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PHOSPHATE BASED LINKERS FOR INTRACELLULAR DELIVERY OF DRUG CONJUGATES
专利权人:
MERCK SHARP & DOHME CORP.;AMBRX, INC.
发明人:
Robert M. Garbaccio,Jeffrey Kern,Philip E. Brandish,Sanjiv Shah,Linda Liang,Ying Sun,Jianing Wang,Nick Knudsen,Andrew Beck,Anthony Manibusan,Dennis Gately
申请号:
US15301564
公开号:
US20170182181A1
申请日:
2015.03.30
申请国别(地区):
US
年份:
2017
代理人:
摘要:
Phosphate-based linkers with tunable stability for intracellular delivery of drug conjugates are described. The phosphate-based linkers comprise a monophosphate, diphosphate, triphosphate, or tetraphosphate group (phosphate group) and a linker arm comprising a tuning element and optionally a spacer. A payload is covalently linked to the phosphate group at the distal end of the linker arm and the functional group at the proximal end of the linker arm is covalently linked to a cell-specific targeting ligand such as an antibody. These phosphate-based linkers have a differentiated and tunable stability in blood vs. an intracellular environment (e.g. lysosomal compartment).
来源网站:
中国工程科技知识中心
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http://www.ckcest.cn/home/

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