JP2002517245A - 治療的および診断的ドメイン1β2GPIポリペプチドおよびその使用の方法 - Google Patents
治療的および診断的ドメイン1β2GPIポリペプチドおよびその使用の方法Info
- Publication number
- JP2002517245A JP2002517245A JP2000553585A JP2000553585A JP2002517245A JP 2002517245 A JP2002517245 A JP 2002517245A JP 2000553585 A JP2000553585 A JP 2000553585A JP 2000553585 A JP2000553585 A JP 2000553585A JP 2002517245 A JP2002517245 A JP 2002517245A
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- Prior art keywords
- gpi
- polypeptide
- domain
- antibody
- conjugate
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Classifications
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- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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- A61K47/50—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
- A61K47/51—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
- A61K47/56—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
- A61K47/59—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes
- A61K47/60—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
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- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4713—Autoimmune diseases, e.g. Insulin-dependent diabetes mellitus, multiple sclerosis, rheumathoid arthritis, systemic lupus erythematosus; Autoantigens
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/775—Apolipopeptides
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Peptides Or Proteins (AREA)
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- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Magnetic Resonance Imaging Apparatus (AREA)
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Applications Claiming Priority (7)
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| US8865698P | 1998-06-09 | 1998-06-09 | |
| US60/088,656 | 1998-06-09 | ||
| US10308898P | 1998-10-05 | 1998-10-05 | |
| US60/103,088 | 1998-10-05 | ||
| US09/328,199 | 1999-06-08 | ||
| US09/328,199 US6858210B1 (en) | 1998-06-09 | 1999-06-08 | Therapeutic and diagnostic domain 1 β2GPI polypeptides and methods of using same |
| PCT/US1999/013194 WO1999064595A1 (en) | 1998-06-09 | 1999-06-09 | THERAPEUTIC AND DIAGNOSTIC DOMAIN 1 β2GPI POLYPEPTIDES AND METHODS OF USING SAME |
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| JP2002517245A true JP2002517245A (ja) | 2002-06-18 |
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| US (2) | US6858210B1 (enExample) |
| EP (1) | EP1092027B1 (enExample) |
| JP (1) | JP2002517245A (enExample) |
| KR (1) | KR20010052713A (enExample) |
| CN (1) | CN1310759A (enExample) |
| AT (1) | ATE346922T1 (enExample) |
| AU (1) | AU772851B2 (enExample) |
| CA (1) | CA2329942A1 (enExample) |
| DE (1) | DE69934228T2 (enExample) |
| ES (1) | ES2275348T3 (enExample) |
| PT (1) | PT1092027E (enExample) |
| WO (1) | WO1999064595A1 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006507232A (ja) * | 2002-07-19 | 2006-03-02 | ザ ジェネラル ホスピタル コーポレイション | オキシム結合体、およびそれらの形成および用途 |
| JP2007535468A (ja) * | 2003-03-07 | 2007-12-06 | カーテーベー トゥモーアフォルシュングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | タンパク質結合性のドキソルビシン−ペプチド−誘導体 |
| JP2025532422A (ja) * | 2022-10-10 | 2025-09-29 | 深▲せん▼市迪克曼生物科技有限公司 | 新規なセラミド、その調製方法及び使用 |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5268454A (en) * | 1991-02-08 | 1993-12-07 | La Jolla Pharmaceutical Company | Composition for inducing humoral anergy to an immunogen comprising a t cell epitope-deficient analog of the immunogen conjugated to a nonimmunogenic carrier |
| KR100361933B1 (ko) * | 1993-09-08 | 2003-02-14 | 라 졸라 파마슈티칼 컴파니 | 화학적으로정의된비중합성결합가플랫폼분자및그것의콘주게이트 |
| US6858210B1 (en) | 1998-06-09 | 2005-02-22 | La Jolla Pharmaceutical Co. | Therapeutic and diagnostic domain 1 β2GPI polypeptides and methods of using same |
| US6458953B1 (en) | 1998-12-09 | 2002-10-01 | La Jolla Pharmaceutical Company | Valency platform molecules comprising carbamate linkages |
