EA201100687A1 - Соединения и композиции в качестве ингибиторов протеинкиназы - Google Patents

Соединения и композиции в качестве ингибиторов протеинкиназы

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Publication number
EA201100687A1
EA201100687A1 EA201100687A EA201100687A EA201100687A1 EA 201100687 A1 EA201100687 A1 EA 201100687A1 EA 201100687 A EA201100687 A EA 201100687A EA 201100687 A EA201100687 A EA 201100687A EA 201100687 A1 EA201100687 A1 EA 201100687A1
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EA
Eurasian Patent Office
Prior art keywords
compounds
compositions
pyrimidine
kinase
pyridine
Prior art date
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EA201100687A
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English (en)
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EA019966B1 (ru
Inventor
Пьер-Ив Мишелли
Вэй Пэй
Томас Х. Марсилдж
Вэньшо Лу
Бэй Чэнь
Тецуо Уно
Юнхо Джин
Тао Цзян
Original Assignee
АйАрЭм ЭлЭлСи
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Application filed by АйАрЭм ЭлЭлСи filed Critical АйАрЭм ЭлЭлСи
Publication of EA201100687A1 publication Critical patent/EA201100687A1/ru
Publication of EA019966B1 publication Critical patent/EA019966B1/ru

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    • A61K31/33Heterocyclic compounds
    • 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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    • A61K31/535Heterocyclic 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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Abstract

Изобретение относится к новым производным пиримидина и пиридина, к их фармацевтическим композициям и к способам применения таких соединений. Например, производные пиримидина и пиридина согласно изобретению могут быть использованы для лечения, улучшения или предотвращения состояния, которое отвечает на ингибирование активности киназы анапластической лимфомы (ALK), очагово-адгезивной киназы (FAK), дзета-цепь-ассоциированной протеинкиназы 70 (ZAP-70), инсулинподобного фактора роста (IGF-1R) или их комбинаций.
EA201100687A 2006-12-08 2007-11-20 Соединения и композиции в качестве ингибиторов протеинкиназы EA019966B1 (ru)

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US86929906P 2006-12-08 2006-12-08

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EA019966B1 EA019966B1 (ru) 2014-07-30

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EA201100688A EA019941B1 (ru) 2006-12-08 2007-11-20 Соединения и композиции в качестве ингибиторов протеинкиназы
EA201100687A EA019966B1 (ru) 2006-12-08 2007-11-20 Соединения и композиции в качестве ингибиторов протеинкиназы

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US (6) US8039479B2 (ru)
EP (3) EP3012249A1 (ru)
KR (1) KR101364277B1 (ru)
CN (1) CN101616895A (ru)
AR (3) AR064197A1 (ru)
BR (2) BRPI0722383A2 (ru)
CL (2) CL2007003552A1 (ru)
CU (1) CU23829B1 (ru)
CY (1) CY1115898T1 (ru)
DO (1) DOP2011000074A (ru)
EA (2) EA019941B1 (ru)
EC (1) ECSP109500A (ru)
ES (2) ES2524009T3 (ru)
GE (2) GEP20125691B (ru)
HK (1) HK1134290A1 (ru)
HN (1) HN2009001145A (ru)
HR (1) HRP20141260T1 (ru)
IL (1) IL230972A (ru)
JO (2) JO2980B1 (ru)
LU (1) LU92785I2 (ru)
MY (1) MY148427A (ru)
NZ (2) NZ590601A (ru)
PE (2) PE20120814A1 (ru)
RS (1) RS53588B1 (ru)
SI (1) SI2091918T1 (ru)
SM (1) SM201000108B (ru)
TW (2) TWI410416B (ru)
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ES2524009T3 (es) 2014-12-03
PE20120814A1 (es) 2012-07-26
HRP20141260T1 (en) 2015-03-13
AR077849A2 (es) 2011-09-28
KR20110117195A (ko) 2011-10-26
MY148427A (en) 2013-04-30
US20110257155A1 (en) 2011-10-20
GEP20156282B (en) 2015-05-11
US20150105390A1 (en) 2015-04-16
CL2007003552A1 (es) 2008-07-18
SM201000108B (it) 2012-01-18
HK1134290A1 (en) 2010-04-23
TWI413641B (zh) 2013-11-01
LU92785I2 (fr) 2015-11-03
ES2559528T3 (es) 2016-02-12
US8372858B2 (en) 2013-02-12
CY1115898T1 (el) 2016-04-13
US20110257154A1 (en) 2011-10-20
ZA201005313B (en) 2011-05-25
JO2980B1 (en) 2016-03-15
EA019966B1 (ru) 2014-07-30

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