MX357305B - Compuestos y composiciones para inhibir la actividad de abl-1, abl-2, y bcr-abl1. - Google Patents

Compuestos y composiciones para inhibir la actividad de abl-1, abl-2, y bcr-abl1.

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Publication number
MX357305B
MX357305B MX2014013375A MX2014013375A MX357305B MX 357305 B MX357305 B MX 357305B MX 2014013375 A MX2014013375 A MX 2014013375A MX 2014013375 A MX2014013375 A MX 2014013375A MX 357305 B MX357305 B MX 357305B
Authority
MX
Mexico
Prior art keywords
abl1
compounds
bcr
inhibiting
activity
Prior art date
Application number
MX2014013375A
Other languages
English (en)
Other versions
MX2014013375A (es
Inventor
Furet Pascal
Martin Grotzfeld Robert
Brynley Jones Darryl
Manley Paul
Marzinzik Andreas
Francois Andre Pelle Xavier
Salem Bahaa
Schoepfer Joseph
Jahnke Wolfgang
Moussaoui Saliha
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of MX2014013375A publication Critical patent/MX2014013375A/es
Publication of MX357305B publication Critical patent/MX357305B/es

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    • C07D403/04Heterocyclic 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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    • A61K31/357Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having two or more oxygen atoms in the same ring, e.g. crown ethers, guanadrel
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    • A61K31/4025Heterocyclic 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 not condensed and containing further heterocyclic rings, e.g. cromakalim
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Abstract

La presente invención se refiere a compuestos de la fórmula ): (ver Fórmula) en donde Y, Y1, Y4, Y5, Y6, R1, R3 y R4 se definen en la Breve Descripción de la Invención; capaces de inhibir la actividad de BCR-ABL1 y de los mutantes del mismo. La invención proporciona además un proceso para la preparación de los compuestos de la invención, preparaciones farmacéuticas que comprenden tales compuestos, y métodos para usar estos compuestos en el tratamiento de cánceres.
MX2014013375A 2012-05-15 2013-05-09 Compuestos y composiciones para inhibir la actividad de abl-1, abl-2, y bcr-abl1. MX357305B (es)

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KR102190848B1 (ko) 2020-12-15
EP2900637B1 (en) 2017-08-09
CA2870339C (en) 2020-06-02
BR112014027584A2 (pt) 2017-06-27
EA026559B1 (ru) 2017-04-28
CA2870339A1 (en) 2013-11-21
BR112014027584B1 (pt) 2023-01-24
ES2646777T3 (es) 2017-12-15
JP2015520157A (ja) 2015-07-16
US20150141427A1 (en) 2015-05-21
EP2900637A1 (en) 2015-08-05
US9458112B2 (en) 2016-10-04
AU2013261129A1 (en) 2014-10-23
AU2013261129B2 (en) 2016-05-12
CN104334529B (zh) 2017-03-15
WO2013171641A1 (en) 2013-11-21
CN104334529A (zh) 2015-02-04
EA201492092A1 (ru) 2015-03-31
PT2900637T (pt) 2017-11-15
KR20150014452A (ko) 2015-02-06
US20160185733A1 (en) 2016-06-30
MX2014013375A (es) 2015-08-14
PL2900637T3 (pl) 2018-01-31
US9315489B2 (en) 2016-04-19
JP6080947B2 (ja) 2017-02-15

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