| US6399578B1 (en) | 1998-12-09 | 2002-06-04 | La Jolla Pharmaceutical Company | Conjugates comprising galactose α1,3 galactosyl epitopes and methods of using same |
| KR20020022691A (ko) * | 1999-06-08 | 2002-03-27 | 와이즈먼 앤드루 | 아미노옥시기를 포함하는 원자가 플랫폼 분자 |
| JP2003505519A (ja) * | 1999-07-29 | 2003-02-12 | エピックス メディカル, インコーポレイテッド | 多座結合を介した多量体画像化剤の標的化 |
| HK1045944A1 (zh) | 1999-11-28 | 2002-12-20 | La Jolla Pharmaceutical Company | 基於抗体亲和力的狼疮治疗方法和筛选方法及用於其的组合物 |
| CA2414076A1 (en) * | 2000-06-08 | 2001-12-13 | La Jolla Pharmaceutical Company | Multivalent platform molecules comprising high molecular weight polyethylene oxide |
| DK1360207T3 (da) * | 2000-12-13 | 2011-09-05 | Bac Ip B V | Proteinarray af variable domæner af tunge immunoglobulinkæder fra kameler |
| TWI221406B (en) | 2001-07-30 | 2004-10-01 | Epix Medical Inc | Systems and methods for targeted magnetic resonance imaging of the vascular system |
| US20030114405A1 (en) * | 2001-08-13 | 2003-06-19 | Linnik Matthew D. | Methods of treating systemic lupus erythematosus in individuals having significantly impaired renal function |
| US20040208864A1 (en) * | 2002-12-27 | 2004-10-21 | Vibeke Strand | Methods of improving health-related quality of life in individuals with systemic lupus erythematosus |
| US20040258683A1 (en) * | 2003-03-30 | 2004-12-23 | Linnik Matthew D. | Methods of treating and monitoring systemic lupus erythematosus in individuals |
| SG158919A1 (en) * | 2005-01-24 | 2010-02-26 | Univ Texas | Constructs binding to phosphatidylserine and their use in disease treatment |
| WO2006113720A2 (en) | 2005-04-18 | 2006-10-26 | Bio-Rad Laboratories, Inc. | Solid phase immobilization of phospholipids and cofactor proteins via covalent attachment |
| US20100021379A1 (en) * | 2006-06-29 | 2010-01-28 | The Regents Of The University Of California | Chemical Antibodies for Immunotherapy and Imaging |
| US20080015145A1 (en) * | 2006-07-11 | 2008-01-17 | Maria Gyongyossy-Issa | Mimotope receptors and inhibitors for platelet-platelet and platelet-endothelium interactions |
| AU2009335585B2 (en) * | 2009-01-02 | 2013-09-19 | Flysun Development Co. Ltd | Synthetic peptides, methods and kits for diagnosing autoimmune diseases |
| WO2011163572A2 (en) * | 2010-06-24 | 2011-12-29 | University Of Kansas | Bifunctional conjugate compositions and associated methods |
| CN105273080A (zh) * | 2014-07-14 | 2016-01-27 | 于珮 | 一种还原型β2-糖蛋白Ⅰ的制备方法 |
| US10098960B2 (en) | 2015-04-03 | 2018-10-16 | Ucl Business Plc | Polymer conjugate |
| TWI572617B (zh) * | 2016-01-20 | 2017-03-01 | 國立陽明大學 | 重組β-醣蛋白胜肽及其於抗腫瘤之應用 |
| CN105801694A (zh) * | 2016-05-03 | 2016-07-27 | 上海科新生物技术股份有限公司 | 一种抗心磷脂/β2糖蛋白I复合物的嵌合抗体 |
| WO2019028336A1 (en) * | 2017-08-03 | 2019-02-07 | The Cleveland Clinic Foundation | IMPROVED PEPTIDE EXPRESSION AND ANTIBODY DETECTION OF APO-H SPECIFIC SUBJECT |
| EP4308602A1 (en) * | 2021-03-18 | 2024-01-24 | Université de Genève | Peptides and use thereof for diagnosing and treating antiphospholipid syndrome |
Family Cites Families (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4191668A (en) | 1977-02-03 | 1980-03-04 | Scripps Clinic And Research Foundation | Induction of immunological tolerance |
| US5126131A (en) | 1983-01-24 | 1992-06-30 | The Johns Hopkins University | Therapeutic suppression of specific immune responses by administration of antigen-competitive conjugates. |
| US5370871A (en) | 1983-01-24 | 1994-12-06 | The Johns Hopkins University | Therapeutic suppression of specific immune responses by administration of oligomeric forms of antigen of controlled chemistry |
| US6022544A (en) | 1983-01-24 | 2000-02-08 | The John Hopkins University | Therapeutic suppression of specific immune responses by administration of oligomeric forms of antigen of controlled chemistry |
