JP2013512956A5 - - Google Patents

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JP2013512956A5
JP2013512956A5 JP2012543183A JP2012543183A JP2013512956A5 JP 2013512956 A5 JP2013512956 A5 JP 2013512956A5 JP 2012543183 A JP2012543183 A JP 2012543183A JP 2012543183 A JP2012543183 A JP 2012543183A JP 2013512956 A5 JP2013512956 A5 JP 2013512956A5
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Japan
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diffraction pattern
ray powder
powder diffraction
crystalline
peaks
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JP2012543183A
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JP5714024B2 (ja
JP2013512956A (ja
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Priority claimed from PCT/US2010/059108 external-priority patent/WO2011071821A1/en
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JP2012543183A 2009-12-07 2010-12-06 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩 Active JP5714024B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26715509P 2009-12-07 2009-12-07
US61/267,155 2009-12-07
PCT/US2010/059108 WO2011071821A1 (en) 2009-12-07 2010-12-06 Crystalline forms of 3-(2,6-dichloro-3,5-dimethoxy-phenyl)-1-{6-[4-(4-ethyl-piperazin-1-yl)-phenylamino]-pyrimidin-4-yl}-1-methyl-urea and salts thereof.

Related Child Applications (1)

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JP2015008550A Division JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

Publications (3)

Publication Number Publication Date
JP2013512956A JP2013512956A (ja) 2013-04-18
JP2013512956A5 true JP2013512956A5 (enExample) 2014-01-16
JP5714024B2 JP5714024B2 (ja) 2015-05-07

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JP2012543183A Active JP5714024B2 (ja) 2009-12-07 2010-12-06 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩
JP2015008550A Active JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

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JP2015008550A Active JP6019142B2 (ja) 2009-12-07 2015-01-20 3−(2,6−ジクロロ−3,5−ジメトキシ−フェニル)−1−{6−[4−(4−エチル−ピペラジン−1−イル)−フェニルアミノ]−ピリミジン−4−イル}−1−メチル−尿素の結晶形態およびその塩

Country Status (32)

Country Link
US (1) US9067896B2 (enExample)
EP (1) EP2509963B1 (enExample)
JP (2) JP5714024B2 (enExample)
KR (1) KR101787784B1 (enExample)
CN (5) CN111100078A (enExample)
AR (2) AR079257A1 (enExample)
AU (1) AU2010328391B2 (enExample)
BR (1) BR112012013784B1 (enExample)
CA (1) CA2781431C (enExample)
CL (1) CL2012001480A1 (enExample)
DK (1) DK2509963T3 (enExample)
EC (1) ECSP12012026A (enExample)
ES (1) ES2562462T3 (enExample)
GT (1) GT201200181A (enExample)
HR (1) HRP20160126T1 (enExample)
HU (1) HUE026983T2 (enExample)
IL (1) IL220012B (enExample)
JO (1) JO3061B1 (enExample)
MA (1) MA33849B1 (enExample)
MX (1) MX2012006562A (enExample)
MY (1) MY158333A (enExample)
NZ (3) NZ700778A (enExample)
PE (1) PE20121499A1 (enExample)
PH (2) PH12014502593A1 (enExample)
PL (1) PL2509963T3 (enExample)
RU (1) RU2572848C2 (enExample)
SG (1) SG10201408063SA (enExample)
SI (1) SI2509963T1 (enExample)
TN (1) TN2012000263A1 (enExample)
TW (1) TWI526440B (enExample)
WO (1) WO2011071821A1 (enExample)
ZA (1) ZA201203612B (enExample)

