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pubmed-article:18032042pubmed:abstractTextThe absolute stereochemistry of melleumin A (1) and B (2), novel peptide compounds isolated from the myxomycete Physarum melleum, was determined by synthesis of their segments and by a modified Mosher's method. Total synthesis of melleumin B (2) was achieved by a stereoselective method, which provided further evidence for all the absolute stereochemistries of melleumin B (2). The Wnt signal inhibitory activities of 2 and its 10R-epimer 19 were evaluated. Compound 19 showed moderate inhibition of Wnt signal transcription, which suggests that melleumin analogues might be useful as Wnt signal inhibitors.lld:pubmed
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pubmed-article:18032042pubmed:articleTitleDetermination of absolute stereochemistry, total synthesis, and evaluation of peptides from the myxomycete Physarum melleum.lld:pubmed
pubmed-article:18032042pubmed:affiliationGraduate School of Pharmaceutical Sciences, Chiba University, Chiba 263-8522, Japan.lld:pubmed
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