JP2017527549A5 - - Google Patents

Download PDF

Info

Publication number
JP2017527549A5
JP2017527549A5 JP2017508087A JP2017508087A JP2017527549A5 JP 2017527549 A5 JP2017527549 A5 JP 2017527549A5 JP 2017508087 A JP2017508087 A JP 2017508087A JP 2017508087 A JP2017508087 A JP 2017508087A JP 2017527549 A5 JP2017527549 A5 JP 2017527549A5
Authority
JP
Japan
Prior art keywords
compound
formula
single crystal
crystal form
ray powder
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
JP2017508087A
Other languages
English (en)
Japanese (ja)
Other versions
JP6777626B2 (ja
JP2017527549A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/045395 external-priority patent/WO2016025904A1/en
Publication of JP2017527549A publication Critical patent/JP2017527549A/ja
Publication of JP2017527549A5 publication Critical patent/JP2017527549A5/ja
Application granted granted Critical
Publication of JP6777626B2 publication Critical patent/JP6777626B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017508087A 2014-08-15 2015-08-14 セリネクソールの多形体 Active JP6777626B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462038069P 2014-08-15 2014-08-15
US62/038,069 2014-08-15
PCT/US2015/045395 WO2016025904A1 (en) 2014-08-15 2015-08-14 Polymorphs of selinexor

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2020093874A Division JP7218323B2 (ja) 2014-08-15 2020-05-29 セリネクソールの多形体

Publications (3)

Publication Number Publication Date
JP2017527549A JP2017527549A (ja) 2017-09-21
JP2017527549A5 true JP2017527549A5 (enExample) 2018-09-27
JP6777626B2 JP6777626B2 (ja) 2020-10-28

Family

ID=53969460

Family Applications (3)

Application Number Title Priority Date Filing Date
JP2017508087A Active JP6777626B2 (ja) 2014-08-15 2015-08-14 セリネクソールの多形体
JP2020093874A Active JP7218323B2 (ja) 2014-08-15 2020-05-29 セリネクソールの多形体
JP2023009361A Active JP7558310B2 (ja) 2014-08-15 2023-01-25 セリネクソールの多形体

Family Applications After (2)

Application Number Title Priority Date Filing Date
JP2020093874A Active JP7218323B2 (ja) 2014-08-15 2020-05-29 セリネクソールの多形体
JP2023009361A Active JP7558310B2 (ja) 2014-08-15 2023-01-25 セリネクソールの多形体

Country Status (18)

