JP2013532126A - クロロトキシン変異体、コンジュゲート、およびそれらを使用する方法 - Google Patents
クロロトキシン変異体、コンジュゲート、およびそれらを使用する方法 Download PDFInfo
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- JP2013532126A JP2013532126A JP2013510087A JP2013510087A JP2013532126A JP 2013532126 A JP2013532126 A JP 2013532126A JP 2013510087 A JP2013510087 A JP 2013510087A JP 2013510087 A JP2013510087 A JP 2013510087A JP 2013532126 A JP2013532126 A JP 2013532126A
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- Prior art keywords
- chlorotoxin
- modified
- peptide
- modified chlorotoxin
- imaging
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Cited By (4)
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| JP2013518905A (ja) * | 2010-02-04 | 2013-05-23 | モルフォテック, インコーポレイテッド | クロロトキシンポリペプチドおよびコンジュゲートならびにその使用 |
| JP2016534147A (ja) * | 2013-09-17 | 2016-11-04 | ブレイズ バイオサイエンス, インコーポレイテッド | クロロトキシンコンジュゲート及びその使用方法 |
| CN109963597A (zh) * | 2016-11-10 | 2019-07-02 | 北京普罗吉生物科技发展有限公司 | 聚乙二醇化血管内皮抑制素类似物及其应用 |
| US12048732B2 (en) | 2016-04-15 | 2024-07-30 | Blaze Bioscience, Inc. | Methods of treating breast cancer |
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| ES2360519T3 (es) | 2005-04-22 | 2011-06-06 | University Of Washington | Conjugado de cianina-clorotoxina y procedimiento para la visualización intraquirúrgica del cáncer. |
| AU2009205950C1 (en) | 2008-01-18 | 2015-08-06 | Visen Medical, Inc. | Fluorescent imaging agents |
| BRPI0912683A2 (pt) | 2008-05-15 | 2016-01-26 | Transmolecular Inc | tratamento de tumores metastáticos |
| WO2011142858A2 (en) | 2010-05-11 | 2011-11-17 | Fred Hutchinson Cancer Research Center | Chlorotoxin variants, conjugates, and methods for their use |
| CN102688496B (zh) * | 2012-01-15 | 2013-12-11 | 河南科技大学 | 一种ctx介导的靶向纳米载体及纳米载药体系 |
| US20140179560A1 (en) | 2012-12-10 | 2014-06-26 | Fred Hutchinson Cancer Research Center | Drug discovery methods and platforms |
| US9784730B2 (en) | 2013-03-21 | 2017-10-10 | University Of Washington Through Its Center For Commercialization | Nanoparticle for targeting brain tumors and delivery of O6-benzylguanine |
| US11559580B1 (en) * | 2013-09-17 | 2023-01-24 | Blaze Bioscience, Inc. | Tissue-homing peptide conjugates and methods of use thereof |
| WO2015187651A1 (en) | 2014-06-02 | 2015-12-10 | Li-Cor, Inc. | Therapeutic and diagnostic probes |
| BR112017027985A2 (pt) * | 2015-06-26 | 2018-08-28 | Hutchinson Fred Cancer Res | peptídeos terapêuticos e métodos de uso dos mesmos |
| CN108135970B (zh) | 2015-09-09 | 2023-09-01 | 弗莱德哈钦森癌症中心 | 软骨归巢肽 |
| EP3360066A1 (en) * | 2015-10-07 | 2018-08-15 | Genentech, Inc. | Systems and methods for predicting vitreal half-life of therapeutic agent-polymer conjugates |
| WO2017180789A2 (en) | 2016-04-12 | 2017-10-19 | Blaze Bioscience, Inc. | Methods of treatment using chlorotoxin conjugates |
| WO2018075993A1 (en) * | 2016-10-21 | 2018-04-26 | Da Zen Theranostics, Inc | Compounds and methods to sensitize cancer cells to tyrosine kinase inhibitors |
| CA3044682A1 (en) | 2016-12-02 | 2018-06-07 | University Of Southern California | Synthetic immune receptors and methods of use thereof |
| AU2018210157B2 (en) | 2017-01-18 | 2022-10-06 | Fred Hutchinson Cancer Center | Peptide compositions and methods of use thereof for disrupting TEAD interactions |
