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公开(公告)号:US20120148610A1
公开(公告)日:2012-06-14
申请号:US13397656
申请日:2012-02-15
申请人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
发明人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
IPC分类号: A61K39/395 , A61P35/00 , C07K16/00
CPC分类号: C07K16/32 , A61K38/00 , A61K47/6803 , A61K47/6811 , A61K47/6849 , A61K47/6851 , A61K47/6855 , A61K2039/505 , C07K7/02 , C07K2317/24 , Y02A50/414 , Y02A50/423 , Y02A50/469 , Y10T428/13
摘要: Auristatin peptides, including MeVal-Val-Dil-Dap-Norephedrine (MMAE) and MeVal-Val-Dil-Dap-Phe (MMAF), were prepared and attached to Ligands through various linkers, including maleimidocaproyl-val-cit-PAB. The resulting ligand drug conjugates were active in vitro and in vivo.
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公开(公告)号:US20120148608A1
公开(公告)日:2012-06-14
申请号:US13397644
申请日:2012-02-15
申请人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
发明人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
IPC分类号: A61K39/395 , C07K16/00
CPC分类号: C07K16/32 , A61K38/00 , A61K47/6803 , A61K47/6811 , A61K47/6849 , A61K47/6851 , A61K47/6855 , A61K2039/505 , C07K7/02 , C07K2317/24 , Y02A50/414 , Y02A50/423 , Y02A50/469 , Y10T428/13
摘要: Auristatin peptides, including MeVal-Val-Dil-Dap-Norephedrine (MMAE) and MeVal-Val-Dil-Dap-Phe (MMAF), were prepared and attached to Ligands through various linkers, including maleimidocaproyl-val-cit-PAB. The resulting ligand drug conjugates were active in vitro and in vivo.
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公开(公告)号:US20120003248A1
公开(公告)日:2012-01-05
申请号:US13098393
申请日:2011-04-29
申请人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
发明人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
IPC分类号: A61K39/395 , A61P35/00 , C07K19/00
CPC分类号: C07K16/32 , A61K38/00 , A61K47/6811 , A61K47/6849 , A61K47/6851 , A61K47/6855 , A61K2039/505 , C07K7/02 , C07K2317/24 , Y02A50/414 , Y02A50/423 , Y02A50/469 , Y02A50/491 , Y02A50/492 , Y10T428/13
摘要: Auristatin peptides, including MeVal-Val-Dil-Dap-Norephedrine (MMAE) and MeVal-Val-Dil-Dap-Phe (MMAF), were prepared and attached to Ligands through various linkers, including maleimidocaproyl-val-cit-PAB. The resulting ligand drug conjugates were active in vitro and in vivo.
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公开(公告)号:US07745394B2
公开(公告)日:2010-06-29
申请号:US11833964
申请日:2007-08-03
申请人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
发明人: Svetlana O. Doronina , Peter D. Senter , Brian E. Toki , Allen J. Ebens , Toni Beth Kline , Paul Polakis , Mark X. Sliwkowski , Susan D. Spencer
IPC分类号: A61K38/00
CPC分类号: C07K16/32 , A61K38/00 , A61K47/6811 , A61K47/6849 , A61K47/6851 , A61K47/6855 , A61K2039/505 , C07K7/02 , C07K2317/24 , Y02A50/414 , Y02A50/423 , Y02A50/469 , Y02A50/491 , Y02A50/492 , Y10T428/13
摘要: Auristatin peptides, including MeVal-Val-Dil-Dap-Norephedrine (MMAE) and MeVal-Val-Dil-Dap-Phe (MMAF), were prepared and attached to Ligands through various linkers, including maleimidocaproyl-val-cit-PAB. The resulting ligand drug conjugates were active in vitro and in vivo.
