WO2005037257A3 - Neue alanyl-aminopeptidasen-inhibitoren zur funktionellen beeinflussung unterschiedlicher zellen und zur behandlung immunologischer, entzündlicher, neuronaler und anderer erkrankungen - Google Patents

Neue alanyl-aminopeptidasen-inhibitoren zur funktionellen beeinflussung unterschiedlicher zellen und zur behandlung immunologischer, entzündlicher, neuronaler und anderer erkrankungen Download PDF

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WO2005037257A3
WO2005037257A3 PCT/EP2004/011643 EP2004011643W WO2005037257A3 WO 2005037257 A3 WO2005037257 A3 WO 2005037257A3 EP 2004011643 W EP2004011643 W EP 2004011643W WO 2005037257 A3 WO2005037257 A3 WO 2005037257A3
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Prior art keywords
diseases
neuronal
alanyl
inflammatory
novel
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PCT/EP2004/011643
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English (en)
French (fr)
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WO2005037257A2 (de
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Siegfried Ansorge
Ute Bank
Karsten Nordhoff
Michael Taeger
Frank Striggow
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Imtm Gmbh
Keyneurotek Ag
Siegfried Ansorge
Ute Bank
Karsten Nordhoff
Michael Taeger
Frank Striggow
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Application filed by Imtm Gmbh, Keyneurotek Ag, Siegfried Ansorge, Ute Bank, Karsten Nordhoff, Michael Taeger, Frank Striggow filed Critical Imtm Gmbh
Priority to AU2004281536A priority Critical patent/AU2004281536B9/en
Priority to CA002542723A priority patent/CA2542723A1/en
Priority to US10/575,882 priority patent/US20070037752A1/en
Priority to JP2006534706A priority patent/JP2007508349A/ja
Priority to EP04790485A priority patent/EP1673075A2/de
Publication of WO2005037257A2 publication Critical patent/WO2005037257A2/de
Publication of WO2005037257A3 publication Critical patent/WO2005037257A3/de

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Abstract

Die vorliegende Erfindung betrifft Substanzen, die Ala-p-Nitroanilid spaltende Peptidasen spezifisch inhibieren, für die Verwendung in der Medizin. Weiter betrifft die Erfindung die Verwendung mindestens einer derartigen Substanz oder mindestens einer mindestens eine derartige Substanz enthaltenden pharmazeutischen oder kosmetischen Zusammensetzung zur Prophylaxe und Therapie von Erkrankungen, insbesondere zur Prophylaxe und Therapie von Erkrankungen mit überschiessender Immunantwort (Autoimmunerkrankungen, Allergien und Transplantatrejektionen), von anderen chronisch-entzündlichen Erkrankungen, neuronalen Erkrankungen und zerebralen Schädigungen, Hauterkrankungen (u. a. Akne und Schuppenflechte), Tumorerkrankungen und speziellen Virusinfektionen (u. a. SARS).
PCT/EP2004/011643 2003-10-15 2004-10-15 Neue alanyl-aminopeptidasen-inhibitoren zur funktionellen beeinflussung unterschiedlicher zellen und zur behandlung immunologischer, entzündlicher, neuronaler und anderer erkrankungen WO2005037257A2 (de)

Priority Applications (5)

Application Number Priority Date Filing Date Title
AU2004281536A AU2004281536B9 (en) 2003-10-15 2004-10-15 Novel alanyl-amino peptidase inhibitors for functionally influencing different cells and treating immunological, inflammatory, neuronal, and other diseases
CA002542723A CA2542723A1 (en) 2003-10-15 2004-10-15 Novel alanyl-amino peptidase inhibitors for functionally influencing different cells and treating immunological, inflammatory, neuronal, and other diseases
US10/575,882 US20070037752A1 (en) 2003-10-15 2004-10-15 Novel alanyl-amino peptidase inhibitors for functionally influencing different cells and treating immunological, inflammatory, neuronal, and other diseases
JP2006534706A JP2007508349A (ja) 2003-10-15 2004-10-15 異なるタイプの細胞に機能的に影響を及ぼし、免疫性疾患、炎症性疾患、神経疾患、およびその他の疾患を治療するための新規なアラニルアミノペプチダーゼ阻害剤
EP04790485A EP1673075A2 (de) 2003-10-15 2004-10-15 Neue alanyl-aminopeptidasen-inhibitoren zur funktionellen beeinflussung unterschiedlicher zellen und zur behandlung immunologischer, entz ndlicher, neuronaler und anderer erkrankungen

