A1 Vertaisarvioitu alkuperäisartikkeli tieteellisessä lehdessä
Synthesis of an Alkyne-Modified Bleomycin Disaccharide Precursor, Conversion to a F-18-Labeled Radiotracer, and Preliminary in vivo-PET Imaging Studies
Tekijät: Sajal K. Maity, Cheng-Bin Yim, Satish Jadhav, Alejandra Verhassel, Johanna Tuomela, Olof Solin, Tove J. Grönroos, Pasi Virta
Kustantaja: WILEY-V C H VERLAG GMBH
Julkaisuvuosi: 2019
Journal: European Journal of Organic Chemistry
Tietokannassa oleva lehden nimi: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Lehden akronyymi: EUR J ORG CHEM
Vuosikerta: 2019
Numero: 1
Aloitussivu: 156
Lopetussivu: 163
Sivujen määrä: 8
ISSN: 1434-193X
eISSN: 1099-0690
DOI: https://doi.org/10.1002/ejoc.201801488
Rinnakkaistallenteen osoite: https://research.utu.fi/converis/portal/detail/Publication/39298097
The bleomycins (BLMs) are known antitumor antibiotics composed of the tumoricidal and tumor seeking domains. The peptide structure of BLMs is responsible for the cytotoxicity by selective oxidative cleavage of DNA (and RNA), while the tumor cell selectivity and internalization resides in the disaccharide moiety (i.e. BLM disaccharide). This has prompted researchers to utilize BLM disaccharide and its derivatives as constituents for the selective recognition of tumor cells, which may find further applications as new tumor imaging tools or drug delivery vehicles. In the present study a high yielding synthesis of an alkyne modified BLM disaccharide precursor that may be used as a useful agent for the click conjugation, its conversion to a F-18-labeled radiotracer, and preliminary in vivo PET imaging studies of the tracer with breast cancer (MCF-7) xenograft mouse models are described.
Ladattava julkaisu This is an electronic reprint of the original article. |  |