摘要翻译: 制备包括MeVal-Val-Dil-Dap-Norephedrine(MMAE)和MeVal-Val-Dil-Dap-Phe(MMAF)的Auristatin肽,并通过各种接头包括马来酰亚胺酰基val-cit-PAB连接到配体上。 所得配体药物偶联物在体外和体内都是活性的。
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公开(公告)号:US20080317747A1
公开(公告)日:2008-12-25
申请号:US12116660
申请日:2008-05-07
申请人: Joseph A. Francisco , Grant Risdon , Alan F. Wahl , Clay Siegall , Peter D. Senter , Sveltana Doronina , Brian E. Toki
发明人: Joseph A. Francisco , Grant Risdon , Alan F. Wahl , Clay Siegall , Peter D. Senter , Sveltana Doronina , Brian E. Toki
IPC分类号: A61K39/395 , C07K16/28
CPC分类号: C07K16/2878 , A61K39/39558 , A61K45/06 , A61K47/64 , A61K47/642 , A61K47/6849 , A61K2039/505 , C07K2317/24 , C07K2317/73
摘要: The present invention relates to methods and compositions for the treatment of Hodgkin's Disease, comprising administering proteins characterized by their ability to bind to CD30, or compete with monoclonal antibodies AC10 or HeFi-1 for binding to CD30, and exert a cytostatic or cytotoxic effect on Hodgkin's disease cells in the absence of effector cells or complement. Such proteins include derivatives of monoclonal antibodies AC10 and HeFi-1. The proteins of the invention can be human, humanized, or chimeric antibodies; further, they can be conjugated to cytotoxic agents such as chemotherapeutic drugs. The invention further relates to nucleic acids encoding the proteins of the invention. The invention yet further relates to a method for identifying an anti-CD30 antibody useful for the treatment or prevention of Hodgkin's Disease.
摘要翻译: 本发明涉及用于治疗霍奇金病的方法和组合物,其包括给予特征为结合CD30的能力的蛋白质,或与单克隆抗体AC10或HeFi-1竞争结合CD30,并对细胞生长抑制或细胞毒性作用 霍奇金病细胞在没有效应细胞或补体的情况下。 这些蛋白质包括单克隆抗体AC10和HeFi-1的衍生物。 本发明的蛋白质可以是人,人源化或嵌合抗体; 此外,它们可以与细胞毒性剂如化学治疗药物缀合。 本发明还涉及编码本发明蛋白质的核酸。 本发明还涉及用于鉴定可用于治疗或预防霍奇金病的抗CD30抗体的方法。
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公开(公告)号:US07423116B2
公开(公告)日:2008-09-09
申请号:US11451147
申请日:2006-06-12
IPC分类号: C07K7/06
CPC分类号: C07K5/0205 , A61K38/00 , C07K5/0202 , C07K7/02
摘要: Pentapeptide compounds are disclosed. The compounds have biological activity, e.g., cytotoxicity. Prodrugs having targeting groups and pentapeptide moieties, as well as precursors thereof are also disclosed. For example, precursors having a reactive linker that can serve as a reaction site for joining to a targeting agent, e.g., an antibody, as disclosed.
摘要翻译: 公开了五肽化合物。 这些化合物具有生物活性,例如细胞毒性。 还公开了具有靶向基团和五肽部分的前体药物及其前体。 例如,具有可用作连接靶向试剂(例如抗体)的反应位点的反应性连接体的前体,如所公开的。
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公开(公告)号:US07256257B2
公开(公告)日:2007-08-14
申请号:US10476391
申请日:2002-04-30
IPC分类号: C07K7/06
CPC分类号: C07K5/0205 , A61K38/00 , C07K5/0202 , C07K7/02
摘要: Pentapeptide compounds are disclosed. The compounds have biological activity, e.g., cytotoxicity. Prodrugs having targeting groups and pentapeptide moieities, as well as precursors thereof are also disclosed. For example, precursors having a reactive linker that can serve as a reaction site for joining to a targeting agent, e.g., an antibody, as disclosed.
