JP2015078199A5 - - Google Patents

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Publication number
JP2015078199A5
JP2015078199A5 JP2014231450A JP2014231450A JP2015078199A5 JP 2015078199 A5 JP2015078199 A5 JP 2015078199A5 JP 2014231450 A JP2014231450 A JP 2014231450A JP 2014231450 A JP2014231450 A JP 2014231450A JP 2015078199 A5 JP2015078199 A5 JP 2015078199A5
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JP
Japan
Prior art keywords
cancer
diseases
mek
heptane
ethyl acetate
Prior art date
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JP2014231450A
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English (en)
Japanese (ja)
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JP2015078199A (ja
JP6309880B2 (ja
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Priority claimed from US11/830,733 external-priority patent/US8101799B2/en
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Publication of JP2015078199A publication Critical patent/JP2015078199A/ja
Publication of JP2015078199A5 publication Critical patent/JP2015078199A5/ja
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Publication of JP6309880B2 publication Critical patent/JP6309880B2/ja
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JP2014231450A 2007-07-30 2014-11-14 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法 Expired - Fee Related JP6309880B2 (ja)

Applications Claiming Priority (8)

Application Number Priority Date Filing Date Title
US11/830,733 US8101799B2 (en) 2005-07-21 2007-07-30 Derivatives of N-(arylamino) sulfonamides as inhibitors of MEK
US11/830,733 2007-07-30
US3446408P 2008-03-06 2008-03-06
US3446608P 2008-03-06 2008-03-06
US61/034,466 2008-03-06
US61/034,464 2008-03-06
US4488608P 2008-04-14 2008-04-14
US61/044,886 2008-04-14

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2010520118A Division JP2010535232A (ja) 2007-07-30 2008-07-28 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017018477A Division JP2017125021A (ja) 2007-07-30 2017-02-03 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法

Publications (3)

Publication Number Publication Date
JP2015078199A JP2015078199A (ja) 2015-04-23
JP2015078199A5 true JP2015078199A5 (cg-RX-API-DMAC10.html) 2016-05-26
JP6309880B2 JP6309880B2 (ja) 2018-04-11

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Family Applications (3)

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JP2010520118A Pending JP2010535232A (ja) 2007-07-30 2008-07-28 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法
JP2014231450A Expired - Fee Related JP6309880B2 (ja) 2007-07-30 2014-11-14 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法
JP2017018477A Pending JP2017125021A (ja) 2007-07-30 2017-02-03 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法

Family Applications Before (1)

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JP2010520118A Pending JP2010535232A (ja) 2007-07-30 2008-07-28 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2017018477A Pending JP2017125021A (ja) 2007-07-30 2017-02-03 Mekの阻害剤としての多形体を含む、n−(アリールアミノ)スルホンアミドの誘導体、および組成物、使用方法、ならびにその調製方法

Country Status (22)

Country Link
EP (1) EP2184984A4 (cg-RX-API-DMAC10.html)
JP (3) JP2010535232A (cg-RX-API-DMAC10.html)
KR (3) KR20100092424A (cg-RX-API-DMAC10.html)
CN (2) CN103479604B (cg-RX-API-DMAC10.html)
AP (1) AP2817A (cg-RX-API-DMAC10.html)
AU (2) AU2008282338B2 (cg-RX-API-DMAC10.html)
BR (1) BRPI0815659A2 (cg-RX-API-DMAC10.html)
CA (1) CA2693390C (cg-RX-API-DMAC10.html)
CO (1) CO6470808A2 (cg-RX-API-DMAC10.html)
CR (1) CR11244A (cg-RX-API-DMAC10.html)
DO (1) DOP2010000045A (cg-RX-API-DMAC10.html)
EA (2) EA032294B1 (cg-RX-API-DMAC10.html)
EC (1) ECSP109910A (cg-RX-API-DMAC10.html)
HN (1) HN2010000203A (cg-RX-API-DMAC10.html)
IL (1) IL203296A (cg-RX-API-DMAC10.html)
MA (1) MA31881B1 (cg-RX-API-DMAC10.html)
MX (1) MX2010001244A (cg-RX-API-DMAC10.html)
NZ (1) NZ582929A (cg-RX-API-DMAC10.html)
PH (1) PH12015501914A1 (cg-RX-API-DMAC10.html)
SV (1) SV2010003469A (cg-RX-API-DMAC10.html)
TN (1) TN2010000049A1 (cg-RX-API-DMAC10.html)
WO (1) WO2009018233A1 (cg-RX-API-DMAC10.html)

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TWI535445B (zh) 2010-01-12 2016-06-01 安可美德藥物股份有限公司 Wnt拮抗劑及治療和篩選方法
CN102020651B (zh) 2010-11-02 2012-07-18 北京赛林泰医药技术有限公司 6-芳基氨基吡啶酮甲酰胺mek抑制剂
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EA201391587A1 (ru) * 2011-04-28 2014-08-29 Слоан-Кеттеринг Инститьют Фор Кэнсер Рисерч Комбинированная терапия на основе hsp90
AR086553A1 (es) * 2011-05-27 2014-01-08 Bayer Ip Gmbh Sintesis quiral de n-{3,4-difluoro-2-[(2-fluoro-4-yodofenil)amino]-6-metoxifenil}-1-[2,3-dihidroxi-propil]ciclopropano sulfonamidas
JP2015502958A (ja) * 2011-12-09 2015-01-29 オンコメッド ファーマシューティカルズ インコーポレイテッド がんの処置のための併用療法
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MX348290B (es) 2012-06-04 2017-06-05 Pharmacyclics Llc Formas cristalinas de un inhibidor de tirosina quinasa de bruton.
FI3702351T3 (fi) * 2012-10-19 2024-01-24 Array Biopharma Inc MEK-inhibiittorin käsittävä koostumus
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JP2016510411A (ja) 2013-02-04 2016-04-07 オンコメッド ファーマシューティカルズ インコーポレイテッド Wnt経路インヒビターによる処置の方法およびモニタリング
EP2848246A1 (en) 2013-09-13 2015-03-18 Bayer Pharma Aktiengesellschaft Pharmaceutical compositions containing refametinib
EP3046557A1 (en) 2013-09-20 2016-07-27 Stichting Het Nederlands Kanker Instituut Rock in combination with mapk-pathway
WO2015041534A1 (en) 2013-09-20 2015-03-26 Stichting Het Nederlands Kanker Instituut P90rsk in combination with raf/erk/mek
US20170027940A1 (en) 2014-04-10 2017-02-02 Stichting Het Nederlands Kanker Instituut Method for treating cancer
WO2015178770A1 (en) 2014-05-19 2015-11-26 Stichting Het Nederlands Kanker Instituut Compositions for cancer treatment
US20170114323A1 (en) 2014-06-19 2017-04-27 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
AU2015306683B2 (en) 2014-08-25 2021-11-25 Societe Des Produits Nestle S.A. Egg protein formulations and methods of manufacture thereof
IL315294A (en) 2015-03-03 2024-10-01 Pharmacyclics Llc Pharmaceutical formulations of bruton's tyrosine kinase inhibitor
BR112019026483A2 (pt) * 2017-06-16 2020-07-14 Beta Pharma, Inc. formulação farmacêutica de n-(2-(2-(dimetilamina)etoxi)-4-metoxi-5-((4-(1-metil-1h-indol-3-il)pirimidin-2-il)amina)fenil)acrilamida e seus sais
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