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PE20130457A1 - INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT - Google Patents

INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT

Info

Publication number
PE20130457A1
PE20130457A1 PE2012002515A PE2012002515A PE20130457A1 PE 20130457 A1 PE20130457 A1 PE 20130457A1 PE 2012002515 A PE2012002515 A PE 2012002515A PE 2012002515 A PE2012002515 A PE 2012002515A PE 20130457 A1 PE20130457 A1 PE 20130457A1
Authority
PE
Peru
Prior art keywords
mtor
pirazin
kinase inhibitors
pi3k
akt
Prior art date
Application number
PE2012002515A
Other languages
English (en)
Inventor
Jan Elsner
Roy L Harris
Branden Lee
Deborah Mortensen
Garrick Packard
Patrick Papa
Rama K Narla
Kimberly Fultz
Loui Madakamutil
Jason Parnes
Jingjing Zhao
Weiming Xu
Sophie Perrin-Ninkovic
Lida Tehrani
Graziella Shevlin
John Sapienza
Sabita Sankar
Jennifer Riggs
Original Assignee
Signal Pharm Llc
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41490345&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20130457(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Signal Pharm Llc filed Critical Signal Pharm Llc
Publication of PE20130457A1 publication Critical patent/PE20130457A1/es

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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
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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE 3,4-DIHIDROPIRAZINO[2,3-b]PIRAZIN-2(1H)-ONA DE FORMULA (II) DONDE R1 ES HETEROCICLILO O HETEROARILO TALES COMO PIRIDILO, PIRIMIDILO, 1H-PIRROLO[2,3-b]PIRIDILO, ENTRE OTROS; R2 ES H, ALQUILO(C1-C8), CICLOALQUILO(C3-C10), HETEROCICLILO, ENTRE OTROS; R3 ES H O ALQUILO(C1-C8). SON COMPUESTOS PREFERIDOS: 7-(6-(1H-1,2,4-TRIAZOL-3-IL)PIRIDIN-3-IL)-1-(CIS-4-METOXICICLOHEXILO)-3,4-DIHIDROPIRAZINO[2,3-b]PIRAZIN-2(1H)-ONA; 7-(1H-BENZO[d]IMIDAZOL-4-IL)-1-(2-(TETRAHIDRO-2H-PIRAN-4-IL)ETIL)-3,4-DIHIDROPIRAZINO[2,3-b]PIRAZIN-2(1H)-ONA; 5-(8-ISOPROPILO-7-OXO-5,6,7,8-TETRAHIDROPIRAZINO[2,3-b]PIRAZIN-2-IL)-4-METILPICOLINAMIDA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE CINASA SIENDO UTILES EN EL TRATAMIENTO DEL CANCER, TRANSTORNOS INFLAMATORIOS, INMUNOLOGICOS
PE2012002515A 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT PE20130457A1 (es)

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Application Number Priority Date Filing Date Title
US10862708P 2008-10-27 2008-10-27

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PE20130457A1 true PE20130457A1 (es) 2013-04-17

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ID=41490345

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Application Number Title Priority Date Filing Date
PE2014000555A PE20141197A1 (es) 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT
PE2011000936A PE20110575A1 (es) 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT
PE2012002515A PE20130457A1 (es) 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT

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PE2014000555A PE20141197A1 (es) 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT
PE2011000936A PE20110575A1 (es) 2008-10-27 2009-10-27 INHIBIDORES DE mTOR CINASA PARA INDICADORES DE ONCOLOGIA Y ENFERMEDADES ASOCIADAS CON LA TRAYECTORIA mTOR/PI3K/AKT

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US (10) US8110578B2 (es)
EP (5) EP2358718B1 (es)
JP (3) JP5689420B2 (es)
KR (2) KR101896855B1 (es)
CN (3) CN104744475B (es)
AR (2) AR073995A1 (es)
AU (1) AU2009320137C1 (es)
BR (1) BRPI0920254A2 (es)
CA (1) CA2740975C (es)
CO (1) CO6501147A2 (es)
CR (1) CR20110223A (es)
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HR (2) HRP20160084T1 (es)
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MX (2) MX2011004401A (es)
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NI (1) NI201100080A (es)
NZ (4) NZ708183A (es)
PE (3) PE20141197A1 (es)
PL (2) PL2740732T3 (es)
PT (1) PT2740732T (es)
RU (2) RU2546658C2 (es)
SG (3) SG10201402267VA (es)
SI (2) SI2740733T1 (es)
SM (2) SMT201700341T1 (es)
TW (3) TWI535722B (es)
UA (1) UA108601C2 (es)
WO (1) WO2010062571A1 (es)
ZA (1) ZA201102813B (es)

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* Cited by examiner, † Cited by third party
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BRPI0908637B8 (pt) 2008-05-21 2021-05-25 Ariad Pharma Inc composto e composição farmacêutica do mesmo
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
US8110578B2 (en) 2008-10-27 2012-02-07 Signal Pharmaceuticals, Llc Pyrazino[2,3-b]pyrazine mTOR kinase inhibitors for oncology indications and diseases associated with the mTOR/PI3K/Akt pathway
JP5590040B2 (ja) 2008-11-12 2014-09-17 アリアド・ファーマシューティカルズ・インコーポレイテッド キナーゼ阻害剤としてのピラジノピラジンおよび誘導体
DE102009043260A1 (de) 2009-09-28 2011-04-28 Merck Patent Gmbh Pyridinyl-imidazolonderivate
EP2493472B1 (en) * 2009-10-26 2016-12-07 Signal Pharmaceuticals, LLC Methods of synthesis and purification of heteroaryl compounds
SG183155A1 (en) * 2010-02-03 2012-09-27 Signal Pharm Llc Identification of lkb1 mutation as a predictive biomarker for sensitivity to tor kinase inhibitors
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