摘要翻译: 公开了五肽化合物。 这些化合物具有生物活性,例如细胞毒性。 还公开了具有靶向基团和五肽阴离子的前体药物及其前体物质。 例如,具有可用作连接靶向试剂(例如抗体)的反应位点的反应性连接体的前体,如所公开的。
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公开(公告)号:US6132722A
公开(公告)日:2000-10-17
申请号:US070637
申请日:1998-04-30
IPC分类号: C12N15/09 , A61K31/131 , A61K31/337 , A61K31/407 , A61K31/704 , A61K38/00 , A61K45/06 , A61K47/48 , A61P35/00 , A61P43/00 , C07K16/30 , C07K19/00 , C12N9/78 , A61K39/395 , A61K47/16 , C12N9/96
CPC分类号: B82Y5/00 , A61K47/4843 , A61K47/48623 , A61K47/48723 , A61K47/48761 , C07K16/3053 , A61K2039/505 , C07K2319/00 , Y10S530/866 , Y10S530/867
摘要: The invention is related to recombinantly produced fusion polypeptides comprising antibody V.sub.H and V.sub.L sequences operatively linked to a .beta.-lactamase for use in the delivery of cytotoxic drugs to tumor cells.
摘要翻译: 本发明涉及重组产生的融合多肽,其包含与β-内酰胺酶有效连接的抗体VH和VL序列,用于向肿瘤细胞递送细胞毒性药物。
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公开(公告)号:US5041424A
公开(公告)日:1991-08-20
申请号:US450718
申请日:1989-12-14
申请人: Mark G. Saulnier , Peter D. Senter , John F. Kadow
发明人: Mark G. Saulnier , Peter D. Senter , John F. Kadow
IPC分类号: C07H17/04 , A61K20060101 , A61K31/365 , A61K31/366 , A61K31/44 , A61K31/66 , A61K31/661 , A61K31/70 , A61K31/7042 , A61K31/7048 , A61P35/00 , A61P35/04 , C07F20060101 , C07H20060101 , C07H3/02 , C07H15/00 , C07H15/24
CPC分类号: C07H17/04 , Y10S514/908
摘要: Phosphate derivatives of 4'-demethylepipodophyllotoxin glucosides are novel antitumor agents and the salts thereof offer the pharmaceutical advantage of high water solubility.
摘要翻译: 4'-去甲表鬼臼毒素葡糖苷的磷酸酯衍生物是新的抗肿瘤剂,其盐提供高水溶性的药物优点。
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公开(公告)号:US4618492A
公开(公告)日:1986-10-21
申请号:US733479
申请日:1985-05-13
IPC分类号: C07K14/00 , A61K31/194 , A61K31/195 , A61K31/70 , A61K31/7028 , A61K31/7034 , A61K31/704 , A61K38/00 , A61K38/36 , A61K39/00 , A61K39/395 , A61K45/00 , A61K47/48 , A61P35/00 , C07C229/42 , C07C323/36 , C07D207/44 , C07D207/452 , C07D405/00 , C07D405/12 , C07H15/252 , C07K1/107 , C07K1/113 , C07K9/00 , C07K14/415 , C07K16/00 , C07D519/00 , C07D521/00
CPC分类号: C07D207/452 , C07D405/12
摘要: Amino-sulfhydryl cross-linking reagents that are cleavable under mildly acidic conditions are disclosed. Also disclosed are methods of making the cross-linkers, as well as methods of using the cross-linkers, e.g., to deliver a biologically active substance across the membranes of selected cells in a heterogeneous cell population; once inside the cell the active substance is released, intact, by the transient, mild acidity of certain cell structure. Finally, a method of characterizing complex multi-chain protein structures is disclosed.
摘要翻译: 公开了在弱酸性条件下可切割的氨基 - 巯基交联试剂。 还公开了制备交联剂的方法,以及使用交联剂的方法,例如将生物活性物质跨越异种细胞群体中所选细胞的膜递送; 一旦在细胞内,活性物质被完全释放,通过某些细胞结构的瞬时,温和的酸度。 最后,公开了一种表征复合多链蛋白结构的方法。
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