| EP3595699A4 (en) | 2017-03-16 | 2020-12-23 | Blaze Bioscience, Inc. | PEPTIDIC CONJUGATES OF CARTILAGE ECOTROPISM AND THEIR METHODS OF USE |
| CA3064436A1 (en) | 2017-06-15 | 2018-12-20 | Blaze Bioscience, Inc. | Renal-homing peptide conjugates and methods of use thereof |
| WO2019055840A1 (en) | 2017-09-15 | 2019-03-21 | Eisai Inc. | CHLOROTOXIN AGENTS AND USES THEREOF |
| AU2018388583A1 (en) | 2017-12-19 | 2020-06-11 | Blaze Bioscience, Inc. | Tumor homing and cell penetrating peptide-immuno-oncology agent complexes and methods of use thereof |
| CA3148682A1 (en) * | 2019-12-19 | 2021-06-24 | Alan Cohen | Methods of treating vascular lesions and malformations |
| CA3203901A1 (en) | 2020-12-30 | 2022-07-07 | Sandor Farkas | Chlorotoxin derivatives and use thereof |
Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000009502A1 (en) * | 1998-08-12 | 2000-02-24 | Daiichi Pure Chemicals Co., Ltd. | Fluorescent labelling reagents |
| WO2006115633A2 (en) * | 2005-04-22 | 2006-11-02 | University Of Washington | Cyanine-chlorotoxin conjugate and method for intra-operative fluorescent visualization of cancer |
| JP2008538506A (ja) * | 2005-04-22 | 2008-10-30 | アムジエン・インコーポレーテツド | 延長された血液半減期を有するトキシンペプチド |
| US20090004105A1 (en) * | 2007-06-27 | 2009-01-01 | Zhen Cheng | Molecular imaging of matrix metalloproteinase expression using labeled chlorotoxin |
| WO2009114776A2 (en) * | 2008-03-14 | 2009-09-17 | Visen Medical, Inc. | Integrin targeting agents and methods of using same |
| WO2009133362A2 (en) * | 2008-04-29 | 2009-11-05 | Cambridge Enterprise Limited | Agents for detecting and imaging cell death |
| WO2009140599A1 (en) * | 2008-05-15 | 2009-11-19 | Transmolecular, Inc. | Treatment of metastatic tumors |
| JP2009280567A (ja) * | 2008-02-28 | 2009-12-03 | Kyoto Univ | 多点リン酸化ペプチド(タンパク)認識化合物、それを用いる検出方法 |
| JP2009300110A (ja) * | 2008-06-10 | 2009-12-24 | Olympus Corp | 移植細胞の光学的検出方法又はイメージング方法 |
| WO2010029760A1 (en) * | 2008-09-12 | 2010-03-18 | Nitto Denko Corporation | Imaging agents of fibrotic diseases |
| JP2010085108A (ja) * | 2008-09-29 | 2010-04-15 | Nano Factory:Kk | 生体光イメージング用プローブ |
| WO2011097533A1 (en) * | 2010-02-04 | 2011-08-11 | Transmolecular, Inc. | Chlorotoxin polypeptides and conjugates and uses thereof |
Family Cites Families (96)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4444744A (en) | 1980-03-03 | 1984-04-24 | Goldenberg Milton David | Tumor localization and therapy with labeled antibodies to cell surface antigens |
| DE3407582A1 (de) | 1984-03-01 | 1985-09-05 | Dornier System Gmbh, 7990 Friedrichshafen | Schaltungsanordnung fuer einen regelkreis |
| WO1988002117A1 (en) | 1986-09-19 | 1988-03-24 | Scripps Clinic And Research Foundation | Monoclonal paratopic molecule directed to human ganglioside gd2 |
| US5591829A (en) | 1987-05-29 | 1997-01-07 | Matsushita; Shuzo | Antibodies modified with toxic substance |
| US4904584A (en) * | 1987-12-23 | 1990-02-27 | Genetics Institute, Inc. | Site-specific homogeneous modification of polypeptides |
| US5051364A (en) | 1989-02-16 | 1991-09-24 | The Salk Institute For Biological Studies | Anti-lipocortin-I and anti-lipocortin-II monoclonal antibodies |
