JP2015078199A5 - - Google Patents

Download PDF

Info

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
Authority
JP
Japan
Prior art keywords
cancer
diseases
mek
heptane
ethyl acetate
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2014231450A
Other languages
English (en)
Japanese (ja)
Other versions
JP2015078199A (ja
JP6309880B2 (ja
Filing date
Publication date
Priority claimed from US11/830,733 external-priority patent/US8101799B2/en
Application filed filed Critical
Publication of JP2015078199A publication Critical patent/JP2015078199A/ja
Publication of JP2015078199A5 publication Critical patent/JP2015078199A5/ja
Application granted granted Critical
Publication of JP6309880B2 publication Critical patent/JP6309880B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

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
US61/034,464 2008-03-06
US61/034,466 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 (enExample) 2016-05-26
JP6309880B2 JP6309880B2 (ja) 2018-04-11

Family

ID=40304796

Family Applications (3)

Application Number Title Priority Date Filing Date
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)

Application Number Title Priority Date Filing Date
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 (enExample)
JP (3) JP2010535232A (enExample)
KR (3) KR20140098185A (enExample)
CN (2) CN101808516B (enExample)
AP (1) AP2817A (enExample)
AU (2) AU2008282338B2 (enExample)
BR (1) BRPI0815659A2 (enExample)
CA (1) CA2693390C (enExample)
CO (1) CO6470808A2 (enExample)
CR (1) CR11244A (enExample)
DO (1) DOP2010000045A (enExample)
EA (2) EA032294B1 (enExample)
EC (1) ECSP109910A (enExample)
HN (1) HN2010000203A (enExample)
IL (1) IL203296A (enExample)
MA (1) MA31881B1 (enExample)
MX (1) MX2010001244A (enExample)
NZ (1) NZ582929A (enExample)
PH (1) PH12015501914A1 (enExample)
SV (1) SV2010003469A (enExample)
TN (1) TN2010000049A1 (enExample)
WO (1) WO2009018233A1 (enExample)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7723477B2 (en) 2005-10-31 2010-05-25 Oncomed Pharmaceuticals, Inc. Compositions and methods for inhibiting Wnt-dependent solid tumor cell growth
WO2009129246A2 (en) * 2008-04-14 2009-10-22 Ardea Biosciences, Inc. Compositions and methods for preparing and using same
CA3003213C (en) * 2008-09-09 2021-07-20 F. Hoffmann-La Roche Ag Polymorphs of acyl sulfonamides
ES2663536T3 (es) 2008-09-26 2018-04-13 Oncomed Pharmaceuticals, Inc. Agentes que se unen a receptores frizzled y usos de los mismos
AU2010224044A1 (en) * 2009-03-11 2011-09-22 Ardea Biosciences, Inc. Pharmaceutical combinations comprising RDEA119/BAY 869766 for the treatment of specific cancers
UY32486A (es) * 2009-03-11 2010-10-29 Ardea Biosciences Inc Tratamiento del cáncer de páncreas
US9034861B2 (en) 2009-10-13 2015-05-19 Allomek Therapeutics Llc MEK inhibitors useful in the treatment of diseases
JP2013508318A (ja) * 2009-10-21 2013-03-07 バイエル・ファルマ・アクチェンゲゼルシャフト 置換されたベンゾスルホンアミド誘導体