Country Link
US (6) US10519139B2 (enExample)
EP (2) EP3180331B1 (enExample)
JP (3) JP6777626B2 (enExample)
KR (1) KR102608259B1 (enExample)
CN (3) CN111484483B (enExample)
AU (4) AU2015301484B2 (enExample)
CA (1) CA2957266A1 (enExample)
CO (1) CO2017001884A2 (enExample)
DK (1) DK3180331T3 (enExample)
EA (1) EA201790384A1 (enExample)
ES (1) ES2926377T3 (enExample)
IL (1) IL250328B (enExample)
MA (1) MA40254B1 (enExample)
MX (2) MX388170B (enExample)
SG (2) SG11201700789SA (enExample)
UA (1) UA123535C2 (enExample)
WO (1) WO2016025904A1 (enExample)
ZA (1) ZA201700880B (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX349712B (es) 2011-07-29 2017-08-09 Karyopharm Therapeutics Inc Moduladores del transporte nuclear que contienen hidrazida y sus usos.
KR102223028B1 (ko) 2012-05-09 2021-03-03 바이오젠 엠에이 인코포레이티드 핵 수송 조절인자 및 이의 용도
US10202366B2 (en) 2013-03-15 2019-02-12 Karyopharm Therapeutics Inc. Methods of promoting wound healing using CRM1 inhibitors
EP3492455B1 (en) 2013-06-21 2023-05-17 Karyopharm Therapeutics Inc. 1,2,4-triazoles as nuclear transport modulators and use in the treatment of specific forms of cancer
KR102608259B1 (ko) 2014-08-15 2023-11-29 카리오팜 쎄라퓨틱스, 인코포레이티드 셀리넥소의 다형태
WO2017117535A1 (en) 2015-12-31 2017-07-06 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
US10526295B2 (en) 2015-12-31 2020-01-07 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
WO2017118940A1 (en) 2016-01-08 2017-07-13 Dr. Reddy's Laboratories Limited Solid forms of selinexor and process for their preparation
US11602530B2 (en) 2016-11-28 2023-03-14 Biogen Ma Inc. CRM1 inhibitors for treating epilepsy
WO2018129227A1 (en) 2017-01-05 2018-07-12 Watson Laboratories Inc. Novel crystalline forms of selinexor and process for their preparation
CN106831731B (zh) * 2017-01-17 2019-11-08 广州市闻皓生物科技有限公司 一种Selinexor原料药的合成方法
WO2019232724A1 (en) 2018-06-06 2019-12-12 Xw Laboratories, Inc. Compounds as nuclear transport modulators and uses thereof
WO2020072008A1 (en) * 2018-10-04 2020-04-09 Deva Holding Anonim Sirketi Novel solid dispersions of selinexor
KR20210141936A (ko) * 2019-03-20 2021-11-23 존슨 맛쎄이 퍼블릭 리미티드 컴파니 셀리넥서의 공결정 형태
CR20210590A (es) 2019-05-01 2022-03-11 Karyopharm Therapeutics Inc Proceso para la preparación de inhibidores de xpo1 y productos intermedios para su uso en la preparación de inhibidores de xpo1
WO2020232439A1 (en) * 2019-05-16 2020-11-19 Mayo Foundation For Medical Education And Research Methods and materials for treating cancer
EP3808742A1 (en) 2019-10-16 2021-04-21 Sandoz AG Polymorph of selinexor
WO2022087218A1 (en) 2020-10-21 2022-04-28 Karyopharm Therapeutics Inc. Crystalline form of selinexor
CN112679477B (zh) * 2020-12-17 2021-10-26 佛山奕安赛医药科技有限公司 塞利尼索及其中间体的制备方法
WO2023122014A1 (en) * 2021-12-20 2023-06-29 Raytheon Technologies Corporation Particle enhancement of ceramic matrix composites, method of manufacture thereof and articles comprising the same
CN116675677B (zh) * 2023-08-02 2023-09-26 中国林业科学研究院林产化学工业研究所 一种c8漆酚衍生物及其制备方法和应用