| DE3909799A1 (de) | 1989-03-24 | 1990-09-27 | Behringwerke Ag | Monoklonale antikoerper (mak) gegen tumorassoziierte antigene, ihre herstellung und verwendung |
| ATE135373T1 (de) | 1989-09-08 | 1996-03-15 | Univ Johns Hopkins | Modifikationen der struktur des egf-rezeptor-gens in menschlichen glioma |
| US5223253A (en) | 1989-09-28 | 1993-06-29 | American Home Products Corporation | Bovine vaccine compositions and method for preventing trichomonas infections using same |
| GB2250993B (en) | 1990-11-21 | 1995-02-15 | Inst Nat Sante Rech Med | Stromelysin-3 and its application in the diagnosis and treatment of malignant breast cancer |
| US5750376A (en) | 1991-07-08 | 1998-05-12 | Neurospheres Holdings Ltd. | In vitro growth and proliferation of genetically modified multipotent neural stem cells and their progeny |
| MX9205293A (es) | 1991-09-20 | 1993-05-01 | Syntex Sinergen Neuroscience J | Factores neurotrofico derivado del glial |
| US5314992A (en) | 1991-11-25 | 1994-05-24 | Trustees Of Dartmouth College | Lipocortin-1 receptor protein and its uses |
| WO1993023075A1 (en) | 1992-05-14 | 1993-11-25 | Oncologix, Inc. | Treatment of vascular leakage syndrome and collagenase induced disease by administration of matrix metalloproteinase inhibitors |
| AU5838494A (en) | 1993-01-14 | 1994-08-15 | Cancer Research Campaign Technology Limited | Potentiation of temozolomide in human tumour cells |
| US5626862A (en) | 1994-08-02 | 1997-05-06 | Massachusetts Institute Of Technology | Controlled local delivery of chemotherapeutic agents for treating solid tumors |
| US5688773A (en) | 1994-08-17 | 1997-11-18 | The General Hospital Corporation | Method of selectively destroying neoplastic cells |
| US5985822A (en) | 1994-12-09 | 1999-11-16 | The Scripps Research Institute | Inhibition of glial cell proliferation with N-CAM homophilic peptides |
| US5756340A (en) | 1995-05-08 | 1998-05-26 | The Regents Of The University Of California | Insect control with multiple toxins |
| JP3809502B2 (ja) | 1995-05-30 | 2006-08-16 | 二郎 有川 | ハンタウィルス抗原蛋白質およびモノクローナル抗体 |
| JPH0971599A (ja) | 1995-09-06 | 1997-03-18 | Nippon Seibutsu Kagaku Kenkyusho | 鶏貧血ウイルス(cav)感染鶏血清と高い反応性を示すポリペプチド及びこのポリペプチドに対する抗体、鶏貧血ウイルス感染の診断法及びワクチン |
| US6667156B2 (en) | 1995-12-27 | 2003-12-23 | Uab Research Foundation | Diagnosis and treatment of neuroectodermal tumors |
| US5905027A (en) | 1995-12-27 | 1999-05-18 | Uab Research Foundation | Method of diagnosing and treating gliomas |
| US6130101A (en) | 1997-09-23 | 2000-10-10 | Molecular Probes, Inc. | Sulfonated xanthene derivatives |
| NZ504938A (en) | 1997-12-05 | 2002-10-25 | Kyogo Itoh | Tumor antigen peptide derivatives capable of binding to HLA-A24 antigen |
| GB9809776D0 (en) | 1998-05-07 | 1998-07-08 | Nycomed Imaging As | Method |
| US6703381B1 (en) | 1998-08-14 | 2004-03-09 | Nobex Corporation | Methods for delivery therapeutic compounds across the blood-brain barrier |
| US6214986B1 (en) | 1998-10-07 | 2001-04-10 | Isis Pharmaceuticals, Inc. | Antisense modulation of bcl-x expression |
| SE9901387D0 (sv) | 1999-04-19 | 1999-04-19 | Astra Ab | New pharmaceutical foromaulations |
| US6849714B1 (en) | 1999-05-17 | 2005-02-01 | Conjuchem, Inc. | Protection of endogenous therapeutic peptides from peptidase activity through conjugation to blood components |
