-amino-(alquilo C1-4), fluoro, cloro, bromo, yodo y -CF3. (alquil C1-4)-heterocicloalquilo, (alquil C1-4)-heterocicloalquilo sustituido con 1 a 3 sustituyentes independientemente seleccionados de: alquilo C1-4, di-(alquil C1-4)-amino-(alquilo C1-4), fluoro, cloro, bromo, yodo y -CF3, heteroarilo, y heteroarilo sustituido con 1 a 3 sustituyentes independientemente seleccionados de: alquilo C1-4, di-(alquil C1-4)-amino-(alquilo C1-4), fluoro, cloro, bromo, yodo y -CF3; R2 se selecciona de: arilo, arilo sustituido con 1 a 5 sustituyentes independientemente seleccionados de: fluoro, cloro, bromo, yodo, alquilo C1-4, alquiloxi C1-4, -OH, -COOH, -CONH2, -CF3, -(alquil C1-4)-O-(alquilo C1-4), -NO2, -NH2 y - CN, heteroarilo, heteroarilo sustituido con 1 a 5 sustituyentes independientemente seleccionados de: fluoro, cloro, bromo, yodo, alquilo C1-4, alquiloxi C1-4, -OH, -COOH, -CONH2, -CF3, -(alquil C1-4)-O-(alquilo C1-4), -NO2, -NH2 y -CN, cicloalquilo, y cicloalquilo sustituido con 1 a 5 sustituyentes independientemente seleccionados de: fluoro, cloro, bromo, yodo, alquilo C1-4, alquiloxi C1-4, -OH, -COOH, -CONH2, -CF3, -(alquil C1-4)-O-(alquilo C1-4), -NO2, -NH2 y -CN;6 se selecciona entre: hidrogeno, fluoro, cloro, bromo y yodo; o una sal del mismo incluyendo una sal farmacéuticamente aceptable del mismo. Composicion farmacéutica que lo comprende. Su uso para preparar un medicamento util para la inhibicion de la actividad de PERK y para tratar o reducir la gravedad del cáncer, síndromes precancerosos, enfermedad de Alzheimer, accidente cerebrovascular, diabetes de tipo 1 enfermedad de Parkinson, enfermedad de Huntington, esclerosis lateral amiotrofica, infarto de miocardio, enfermedad cardiovascular, aterosclerosis, arritmias, y degeneracion macular asociada a la edad.
ARP110100955A 2010-03-25 2011-03-23 Compuesto de 1-acetil-indol, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para la inhibicion de la actividad de perk y para tratar o reducir la gravedad del cancer y otras dolencias. AR080792A1 (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US31747610P 2010-03-25 2010-03-25
US35286310P 2010-06-09 2010-06-09
US38148010P 2010-09-10 2010-09-10
US38815110P 2010-09-30 2010-09-30
US41906810P 2010-12-02 2010-12-02

Publications (1)

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AR080792A1 true AR080792A1 (es) 2012-05-09

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ARP110100955A AR080792A1 (es) 2010-03-25 2011-03-23 Compuesto de 1-acetil-indol, composicion farmaceutica que lo comprende y su uso para preparar un medicamento util para la inhibicion de la actividad de perk y para tratar o reducir la gravedad del cancer y otras dolencias.

Country Status (15)

Country Link
US (1) US20120077828A1 (es)
EP (1) EP2549868B1 (es)
JP (1) JP5876031B2 (es)
KR (1) KR101676077B1 (es)
CN (1) CN102917588B (es)
AR (1) AR080792A1 (es)
AU (1) AU2011232516B2 (es)
EA (1) EA022325B1 (es)
ES (1) ES2530955T3 (es)
IL (1) IL222120A (es)
MX (1) MX2012011045A (es)
SG (1) SG183954A1 (es)
TW (1) TW201202241A (es)
UY (1) UY33288A (es)
WO (1) WO2011119663A1 (es)

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JOP20170083B1 (ar) * 2016-04-07 2022-03-14 Glaxosmithkline Ip Dev Ltd أميدات هتيروسيكلية مفيدة كمعدلات بروتين
CN115650985B (zh) * 2016-04-15 2024-08-02 癌症研究科技有限公司 作为ret激酶抑制剂的杂环化合物
US11026945B2 (en) * 2016-04-29 2021-06-08 The Trustees Of The University Of Pennsylvania Protein kinase RNA-like endoplasmic reticulum kinase (PERK) inhibitors for prevention and/or treatment of lung injury and/or inflammation
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CN109982693A (zh) * 2016-09-22 2019-07-05 香港大学 细胞异常分化和isr相关疾病的预防和治疗方法
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CN106974910B (zh) * 2017-03-02 2019-11-12 深圳大学 含索拉非尼和gsk2656157的药物组合物及用途
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