Family Cites Families (73)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1017398A (en) 1911-01-16 1912-02-13 John E Folsom Telegraph-key.
KR840000529A (ko) 1981-07-07 1984-02-25 콘스탄틴 루이스 클레멘트 인돌 유도체의 제조방법
CS229934B2 (en) 1981-07-07 1984-07-16 Pfizer Production method subst.indolylacryte acid derivative
US4778796A (en) 1985-07-19 1988-10-18 Dainippon Pharmaceutical Co., Ltd. ω-(3-pyridyl)alkenamide derivatives and anti-allergenic pharmaceutical compositions containing same
JP3111321B2 (ja) 1990-02-23 2000-11-20 武田薬品工業株式会社 縮合チアゾール化合物
IL97249A (en) 1990-02-23 1995-01-24 Takeda Chemical Industries Ltd Compounds of 7,6,5,4-tetrahydrothiazole] B-5,4 [pyridine and compounds of 5,6-dihydro-H4-pyrrolo] D-3,2 [thiazole, their manufacture, and pharmaceutical compositions including or
US5541213A (en) 1993-06-24 1996-07-30 Eisai Co., Ltd. Propenoic acid derivatives diazole propenoic acid compounds which have useful pharmaceutical utility
US5468353A (en) 1994-05-05 1995-11-21 Minnesota Mining And Manufacturing Company Mist suppressant for solvent extraction metal electrowinning
CN1088062C (zh) 1994-11-23 2002-07-24 纽罗根公司 某些4-氨基甲基-2-取代的咪唑衍生物2-氨基甲基-4-取代的咪唑衍生物新的一族多巴胺受体亚型特异性配体
US20030018025A1 (en) 1995-06-07 2003-01-23 Neurogen Corporation, Corporation Of The State Of Delaware Certain 4-aminomethyl-2-substituted imidazole derivatives and 2-aminomethyl-4-substituted imidazole derivatives: new classes of dopamine receptor subtype specific ligands
CA2229617A1 (en) 1995-10-20 1997-05-01 Dr. Karl Thomae Gmbh 5-membered heterocycles, medicaments containing these compounds, their use and processes for their preparation
ATE341554T1 (de) 1996-04-04 2006-10-15 Shionogi & Co Cephemverbindungen und medikamente die diese verbindungen enthalten
JP4054992B2 (ja) 1996-04-25 2008-03-05 日産化学工業株式会社 エチレン誘導体および有害生物防除剤
IL126728A (en) 1996-04-25 2009-12-24 Nissan Chemical Ind Ltd Ethylene derivatives and agrochemical compositions containing said derivatives as an active ingredient
DE19624659A1 (de) 1996-06-20 1998-01-08 Klinge Co Chem Pharm Fab Neue Pyridylalken- und Pyridylalkinsäureamide
US5994398A (en) 1996-12-11 1999-11-30 Elan Pharmaceuticals, Inc. Arylsulfonamides as phospholipase A2 inhibitors
JP4416198B2 (ja) 1997-12-19 2010-02-17 武田薬品工業株式会社 アニリド誘導体、その製造法および用途
AU2960599A (en) 1998-03-30 1999-10-18 Akira Karasawa Quinazoline derivatives
US6743585B2 (en) 1999-09-16 2004-06-01 Agilent Technologies, Inc. Methods for preparing conjugates
AR029803A1 (es) 2000-02-21 2003-07-16 Smithkline Beecham Plc Imidazoles sustituidos con piridilo y composiciones farmaceuticas que las comprenden
US7569724B2 (en) 2000-09-29 2009-08-04 Topotarget Uk Limited Carbamic acid compounds comprising an amide linkage as HDAC inhibitors
CA2465978C (en) 2001-09-14 2015-04-07 Soon Hyung Woo Inhibitors of histone deacetylase
AU2003287965A1 (en) 2002-10-24 2004-05-13 Carex Sa Modulation of peroxisome proliferator activated receptors activity
DE10250743A1 (de) 2002-10-31 2004-05-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Amid-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
US7423159B2 (en) 2002-11-01 2008-09-09 Takeda Pharmaceutical Company Limited Agent for preventing or treating neuropathy
JP4145230B2 (ja) 2002-11-01 2008-09-03 武田薬品工業株式会社 神経障害の予防・治療剤
EP1565452B1 (en) 2002-11-08 2012-04-04 Novartis International Pharmaceutical Ltd. 3-substituted-6-aryl pyridines as ligands of c5a receptors
CA2512886A1 (en) 2003-02-28 2004-09-10 Galderma Research & Development, S.N.C. Ligands that modulate lxr-type receptors
KR100966749B1 (ko) 2004-05-26 2010-06-30 에자이 알앤드디 매니지먼트 가부시키가이샤 신나미드 화합물
US7902367B2 (en) 2004-08-11 2011-03-08 Kyorin Pharmaceutical Co., Ltd. Cyclic amino benzoic acid derivative
WO2006019020A1 (ja) 2004-08-16 2006-02-23 Sankyo Company, Limited 置換されたウレア化合物
EP1849465A4 (en) 2005-02-18 2008-12-24 Takeda Pharmaceutical AGENS TO CONTROL THE FUNCTION OF THE GPR34 RECEPTOR
AU2006316079B2 (en) 2005-11-15 2012-03-29 Otsuka Pharmaceutical Co., Ltd. Oxazole compound and pharmaceutical composition
JP2007210929A (ja) 2006-02-09 2007-08-23 Sankyo Co Ltd ウレア化合物を含有する医薬
MX2008011221A (es) 2006-03-09 2008-09-11 Eisai R&D Man Co Ltd Compuestos de cinamida policiclicos.
