JP2015506363A5 - - Google Patents

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Publication number
JP2015506363A5
JP2015506363A5 JP2014552326A JP2014552326A JP2015506363A5 JP 2015506363 A5 JP2015506363 A5 JP 2015506363A5 JP 2014552326 A JP2014552326 A JP 2014552326A JP 2014552326 A JP2014552326 A JP 2014552326A JP 2015506363 A5 JP2015506363 A5 JP 2015506363A5
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JP
Japan
Prior art keywords
compound
pharmaceutically acceptable
composition according
acceptable salt
disease
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.)
Pending
Application number
JP2014552326A
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English (en)
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JP2015506363A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2013/021223 external-priority patent/WO2013106702A1/en
Publication of JP2015506363A publication Critical patent/JP2015506363A/ja
Publication of JP2015506363A5 publication Critical patent/JP2015506363A5/ja
Pending legal-status Critical Current

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Claims (12)

  1. 下記式の化合物:

    またはその薬学的に許容される塩。
  2. 前記化合物は下記式の化合物:
    またはその薬学的に許容される塩である、請求項1に記載の化合物。
  3. 前記化合物は下記式の化合物:
    またはその薬学的に許容される塩である、請求項1に記載の化合物。
  4. 前記化合物は他のジアステレオマーを実質的に含まない、請求項1〜のいずれか一項に記載の化合物。
  5. 請求項1〜のいずれか一項に記載の化合物またはその薬学的に許容される塩;および任意選択的に薬学的に許容される賦形剤を含む医薬組成物。
  6. 請求項1〜のいずれか一項に記載の化合物またはその塩;および任意選択的に化粧品として許容される賦形剤を含む化粧料組成物。
  7. ルタミル−プロリルtRNAシンテターゼを阻害するために用いる、請求項1〜4のいずれか一項に記載の化合物、または請求項5もしくは6に記載の組成物
  8. Th17介在性状態、グルタミル−プロリルtRNAシンテターゼ介在性状態、またはAAR介在性状態を処置するための、請求項1〜4のいずれか一項に記載の化合物、または請求項5もしくは6に記載の組成物
  9. 前記Th17介在性状態は自己免疫疾患、ドライアイ症候群、線維症、瘢痕形成、血管新生、虚血障害、炎症性疾患神経変性疾患、セルライトおよび皮膚線条からなる群から選択される請求項に記載の化合物または組成物
  10. 移植用のドナー臓器を保護するための、請求項1〜4のいずれか一項に記載の化合物、または請求項5もしくは6に記載の組成物
  11. 前記AAR介在性状態は線維症、瘢痕形成、自己免疫疾患、ドライアイ症候群、移植片対宿主病、血管新生、癌、黄斑変性、脈絡膜血管新生、喘息、慢性炎症、循環器疾患、糖尿病、ウイルス感染、マラリア、原虫感染症、真菌感染、セルライト、多発性硬化症、関節リウマチ、ループス、乾癬、強皮症および皮膚線条からなる群から選択される、請求項に記載の化合物または組成物
  12. T細胞新生物を処置するための、請求項1〜4のいずれか一項に記載の化合物、または請求項5もしくは6に記載の組成物
JP2014552326A 2012-01-13 2013-01-11 ハロフジノール誘導体、および化粧料組成物および医薬組成物におけるその使用 Pending JP2015506363A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261586271P 2012-01-13 2012-01-13
US61/586,271 2012-01-13
PCT/US2013/021223 WO2013106702A1 (en) 2012-01-13 2013-01-11 Halofuginol derivatives and their use in cosmetic and pharmaceutical compositions

Publications (2)

Publication Number Publication Date
JP2015506363A JP2015506363A (ja) 2015-03-02
JP2015506363A5 true JP2015506363A5 (ja) 2016-03-03

Family

ID=47844437

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2014552326A Pending JP2015506363A (ja) 2012-01-13 2013-01-11 ハロフジノール誘導体、および化粧料組成物および医薬組成物におけるその使用

Country Status (7)

