JP2020517707A5 - - Google Patents

Download PDF

Info

Publication number
JP2020517707A5
JP2020517707A5 JP2019558443A JP2019558443A JP2020517707A5 JP 2020517707 A5 JP2020517707 A5 JP 2020517707A5 JP 2019558443 A JP2019558443 A JP 2019558443A JP 2019558443 A JP2019558443 A JP 2019558443A JP 2020517707 A5 JP2020517707 A5 JP 2020517707A5
Authority
JP
Japan
Prior art keywords
composition
pharmaceutically acceptable
treatment
item
composition according
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
JP2019558443A
Other languages
English (en)
Japanese (ja)
Other versions
JP7179015B2 (ja
JP2020517707A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2018/029288 external-priority patent/WO2018200625A1/en
Publication of JP2020517707A publication Critical patent/JP2020517707A/ja
Publication of JP2020517707A5 publication Critical patent/JP2020517707A5/ja
Application granted granted Critical
Publication of JP7179015B2 publication Critical patent/JP7179015B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2019558443A 2017-04-26 2018-04-25 Sestrin-GATOR2相互座用のモジュレーターおよびその使用 Active JP7179015B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762490280P 2017-04-26 2017-04-26
US62/490,280 2017-04-26
PCT/US2018/029288 WO2018200625A1 (en) 2017-04-26 2018-04-25 Modulators of sestrin-gator2 interaction and uses thereof

Publications (3)

Publication Number Publication Date
JP2020517707A JP2020517707A (ja) 2020-06-18
JP2020517707A5 true JP2020517707A5 (enExample) 2021-07-29
JP7179015B2 JP7179015B2 (ja) 2022-11-28

Family

ID=63920059

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2019558443A Active JP7179015B2 (ja) 2017-04-26 2018-04-25 Sestrin-GATOR2相互座用のモジュレーターおよびその使用

Country Status (9)

Country Link
US (3) US10912750B2 (enExample)
EP (2) EP4556069A3 (enExample)
JP (1) JP7179015B2 (enExample)
CN (2) CN116370448A (enExample)
AU (2) AU2018258355B2 (enExample)
CA (1) CA3061611A1 (enExample)
ES (1) ES3040534T3 (enExample)
TW (1) TWI776886B (enExample)
WO (1) WO2018200625A1 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI3364958T1 (sl) 2015-10-23 2023-05-31 Navitor Pharmaceuticals, Inc. Modulatorji interakcije sestrina in gator2 ter njihova uporaba
WO2018200625A1 (en) * 2017-04-26 2018-11-01 Navitor Pharmaceuticals, Inc. Modulators of sestrin-gator2 interaction and uses thereof
EP3870158A4 (en) 2018-10-24 2022-08-10 Navitor Pharmaceuticals, Inc. Polymorphic compounds and uses thereof
CN112969687B (zh) 2018-10-30 2024-08-23 吉利德科学公司 作为α4β7整合素抑制剂的喹啉衍生物
ES3003232T3 (en) 2018-10-30 2025-03-10 Gilead Sciences Inc Compounds for inhibition of alpha4beta7 integrin
ES2987796T3 (es) 2018-10-30 2024-11-18 Gilead Sciences Inc Derivados de N-benzoil-fenilalanina como inhibidores de la integrina alfa4beta7 para el tratamiento de enfermedades inflamatorias
CA3114240C (en) 2018-10-30 2023-09-05 Gilead Sciences, Inc. Imidazopyridine derivatives as alpha4beta7 integrin inhibitors
CN111689993B (zh) * 2019-03-11 2023-04-14 凯特立斯(深圳)科技有限公司 一种新的含硼类佐米药物关键中间体手性α-氨基硼酸酯的制备方法
CN114222730B (zh) 2019-08-14 2024-09-10 吉利德科学公司 用于抑制α4β7整合素的化合物
TWI870497B (zh) * 2019-11-01 2025-01-21 美商奈維特製藥公司 使用mtorc1調節劑的治療方法
CN113876784B (zh) * 2021-09-27 2023-07-21 潍坊博创国际生物医药研究院 硼代亮氨酸类化合物的新用途
CN115927459A (zh) * 2022-07-19 2023-04-07 华南农业大学 猪ctns基因在促进动物骨骼肌生长中的应用
EP4612120A1 (en) * 2022-11-01 2025-09-10 Navitor Pharmaceuticals, Inc. Modulators of mtorc1 activity and uses thereof

