102988-95-4Relevant articles and documents
Direct N-glycan profiling in the presence of tryptic peptides on MALDI-TOF by controlled ion enhancement and suppression upon glycan-selective derivatization
Shinohara, Yasuro,Furukawa, Jun-Ichi,Niikura, Kenichi,Miura, Nobuaki,Nishimura, Shin-Ichiro
, p. 6989 - 6997 (2007/10/03)
Even though the formidably laborious and time-consuming nature of oligosaccharide analysis limits certain attempts to analyze the glycosylation profile, the significant elucidation of carbohydrate modifications is largely dependent on it. Aiming to substa
New amino acid porphyrin derivatives. Part I: Synthesis
Perree-Fauvet, Martine,Verchere-Beaur, Catherine,Tarnaud, Eric,Anneheim-Herbelin, Gilles,Bone, Nathalie,Gaudemer, Alain
, p. 13569 - 13588 (2007/10/03)
In order to obtain molecules that can bind to specific DNA-sequences, several new tri-(N-methyl-4-pyridiniumyl)porphyrins bearing an amino acid or peptide side-chain on the fourth meso aromatic substituent have been synthesized by efficient coupling of a
Synthesis and inhibiting activities of 1-peptidyl-2-haloacetyl hydrazines toward cathepsin B and calpains
Giordano, C,Calabretta, R,Gallina, C,Consalvi, V,Scandurra, R,et al.
, p. 297 - 311 (2007/10/02)
Twenty-four 1-peptidyl-2-haloacetyl hydrazines which can be considered azapeptide halomethanes were synthesized and tested as models of cathepsin B, calpain I and calpain II inhibitors.Reagents designed for cathepsin B inactivation include Z-Tyr, Z-Tyr(I)