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
CN102649773A (zh) * 2011-02-23 2012-08-29 苏州波锐生物医药科技有限公司 氨基芳香烃类化合物及其在制备抗恶性肿瘤药物中的用途
US20140315929A1 (en) * 2011-04-28 2014-10-23 Sloan-Kettering Institute For Cancer Research Hsp90 combination therapy
CA2837162C (en) * 2011-05-27 2019-04-02 Bayer Intellectual Property Gmbh Chiral synthesis of n-{3,4-difluoro-2-[(2-fluoro-4-iodophenyl)amino]-6-methoxyphenyl}-1-[2,3-dihydroxy-propyl]cyclopropanesulfonamides
WO2013086260A2 (en) * 2011-12-09 2013-06-13 Oncomed Pharmaceuticals, Inc. Combination therapy for treatment of cancer
WO2013109142A1 (en) 2012-01-16 2013-07-25 Stichting Het Nederlands Kanker Instituut Combined pdk and mapk/erk pathway inhibition in neoplasia
CN104394855A (zh) * 2012-05-31 2015-03-04 拜耳医药股份有限公司 用于测定肝细胞癌(hcc)患者的治疗的有效响应的生物标记
EA201492082A1 (ru) 2012-06-04 2015-03-31 Фармасайкликс, Инк. Кристаллические формы ингибитора тирозинкиназы брутона
HRP20240033T1 (hr) * 2012-10-19 2024-03-29 Array Biopharma, Inc. Formulacija koja sadrži inhibitor mek
CA2890238A1 (en) 2012-11-02 2014-05-08 Merck Patent Gmbh Method of reducing adverse effects in a cancer patient undergoing treatment with a mek inhibitor
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
WO2015041533A1 (en) 2013-09-20 2015-03-26 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
WO2015156674A2 (en) 2014-04-10 2015-10-15 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
WO2015196072A2 (en) 2014-06-19 2015-12-23 Whitehead Institute For Biomedical Research Uses of kinase inhibitors for inducing and maintaining pluripotency
CN106535931A (zh) * 2014-08-25 2017-03-22 艾慕恩治疗公司 卵蛋白制剂及其制备方法
IL315294A (en) 2015-03-03 2024-10-01 Pharmacyclics Llc Pharmaceutical formulations of bruton's tyrosine kinase inhibitor
MX2019015177A (es) 2017-06-16 2020-02-07 Beta Pharma Inc Formulaciones farmaceuticas de n-(2-(2-(dimetilamino)etoxi)-4-meto xi-5((4-(1-metil-1h-indol-3-il)pirimidin-2-il)amino)fenil)acrilam ida y las sales de ellas.
BR112021018168B1 (pt) 2019-03-21 2023-11-28 Onxeo Composição farmacêutica, combinação e kit compreendendo uma molécula dbait e um inibidor de quinase para o tratamento de câncer
WO2021067772A1 (en) * 2019-10-04 2021-04-08 Sumitomo Dainippon Pharma Oncology, Inc. Axl inhibitor formulations
CA3159348A1 (en) 2019-11-08 2021-05-14 Inserm (Institut National De La Sante Et De La Recherche Medicale) Methods for the treatment of cancers that have acquired resistance to kinase inhibitors
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
US12371667B2 (en) 2021-05-13 2025-07-29 Washington University Enhanced methods for inducing and maintaining naive human pluripotent stem cells
WO2025073765A1 (en) 2023-10-03 2025-04-10 Institut National de la Santé et de la Recherche Médicale Methods of prognosis and treatment of patients suffering from melanoma
CN118834328B (zh) * 2024-07-02 2025-09-16 江苏海洋大学 金属蛋白酶9抗原决定基印迹纳米颗粒的制备方法及应用