Family Cites Families (77)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4110368A (en) 1972-07-24 1978-08-29 American Cyanamid Company Hydro substituted prostanoic acids and esters
US4346110A (en) * 1981-06-01 1982-08-24 Merrell Toraude Et Compagnie Method for treating depression
JPS61149964A (ja) 1984-12-25 1986-07-08 Canon Inc 電子写真感光体
US4670196A (en) 1985-09-05 1987-06-02 Norton Company Tower packing element
ES2029799T3 (es) 1986-01-24 1992-10-01 Toray Industries, Inc. Derivados de 2,5,6,7 tetranor-4,8-inter-m-fenilen pg12.
GB8827885D0 (en) 1988-11-30 1989-01-05 Wellcome Found Novel heterocyclic pesticidal compounds
US5639600A (en) 1994-08-05 1997-06-17 The Regents Of The University Of California Diagnosis and treatment of cell proliferative disease having clonal macrophage involvement
DE19623142A1 (de) 1996-06-10 1997-12-11 Huels Chemische Werke Ag Enantiomerenangereicherte, durch einen tertiären Kohlenwasserstoffrest substituierte Malonsäuremonoester sowie deren Herstellung
WO1998008853A1 (en) * 1996-08-28 1998-03-05 The Procter & Gamble Company Phosphinic acid amides as matrix metalloprotease inhibitors
US7087648B1 (en) 1997-10-27 2006-08-08 The Regents Of The University Of California Methods for modulating macrophage proliferation using polyamine analogs
AU3459999A (en) 1998-04-27 1999-11-16 Warner-Lambert Company Substituted diarylalkyl amides as calcium channel antagonists
CN1146585C (zh) 1998-11-04 2004-04-21 蒙特尔技术有限公司 用于烯烃聚合的催化剂组分和催化剂
US6329546B1 (en) 1999-01-12 2001-12-11 Laboratory Of Molecular Biophotonics Caged amino acids
US20030203900A1 (en) 1999-05-18 2003-10-30 Martin Quibell Cysteine protease inhibitors
HRP20020025A2 (en) 1999-06-10 2003-12-31 Warner Lambert Co Mono- and disubstituted 3-propyl gamma-aminobutyric acids
US20020155170A1 (en) * 2000-11-30 2002-10-24 Walsh William John Nutrient supplements and methods for treating autism and for preventing the onset of autism
JP5076257B2 (ja) 2001-02-01 2012-11-21 旭硝子株式会社 撥水性組成物、表面処理された基材、その製造方法および輸送機器用物品
PT1389617E (pt) 2001-04-27 2007-04-30 Zenyaku Kogyo Kk Composto heterocíclico e agente antitumoral contendo o mesmo como igrediente activo
TWI329105B (en) 2002-02-01 2010-08-21 Rigel Pharmaceuticals Inc 2,4-pyrimidinediamine compounds and their uses
EP2055310B1 (en) 2002-08-14 2015-12-16 Silence Therapeutics GmbH Protein kinase N beta for the diagnosis and the treatment of late stage tumor
US6787664B2 (en) 2002-09-17 2004-09-07 Warner-Lambert Company Llc Process for preparing single enantiomers of 5,5,5,5′,5′,5′-hexafluoroleucine and protected analogs
AU2002953255A0 (en) 2002-12-11 2003-01-02 Cytopia Research Pty Ltd Protein kinase inhibitors
EP1611119A1 (en) 2003-04-03 2006-01-04 Semafore Pharmaceuticals, Inc. Pi-3 kinase inhibitor prodrugs
PT1644363E (pt) 2003-05-30 2012-05-18 Gemin X Pharmaceuticals Canada Inc Compostos tri-heterocíclicos, composições e métodos para tratamento de cancro ou doenças virais
EP2371835A1 (en) 2003-07-03 2011-10-05 The Trustees Of The University Of Pennsylvania Inhibition of syk kinase expression
ES2607804T3 (es) 2004-05-13 2017-04-04 Icos Corporation Quinazolinones como inhibidores de la fosfatidilinositol humana 3-quinasa delta
US20070212428A1 (en) * 2004-06-04 2007-09-13 Mood Management Sciences, Inc. Methods and compositions for treating mood disorder
DE102004053407A1 (de) 2004-11-05 2006-05-11 Bayer Healthcare Ag Acylierte Nonadepsipeptide II
EP1856135B1 (en) 2005-01-19 2009-12-09 Rigel Pharmaceuticals, Inc. Prodrugs of 2,4-pyrimidinediamine compounds and their uses
