| Literature DB >> 24900208 |
Scott C Jeffrey1, Jef De Brabander2, Jamie Miyamoto1, Peter D Senter1.
Abstract
The β-glucuronide linker has been used for antibody-drug conjugates (ADCs) to deliver amine-containing cytotoxic agents. The linker is stable in circulation, hydrophilic and provides ADCs that are highly active in vitro and in vivo. To extend the utility of the β-glucuronide linker toward phenol-containing drugs, an N,N'-dimethylethylene diamine self-immolative spacer was incorporated with the linker for release of the potent cytotoxic phenol psymberin A. Exposure of the drug-linker to β-glucuronidase resulted in facile drug release. The corresponding ADCs were active and immunologically selective against CD30-positive L540cy and CD70-positive Caki-1 cell lines.Entities:
Keywords: CD30-positive L540cy cell line; CD70-positive Caki-1 cell line; N,N′-dimethylethylene diamine; antibody−drug conjugates; phenolic cytotoxic agents; β-Glucuronide linker
Year: 2010 PMID: 24900208 PMCID: PMC4007898 DOI: 10.1021/ml100039h
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345