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10348023A DE10348023A1 (de) 2003-10-15 2003-10-15 Neue Alanyl-Aminopeptidasen-Inhibitoren zur funktionellen Beeinflussung unterschiedlicher Zellen und zur Behandlung immunologischer, entzündlicher, neuronaler und anderer Erkrankungen
DE10348023.4 2003-10-15

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WO2005037257A2 WO2005037257A2 (de) 2005-04-28
WO2005037257A3 true WO2005037257A3 (de) 2006-09-14

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US (1) US20070037752A1 (de)
EP (1) EP1673075A2 (de)
JP (1) JP2007508349A (de)
CN (1) CN1897928A (de)
AU (1) AU2004281536B9 (de)
CA (1) CA2542723A1 (de)
DE (1) DE10348023A1 (de)
WO (1) WO2005037257A2 (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9217024B2 (en) 2007-12-18 2015-12-22 Acumen Pharmaceuticals, Inc. ADDL receptor polypeptides, polynucleotides and host cells for recombinant production
US9415043B2 (en) 2013-03-15 2016-08-16 Aerie Pharmaceuticals, Inc. Combination therapy
US9512101B2 (en) 2008-07-25 2016-12-06 Aerie Pharmaceuticals, Inc. Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
US11590123B2 (en) 2016-08-31 2023-02-28 Aerie Pharmaceuticals, Inc. Ophthalmic compositions