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CA2876689C (en) 2012-06-13 2022-04-26 Incyte Corporation Substituted tricyclic compounds as fgfr inhibitors
US9388185B2 (en) 2012-08-10 2016-07-12 Incyte Holdings Corporation Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors
US9266892B2 (en) 2012-12-19 2016-02-23 Incyte Holdings Corporation Fused pyrazoles as FGFR inhibitors
AR094812A1 (es) 2013-02-20 2015-08-26 Eisai R&D Man Co Ltd Derivado de piridina monocíclico como inhibidor del fgfr
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TWI647220B (zh) 2013-03-15 2019-01-11 美商西建卡爾有限責任公司 雜芳基化合物及其用途
WO2014155268A2 (en) 2013-03-25 2014-10-02 Novartis Ag Fgf-r tyrosine kinase activity inhibitors - use in diseases associated with lack of or reduced snf5 activity
PH12015502383B1 (en) 2013-04-19 2023-02-03 Incyte Holdings Corp Bicyclic heterocycles as fgfr inhibitors
AU2014287209B2 (en) * 2013-07-09 2019-01-24 Dana-Farber Cancer Institute, Inc. Kinase inhibitors for the treatment of disease
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MA38393B1 (fr) 2014-03-13 2018-11-30 Sanofi Sa Composés hétéroaryle et utilisations associées
WO2016027781A1 (ja) 2014-08-18 2016-02-25 エーザイ・アール・アンド・ディー・マネジメント株式会社 単環ピリジン誘導体の塩およびその結晶
WO2016055916A1 (en) 2014-10-06 2016-04-14 Novartis Ag Therapeutic combination for the treatment of cancer
US10851105B2 (en) 2014-10-22 2020-12-01 Incyte Corporation Bicyclic heterocycles as FGFR4 inhibitors
MA41551A (fr) 2015-02-20 2017-12-26 Incyte Corp Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4
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WO2016151501A1 (en) 2015-03-25 2016-09-29 Novartis Ag Pharmaceutical combinations
CN114984013A (zh) 2015-03-25 2022-09-02 国立癌症研究中心 胆管癌治疗剂
CN107660200B (zh) 2015-04-14 2022-01-11 卫材R&D管理有限公司 结晶fgfr4抑制剂化合物和其用途
CN104803925B (zh) * 2015-04-16 2018-01-12 温州医科大学 一类以fgfr为靶点的2,4,5‑三取代嘧啶类化合物及其制备方法和用途
WO2016189472A1 (en) 2015-05-28 2016-12-01 Novartis Ag Fgfr inhibitor for use in the treatment of the phosphaturic mesenchymal tumor
AU2016374441B2 (en) 2015-12-17 2021-10-21 Eisai R&D Management Co., Ltd. Therapeutic agent for breast cancer
JP7372740B2 (ja) 2016-05-10 2023-11-01 エーザイ・アール・アンド・ディー・マネジメント株式会社 細胞生存性及び/又は細胞増殖を低減するための薬物の組み合わせ
TWI669300B (zh) * 2016-05-20 2019-08-21 浙江海正藥業股份有限公司 嘧啶類衍生物、其製備方法、其藥物組合物以及其在醫藥上的用途
BR112019003722A2 (pt) * 2016-08-23 2019-05-28 Eisai R&D Man Co Ltd terapias de combinação para o tratamento de carcinoma hepatocelular
AR111960A1 (es) 2017-05-26 2019-09-04 Incyte Corp Formas cristalinas de un inhibidor de fgfr y procesos para su preparación
CN107176954B (zh) * 2017-06-02 2019-01-11 无锡双良生物科技有限公司 一种egfr抑制剂的药用盐及其晶型、制备方法和应用
AU2018361264B2 (en) 2017-11-01 2021-04-01 Guangdong Xianqiang Pharmaceutical Co., Ltd Salt form and crystal form of compound as FGFR4 inhibitor and preparation method thereof
BR112020017922A2 (pt) 2018-03-28 2020-12-22 Eisai R&D Management Co., Ltd. Agente terapêutico para carcinoma hepatocelular
KR102956194B1 (ko) 2018-05-04 2026-04-23 인사이트 코포레이션 Fgfr 억제제의 염
RS66310B1 (sr) 2018-05-04 2025-01-31 Incyte Corp Čvrsti oblici inhibitora fgfr i procesi za njegovu pripremu
WO2020185532A1 (en) 2019-03-08 2020-09-17 Incyte Corporation Methods of treating cancer with an fgfr inhibitor
WO2021007269A1 (en) 2019-07-09 2021-01-14 Incyte Corporation Bicyclic heterocycles as fgfr inhibitors
US12122767B2 (en) 2019-10-01 2024-10-22 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
GEP20247679B (en) 2019-10-14 2024-10-10 Incyte Corp Bicyclic heterocycles as fgfr inhibitors
CN119751422A (zh) * 2019-10-14 2025-04-04 和记黄埔医药(上海)有限公司 化合物的盐及其晶型
US11566028B2 (en) 2019-10-16 2023-01-31 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
WO2021113479A1 (en) 2019-12-04 2021-06-10 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
MX2022006691A (es) 2019-12-04 2022-09-19 Incyte Corp Derivados de un inhibidor de receptores del factor de crecimiento de fibroblastos (fgfr).
US12012409B2 (en) 2020-01-15 2024-06-18 Incyte Corporation Bicyclic heterocycles as FGFR inhibitors
CA3202267A1 (en) * 2020-12-18 2022-06-23 Riccardo Panicucci Methods of treating achondroplasia
EP4323405A1 (en) 2021-04-12 2024-02-21 Incyte Corporation Combination therapy comprising an fgfr inhibitor and a nectin-4 targeting agent
CA3220274A1 (en) 2021-06-09 2022-12-15 Incyte Corporation Tricyclic heterocycles as fgfr inhibitors
TW202313610A (zh) 2021-06-09 2023-04-01 美商英塞特公司 作為fgfr抑制劑之三環雜環
US11583602B2 (en) 2021-06-23 2023-02-21 Kimtron, Inc. System and method for ultra-close proximity irradiation of rotating biomass
WO2023174400A1 (zh) * 2022-03-18 2023-09-21 上海润石医药科技有限公司 一种取代的氨基六元氮杂环类化合物的盐及其晶型、制备方法和应用
CN115785001B (zh) * 2022-11-23 2023-09-15 斯坦德药典标准物质研发(湖北)有限公司 一种英菲格拉替尼的制备方法
WO2024186882A1 (en) 2023-03-06 2024-09-12 Qed Therapeutics, Inc. Methods of treating skeletal dysplasias
AU2024345848A1 (en) * 2023-09-18 2026-04-09 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Pharmaceutical composition containing heteroaryl oxynaphthalene compound, preparation method therefor, and use thereof
WO2025090870A1 (en) 2023-10-27 2025-05-01 Qed Therapeutics, Inc. Infigratinib and metabolites thereof for use in methods of treating skeletal disorders

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GB0512324D0 (en) * 2005-06-16 2005-07-27 Novartis Ag Organic compounds
CN101242843A (zh) * 2005-06-10 2008-08-13 詹森药业有限公司 作为激酶调节剂的氨基嘧啶类化合物
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ME00011A (me) * 2005-12-21 2009-02-10 Novartis Ag Derivati pirimidinilaril uree kao fgf inhibitori
BRPI0911491A2 (pt) * 2008-04-29 2016-01-05 Novartis Ag métodos de monitoramento da modulação de atividade de quinase de receptor de fator de crescimento de fibroblasto e usos dos ditos métodos.
AR079257A1 (es) * 2009-12-07 2012-01-04 Novartis Ag Formas cristalinas de 3-(2,6-dicloro-3-5-dimetoxi-fenil)-1-{6-[4-(4-etil-piperazin-1-il)-fenil-amino]-pirimidin-4-il}-1-metil-urea y sales de las mismas

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