Charge-Compensated Metallacarborane Building Blocks for Conjugation with Peptides

被引:27
作者
Frank, Rene [1 ]
Ahrens, Verena M. [2 ]
Boehnke, Solveig [1 ]
Beck-Sickinger, Annette G. [2 ]
Hey-Hawkins, Evamarie [1 ]
机构
[1] Univ Leipzig, Fak Chem & Mineral, Inst Anorgan Chem, Johannisallee 29, D-04103 Leipzig, Germany
[2] Univ Leipzig, Inst Biochem, Fak Biochem Pharm & Psychol, Bruderstr 34, D-04103 Leipzig, Germany
关键词
boron neutron capture therapy; carboranes; metallacarboranes; peptides; zwitterions; NEUTRON-CAPTURE THERAPY; EPIDERMAL-GROWTH-FACTOR; NEUROPEPTIDE-Y ANALOGS; COBALT BIS(DICARBOLLIDE); BORON; DERIVATIVES; RECEPTOR; CHEMISTRY; RECOMMENDATIONS; NOMENCLATURE;
D O I
10.1002/cbic.201500569
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cobalt bis(dicarbollide) complex [commo-3,3-Co(1,2-C2B9H11)(2)](-) has captured much attention in biochemical and medical contexts, in particular for the treatment of tumors by boron neutron capture therapy (BNCT). Derivatives of cobalt bis(dicarbollide) are commonly prepared through ring-opening reactions of cyclic oxonium ions, so the corresponding products are usually charged. Furthermore, attempts to incorporate cobalt bis(dicarbollide) into peptides are rare, despite obvious potential advantages. Here the synthesis of an imidazolium-based charge-compensated cobalt bis(dicarbollide) building block, which allows additional modifications with moieties of biochemical relevance, such as monosaccharides, is reported. Furthermore, conjugates of these building blocks with the Y-1-receptor-selective derivative of neuropeptideY ([F-7,P-34]-NPY) retained excellent response to hY(1) receptors found to be overexpressed in breast tumors and metastases.
引用
收藏
页码:308 / 317
页数:10
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