CA2648804C (en) 2006-04-07 2014-05-27 Methylgene Inc. Benzamide derivatives as inhibitors of histone deacetylase
RU2435764C2 (ru) 2006-04-18 2011-12-10 Ниппон Кемифар Ко., Лтд. АГЕНТ, АКТИВИРУЮЩИЙ РЕЦЕПТОР, АКТИВИРУЕМЫЙ ПРОЛИФЕРАТОРАМИ ПЕРОКСИСОМ δ
EP2030974B1 (en) 2006-06-13 2016-02-17 Shanghai Institute of Materia Medica, Chinese Academy of Sciences Thiazole non-nucleoside compounds, their preparation, pharmaceutical composition and their use as antiviral agents
PL2054411T3 (pl) 2006-07-27 2015-02-27 Amorepacific Corp Nowe związki, ich izomery lub ich farmaceutycznie dopuszczalne sole jako antagoniści receptora waniloidowego oraz zawierające je kompozycje farmaceutyczne
KR101404360B1 (ko) 2006-09-05 2014-06-09 교와 핫꼬 기린 가부시키가이샤 이미다졸 유도체
EP1939180A1 (en) 2006-12-20 2008-07-02 sanofi-aventis Heteroarylacrylamides and their use as pharmaceuticals for the stimulation of the expression of endothelial NO synthase
EP1942104A1 (en) 2006-12-20 2008-07-09 sanofi-aventis Heteroarylcyclopropanecarboxamides and their use as pharmaceuticals
CN101711154A (zh) 2007-02-26 2010-05-19 科森生物科学公司 氨基甲酸酯化合物
EP2003118A1 (de) 2007-06-13 2008-12-17 Bayer Schering Pharma Aktiengesellschaft Zimtsäurederivate als Modulatoren des EP2-Rezeptors
US8106083B2 (en) 2008-08-08 2012-01-31 Synta Pharmaceuticals Corp. Triazole compounds that modulate HSP90 activity
JP2012532889A (ja) 2009-07-09 2012-12-20 クレッシェンド セラピューティクス、エルエルシー 創傷治療方法及び傷跡変性方法
US8518968B2 (en) 2009-12-04 2013-08-27 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Hydrazone and diacyl hydrazine compounds and methods of use
CN103002742B (zh) 2010-03-05 2016-07-13 卡尔约药物治疗公司 核转运调节剂及其应用
CN103402359B (zh) 2011-01-17 2016-08-24 卡尔约药物治疗公司 含烯烃核运输调节剂及其用途
KR102022715B1 (ko) 2011-07-29 2019-09-18 카리오팜 쎄라퓨틱스, 인코포레이티드 핵 수송 조절인자 및 이의 용도
MX349712B (es) 2011-07-29 2017-08-09 Karyopharm Therapeutics Inc Moduladores del transporte nuclear que contienen hidrazida y sus usos.
WO2013020024A2 (en) 2011-08-03 2013-02-07 Karyopharm Therapeutics, Inc. Maleimide compounds and methods of treatment
KR102223028B1 (ko) 2012-05-09 2021-03-03 바이오젠 엠에이 인코포레이티드 핵 수송 조절인자 및 이의 용도
US10202366B2 (en) * 2013-03-15 2019-02-12 Karyopharm Therapeutics Inc. Methods of promoting wound healing using CRM1 inhibitors
US20160016916A1 (en) 2013-03-15 2016-01-21 Karyopharm Therapeutics Inc. Exo Olefin-Containing Nuclear Transport Modulators and Uses Thereof
WO2014205393A1 (en) 2013-06-21 2014-12-24 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
EP3492455B1 (en) 2013-06-21 2023-05-17 Karyopharm Therapeutics Inc. 1,2,4-triazoles as nuclear transport modulators and use in the treatment of specific forms of cancer
US11567063B2 (en) * 2013-11-15 2023-01-31 H. Lee Moffitt Cancer Center And Research Institute, Inc. Methods for assessing cell viability or predicting cell response to a treatment using cell movement
JP6805137B2 (ja) 2014-07-11 2020-12-23 アンセルム(アンスティチュ ナショナル ドゥ ラ サンテ エ ドゥ ラ ルシェルシュ メディカル) 血液学的癌を診断するための方法
CN105294682B (zh) * 2014-07-26 2017-07-07 广东东阳光药业有限公司 Cdk类小分子抑制剂的化合物及其用途
KR102608259B1 (ko) * 2014-08-15 2023-11-29 카리오팜 쎄라퓨틱스, 인코포레이티드 셀리넥소의 다형태
CN108348547B (zh) 2015-08-28 2023-09-22 纽约市哥伦比亚大学信托人 用于匹配肿瘤学特征的系统和方法
US10526295B2 (en) 2015-12-31 2020-01-07 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
WO2017117535A1 (en) 2015-12-31 2017-07-06 Karyopharm Therapeutics Inc. Nuclear transport modulators and uses thereof
WO2017118940A1 (en) 2016-01-08 2017-07-13 Dr. Reddy's Laboratories Limited Solid forms of selinexor and process for their preparation
JP6765198B2 (ja) 2016-03-10 2020-10-07 パナソニック株式会社 潜熱蓄熱材及びそれを用いる蓄熱システム
US11602530B2 (en) 2016-11-28 2023-03-14 Biogen Ma Inc. CRM1 inhibitors for treating epilepsy
WO2018129227A1 (en) * 2017-01-05 2018-07-12 Watson Laboratories Inc. Novel crystalline forms of selinexor and process for their preparation
CN106831731B (zh) 2017-01-17 2019-11-08 广州市闻皓生物科技有限公司 一种Selinexor原料药的合成方法
CA3131720A1 (en) 2019-03-27 2020-10-01 Andrea Califano Biomarkers for selinexor
EP3808742A1 (en) 2019-10-16 2021-04-21 Sandoz AG Polymorph of selinexor
GB2591846B (en) 2019-12-06 2024-08-14 Bae Systems Plc Light source
WO2022087218A1 (en) 2020-10-21 2022-04-28 Karyopharm Therapeutics Inc. Crystalline form of selinexor

