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- Problems in the synthesis of cyclic peptides through use of the Dmab protecting group . Tony Johnson, Mark Liley, Timothy J. Cheeseright, Farida Begum
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2811
- Enzyme-triggered delivery of chlorambucil from conjugates based on the cell-penetrating peptide BP16. Marta Soler, Marta González-Bártulos, Eduard Figueras, Xavi Ribas, Miquel Costas, Anna Massaguer, Marta Planas, Lidia Feliu
, Org. Biomol. Chem.
, 2015
, 13
, 1470
- Discovery of lixisenatide analogues as long-acting hypoglycemic agents using novel peptide half-life extension technology based on mycophenolic acid. Chunli Tang, Qing Li, Xiaoyan Deng, Weiwei Wu, Liufeng Liao, Kai Liang, Rongrui Huo, Chenglin Li, Jing Han, Weizhong Tang, Neng Jiang
, RSC Adv.
, 2020
, 10
, 12089
- Synthesis of fluorescein-labelled O-mannosylated peptides as components for synthetic vaccines: comparison of two synthetic strategies. Margaret A. Brimble, Renata Kowalczyk, Paul W. R. Harris, P. Rod Dunbar, Victoria J. Muir
, Org. Biomol. Chem.
, 2008
, 6
, 112
- Synthesis and pharmaceutical characterization of site specific mycophenolic acid-modified Xenopus glucagon-like peptide-1 analogs. Jing Han, Junjie Fu, Lidan Sun, Yue Han, Qiuyi Mao, Fang Liao, Xinshi Zheng, Ke Zhu
, Med. Chem. Commun.
, 2018
, 9
, 67
- Activation of monocytic cells by immunostimulatory lipids conjugated to peptide antigens. Stefania Galdiero, Mariateresa Vitiello, Emiliana Finamore, Rosalba Mansi, Marilena Galdiero, Giancarlo Morelli, Diego Tesauro
, Mol. BioSyst.
, 2012
, 8
, 3166
- Delivering aminopyridine ligands into cancer cells through conjugation to the cell-penetrating peptide BP16. M. Soler, M. González-Bártulos, E. Figueras, A. Massaguer, L. Feliu, M. Planas, X. Ribas, M. Costas
, Org. Biomol. Chem.
, 2016
, 14
, 4061
- Access to a stabilized i-motif DNA structure through four successive ligation reactions on a cyclopeptide scaffold. Alexandre Devaux, Laureen Bonnat, Thomas Lavergne, Eric Defrancq
, Org. Biomol. Chem.
, 2020
, 18
, 6394
- Antimicrobial activity of levofloxacin – M33 peptide conjugation or combination. Federica Ceccherini, Chiara Falciani, Martina Onori, Silvia Scali, Simona Pollini, Gian Maria Rossolini, Luisa Bracci, Alessandro Pini
, Med. Chem. Commun.
, 2016
, 7
, 258
- Eliminating caspase-7 and cathepsin B cross-reactivity on fluorogenic caspase-3 substrates. Martha Mackay, Ana M. Pérez-López, Mark Bradley, Annamaria Lilienkampf
, Mol. BioSyst.
, 2016
, 12
, 693