| US4650675A (en) | 1983-08-18 | 1987-03-17 | The Children's Medical Center Corporation | Oligonucleotide conjugates |
| US4751181A (en) | 1984-12-31 | 1988-06-14 | Duke University | Methods and compositions useful in the diagnosis and treatment of autoimmune diseases |
| DE3676670D1 (de) | 1985-06-26 | 1991-02-07 | Cetus Corp | Solubilisierung von proteinen fuer pharmazeutische zusammensetzungen mittels polymerkonjugierung. |
| US4904582A (en) | 1987-06-11 | 1990-02-27 | Synthetic Genetics | Novel amphiphilic nucleic acid conjugates |
| AU633488B2 (en) | 1988-04-04 | 1993-02-04 | Northwestern University | Binding of immune complexes by modified forms of c-reactive protein |
| EP0450099B1 (en) | 1989-10-19 | 1996-09-11 | Yamasa Shoyu Kabushiki Kaisha | Carrier for binding antiphospholipid antibody, immunoassay using the same, and kit therefor |
| US5552391A (en) | 1990-01-16 | 1996-09-03 | La Jolla Pharmaceutical Company | Chemically-defined non-polymeric valency platform molecules and conjugates thereof |
| US5268454A (en) | 1991-02-08 | 1993-12-07 | La Jolla Pharmaceutical Company | Composition for inducing humoral anergy to an immunogen comprising a t cell epitope-deficient analog of the immunogen conjugated to a nonimmunogenic carrier |
| US5162515A (en) | 1990-01-16 | 1992-11-10 | La Jolla Pharmaceutical Company | Conjugates of biologically stable polymers and polynucleotides for treating systemic lupus erythematosus |
| JPH04218000A (ja) | 1990-02-13 | 1992-08-07 | Kirin Amgen Inc | 修飾ポリペプチド |
| US5498538A (en) | 1990-02-15 | 1996-03-12 | The University Of North Carolina At Chapel Hill | Totally synthetic affinity reagents |
| WO1991015772A1 (en) | 1990-04-06 | 1991-10-17 | Yamasa Shoyu Co. Ltd. | Methods for determining phospholipids and antibodies thereof |
| CA2098281A1 (en) | 1990-12-17 | 1992-06-18 | Howard M. Dintzis | Suppression of immune responses of oligomeric forms of antigen of controlled chemistry |
| WO1993002093A1 (en) | 1991-07-15 | 1993-02-04 | La Jolla Pharmaceutical Company | Modified phosphorous intermediates for providing functional groups on the 5' end of oligonucleotides |
| DE69322842T2 (de) | 1992-02-05 | 1999-05-20 | Koike, Takao, Sapporo, Hokkaido | Festphasenreagenz und selbiges verwendendes antikörpertestverfahren |
| FR2701263B1 (fr) | 1993-02-09 | 1995-04-21 | Elie Stefas | Procédé d'obtention d'une composition aqueuse protéinique, composition correspondante, glycoprotéine contenue et son utilisation pour la stabilisation de l'albumine et la détection ou le dosage d'anticorps. |
| ATE359830T1 (de) | 1993-09-08 | 2007-05-15 | Jolla Pharma | Chemisch definierten nicht-polymer wertigen plattformmolokülen und ihren konjugaten |
| US5998223A (en) * | 1993-11-16 | 1999-12-07 | Yamasa Corporation | Method of assaying autoimmune anticardiolipin antibody and kit therefor |
| FR2722991B1 (fr) | 1994-08-01 | 1996-10-11 | Orstom | Utilisation de la beta2-glycoproteine i sous au moins une de ses formes comme agent anti-infectueux et composition pharmaceutique corrrespondante |
| JPH08333390A (ja) | 1995-04-07 | 1996-12-17 | Hoechst Japan Ltd | ペプチド及びそれからなる自己免疫疾患治療剤 |
| US5874409A (en) | 1995-06-07 | 1999-02-23 | La Jolla Pharmaceutical Company | APL immunoreactive peptides, conjugates thereof and methods of treatment for APL antibody-mediated pathologies |
| US5780319A (en) | 1996-04-19 | 1998-07-14 | Pasteur Sanofi Diagnostics | Immunoassays to detect antiphospholipid antibodies |
| EP0954531A1 (en) | 1996-06-06 | 1999-11-10 | Lajolla Pharmaceutical Company | aPL IMMUNOREACTIVE PEPTIDES, CONJUGATES THEREOF AND METHODS OF TREATMENT FOR aPL ANTIBODY-MEDIATED PATHOLOGIES |
| DE19637770A1 (de) | 1996-09-16 | 1998-03-19 | Koenig & Bauer Albert Ag | Verfahren und Anlage zum automatischen Zu- und Abführen von Rollen |
| CA2271784A1 (en) | 1996-11-12 | 1998-05-22 | City Of Hope | Immuno-reactive peptide ctl epitopes of human cytomegalovirus |