Country Link
US (1) US10155742B2 (ja)
EP (1) EP2802572B1 (ja)
JP (1) JP2015506363A (ja)
AU (1) AU2013207796B2 (ja)
CA (1) CA2861840C (ja)
HK (1) HK1203947A1 (ja)
WO (1) WO2013106702A1 (ja)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9284297B2 (en) 2008-08-11 2016-03-15 President And Fellows Of Harvard College Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
JP2015506363A (ja) 2012-01-13 2015-03-02 プレジデント アンド フェローズ オブ ハーバード カレッジ ハロフジノール誘導体、および化粧料組成物および医薬組成物におけるその使用
PT3159335T (pt) 2014-06-23 2020-06-05 Dae Woong Pharma Novo composto heterocíclico
KR102277538B1 (ko) * 2015-06-08 2021-07-14 주식회사 대웅제약 신규한 헤테로 고리 화합물, 이의 제조 방법 및 이를 포함하는 약학적 조성물
JP2019196307A (ja) 2016-09-15 2019-11-14 武田薬品工業株式会社 複素環アミド化合物
US20190365760A1 (en) * 2016-11-14 2019-12-05 Keio University A therapeutic or prophylactic agent for ischemic disease, glaucoma, optic nerve disease, retinal degenerative disease, angiogenic retinal disease, cancer, neurodegenerative or autoimmune disease, and a hypoxia inducing factor inhibitor
WO2019237125A1 (en) 2018-06-08 2019-12-12 The General Hospital Corporation Inhibitors of prolyl-trna-synthetase
CN109134437B (zh) * 2018-08-24 2021-05-25 中山大学 一种去氧常山酮类化合物及其制备方法和应用
WO2021163304A1 (en) * 2020-02-11 2021-08-19 Tufts Medical Center, Inc. Activation of neuropeptide receptors on plasmacytoid dendritic cells to treat or prevent ocular diseases associated with neovascularization and inflammation
AU2022316021A1 (en) * 2021-07-23 2024-01-18 Daewoong Pharmaceutical Co., Ltd. Pharmaceutical composition for preventing or treating systemic sclerosis
WO2023140505A1 (ko) * 2022-01-18 2023-07-27 (주)큐라미스 할로푸지논을 유효성분으로 함유하는 신경퇴행성 또는 운동신경 질환 예방 또는 치료용 조성물
CN114288300B (zh) * 2022-01-29 2023-04-21 中国科学技术大学 常山酮在治疗和预防脂肪肝、肥胖的药物中的应用

