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 PDFInfo
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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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Abstract
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 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2005037257A2 WO2005037257A2 (de) | 2005-04-28 |
WO2005037257A3 true WO2005037257A3 (de) | 2006-09-14 |
Family
ID=34441990
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP2004/011643 WO2005037257A2 (de) | 2003-10-15 | 2004-10-15 | Neue alanyl-aminopeptidasen-inhibitoren zur funktionellen beeinflussung unterschiedlicher zellen und zur behandlung immunologischer, entzündlicher, neuronaler und anderer erkrankungen |
Country Status (8)
Country | Link |
---|---|
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)
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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 |
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Publication number | Priority date | Publication date | Assignee | Title |
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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 |
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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 |
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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 |
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US11084807B2 (en) | 2016-08-18 | 2021-08-10 | Vidac Pharama Ltd. | Piperazine derivatives, pharmaceutical compositions and methods of use thereof |
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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)
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)
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 |
-
2003
- 2003-10-15 DE DE10348023A patent/DE10348023A1/de not_active Ceased
-
2004
- 2004-10-15 US US10/575,882 patent/US20070037752A1/en not_active Abandoned
- 2004-10-15 AU AU2004281536A patent/AU2004281536B9/en not_active Ceased
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- 2004-10-15 EP EP04790485A patent/EP1673075A2/de not_active Withdrawn
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Patent Citations (1)
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)
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 * |
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AU2004281536B2 (en) | 2009-07-09 |
WO2005037257A2 (de) | 2005-04-28 |
US20070037752A1 (en) | 2007-02-15 |
DE10348023A1 (de) | 2005-05-19 |
CA2542723A1 (en) | 2005-04-28 |
AU2004281536B9 (en) | 2009-10-08 |
AU2004281536A1 (en) | 2005-04-28 |
JP2007508349A (ja) | 2007-04-05 |
EP1673075A2 (de) | 2006-06-28 |
CN1897928A (zh) | 2007-01-17 |
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