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- W2000566006 abstract "A cyclic heptapeptide, cyclo-(L-Val-L-Orn-L-Leu-D-Phe-L-Pro-Gly-Gly-), was synthesized in order to investigate a contribution for an antibacterial activity of a ring size of a cyclic peptide. A linear heptapeptide p-nitrophenyl ester, in which an δ-amino function of ornithine residue was protected with benzyloxycarbonyl group, was transformed to the cyclic benzyloxycarbonyl-substituted heptapeptide which was hydrogenated to afford the desired cyclic heptapeptide as hydrochloride. The cyclic peptide thus obtained showed no activity against any of microorganisms tested." @default.
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- W2000566006 date "1970-03-01" @default.
- W2000566006 modified "2023-09-26" @default.
- W2000566006 title "Studies of Peptide Antibiotics. XV. The Synthesis of<i>cyclo</i>-(L-Valyl-L-ornithyl-L-leueyl-D-phenylalanyl-L-prolyl-glycyl-glycyl)" @default.
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- W2000566006 doi "https://doi.org/10.1246/bcsj.43.914" @default.
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