Families Citing this family (85)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2520172C (en) 2003-03-27 2012-10-02 Lankenau Institute For Medical Research Novel methods for the treatment of cancer with an indoleamine 2, 3-dioxygenase inhibitor
US8134015B2 (en) 2003-03-27 2012-03-13 Kyowa Hakko Kirin Co., Ltd. Compound inhibiting in vivo phosphorous transport and medicine containing the same
DE10348022A1 (de) * 2003-10-15 2005-05-25 Imtm Gmbh Neue Dipeptidylpeptidase IV-Inhibitoren zur funktionellen Beeinflussung unterschiedlicher Zellen und zur Behandlung immunologischer, entzündlicher, neuronaler und anderer Erkrankungen
US20060194810A1 (en) * 2004-04-30 2006-08-31 Bijan Almassian Methods of treating ischemic related conditions
EP1802634A2 (de) * 2004-10-20 2007-07-04 Compass Pharmaceuticals LLC Thiophene und ihre verwendung als antitumormittel
US7994221B2 (en) 2004-12-06 2011-08-09 Siga Technologies, Inc. Sulfonyl semicarbazides, carbonyl semicarbazides, semicarbazides and ureas, pharmaceutical compositions thereof, and methods for treating hemorrhagic fever viruses, including infections associated with arenaviruses
US8642596B2 (en) 2004-12-06 2014-02-04 Siga Technologies, Inc. Sulfonyl semicarbazides, semicarbazides and ureas, pharmaceutical compositions thereof, and methods for treating hemorrhagic fever viruses, including infections associated with arena viruses
US8410149B2 (en) 2004-12-06 2013-04-02 Siga Technologies Inc. Sulfonyl semicarbazides, semicarbazides and ureas, pharmaceutical compositions thereof, and methods for treating hemorrhagic fever viruses, including infections associated with arenaviruses
US7544838B2 (en) * 2005-01-21 2009-06-09 City Of Hope Ligands for estrogen related receptors and methods for synthesis of said ligands
ITMI20050261A1 (it) * 2005-02-21 2006-08-22 Carlo Ghisalberti Analoghi strutturali di avenatramidi loro uso in composizioni utili nel trattamento di disordini dermatologici
WO2006094248A1 (en) * 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Aryl-substituted cyclic sirtuin modulators
CA2599987A1 (en) 2005-03-03 2006-09-08 Sirtris Pharmaceuticals, Inc. Fused heterocyclic compounds and their use as sirtuin modulators
AU2006244068B9 (en) 2005-05-10 2012-10-25 Incyte Holdings Corporation Modulators of indoleamine 2,3-dioxygenase and methods of using the same
WO2006132583A1 (en) * 2005-06-07 2006-12-14 Innate Pharmaceuticals Ab Method and means for preventing and inhibiting respiratory disease, atherosclerosis and osteoporosis caused by chlamydia pneumoniae infection
AU2006259574A1 (en) * 2005-06-14 2006-12-28 Schering Corporation The preparation and use of compounds as aspartyl protease inhibitors
WO2007008942A2 (en) * 2005-07-11 2007-01-18 Aerie Pharmaceuticals, Inc. Phenylamino-acetic acid [1-(pyridin-4-yl)-methylidene]-hydrazide derivatives and related compounds as modulators of g protein-coupled receptor kinases for the treatment of eye diseases
WO2007008926A1 (en) 2005-07-11 2007-01-18 Aerie Pharmaceuticals, Inc. Isoquinoline compounds
CA2634005C (en) * 2005-12-15 2012-01-03 Vicuron Pharmaceuticals Inc. N-hydroxyamide derivatives possessing antibacterial activity
US8450351B2 (en) 2005-12-20 2013-05-28 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
JP2009525338A (ja) 2006-02-01 2009-07-09 サイガ・テクノロジーズ・インコーポレーテッド 抗アレナウイルス化合物
US8791110B2 (en) 2006-02-01 2014-07-29 Siga Technologies, Inc. Anti-arenaviral compounds
US8871746B2 (en) 2006-03-02 2014-10-28 Kineta Four, LLC Antiviral drugs for treatment of arenavirus infection
US8148428B2 (en) 2006-03-02 2012-04-03 Siga Technologies, Inc. Antiviral drugs for treatment of arenavirus infection
US7872037B2 (en) 2006-03-02 2011-01-18 Siga Technologies, Inc. Antiviral drugs for treatment of arenavirus infection
US7977365B2 (en) 2006-03-02 2011-07-12 Siga Technologies, Inc. Antiviral drugs for treatment of arenavirus infection
DE102006028862A1 (de) * 2006-06-23 2007-12-27 Merck Patent Gmbh 3-Amino-imidazo[1,2-a]pyridinderivate
WO2008036642A2 (en) 2006-09-19 2008-03-27 Incyte Corporation N-hydroxyamidinoheterocycles as modulators of indoleamine 2,3-dioxygenase
CL2007002650A1 (es) * 2006-09-19 2008-02-08 Incyte Corp Compuestos derivados de heterociclo n-hidroxiamino; composicion farmaceutica, util para tratar cancer, infecciones virales y desordenes neurodegenerativos entre otras.
CA2664335C (en) 2006-09-20 2014-12-02 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
US8455513B2 (en) 2007-01-10 2013-06-04 Aerie Pharmaceuticals, Inc. 6-aminoisoquinoline compounds
PT2155747E (pt) * 2007-05-10 2012-12-19 Ge Healthcare Ltd Imidazol(1,2-a)piridinas e compostos relacionados com actividade nos receptores de canabinóides cb2
EP2003125A1 (de) * 2007-06-14 2008-12-17 Total Petrochemicals Research Feluy Neue Tridentat-Ligandverbindungen mit Iminofuraneinheiten, Verfahren zur Herstellung dieser Verbindungen und ihre Verwendung bei der Herstellung von Katalysatoren zur Homopolymerisation und Copolymerisation von Ethylen und Alpha-Olefinen
US9006283B2 (en) 2007-07-12 2015-04-14 Acumen Pharmaceuticals, Inc. Methods of modifying amyloid β oligomers using non-peptidic compounds
WO2009009768A2 (en) * 2007-07-12 2009-01-15 Acumen Pharmaceuticals, Inc. METHODS OF INHIBITING THE FORMATION OF AMYLOID-β DIFFUSABLE LIGANDS USING A ACYLHYDRAZIDE COMPOUDS
US8962677B2 (en) * 2007-07-12 2015-02-24 Acumen Pharmaceuticals, Inc. Methods of restoring cognitive ability using non-peptidic compounds
WO2009011910A2 (en) * 2007-07-18 2009-01-22 Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Serices Imidazolidinone compounds, methods to inhibit deubiquitination and methods of treatment
JP2011502998A (ja) * 2007-11-01 2011-01-27 ザ ユーエイビー リサーチ ファウンデイション ウイルス感染の治療および予防
