UA101098C2 - Заміщені оксазолом індазоли як інгібітори pi3-кінази$замещенные оксазолом индазолы как ингибиторы pi3-киназы - Google Patents

Заміщені оксазолом індазоли як інгібітори pi3-кінази$замещенные оксазолом индазолы как ингибиторы pi3-киназы Download PDF

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Publication number
UA101098C2
UA101098C2 UAA201112776A UAA201112776A UA101098C2 UA 101098 C2 UA101098 C2 UA 101098C2 UA A201112776 A UAA201112776 A UA A201112776A UA A201112776 A UAA201112776 A UA A201112776A UA 101098 C2 UA101098 C2 UA 101098C2
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UA
Ukraine
Prior art keywords
methyl
pharmaceutically acceptable
oxazol
pyridinyl
acceptable salt
Prior art date
Application number
UAA201112776A
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English (en)
Russian (ru)
Ukrainian (uk)
Inventor
Джули Николь Амбли
Пол Спенсер Джонс
Сюзанн Элейн Килинг
Джоэлль Ли
Шарлотт Джейн Митчелл
Найджел Джеймс Парр
Original Assignee
Глаксо Груп Лимитед
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Application filed by Глаксо Груп Лимитед filed Critical Глаксо Груп Лимитед
Publication of UA101098C2 publication Critical patent/UA101098C2/uk

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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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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    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/4965Non-condensed pyrazines
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UAA201112776A 2009-04-30 2010-04-28 Заміщені оксазолом індазоли як інгібітори pi3-кінази$замещенные оксазолом индазолы как ингибиторы pi3-киназы UA101098C2 (xx)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US17403309P 2009-04-30 2009-04-30
PCT/EP2010/055666 WO2010125082A1 (en) 2009-04-30 2010-04-28 Oxazole substituted indazoles as pi3-kinase inhibitors

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Publication Number Publication Date
UA101098C2 true UA101098C2 (xx) 2013-02-25

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US (14) US8575162B2 (OSRAM)
EP (3) EP3260453B1 (OSRAM)
JP (1) JP5570589B2 (OSRAM)
KR (2) KR101679642B1 (OSRAM)
CN (1) CN102459253B (OSRAM)
AR (2) AR076435A1 (OSRAM)
AU (1) AU2010243613B2 (OSRAM)
BR (1) BRPI1016219B8 (OSRAM)
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SI (2) SI2899191T1 (OSRAM)
SM (2) SMT201700481T1 (OSRAM)
TW (3) TWI516487B (OSRAM)
UA (1) UA101098C2 (OSRAM)
UY (1) UY32585A (OSRAM)
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JP5502076B2 (ja) 2008-06-05 2014-05-28 グラクソ グループ リミテッド 新規化合物
ATE552255T1 (de) * 2008-06-05 2012-04-15 Glaxo Group Ltd 4-aminoindazole
JP5656880B2 (ja) 2009-03-09 2015-01-21 グラクソ グループ リミテッドGlaxo Group Limited Pi3キナーゼの阻害剤としての4−オキサジアゾール−2−イル−インダゾール
JO3025B1 (ar) 2009-04-30 2016-09-05 Glaxo Group Ltd الأندازولات المستبدلة بالأوكسازول كمثبطات كيناز pi3
CN102372675B (zh) * 2010-08-14 2013-12-18 王娜 6-氯-4-碘吲唑及其制备方法与应用
US9102668B2 (en) 2010-09-08 2015-08-11 Glaxo Group Limited Polymorphs and salts
EP2614058B1 (en) * 2010-09-08 2015-07-08 GlaxoSmithKline Intellectual Property Development Limited POLYMORPHS AND SALTS OF N-[5-[4-(5-{[(2R,6S)-2,6-DIMETHYL-4-MORPHOLINYL]METHYL}-& xA;1,3-OXAZOL-2-YL)-1H-INDAZOL-6-YL]-2-(METHYLOXY)-3-PYRIDINYL]METHANESULFONAMIDE
JP5876051B2 (ja) * 2010-09-08 2016-03-02 グラクソスミスクライン、インテレクチュアル、プロパティー、ディベロップメント、リミテッドGlaxosmithkline Intellectual Property Development Limited インフルエンザウィルス感染の治療に使用するためのインダゾール誘導体
GB201018124D0 (en) 2010-10-27 2010-12-08 Glaxo Group Ltd Polymorphs and salts
US9512111B2 (en) 2010-11-08 2016-12-06 Lycera Corporation N-sulfonylated tetrahydroquinolines and related bicyclic compounds for inhibition of RORγ activity and the treatment of disease
AU2012354094C1 (en) 2011-12-15 2015-10-15 Novartis Ag Use of inhibitors of the activity or function of PI3K
US9394315B2 (en) 2012-05-08 2016-07-19 Lycera Corporation Tetrahydro[1,8]naphthyridine sulfonamide and related compounds for use as agonists of RORγ and the treatment of disease
BR112014028017A2 (pt) 2012-05-08 2017-06-27 Lycera Corp composto, composição farmacêutica, método para tratar um distúrbio, método para reduzir a quantidade il-17 em um indivíduo e método para inibir a atividade de ror
CN104703604A (zh) 2012-07-16 2015-06-10 神经孔疗法股份有限公司 作为蛋白质聚集抑制剂的二-和三-杂芳基衍生物
WO2014068070A1 (en) 2012-10-31 2014-05-08 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for preventing antiphospholipid syndrome (aps)
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