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- Successful development of a method for the incorporation of Fmoc-Arg(Pbf)-OH in solid-phase peptide synthesis using N-butylpyrrolidinone (NBP) as solvent. Beatriz G. de la Torre, Ashish Kumar, Mahama Alhassan, Christoph Bucher, Fernando Albericio, John Lopez
, Green Chem.
, 2020
, 22
, 3162
- Resin-free peptide synthesis mediated by tri(4-benzoylphenyl) phosphate (TBP) derivatives as small-molecule supports. Haidi Li, Jie Chao, Guang Tian, Jaafar Hasan, Yatao Jin, Zixin Zhang, Chuanguang Qin
, Org. Chem. Front.
, 2020
, 7
, 689
- Greener liquid-phase synthesis and the ACE inhibitory structure–activity relationship of an anti-SARS octapeptide. Haidi Li, Jin Ren, Junyou Li, Zixin Zhang, Ninghui Chang, Chuanguang Qin
, Org. Biomol. Chem.
, 2020
, 18
, 8433
- The phenacyl group as an efficient thiol protecting group in a peptide condensation reaction by the thioester method. Hidekazu Katayama, Hironobu Hojo
, Org. Biomol. Chem.
, 2013
, 11
, 4405
- Enhancement of the T140-based pharmacophores leads to the development of more potent and bio-stable CXCR4 antagonists. Hirokazu Tamamura, Kenichi Hiramatsu, Makiko Mizumoto, Satoshi Ueda, Shuichi Kusano, Shigemi Terakubo, Miki Akamatsu, Naoki Yamamoto, John O. Trent, Zixuan Wang, Stephen C. Peiper, Hideki Nakashima, Akira Otaka, Nobutaka Fujii
, Org. Biomol. Chem.
, 2003
, 1
, 3663
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Cell permeable ITAM constructs for the modulation of mediator release in mast cells. Joeri Kuil, Marcel J. E. Fischer, Nico J. de Mol, Rob M. J. Liskamp
, Org. Biomol. Chem.
, 2011
, 9
, 820
- Replacing DMF in solid-phase peptide synthesis: varying the composition of green binary solvent mixtures as a tool to mitigate common side-reactions. Sandip Jadhav, Vincent Martin, Peter H. G. Egelund, Henrik Johansson Castro, Tobias Krüger, Franziska Richner, Sebastian Thordal Le Quement, Fernando Albericio, Frank Dettner, Carolin Lechner, Ralph Schönleber, Daniel Sejer Pedersen
, Green Chem.
, 2021
, 23
, 3312
- Structure activity relationship study on the peptide hormone preptin, a novel bone-anabolic agent for the treatment of osteoporosis. Zaid Amso, Renata Kowalczyk, Maureen Watson, Young-Eun Park, Karen E. Callon, David S. Musson, Jillian Cornish, Margaret A. Brimble
, Org. Biomol. Chem.
, 2016
, 14
, 9225
- Metabolically stable apelin-analogues, incorporating cyclohexylalanine and homoarginine, as potent apelin receptor activators. Kleinberg X. Fernandez, Conrad Fischer, Jennie Vu, Mahmoud Gheblawi, Wang Wang, Samantha Gottschalk, Xavier Iturrioz, Catherine Llorens-Cortés, Gavin Y. Oudit, John C. Vederas
, RSC Med. Chem.
, 2021
, 12
, 1402
- N-Methyl-phenacyloxycarbamidomethyl (Pocam) group: a novel thiol
protecting group for solid-phase peptide synthesis and peptide condensation reactions. Hidekazu Katayama, Yoshiaki Nakahara, Hironobu Hojo
, Org. Biomol. Chem.
, 2011
, 9
, 4653