AU2006242851A1 (en) 2005-02-18 2006-11-09 Centre National De La Recherche Scientifique (C.N.R.S.) Diastereoisomers of 4-hydroxyisoleucine and uses thereof
TWI337608B (en) 2005-05-12 2011-02-21 Abbott Lab Apoptosis promoters
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
US7402325B2 (en) 2005-07-28 2008-07-22 Phoenix Biotechnology, Inc. Supercritical carbon dioxide extract of pharmacologically active components from Nerium oleander
RS53627B1 (sr) 2005-10-07 2015-04-30 Exelixis Inc. Derivati n-(3-amino-hinoksalin-2-il)-sulfonamida i njihova upotreba kao inhibitora fosfatidilinozitol3-kinaze
DK1951684T3 (en) 2005-11-01 2016-10-24 Targegen Inc BIARYLMETAPYRIMIDIN kinase inhibitors
DK3184526T3 (en) 2005-12-13 2019-01-14 Incyte Holdings Corp PYRROLO [2,3-D] PYRIMIDINE DERIVATIVES AS A JANUS-KINASE INHIBITOR
JO2660B1 (en) 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
BRPI0710874A2 (pt) 2006-04-26 2012-02-14 Hoffmann La Roche compostos de tienopirimidina, processos de produção dos referidos compostos, composições farmacêuticas contendo os mesmos, kit, produto, e usos dos compostos
US20100093706A1 (en) * 2006-08-21 2010-04-15 Prexa Pharmaceuticals, Inc. Multimediator transporter inhibitors for use in treatment of central nervous system disorders
SG166093A1 (en) 2006-09-22 2010-11-29 Pharmacyclics Inc Inhibitors of brutonæs tyrosine kinase
KR20130095850A (ko) 2006-09-25 2013-08-28 욱크하르트 리미티드 치환된 피페리디노페닐 옥사졸리디논
TWI397418B (zh) 2006-10-10 2013-06-01 Otsuka Pharma Co Ltd 抗憂鬱劑
RU2009118935A (ru) 2006-10-20 2010-11-27 Мерк энд Ко., Инк. (US) Земещенные имидазолы в качестве модуляторов подтипа 3 бомбезиновых рецепторов
HUE029188T2 (en) 2007-03-12 2017-03-28 Ym Biosciences Australia Pty Phenylamino-pyrimidine compounds and their use
WO2008118802A1 (en) 2007-03-23 2008-10-02 Regents Of The University Of Minnesota Therapeutic compounds
TW200902019A (en) 2007-04-26 2009-01-16 Ono Pharmaceutical Co Dicyclic heterocyclic compound
PE20090717A1 (es) 2007-05-18 2009-07-18 Smithkline Beecham Corp Derivados de quinolina como inhibidores de la pi3 quinasa
US8431608B2 (en) 2007-08-17 2013-04-30 Icagen Inc. Heterocycles as potassium channel modulators
EP2193119B1 (en) 2007-08-27 2014-01-01 Abbvie Deutschland GmbH & Co. KG 4-(4-pyridinyl)-benzamides and their use as rock activity modulators
ES2602577T3 (es) 2008-03-11 2017-02-21 Incyte Holdings Corporation Derivados de azetidina y ciclobutano como inhibidores de JAK
US8613951B2 (en) 2008-06-16 2013-12-24 Bind Therapeutics, Inc. Therapeutic polymeric nanoparticles with mTor inhibitors and methods of making and using same
CN102256966B (zh) * 2008-10-17 2016-02-10 白头生物医学研究所 可溶性mTOR复合物和其调节剂
WO2010146172A2 (en) 2009-06-19 2010-12-23 Lek Pharmaceuticals D.D. NEW SYNTHETIC ROUTE FOR THE PREPARATION OF α-AMINO BORONIC ACID DERIVATIVES VIA SUBSTITUTED ALK-1-YNES
WO2011012283A1 (en) * 2009-07-30 2011-02-03 University Of Zurich Injectable formulation for treatment and protection of patients having an inflammatory reaction or an ischemia-reperfusion event
EA201201052A1 (ru) 2010-01-29 2013-02-28 Бёрингер Ингельхайм Интернациональ Гмбх Замещенные нафтиридины и их применение в качестве ингибиторов киназы syk
MY177250A (en) * 2010-06-30 2020-09-10 Fujifilm Corp Novel nicotinamide derivative or salt thereof
CN102464701B (zh) 2010-11-08 2015-10-21 上海医药工业研究院 一类新型化合物、其制备方法及用途
WO2012076063A1 (en) 2010-12-10 2012-06-14 Rottapharm S.P.A. Pyridine amide derivatives as ep4 receptor antagonists
