期刊
TETRAHEDRON
卷 57, 期 29, 页码 6249-6255出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4020(01)00579-8
关键词
cyclopeptides; solid phase synthesis; marine natural product; elastase degranulation
Head-to-tail proline containing cyclopeptide hymenamide C [cyclo(Leu-Trp-Pro(3)-Phe-Gly-Pro(6)-Glu); 1], isolated from a marine sponge and for which a preliminary immunomodulating activity was reported, was efficiently synthesized by a three-dimensional orthogonal solid-phase strategy (Fmoc/tBu/Allyl) via anchoring the omega -carboxyl function of the glutamic acid to the solid support (PAC-PEG-PS). The Linear precursor was entirely assembled and subsequently cyclized on resin, yielding a major product identical to the natural hymenamide C and a minor one, a geometric isomer of hymenamide C (2), differing for the geometry of peptide linkages at Pro residues. Both the 'proline-rich' cyclopeptides were submitted to a multiparametric in vitro screening on immune cells in order to acquire additional information on their biological activity. Indeed, compounds 1 and 2 were shown to exert inhibitory effect on human neutrophil elastase degranulation release at micromolar concentration. (C) 2001 Elsevier Science Ltd. All rights reserved.
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