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5162117A (en) * 1991-11-22 1992-11-10 Schering Corporation Controlled release flutamide composition
JP2575590B2 (ja) * 1992-07-31 1997-01-29 塩野義製薬株式会社 トリアゾリルチオメチルチオセファロスポリン塩酸塩およびその水和物結晶ならびにそれらの製法
DK0810209T3 (da) * 1992-08-25 2002-08-12 Monsanto Co Alpha - and beta-aminosyre-hydroxyethylaminosulfonamider til anvendelse som inhibitorer af retrovirale proteaser
US7115632B1 (en) * 1999-05-12 2006-10-03 G. D. Searle & Co. Sulfonyl aryl or heteroaryl hydroxamic acid compounds
AU2482700A (en) * 1999-01-13 2000-08-01 Warner-Lambert Company 1-heterocycle substituted diarylamines
GB0003224D0 (en) * 2000-02-11 2000-04-05 Glaxo Group Ltd Chemical compounds
US7235567B2 (en) * 2000-06-15 2007-06-26 Schering Corporation Crystalline polymorph of a bisulfate salt of a thrombin receptor antagonist
CN100441176C (zh) * 2001-09-24 2008-12-10 杰西·L·S·奥 测定联合疗法中使用的苏拉明的化学敏感化剂量的方法和组合物
EP1534262A1 (en) * 2002-07-17 2005-06-01 Titan Pharmaceuticals, Inc. Combination of chemotherapeutic drugs for increasing antitumor activity
KR20130016413A (ko) * 2002-07-30 2013-02-14 아에테르나 젠타리스 게엠베하 항종양 약제와 조합하여 사용하기 위한 알킬포스포콜린의 약물 제품
BRPI0607537A2 (pt) * 2005-04-12 2009-09-15 Elan Pharma Int Ltd formulações de derivado de quinazolina nanoparticulado
EP1876167A4 (en) * 2005-04-22 2010-07-07 Kissei Pharmaceutical CRYSTAL POLYMORPHYIS OF 4- {2 - [(1S, 2R) -2-HYDROXY-2- (4-HYDROXYPHENYL) -1-METHYLETHYLAMINO] ETHOXY} -3-ISOPROPYL-3,5-DIMETHYLBIPHENYLCARBOXYLIC ACID HYDROCHLORIDE
ES2481402T3 (es) * 2005-07-21 2014-07-30 Ardea Biosciences, Inc. Inhibidores de N-(arilamino)sulfonamida de MEK
JP2007099763A (ja) * 2005-09-08 2007-04-19 Toyama Chem Co Ltd ピペラシリンナトリウム・1水和物の新規な結晶及びその製造方法
TW200800150A (en) * 2005-12-21 2008-01-01 Organon Nv Compounds with medicinal effects due to interaction with the glucocorticoid receptor

Similar Documents

Publication Publication Date Title
JP2015078199A5 (enExample)
JP2018520205A5 (enExample)
CN115244058A (zh) 嘧啶并二环类衍生物、其制备方法及其在医药上的应用
HRP20192209T1 (hr) Derivati benzofurana, postupci njihove pripreme i njihova uporaba u medicini
JP2017507175A5 (enExample)
JP2019518766A5 (enExample)
JP2013525363A5 (enExample)
RU2016118753A (ru) Производные пиридилкетона, способ их получения и их фармацевтическое применение
HRP20180499T1 (hr) Spojevi i postupci za modulaciju kinaze, te odgovarajuće indikacije
RU2019101220A (ru) Кристаллические формы соединения триазолопиримидина
JP2013525458A5 (enExample)
JP2016501221A5 (enExample)
HRP20140486T1 (hr) Postupci sinteze spojeva spirooksindola
ME02452B (me) Sredstva za induciranje apoptoze namijenjena liječenju raka i imunih i autoimunih bolesti
RU2017136715A (ru) Производное имидазоизоиндола, способ его получения и медицинское применение
JP2022071077A5 (enExample)
JP2016531108A5 (enExample)
CA2796744A1 (en) Synthetic metabolites of fluoro substituted omega-carboxyaryl diphenyl urea for the treatment and prevention of diseases and conditions
JP2016528273A5 (enExample)
RU2016133731A (ru) Функционализованные соединения бензопирана и их применение
JP2013523680A5 (enExample)
JP2016539985A5 (enExample)
JP2016504325A5 (enExample)
RU2017133243A (ru) Частицы n-(5-циано-4-((2-метоксиэтил)амино)пиридин-2-ил)-7-формил-6-((4-метил-2-оксопиперазин-1-ил)метил)-3,4-дигидро-1,8-нафтиридин-1(2h)-карбоксамида
JP2016534048A5 (enExample)