| JP2003509034A (ja) | 1999-09-14 | 2003-03-11 | バイオメディカル アフエレーゼ システム ゲーエムベーハー | 生化学活性を有する磁性ナノ粒子、その製造法と使用 |
| AU4305101A (en) | 1999-11-22 | 2001-06-04 | Research Foundation Of The State University Of New York, The | Magnetic nanoparticles for selective therapy |
| DE10020376A1 (de) | 2000-04-26 | 2001-11-08 | Inst Zelltechnologie E V | Dynamische Marker |
| CA2427858A1 (en) * | 2000-11-03 | 2002-05-10 | University Of Vermont And State Agricultural College | Compositions for inhibiting grb7 |
| US20020077921A1 (en) | 2000-12-15 | 2002-06-20 | Paul-David Morrison | Method and apparatus for an interactive catalog |
| US20040180846A1 (en) | 2001-03-01 | 2004-09-16 | Ruo-Pan Huang | Connexin enhances chemotherapy-induced apoptiosis in human cancer cells inhibiting tumor cell proliferation |
| WO2003008583A2 (en) | 2001-03-02 | 2003-01-30 | Sagres Discovery | Novel compositions and methods for cancer |
| US20030021810A1 (en) | 2001-06-26 | 2003-01-30 | Sontheimer Harald W. | Chlorotoxin inhibition of cell invasion, cancer metastasis, angiogenesis and tissue remodeling |
| WO2003029462A1 (en) | 2001-09-27 | 2003-04-10 | Pieris Proteolab Ag | Muteins of human neutrophil gelatinase-associated lipocalin and related proteins |
| US6972326B2 (en) | 2001-12-03 | 2005-12-06 | Molecular Probes, Inc. | Labeling of immobilized proteins using dipyrrometheneboron difluoride dyes |
| AU2003207835A1 (en) | 2002-02-04 | 2003-09-02 | Auburn University | Peptides for recognition and targeting of glial cell tumors |
| US20030232013A1 (en) | 2002-02-22 | 2003-12-18 | Gary Sieckman | Therapeutic and diagnostic targeting of cancers cells with tumor homing peptides |
| US20060088899A1 (en) | 2002-05-31 | 2006-04-27 | Alvarez Vernon L | Combination chemotherapy with chlorotoxin |
| WO2003101475A1 (en) * | 2002-05-31 | 2003-12-11 | Transmolecular Inc. | Treatment of cell proliferative disorders with chlorotoxin |
| US7560160B2 (en) | 2002-11-25 | 2009-07-14 | Materials Modification, Inc. | Multifunctional particulate material, fluid, and composition |
| US20040101822A1 (en) | 2002-11-26 | 2004-05-27 | Ulrich Wiesner | Fluorescent silica-based nanoparticles |
| KR20060031809A (ko) | 2003-06-09 | 2006-04-13 | 더 리젠츠 오브 더 유니버시티 오브 미시간 | 암 치료 및 진단용 조성물 및 방법 |
| DE10328251A1 (de) | 2003-06-24 | 2005-01-13 | Toximed Gmbh | Pharmazeutischer Wirkstoff |
| WO2005053611A2 (en) | 2003-11-26 | 2005-06-16 | Transmolecular, Inc. | Treatment of phosphatidylinositol phospholipid disorders |
| US20080153746A1 (en) * | 2004-04-06 | 2008-06-26 | Transmolecular, Inc. | Diagnosis and Treatment of Myeloid and Lymphoid Cell Cancers |
| JP2007532879A (ja) | 2004-04-06 | 2007-11-15 | トランスモレキュラー, インコーポレイテッド | 骨髄およびリンパ系細胞癌の診断および処置 |
| CA2565701A1 (en) | 2004-05-06 | 2005-11-17 | Jonathan M. Barasch | Ngal for reduction and amelioration of ischemic and nephrotoxic injuries |
| MX2007000728A (es) | 2004-07-21 | 2007-03-15 | Ambrx Inc | Polipeptidos biosinteticos que utilizan amino acidos no naturalmente codificados. |
| GB0422901D0 (en) | 2004-10-14 | 2004-11-17 | Ares Trading Sa | Lipocalin protein |
| KR100681763B1 (ko) | 2005-02-28 | 2007-02-15 | 재단법인 목암생명공학연구소 | 인간 리포칼린 2를 유효성분으로 포함하는 암 전이 억제용약학적 조성물, 이를 이용한 암 전이 억제 방법 |