US8455514B2 (en) 2008-01-17 2013-06-04 Aerie Pharmaceuticals, Inc. 6-and 7-amino isoquinoline compounds and methods for making and using the same
FR2926463B1 (fr) * 2008-01-22 2010-08-13 Centre Nat Rech Scient Utilisation d'inhibiteurs d'aminopeptidase ou de composes azaindole pour la prevention ou le traitement de metastases cancereuses d'origine epitheliale
TWI490214B (zh) 2008-05-30 2015-07-01 艾德克 上野股份有限公司 苯或噻吩衍生物及該等作為vap-1抑制劑之用途
KR101783004B1 (ko) 2008-07-08 2017-09-28 인사이트 홀딩스 코포레이션 인돌아민 2,3-디옥시게나아제의 억제제로서의 1,2,5-옥사디아졸
WO2010075561A1 (en) * 2008-12-23 2010-07-01 President And Fellows Of Harvard College Small molecule inhibitors of necroptosis
WO2010072807A2 (en) * 2008-12-23 2010-07-01 Fondation Jerome Lejeune Inhibitors of cystathionine beta synthase to reduce the neurotoxic overproduction of endogenous hydrogen sulfide
WO2010080183A1 (en) 2009-01-08 2010-07-15 The Trustees Of Columbia University In The City Of New York Potent non-urea inhibitors of soluble epoxide hydrolase
WO2010101246A1 (ja) 2009-03-05 2010-09-10 塩野義製薬株式会社 Npy y5受容体拮抗作用を有するピペリジンおよびピロリジン誘導体
ES2665277T3 (es) * 2009-03-13 2018-04-25 Katholieke Universiteit Leuven K.U. Leuven R&D Análogos de purina y su uso como agentes inmunosupresores
US20100248365A1 (en) * 2009-03-27 2010-09-30 Zacharon Pharmaceuticals, Inc. Ganglioside biosynthesis modulators
WO2010126002A1 (ja) * 2009-04-28 2010-11-04 塩野義製薬株式会社 ヘテロ環スルホンアミド化合物を含有する医薬
CA2929545C (en) 2009-05-01 2019-04-09 Aerie Pharmaceuticals, Inc. Dual mechanism inhibitors for the treatment of disease
WO2011006158A2 (en) * 2009-07-10 2011-01-13 University Of Maryland, Baltimore Targeting nad biosynthesis in bacterial pathogens
WO2011069039A1 (en) 2009-12-04 2011-06-09 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
US8242282B2 (en) * 2010-05-18 2012-08-14 Taipei Medical University Histone deacetylase inhibitors
TWI457323B (zh) * 2010-05-19 2014-10-21 Univ Taipei Medical 組織蛋白去乙醯酶抑制劑
CN102267923B (zh) * 2010-06-04 2015-07-15 台北医学大学 组蛋白去乙酰化酶抑制剂
US9255088B2 (en) 2010-08-11 2016-02-09 The Regents Of The University Of California Premature-termination-codons readthrough compounds
CN102631664B (zh) * 2011-01-28 2014-10-01 上海来益生物药物研究开发中心有限责任公司 3-氨基-2-羟基-4-苯基-缬氨酰-异亮氨酸的应用
WO2013142346A1 (en) 2012-03-23 2013-09-26 The Regents Of The University Of California Premature-termination-codons readthrough compounds
ES2779748T3 (es) 2012-08-23 2020-08-19 Janssen Biopharma Inc Compuestos para el tratamiento de infecciones víricas por paramixovirus
US9617217B2 (en) * 2013-02-26 2017-04-11 Microbial Chemistry Research Foundation Compound, production method therefor, and use of said compound
EA030611B1 (ru) 2013-03-15 2018-08-31 Кэнсер Рисерч Текнолоджи, Ллк Способы и композиции для модуляции гамма-глутамилового цикла
JP2016514693A (ja) 2013-03-15 2016-05-23 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 ハイブリッド型ネクロトーシス阻害剤
ES2526580B1 (es) * 2013-07-08 2015-10-23 Consejo Superior De Investigaciones Científicas (Csic) Uso de un compuesto de fórmula (I) como bactericida frente a Streptococcus
AU2014308991B2 (en) 2013-08-21 2019-02-14 Janssen Biopharma, Inc. Antiviral compounds
CR20190351A (es) 2013-11-08 2019-10-07 Incyte Holdings Corp PROCESO PARA LA SINTESIS DE UN INHIBIDOR DE INDOLAMINA 2,3-DIOXIGENASA (Divisional 2016-0252)
GB201321749D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic agents
US10653672B2 (en) 2014-02-07 2020-05-19 National University Corporation Tokyo Medical And Dental University Myogenesis promotor, muscle atrophy inhibitor, medical composition and TAZ activator
JP2017518312A (ja) * 2014-06-05 2017-07-06 ユニバーシティ・オブ・カンザス マルメリン類似体および癌治療における使用方法
JP2018502157A (ja) * 2015-01-12 2018-01-25 レビバ ファーマシューティカルズ,インコーポレイティド アルツハイマー病の治療方法
WO2016115150A1 (en) * 2015-01-12 2016-07-21 Reviva Pharmaceuticals Inc. Methods for treating psychosis associated with parkinson's disease
MA41614A (fr) 2015-02-25 2018-01-02 Alios Biopharma Inc Composés antiviraux
EP3108883A1 (de) * 2015-06-22 2016-12-28 Fundació Institut de Recerca Biomèdica de Bellvitge Therapeutische verwendungen von nicht-peptidischen hemmern des calcineurin-nfat-signalwegs
US9643927B1 (en) 2015-11-17 2017-05-09 Aerie Pharmaceuticals, Inc. Process for the preparation of kinase inhibitors and intermediates thereof
JP6832946B2 (ja) 2015-11-17 2021-02-24 アエリエ ファーマシューティカルズ インコーポレイテッド キナーゼ阻害剤およびその中間体の調製方法
JP6752888B2 (ja) * 2015-12-07 2020-09-09 ヒノバ ファーマシューティカルズ インコーポレイテッド キノリン系化合物とその調製方法および尿酸トランスポータ阻害剤類薬物としての使用
US11084807B2 (en) 2016-08-18 2021-08-10 Vidac Pharama Ltd. Piperazine derivatives, pharmaceutical compositions and methods of use thereof
CN106496108B (zh) * 2016-11-01 2019-05-31 上海应用技术大学 具有抗肿瘤活性的酰胺类化合物及其应用
CN110506037A (zh) 2017-03-31 2019-11-26 爱瑞制药公司 芳基环丙基-氨基-异喹啉酰胺化合物
US10471045B2 (en) * 2017-07-21 2019-11-12 The University Of Hong Kong Compounds and methods for the treatment of microbial infections
US11474098B2 (en) 2017-12-22 2022-10-18 The Trustees Of Columbia University In The City Of New York Drug target for preventing pathologic calcium overload in cardiomyocytes and methods of screening for same
AU2019337703B2 (en) 2018-09-14 2023-02-02 Aerie Pharmaceuticals, Inc. Aryl cyclopropyl-amino-isoquinolinyl amide compounds
EP3858342A1 (de) * 2018-09-27 2021-08-04 Consejo Superior de Investigaciones Científicas (CSIC) Acylhydrazone zur behandlung von neurologischen erkrankungen
CN111249283A (zh) * 2018-11-30 2020-06-09 四川大学 具有抗癌作用的嘧啶衍生物
KR20210112316A (ko) * 2019-01-04 2021-09-14 벨부르크 랩스, 엘엘씨 치료제로서의 cgas 활성 억제제
WO2020206109A1 (en) * 2019-04-02 2020-10-08 The University Of Chicago Remodilins for airway remodeling and organ fibrosis
CN113750088A (zh) * 2021-09-16 2021-12-07 中国人民解放军海军特色医学中心 杂环化合物在制备治疗溃疡性结肠炎药物中的应用

