AR110599A1 - Moduladores de la vía de estrés integrada - Google Patents

Moduladores de la vía de estrés integrada

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Publication number
AR110599A1
AR110599A1 ARP170101183A ARP170101183A AR110599A1 AR 110599 A1 AR110599 A1 AR 110599A1 AR P170101183 A ARP170101183 A AR P170101183A AR P170101183 A ARP170101183 A AR P170101183A AR 110599 A1 AR110599 A1 AR 110599A1
Authority
AR
Argentina
Prior art keywords
alkyl
independently
membered
halo
heteroaryl
Prior art date
Application number
ARP170101183A
Other languages
English (en)
Inventor
Michael J Dart
Seungwon Chung
Charles W Hutchins
Yunsong Tong
Qinwei I Zhang
Lei Shi
Ramzi Farah Sweis
Xiangdong Xu
Lawrence A Black
Jennifer M Frost
Marina Pliushchev
Carmela Sidrauski
Original Assignee
Calico Life Sciences Llc
Abbvie Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Calico Life Sciences Llc, Abbvie Inc filed Critical Calico Life Sciences Llc
Publication of AR110599A1 publication Critical patent/AR110599A1/es

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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
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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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    • A61K31/16Amides, e.g. hydroxamic acids
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    • A61K31/167Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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Abstract

Se proporcionan en la presente compuestos, composiciones y métodos de utilidad para modular la respuesta al estrés integrada (ISR) y para tratar enfermedades, trastornos y condiciones relacionados. Reivindicación 1: Un compuesto de la fórmula (1), o una de sus sales, solvatos, hidratos, tautómeros o estereoisómeros farmacéuticamente aceptables, en donde: D es un cicloalquilo monocíclico en puente, heterociclo monocíclico en puente o cubanilo, en donde cada cicloalquilo monocíclico en puente, heterociclo monocíclico en puente o cubanilo está opcionalmente sustituido con 1 - 4 grupos RX; L¹ y L² son cada uno, de modo independiente, alquileno C₁₋₆, alquenileno C₂₋₆ o heteroalquileno de 2 - 7 miembros, en donde cada alquileno C₁₋₆, alquenileno C₂₋₆ o heteroalquileno de 2 - 7 miembros está opcionalmente sustituido con 1 - 5 RX; R¹ y R² son cada uno, de modo independiente, hidrógeno, alquilo C₁₋₆, alcoxi C₁₋₆-alquilo C₁₋₆, hidroxi-alquilo C₁₋₆, sililoxi-alquilo C₁₋₆; A y W son cada uno, de modo independiente, fenilo o heteroarilo de 5 - 6 miembros, en donde cada fenilo o heteroarilo de 5 - 6 miembros está opcionalmente sustituido con 1 - 5 RY; cada RX se selecciona, de modo independiente, del grupo que consiste en alquilo C₁₋₆, hidroxi-alquilo C₁₋₆, halo-alquilo C₁₋₆, amino-alquilo C₁₋₆, ciano-alquilo C₁₋₆, oxo, halo, ciano, -ORA, -NRBRC, -NRBC(O)RD, -C(O)NRBRC, -C(O)RD, -C(O)OH, -C(O)ORD, -SRE, -S(O)RD, -S(O)₂RD, OS(O)RD, -OS(O)₂RD y heteroarilo de 5 - 6 miembros; cada RY se selecciona, de modo independiente, del grupo que consiste en hidrógeno, alquilo C₁₋₆, hidroxi-alquilo C₁₋₆, halo-alquilo C₁₋₆, halo-alcoxi C₁₋₆, amino-alquilo C₁₋₆, ciano-alquilo C₁₋₆, oxo, halo, ciano, -ORA, -NRBRC, -NRBC(O)RD, -C(O)NRBRC, -C(O)RD, -C(O)OH, -C(O)ORD, -S(RF)ₘ, -S(O)RD, -S(O)₂RD y G¹; o 2 grupos RY en átomos adyacentes, junto con los átomos a los que están unidos, forman un anillo cicloalquilo fusionado de 3 - 7 miembros, heterociclilo, arilo o heteroarilo opcionalmente sustituido con 1 - 5 RX; cada G¹ es, de modo independiente, cicloalquilo C₃₋₆, heterociclilo de 4 - 7 miembros, arilo o heteroarilo de 5 - 6 miembros, en donde cada cicloalquilo C₃₋₆, heterociclilo de 4 - 7 miembros, arilo o heteroarilo de 5 - 6 miembros está opcionalmente sustituido con 1 - 3 RZ; cada RZ se selecciona, de modo independiente, del grupo que consiste en alquilo C₁₋₆, hidroxi-alquilo C₁₋₆, halo-alquilo C₁₋₆, halo, ciano, -ORA, -NRBRC, -NRBC(O)RD, -C(O)NRBRC, -C(O)RD, -C(O)OH, -C(O)ORD y -S(O)₂RD; cada RA es, de modo independiente, hidrógeno, alquilo C₁₋₆, halo-alquilo C₁₋₆, -C(O)NRBRC, -C(O)RD, -C(O)OH o -C(O)ORD; cada uno de RB y RC es, de modo independiente, hidrógeno o alquilo C₁₋₆; o RB y RC junto con el átomo al que están unidos forman un anillo heterociclilo de 3 - 7 miembros opcionalmente sustituido con 1 - 3 RZ; cada RD es, de modo independiente, alquilo C₁₋₆, heteroalquilo de 2 - 7 miembros o halo-alquilo C₁₋₆, en donde cada alquilo C₁₋₆, heteroalquilo de 2 - 7 miembros o halo- alquilo C₁₋₆ está opcionalmente sustituido con 1 - 5 RG; cada RE es, de modo independiente, hidrógeno, alquilo C₁₋₆ o halo-alquilo C₁₋₆; cada RF es, de modo independiente, hidrógeno, alquilo C₁₋₆ o halo; cada RG es, de modo independiente, arilo o heteroarilo de 5 - 6 miembros, en donde cada arilo o heteroarilo de 5 - 6 miembros está opcionalmente sustituido con 1 - 5 RH; cada RH es, de modo independiente, alquilo C₁₋₆ o halo-alquilo C₁₋₆; m es 1, 3 ó 5; y t es 0 ó 1.
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