42749-52-0Relevant academic research and scientific papers
Quadruple helix formation of a photoresponsive peptide amphiphile and its light-triggered dissociation into single fibers
Muraoka, Takahiro,Cui, Honggang,Stupp, Samuel I.
, p. 2946 - 2947 (2008/09/19)
Using a peptide amphiphile having a bulky photolabile 2-nitrobenzyl group between the alkyl chain and the peptide segment, we demonstrated quadruple helical fiber formation and its dissociation into single fibrils in response to light. Putting the bulky g
Synthesis, stability and optimized photolytic cleavage of 4-methoxy-2-nitrobenzyl backbone-protected peptides
Johnson, Erik C. B.,Kent, Stephen B. H.
, p. 1557 - 1559 (2008/03/12)
We demonstrate the potential of 4-methoxy-2-nitrobenzyl as a Boc chemistry-compatible fully reversible backbone modification for synthetic peptides. The Royal Society of Chemistry 2006.
Peptide Conformations, 22. - The Conformation of cyclo- in Crystal and Solution by X-ray Analysis and One- and Two-dimensional NMR Spectroscopy
Kessler, Horst,Schuck, Regina,Siegmeier, Rainer,Bats, Jan Willem,Fuess, Hartmut,Foerster, Hans
, p. 231 - 247 (2007/10/02)
The conformation of the cyclic tripeptide cyclo- (NB= o-Nitrobenzyl) was investigated by X-ray analysis and NMR spectroscopy.The backbone conformation is - according to X-ray analysis - a boat for crystals grown from methanol or chloroform.T