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001089569A1 (de) * 2000-05-23 2001-11-29 Institut Für Medizintechnologie Magdeburg Gmbh Imtm Kombinationen von enzyminhibitoren umfassende zubereitungen und deren verwendung

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5639794A (en) * 1995-06-07 1997-06-17 Proguard, Inc. Use of saponin in methods and compositions for pathogen control
DE19823831A1 (de) * 1998-05-28 1999-12-02 Probiodrug Ges Fuer Arzneim Neue pharmazeutische Verwendung von Isoleucyl Thiazolidid und seinen Salzen
CA2436724C (en) * 2001-01-02 2010-03-16 Siegfried Ansorge Use of inhibitors of dipeptidyl peptidase iv (dp iv) in combination with inhibitors of alanyl-aminopeptidase (apn)
DE10100053A1 (de) * 2001-01-02 2002-08-22 Keyneurotek Ag I G Verwendung von Enzyminhibitoren der Dipeptidylpeptidase IV sowie der Aminopeptidase N und pharmazeutischen Zubereitungen daraus zur Prävention und/oder Therapie Ischämie-bedingter akuter und chronischer neurodegenerativer Prozesse und Erkrankungen
PT1368349E (pt) * 2001-02-24 2007-04-30 Boehringer Ingelheim Pharma Derivados de xantina, sua preparação e sua utilização como medicamento
GB0125446D0 (en) * 2001-10-23 2001-12-12 Ferring Bv Novel anti-diabetic agents
JP4771661B2 (ja) * 2001-11-26 2011-09-14 トラスティーズ オブ タフツ カレッジ Post−プロリン開裂酵素の擬ペプチド性阻害剤
DE10211555A1 (de) * 2002-03-15 2003-10-02 Imtm Inst Fuer Medizintechnolo Verwendung der Inhibitoren von Enzymen mit Aktivitäten der Aminopeptidase N und/oder der Dipeptidylpeptidase IV und pharmazeutischen Zubereitungen daraus zur Therapie und Prävention dermatologischer Erkrankungen mit sebozytärer Hyperproliferation und veränderten Differenzierungszuständen
DE10230381A1 (de) * 2002-07-05 2004-01-22 Institut für Medizintechnologie Magdeburg GmbH, IMTM Verwendung von Inhibitoren der Alanyl-Aminopeptidasen und diese umfassende pharmazeutischen Zubereitungen
US7482337B2 (en) * 2002-11-08 2009-01-27 Boehringer Ingelheim Pharma Gmbh & Co. Kg Xanthine derivatives, the preparation thereof and their use as pharmaceutical compositions
DE10337074A1 (de) * 2003-08-12 2005-03-17 Keyneurotek Ag Verwendung der Inhibitoren von Enzymen mit Aktivitäten der Aminopeptidase N und/oder der Dipeptidylpeptidase IV und pharmazeutischen Zubereitungen daraus zur Therapie und Prävention von chronischen neurodegenerativen Erkrankungen