WO2012113847A1 (en) 2011-02-25 2012-08-30 Lonza Ltd Branched linker for protein drug conjugates
US9321727B2 (en) 2011-06-10 2016-04-26 Hoffmann-La Roche Inc. Pyridine derivatives as agonists of the CB2 receptor
WO2013052393A1 (en) 2011-10-05 2013-04-11 Merck Sharp & Dohme Corp. 3-PYRIDYL CARBOXAMIDE-CONTAINING SPLEEN TYROSINE KINASE (Syk) INHIBITORS
EP2589383A1 (en) * 2011-11-06 2013-05-08 Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. Berlin FKBP subtype-specific rapamycin analogue for use in treatment of diseases
WO2013142229A1 (en) 2012-03-19 2013-09-26 President And Fellows Of Harvard College Designing novel peptides for inducing fibronectin matrix assembly
US9790176B2 (en) 2012-08-06 2017-10-17 Pitney Pharmaceuticals Pty Limited Compounds for the treatment of mTOR pathway related diseases
WO2014127052A1 (en) 2013-02-13 2014-08-21 Zondlo Neal Perfluoro-tert-butyl hydroxyproline
WO2014145852A2 (en) 2013-03-15 2014-09-18 Knopp Biosciences Llc Imidazo(4,5-b) pyridin-2-yl amides as kv7 channel activators
WO2014201111A1 (en) 2013-06-14 2014-12-18 The Brigham And Women's Hospital, Inc. Treatment of mtor hyperactive related diseases and disorders
EP3191116B1 (en) * 2014-09-12 2020-11-25 The Whitehead Institute for Biomedical Research Methods of identifying modulators of sestrin-gator2 interaction and use of same to modulate mtorc1
SI3364958T1 (sl) * 2015-10-23 2023-05-31 Navitor Pharmaceuticals, Inc. Modulatorji interakcije sestrina in gator2 ter njihova uporaba
WO2017083823A1 (en) 2015-11-13 2017-05-18 Brandeis University Mtor inhibitors and methods of use thereof
AU2017252563B2 (en) 2016-04-21 2022-07-21 Baylor College Of Medicine Compositions and methods for the treatment of lysosomal storage disorders and disorders characterized by lysosomal dysfunction
WO2018200625A1 (en) 2017-04-26 2018-11-01 Navitor Pharmaceuticals, Inc. Modulators of sestrin-gator2 interaction and uses thereof
JP2021512920A (ja) 2018-02-08 2021-05-20 オービッド・セラピューティクス・インコーポレイテッドOvid Therapeutics Inc. 耳鳴、急性感音性難聴、メニエール病、トゥレット症候群、注意欠陥多動性障害、および嗜癖の治療における(1s,3s)−3−アミノ−4−(ジフルオロメチリデン)シクロペンタン−1−カルボン酸および(s)−3−アミノ−4−(ジフルオロメチルエニル)シクロペンタ−1−エン−1−カルボン酸の使用
EP3870158A4 (en) 2018-10-24 2022-08-10 Navitor Pharmaceuticals, Inc. Polymorphic compounds and uses thereof
US10926803B2 (en) 2019-07-17 2021-02-23 GM Global Technology Operations LLC Four rail front crush structure with load dissemination into eight element support structure
TWI870497B (zh) 2019-11-01 2025-01-21 美商奈維特製藥公司 使用mtorc1調節劑的治療方法
JP6689441B1 (ja) 2019-11-01 2020-04-28 エヌ・ティ・ティ・コミュニケーションズ株式会社 電子マネー管理システムおよび電子マネー管理方法

Similar Documents

Publication Publication Date Title
JP2020517707A5 (enExample)
JP2018538248A5 (enExample)
JP2013532652A5 (enExample)
JP2011529918A5 (enExample)
JP2019520344A5 (enExample)
JP2020507589A5 (enExample)
JP2006505543A5 (enExample)
JP2010506854A5 (enExample)
JP2007529421A5 (enExample)
JP2011509309A5 (enExample)
JP2011529964A5 (enExample)
JP2019529444A5 (enExample)
JP2007527919A5 (enExample)
JP2008535903A5 (enExample)
JP2013515074A5 (enExample)
JP2012530779A5 (enExample)
JP2019518050A5 (enExample)
JP2018524304A5 (enExample)
RU2018127728A (ru) Слитые трициклические гетероциклические соединения в качестве ингибиторов интегразы вич
RU2010119458A (ru) 1,3,5-тризамещенное производное триазола
JP2019500387A5 (enExample)
JP2020533352A5 (enExample)
JP2018527301A5 (ja) アジリジン含有dnaアルキル化剤
JP2015536997A5 (enExample)
JPWO2023099623A5 (enExample)