| GB0504767D0 (en) | 2005-03-08 | 2005-04-13 | Ares Trading Sa | Lipocalin protein |
| US7462446B2 (en) | 2005-03-18 | 2008-12-09 | University Of Washington | Magnetic nanoparticle compositions and methods |
| US20070037232A1 (en) | 2005-03-31 | 2007-02-15 | Barasch Jonathan M | Detection of NGAL in chronic renal disease |
| JP2008535853A (ja) | 2005-04-07 | 2008-09-04 | ノバルティス ヴァクシンズ アンド ダイアグノスティクス インコーポレイテッド | 癌関連遺伝子 |
| US20060286089A1 (en) | 2005-04-08 | 2006-12-21 | Xcyte Therapies, Inc. | Compositions and methods for the treatment of burns and sepsis |
| JP4829969B2 (ja) | 2005-08-18 | 2011-12-07 | アンブルックス,インコーポレイテッド | tRNA組成物、およびその使用 |
| EP2147927A3 (en) | 2006-03-31 | 2010-09-01 | Transmolecular, Inc. | Use of 131i-tm-601 for the diagnosis and treatment of gliomas |
| US8106013B2 (en) | 2006-05-19 | 2012-01-31 | Georgia Tech Research Corporation | ABC transporter ligand GATX1 |
| CN101003788A (zh) | 2006-09-21 | 2007-07-25 | 武汉大学 | 一种蝎抗肿瘤转移肽及其制备方法和应用 |
| CN100564517C (zh) | 2006-09-21 | 2009-12-02 | 武汉大学 | 一种蝎抗神经胶质瘤肽及其制备方法和应用 |
| WO2008088422A2 (en) * | 2006-10-25 | 2008-07-24 | Amgen Inc. | Toxin peptide therapeutic agents |
| DE602008005596D1 (de) | 2007-06-21 | 2011-04-28 | Univ Muenchen Tech | Biologisch aktive proteine mit erhöhter in-vivo- und/oder in-vitro-stabilität |
| CA2696303A1 (en) | 2007-08-07 | 2009-02-12 | Transmolecular, Inc. | Chlorotoxins as drug carriers |
| WO2009029760A1 (en) | 2007-08-31 | 2009-03-05 | Iosemantics, Llc | Quality assurance tools for use with source code and a semantic model |
| CN101918041A (zh) | 2007-10-12 | 2010-12-15 | 超分子有限公司 | 用于肿瘤诊断和治疗的氯毒素剂的系统性给药 |
| US7904868B2 (en) | 2007-10-17 | 2011-03-08 | International Business Machines Corporation | Structures including means for lateral current carrying capability improvement in semiconductor devices |
| US20090176274A1 (en) | 2007-10-19 | 2009-07-09 | Abbott Laboratories | Glycosylated mammalian ngal and use thereof |
| US20090123946A1 (en) | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Immunoassays and kits for the detection of ngal |
| US20090123970A1 (en) | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Glycosylated mammalian ngal and use thereof |
| US20090124022A1 (en) | 2007-10-19 | 2009-05-14 | Abbott Laboratories | Antibodies that bind to mammalian ngal and uses thereof |
| CA2702590A1 (en) | 2007-10-19 | 2009-04-23 | Abbott Laboratories | Glycosylated mammalian ngal and use thereof |
| US20090269777A1 (en) | 2007-10-19 | 2009-10-29 | Abbott Laboratories | Immunoassays and kits for the detection of ngal |
| US8846036B2 (en) | 2007-10-19 | 2014-09-30 | Abbott Laboratories | Antibodies that bind to mammalian NGAL and uses thereof |
| US20100304413A1 (en) | 2007-11-15 | 2010-12-02 | Lars Otto Uttenthal | Diagnostic use of individual molecular forms of a biomarker |
| AU2009205950C1 (en) * | 2008-01-18 | 2015-08-06 | Visen Medical, Inc. | Fluorescent imaging agents |
| WO2009108762A2 (en) | 2008-02-26 | 2009-09-03 | The Penn State Research Foundation | Methods and compositions for treatment of retinoid-responsive conditions |
| CA2718854A1 (en) | 2008-03-20 | 2009-09-24 | Transmolecular, Inc. | Inhibition of angiogenesis |
| CN101270158B (zh) | 2008-04-30 | 2010-12-22 | 武汉大学 | 一种靶向抗神经胶质瘤蛋白及制备方法和用途 |