Family Cites Families (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2694711A (en) 1952-12-02 1954-11-16 American Cyanamid Co Quinazolone antimalarial compounds
US3320124A (en) 1964-07-20 1967-05-16 American Cyanamid Co Method for treating coccidiosis with quinazolinones
DE2020234A1 (de) 1970-04-25 1971-11-18 Cassella Farbwerke Mainkur Ag Basisch substituierte Derivate des 4(3H)-Chinazolinons
GB1541463A (en) 1975-10-11 1979-02-28 Lion Dentifrice Co Ltd Process for prparing a multiple emulsion having a dispersing form of water-phase/oil-phase/water-phase
DE2934069A1 (de) 1979-08-23 1981-03-12 Hoechst Ag, 6000 Frankfurt Mittel gegen theileriosen und seine verwendung.
US4762838A (en) 1985-08-30 1988-08-09 Pfizer Inc. Quinazolin-4(3H)-one derivatives as anticoccidial agents
US4937370A (en) 1987-06-02 1990-06-26 The Procter & Gamble Company Novel chromophores, sunscreen compositions and methods for preventing sunburn
US4999186A (en) 1986-06-27 1991-03-12 The Procter & Gamble Company Novel sunscreen agents, sunscreen compositions and methods for preventing sunburn
US4725599A (en) 1986-09-08 1988-02-16 Pfizer Inc. Heterocyclic ring fused pyrimidine-4 (3H)-ones as anticoccidial agents
US4960764A (en) 1987-03-06 1990-10-02 Richardson-Vicks Inc. Oil-in-water-in-silicone emulsion compositions
US4800197A (en) 1987-07-17 1989-01-24 Richardson-Vicks Inc. Anti-acne composition
US4891228A (en) 1988-02-02 1990-01-02 Richardson-Vicks Inc. Medicated cleansing pads
US4891227A (en) 1988-02-02 1990-01-02 Richardson-Vicks Inc. Medicated cleansing pads
US5223409A (en) 1988-09-02 1993-06-29 Protein Engineering Corp. Directed evolution of novel binding proteins
US4919934A (en) 1989-03-02 1990-04-24 Richardson-Vicks Inc. Cosmetic sticks
US5087445A (en) 1989-09-08 1992-02-11 Richardson-Vicks, Inc. Photoprotection compositions having reduced dermal irritation
US6446032B1 (en) 1990-09-21 2002-09-03 Massachusetts Institute Of Technology Designing compounds specifically inhibiting ribonucleic acid by binding to the minor groove
US5073371A (en) 1990-11-30 1991-12-17 Richardson-Vicks, Inc. Leave-on facial emulsion compositions
US5073372A (en) 1990-11-30 1991-12-17 Richardson-Vicks, Inc. Leave-on facial emulsion compositions
CA2113229C (en) 1994-01-11 1999-04-20 Mark Pines Anti-fibrotic quinazolinone-containing compositions and methods for the use thereof
US5759833A (en) 1994-05-27 1998-06-02 Cubist Pharmaceuticals, Inc. Human isoleucyl-tRNA synthetase proteins, nucleic acids and tester strains comprising same
US20020025316A1 (en) 1995-08-18 2002-02-28 Ferguson Mark Williams James Pharmaceutical composition containing inhibitors of interferon-gamma
US6028075A (en) 1997-02-11 2000-02-22 Pines; Mark Quinazolinone containing pharmaceutical compositions for prevention of neovascularization and for treating malignancies
GB9702944D0 (en) 1997-02-13 1997-04-02 Univ Manchester Reducing fibrosis
CA2285350A1 (en) 1997-03-31 1998-10-08 Hadasit Medical Research Services And Development Company Ltd. Treatment for pulmonary fibrosis
EP1109559B1 (en) 1998-08-13 2005-10-26 Hadasit Medical Research Services & Development Co., Ltd. Inhibition of pathogenic processes related to tissue trauma
ATE279175T1 (de) 1999-08-20 2004-10-15 Howard Murad Pharmazeutische zusammensetzungen und verfahren zur verminderung des cellulite auftretens
ITMI991894A1 (it) 1999-09-09 2001-03-09 Carlo Ghisalberti Acido linoleico coniugato e trigliceride nuovi metodi di sintesi e d'uso
JP3771128B2 (ja) 2000-12-28 2006-04-26 独立行政法人科学技術振興機構 フェブリフジンおよびフェブリフジン化合物の新規合成方法
US20050227935A1 (en) 2001-05-18 2005-10-13 Sirna Therapeutics, Inc. RNA interference mediated inhibition of TNF and TNF receptor gene expression using short interfering nucleic acid (siNA)
AU2002356043A1 (en) 2001-08-14 2003-03-03 Washington University In St. Louis Systems and methods for screening pharmaceutical chemicals
WO2004069793A2 (en) 2003-01-28 2004-08-19 Bristol-Myers Squibb Company Novel 2-substituted cyclic amines as calcium sensing receptor modulators
CN1263753C (zh) 2004-05-21 2006-07-12 厦门大学 一种合成常山碱与ru-19110中间体的方法
EP1855684A4 (en) 2005-02-23 2011-04-06 Collgard Biopharmaceuticals Ltd PHARMACEUTICAL COMPOSITIONS OF THE ISOLATED D-ENANTIOMER OF THE CHINAZOLINONE DERIVATIVE HALOFUGINONE
WO2007058990A2 (en) 2005-11-14 2007-05-24 Kemia, Inc. Therapy using cytokine inhibitors
TWI464148B (zh) 2006-03-16 2014-12-11 Evotec Us Inc 作為p2x7調節劑之雙環雜芳基化合物與其用途
AU2007238816B2 (en) 2006-04-10 2012-12-06 President And Fellows Of Harvard College Methods for modulating formation and progression of cellulite
KR20100110396A (ko) 2006-04-14 2010-10-12 프라나 바이오테크놀로지 리미티드 연령 관련 황반 변성(에이엠디)의 치료 방법
ES2474865T3 (es) 2006-06-22 2014-07-09 Prana Biotechnology Limited Método de tratamiento de un tumor cerebral glioma
WO2008094909A2 (en) 2007-01-29 2008-08-07 Xenon Pharmaceuticals Inc. Quinazolinone and fused pyrimidinone compounds and their use in treating sodium channel-mediated diseases or conditions
US20080188498A1 (en) * 2007-02-05 2008-08-07 Radix Pharmaceuticals, Inc. Pyridopyrimidinone compounds with antimalarial activity
CA2693062C (en) 2007-06-21 2016-08-09 Neuronascent, Inc. Methods and compositions for stimulating neurogenesis and inhibiting neuronal degeneration using isothiazolopyrimidinones
WO2009023267A2 (en) 2007-08-15 2009-02-19 President And Fellows Of Harvard College Methods for modulating development and expansion of il-17 expressing cells
US20090123389A1 (en) 2007-08-15 2009-05-14 Malcolm Whitman Methods for modulating Th17 cell development in the treatment and prevention of cellulite
US9284297B2 (en) 2008-08-11 2016-03-15 President And Fellows Of Harvard College Halofuginone analogs for inhibition of tRNA synthetases and uses thereof
WO2010096170A2 (en) 2009-02-19 2010-08-26 President And Fellows Of Harvard College Inhibition of trna synthetases and therapeutic applications thereof
US8357692B2 (en) * 2010-06-20 2013-01-22 Washington University Methods of treatment of bone degenerative diseases
JP2015506363A (ja) 2012-01-13 2015-03-02 プレジデント アンド フェローズ オブ ハーバード カレッジ ハロフジノール誘導体、および化粧料組成物および医薬組成物におけるその使用

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