| GB9805477D0 (en) | 1998-03-13 | 1998-05-13 | Oxford Glycosciences Limited | Methods and compositions for diagnosis of rheumatoid arthritis |
| US6858210B1 (en) | 1998-06-09 | 2005-02-22 | La Jolla Pharmaceutical Co. | Therapeutic and diagnostic domain 1 β2GPI polypeptides and methods of using same |
| IL125262A0 (en) | 1998-07-07 | 1999-03-12 | Yeda Res & Dev | Synthetic peptides and pharmaceutical compositions comprising them |
| IL126447A (en) | 1998-10-04 | 2004-09-27 | Vascular Biogenics Ltd | An immune preparation that confers tolerance in oral administration and its use in the prevention and / or treatment of atherosclerosis |
| US6458953B1 (en) | 1998-12-09 | 2002-10-01 | La Jolla Pharmaceutical Company | Valency platform molecules comprising carbamate linkages |
| AU5211200A (en) | 1999-05-04 | 2000-11-17 | Genethor Gmbh | Method for diminishing specific immune reactions |
| KR20020022691A (ko) | 1999-06-08 | 2002-03-27 | 와이즈먼 앤드루 | 아미노옥시기를 포함하는 원자가 플랫폼 분자 |
| AUPQ272699A0 (en) | 1999-09-09 | 1999-09-30 | Unisearch Limited | Use of beta2GPI in diagnostic tests for autoimmune diseases |
| HK1045944A1 (zh) | 1999-11-28 | 2002-12-20 | La Jolla Pharmaceutical Company | 基於抗体亲和力的狼疮治疗方法和筛选方法及用於其的组合物 |
| US20010051351A1 (en) | 2000-03-27 | 2001-12-13 | Racis Stanley Paul | Antigen-specific immune complex-based enzyme-linked immunosorbent assay |
| US20020150898A1 (en) | 2000-04-18 | 2002-10-17 | Tang Y. Tom | Novel nucleic acids and polypeptides |
| AU2001263006A1 (en) | 2000-05-18 | 2001-11-26 | Hyseq, Inc. | Novel nucleic acids and polypeptides |
| CA2414076A1 (en) | 2000-06-08 | 2001-12-13 | La Jolla Pharmaceutical Company | Multivalent platform molecules comprising high molecular weight polyethylene oxide |
| DE10048417A1 (de) | 2000-09-29 | 2002-04-11 | Roche Diagnostics Gmbh | Verbindungen mit verzweigtem Linker |
-
1999
- 1999-06-08 US US09/328,199 patent/US6858210B1/en not_active Expired - Lifetime
- 1999-06-09 ES ES99937843T patent/ES2275348T3/es not_active Expired - Lifetime
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- 1999-06-09 AU AU43395/99A patent/AU772851B2/en not_active Ceased
- 1999-06-09 EP EP99937843A patent/EP1092027B1/en not_active Expired - Lifetime
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- 1999-06-09 AT AT99937843T patent/ATE346922T1/de active
- 1999-06-09 DE DE69934228T patent/DE69934228T2/de not_active Expired - Lifetime
- 1999-06-09 CN CN99808415A patent/CN1310759A/zh active Pending
- 1999-06-09 CA CA002329942A patent/CA2329942A1/en not_active Abandoned
- 1999-06-09 KR KR1020007013980A patent/KR20010052713A/ko not_active Ceased
- 1999-06-09 WO PCT/US1999/013194 patent/WO1999064595A1/en not_active Ceased
-
2004
- 2004-07-30 US US10/903,058 patent/US20050004351A1/en not_active Abandoned
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006507232A (ja) * | 2002-07-19 | 2006-03-02 | ザ ジェネラル ホスピタル コーポレイション | オキシム結合体、およびそれらの形成および用途 |
| JP2011105773A (ja) * | 2002-07-19 | 2011-06-02 | General Hospital Corp | オキシム結合体、およびそれらの形成および使用のための方法 |
| JP2007535468A (ja) * | 2003-03-07 | 2007-12-06 | カーテーベー トゥモーアフォルシュングス ゲゼルシャフト ミット ベシュレンクテル ハフツング | タンパク質結合性のドキソルビシン−ペプチド−誘導体 |
| JP2025532422A (ja) * | 2022-10-10 | 2025-09-29 | 深▲せん▼市迪克曼生物科技有限公司 | 新規なセラミド、その調製方法及び使用 |
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| US20050004351A1 (en) | 2005-01-06 |
| WO1999064595A1 (en) | 1999-12-16 |
| CA2329942A1 (en) | 1999-12-16 |
| DE69934228T2 (de) | 2007-10-04 |
| US6858210B1 (en) | 2005-02-22 |
| ATE346922T1 (de) | 2006-12-15 |
| EP1092027B1 (en) | 2006-11-29 |
| AU4339599A (en) | 1999-12-30 |
| PT1092027E (pt) | 2007-02-28 |
| EP1092027A1 (en) | 2001-04-18 |
| ES2275348T3 (es) | 2007-06-01 |
| DE69934228D1 (de) | 2007-01-11 |
| WO1999064595A9 (en) | 2000-09-08 |
| KR20010052713A (ko) | 2001-06-25 |
| CN1310759A (zh) | 2001-08-29 |
| AU772851B2 (en) | 2004-05-06 |
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