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001089569A1 (de) * 2000-05-23 2001-11-29 Institut Für Medizintechnologie Magdeburg Gmbh Imtm Kombinationen von enzyminhibitoren umfassende zubereitungen und deren verwendung

Non-Patent Citations (9)

* Cited by examiner, † Cited by third party
Title
BULL. ACAD. POLON. SCI. SER. SCI., CHIM., GEOL. ET GEOGRAPH. , (6), 235-8, 1958 *
DATABASE BEILSTEIN XP002320599, Database accession no. 7444296 *
DATABASE BEILSTEIN XP002320600, Database accession no. 2121406 *
DATABASE CAPLUS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; ALK'EWICZ, J. ET AL: "Fungistatic activity of some hydroxamic acids", XP002320602, retrieved from STN Database accession no. 1958:56723 *
DATABASE CAPLUS [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; ECKSTEIN, Z. ET AL: "The fungistatic activity of 3,4-dichlorophenoxyacethydroxamic acid on pathogenic fungi in vitro", XP002320601, retrieved from STN Database accession no. 1958:94255 *
ECKSTEIN, URBANSKI, PRZEM. CHEM., vol. 35, 1956, pages 640 *
FUJII, HIDEJI ET AL., BIOL. PHARM. BULL., vol. 19, no. 1, 1996, pages 6 - 10 *
NAGAI, MACHIKO ET AL., J. ANTIBIOT., vol. 50, no. 1, 1997, pages 82 - 84 *
NATURE (LONDON, UNITED KINGDOM) , 180, 1204-5 CODEN: NATUAS; ISSN: 0028-0836, 1957 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9217024B2 (en) 2007-12-18 2015-12-22 Acumen Pharmaceuticals, Inc. ADDL receptor polypeptides, polynucleotides and host cells for recombinant production
US9512101B2 (en) 2008-07-25 2016-12-06 Aerie Pharmaceuticals, Inc. Beta- and gamma-amino-isoquinoline amide compounds and substituted benzamide compounds
US9415043B2 (en) 2013-03-15 2016-08-16 Aerie Pharmaceuticals, Inc. Combination therapy
US11590123B2 (en) 2016-08-31 2023-02-28 Aerie Pharmaceuticals, Inc. Ophthalmic compositions

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