| EP2313430B1 (en) | 2008-06-24 | 2018-05-02 | Technische Universität München | Muteins of hngal and related proteins with affinity for a given target |
| US20100098637A1 (en) * | 2008-09-23 | 2010-04-22 | The Regents Of The University Of Michigan | Dye-loaded nanoparticle |
| CN101381405B (zh) | 2008-09-24 | 2011-07-27 | 武汉摩尔生物科技有限公司 | 基因工程肿瘤靶向kct-w1多肽及制备方法和用途 |
| US20100105150A1 (en) | 2008-10-24 | 2010-04-29 | Abbott Laboratories | Isolated human autoantibodies to neutrophil gelatinase-associated lipocalin (ngal) and methods and kits for the detection of human autoantibodies to ngal |
| US10191060B2 (en) | 2009-11-09 | 2019-01-29 | University Of Washington | Functionalized chromophoric polymer dots and bioconjugates thereof |
| CN101921769B (zh) | 2010-01-11 | 2012-07-25 | 山西大学 | 一种重组腺病毒及其制备方法和应用 |
| WO2011094671A2 (en) | 2010-01-29 | 2011-08-04 | The Uab Research Foundation | N-terminally conjugated polypeptides for targeted therapy and diagnosis |
| CN101824084A (zh) | 2010-04-08 | 2010-09-08 | 山西大学 | 靶向性抗胶质瘤蛋白质及其应用 |
| WO2011142858A2 (en) | 2010-05-11 | 2011-11-17 | Fred Hutchinson Cancer Research Center | Chlorotoxin variants, conjugates, and methods for their use |
| CA2808392C (en) | 2010-08-16 | 2020-03-10 | Pieris Ag | Binding proteins for hepcidin |
| US20140179560A1 (en) | 2012-12-10 | 2014-06-26 | Fred Hutchinson Cancer Research Center | Drug discovery methods and platforms |
| EP3442555A4 (en) * | 2016-04-15 | 2020-04-01 | Blaze Bioscience, Inc. | METHOD FOR TREATING BREAST CANCER |
| US12048732B2 (en) * | 2016-04-15 | 2024-07-30 | Blaze Bioscience, Inc. | Methods of treating breast cancer |
-
2011
- 2011-02-04 WO PCT/US2011/023797 patent/WO2011142858A2/en not_active Ceased
- 2011-02-04 KR KR1020127032307A patent/KR101972173B1/ko active Active
- 2011-02-04 CA CA2799169A patent/CA2799169C/en active Active
- 2011-02-04 EP EP11780950.9A patent/EP2569330B1/en active Active
- 2011-02-04 JP JP2013510087A patent/JP2013532126A/ja active Pending
- 2011-02-04 AU AU2011253424A patent/AU2011253424B2/en active Active
- 2011-02-04 CN CN201710180111.9A patent/CN106957356B/zh active Active
- 2011-02-04 CN CN201180031651.1A patent/CN103097403B/zh active Active
- 2011-02-04 ES ES16189999T patent/ES2811065T3/es active Active
- 2011-02-04 ES ES11780950.9T patent/ES2601182T3/es active Active
- 2011-02-04 EP EP16189999.2A patent/EP3165533B1/en active Active
-
2012
- 2012-11-08 IL IL222930A patent/IL222930B/en active IP Right Grant
- 2012-11-09 US US13/673,779 patent/US9944683B2/en active Active
-
2017
- 2017-02-10 JP JP2017023098A patent/JP6553105B2/ja active Active
-
2018
- 2018-03-02 US US15/911,017 patent/US10822381B2/en active Active
Patent Citations (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000009502A1 (en) * | 1998-08-12 | 2000-02-24 | Daiichi Pure Chemicals Co., Ltd. | Fluorescent labelling reagents |
| WO2006115633A2 (en) * | 2005-04-22 | 2006-11-02 | University Of Washington | Cyanine-chlorotoxin conjugate and method for intra-operative fluorescent visualization of cancer |
| JP2008538506A (ja) * | 2005-04-22 | 2008-10-30 | アムジエン・インコーポレーテツド | 延長された血液半減期を有するトキシンペプチド |
| US20090004105A1 (en) * | 2007-06-27 | 2009-01-01 | Zhen Cheng | Molecular imaging of matrix metalloproteinase expression using labeled chlorotoxin |