Similar Documents

Publication Publication Date Title
JP2017527549A5 (enExample)
JP2018528199A5 (enExample)
ES2778274T3 (es) Síntesis de productos intermedios para producir derivados de prostaciclina
JP2017535550A5 (enExample)
JP2014524442A5 (enExample)
JP2020517611A5 (enExample)
JP6678711B2 (ja) マルトール第二鉄の結晶形態
CN101528762A (zh) 5-氨基-3-(2′,3′-二-O-乙酰基-β-D-呋喃核糖基)-3H-噻唑并[4,5-D]嘧啶-2-酮的马来酸盐的结晶A和B形式
JP2015509973A5 (enExample)
JP2016537346A5 (enExample)
JP6483674B2 (ja) 5−ブロモ−2−(α−ヒドロキシペンチル)安息香酸ナトリウム塩の複数の異なる結晶型及びそれらの調製方法
JP2019516749A5 (enExample)
JP2019505533A5 (enExample)
JP2016190843A5 (enExample)
JP2013541592A5 (enExample)
JP6779972B2 (ja) 呼吸器合胞体ウイルス(rsv)感染症の処置のためのn−[(3−アミノ−3−オキセタニル)メチル]−2−(2,3−ジヒドロ−1,1−ジオキシド−1,4−ベンゾチアゼピン−4(5h)−イル)−6−メチル−4−キナゾリンアミンの結晶形
JP2019505532A5 (enExample)
JP2016510768A5 (enExample)
JP2014506602A5 (enExample)
JP2006151999A5 (enExample)
WO2011050638A1 (zh) 一种比马前列素晶体及其制备方法和用途
TWI808069B (zh) [(1S)-1-[(2S,4R,5R)-5-(5-胺基-2-酮基-噻唑并[4,5-d]嘧啶-3-基)-4-羥基-四氫呋喃-2-基]丙基]乙酸酯之新穎固態形式
JP2020502077A5 (enExample)
CN113348166A (zh) 喹啉衍生物的结晶
CN103193864A (zh) 培哚普利的精氨酸盐的δ晶型、其制备方法和包含它的药物组合物