JO3121B1 - مشتقات 1 - ((5-هيتيرورلثيازول-2-يل) أمينوكاربونيل) بيروليدين-2-كربوكساميد كمثبات الفوسفاتديلينوسيتول 3-كيناس (pi3k) مفيدة في علاج الأمراض التصاعدية - Google Patents

مشتقات 1 - ((5-هيتيرورلثيازول-2-يل) أمينوكاربونيل) بيروليدين-2-كربوكساميد كمثبات الفوسفاتديلينوسيتول 3-كيناس (pi3k) مفيدة في علاج الأمراض التصاعدية

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Publication number
JO3121B1
JO3121B1 JOP/2009/0334A JOP20090334A JO3121B1 JO 3121 B1 JO3121 B1 JO 3121B1 JO P20090334 A JOP20090334 A JO P20090334A JO 3121 B1 JO3121 B1 JO 3121B1
Authority
JO
Jordan
Prior art keywords
kinase
treatment
heteroarylthiazol
pi3k
phosphatidylinositol
Prior art date
Application number
JOP/2009/0334A
Other languages
English (en)
Inventor
Imbach Patricia
Furet Pascal
Caravatti Giorgio
Alec Fairhurst Robin
Guagnano Vito
Original Assignee
Novartis Ag
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Publication date
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40350060&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=JO3121(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Application granted granted Critical
Publication of JO3121B1 publication Critical patent/JO3121B1/ar

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    • 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
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
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Abstract

يتعلق الإختراع الحالي بمركب الصيغة (I) (I) أو ملح من ذلك، الذى به المستبدلات كما عرف في الوصف، إلى التراكيب وإستعمال المركبات في معالجة أمراض المحسنة ameloriated بمنع فوسفاتيديل لينوسيتول 3-كينيز.
JOP/2009/0334A 2008-09-10 2009-09-09 مشتقات 1 - ((5-هيتيرورلثيازول-2-يل) أمينوكاربونيل) بيروليدين-2-كربوكساميد كمثبات الفوسفاتديلينوسيتول 3-كيناس (pi3k) مفيدة في علاج الأمراض التصاعدية JO3121B1 (ar)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP08164104 2008-09-10
US9667408P 2008-09-12 2008-09-12

Publications (1)

Publication Number Publication Date
JO3121B1 true JO3121B1 (ar) 2017-09-20

Family

ID=40350060

Family Applications (1)

Application Number Title Priority Date Filing Date
JOP/2009/0334A JO3121B1 (ar) 2008-09-10 2009-09-09 مشتقات 1 - ((5-هيتيرورلثيازول-2-يل) أمينوكاربونيل) بيروليدين-2-كربوكساميد كمثبات الفوسفاتديلينوسيتول 3-كيناس (pi3k) مفيدة في علاج الأمراض التصاعدية

Country Status (50)

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US (4) US8227462B2 (ar)
EP (1) EP2331537B1 (ar)
JP (1) JP5486601B2 (ar)
KR (1) KR101290844B1 (ar)
CN (1) CN102149711B (ar)
AR (2) AR073369A1 (ar)
AU (1) AU2009290904B2 (ar)
BR (1) BRPI0918750B8 (ar)
CA (1) CA2734819C (ar)
CL (1) CL2011000504A1 (ar)
CO (1) CO6351738A2 (ar)
CR (1) CR20110059A (ar)
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CY (2) CY1117078T1 (ar)
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FI (1) FIC20200046I1 (ar)
GE (1) GEP20135991B (ar)
HN (1) HN2011000699A (ar)
HR (1) HRP20160014T1 (ar)
HU (2) HUE025884T2 (ar)
IL (1) IL210976A (ar)
JO (1) JO3121B1 (ar)
LT (1) LTC2331537I2 (ar)
LU (1) LUC00186I2 (ar)
MA (1) MA32604B1 (ar)
ME (1) ME01284B (ar)
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AR082418A1 (es) 2010-08-02 2012-12-05 Novartis Ag Formas cristalinas de 1-(4-metil-5-[2-(2,2,2-trifluoro-1,1-dimetil-etil)-piridin-4-il]-tiazol-2-il)-amida de 2-amida del acido (s)-pirrolidin-1,2-dicarboxilico
AU2011328227B2 (en) * 2010-11-08 2015-04-09 Novartis Ag Use of 2-carboxamide cycloamino urea derivatives in the treatment of EGFR dependent diseases or diseases that have acquired resistance to agents that target EGFR family members
AU2015203865B2 (en) * 2010-11-08 2016-11-03 Novartis Ag Use of 2-carboxamide cycloamino urea derivatives in the treatment of EGFR dependent diseases or diseases that have acquired resistance to agents that target EGFR family members
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BR112013027486A2 (pt) 2011-04-25 2017-02-14 Novartis Ag combinação de um inibidor de fosfatidilinositol-3-cinase (pi3k) e um inibidor de mtor
JP2014517049A (ja) * 2011-06-21 2014-07-17 ノバルティス アーゲー (s)−ピロリジン−1,2−ジカルボン酸2−アミド1−({4−メチル−5−[2−(2,2,2−トリフルオロ−1,1−ジメチル−エチル)−ピリジン−4−イル]−チアゾール−2−イル}−アミドの多形
AU2012279117A1 (en) * 2011-07-01 2014-01-09 Novartis Ag Combination therapy comprising a CDK4/6 inhibitor and a PI3K inhibitor for use in the treatment of cancer
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BR112014009993A2 (pt) * 2011-10-28 2017-04-25 Novartis Ag método para o tratamento de tumores do estroma gastrointestinal
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BR112014023530A2 (pt) * 2012-03-29 2017-07-18 Novartis Ag diagnóstico farmacêutico
US20150051252A1 (en) * 2012-03-30 2015-02-19 Xizhong Huang Compounds for use in the treatment of neuroblastoma, ewing's sarcoma or rhabdomyosarcoma
RU2014149145A (ru) 2012-05-23 2016-07-20 Ф. Хоффманн-Ля Рош Аг Композиции и способы получения и применения эндодермальных клеток и гепатоцитов
US8980259B2 (en) 2012-07-20 2015-03-17 Novartis Ag Combination therapy
SG11201500321YA (en) * 2012-08-07 2015-04-29 Novartis Ag Pharmaceutical combinations comprising a b-raf inhibitor, an egfr inhibitor and optionally a pi3k-alpha inhibitor
IN2015DN00528A (ar) * 2012-08-16 2015-06-26 Novartis Ag
ES2686689T3 (es) * 2012-09-20 2018-10-19 Novartis Ag Combinación farmacéutica que comprende un inhibidor de fosfatidilinositol 3-quinasa y un inhibidor de aromatasa
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