| JP2009280567A (ja) * | 2008-02-28 | 2009-12-03 | Kyoto Univ | 多点リン酸化ペプチド(タンパク)認識化合物、それを用いる検出方法 |
| WO2009114776A2 (en) * | 2008-03-14 | 2009-09-17 | Visen Medical, Inc. | Integrin targeting agents and methods of using same |
| WO2009133362A2 (en) * | 2008-04-29 | 2009-11-05 | Cambridge Enterprise Limited | Agents for detecting and imaging cell death |
| WO2009140599A1 (en) * | 2008-05-15 | 2009-11-19 | Transmolecular, Inc. | Treatment of metastatic tumors |
| JP2009300110A (ja) * | 2008-06-10 | 2009-12-24 | Olympus Corp | 移植細胞の光学的検出方法又はイメージング方法 |
| WO2010029760A1 (en) * | 2008-09-12 | 2010-03-18 | Nitto Denko Corporation | Imaging agents of fibrotic diseases |
| JP2010085108A (ja) * | 2008-09-29 | 2010-04-15 | Nano Factory:Kk | 生体光イメージング用プローブ |
| WO2011097533A1 (en) * | 2010-02-04 | 2011-08-11 | Transmolecular, Inc. | Chlorotoxin polypeptides and conjugates and uses thereof |
Non-Patent Citations (6)
| Title |
|---|
| JPN6015011611; Cancer Res., 2007, 67(14), pp.6882-6888 * |
| JPN6015011614; Nano Lett., 2005, 5(6), pp.1003-1008 * |
| JPN6015011617; Cancer Res., 2009, 69(15), pp.6200-6207 * |
| JPN6015011620; J. Chromatogr. B, 2004, 803(1), pp.67-73 * |
| JPN6015011623; FEBS Lett., 1998, 441(3), PP.387-391 * |
| JPN6016038544; J. Med. Invest., 2006, 53(1-2), pp.52-60 * |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015212307A (ja) * | 2010-02-04 | 2015-11-26 | モルフォテック, インコーポレイテッド | クロロトキシンポリペプチドおよびコンジュゲートならびにその使用 |
| JP2017031205A (ja) * | 2010-02-04 | 2017-02-09 | モルフォテック, インコーポレイテッド | クロロトキシンポリペプチドおよびコンジュゲートならびにその使用 |
| US10183975B2 (en) | 2010-02-04 | 2019-01-22 | Morphotek, Inc. | Chlorotoxin polypeptides and conjugates and uses thereof |
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| JP2020019779A (ja) * | 2013-09-17 | 2020-02-06 | ブレイズ バイオサイエンス, インコーポレイテッド | クロロトキシンコンジュゲート及びその使用方法 |
| US12048732B2 (en) | 2016-04-15 | 2024-07-30 | Blaze Bioscience, Inc. | Methods of treating breast cancer |
| JP2019535700A (ja) * | 2016-11-10 | 2019-12-12 | ベイジン プロトゲン リミテッドBeijing Protgen Ltd. | ペグ化エンドスタチン類似体およびその適用 |
| CN109963597B (zh) * | 2016-11-10 | 2022-08-26 | 北京普罗吉生物科技发展有限公司 | 聚乙二醇化血管内皮抑制素类似物及其应用 |
| JP7140454B2 (ja) | 2016-11-10 | 2022-09-21 | ベイジン プロトゲン リミテッド | ペグ化エンドスタチン類似体およびその適用 |
| CN115721730A (zh) * | 2016-11-10 | 2023-03-03 | 北京普罗吉生物科技发展有限公司 | 聚乙二醇化血管内皮抑制素类似物及其应用 |
| CN109963597A (zh) * | 2016-11-10 | 2019-07-02 | 北京普罗吉生物科技发展有限公司 | 聚乙二醇化血管内皮抑制素类似物及其应用 |
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| EP2569330B1 (en) | 2016-09-28 |
| JP2017137316A (ja) | 2017-08-10 |
| AU2011253424B2 (en) | 2016-02-04 |
| CA2799169C (en) | 2019-07-23 |
| EP3165533B1 (en) | 2020-04-08 |
| KR101972173B1 (ko) | 2019-04-24 |
| US20180194818A1 (en) | 2018-07-12 |
| EP2569330A4 (en) | 2013-11-13 |
| CN103097403B (zh) | 2017-04-19 |
| EP2569330A2 (en) | 2013-03-20 |
| EP3165533A1 (en) | 2017-05-10 |
| KR20130113938A (ko) | 2013-10-16 |
| WO2011142858A9 (en) | 2012-03-22 |
| IL222930A0 (en) | 2012-12-31 |
| CN103097403A (zh) | 2013-05-08 |
| ES2601182T3 (es) | 2017-02-14 |
| ES2811065T3 (es) | 2021-03-10 |
| JP6553105B2 (ja) | 2019-07-31 |
| CA2799169A1 (en) | 2011-11-17 |
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