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- W2029897481 abstract "Four pentapeptide N-hydroxysuccinimide esters [X–Orn(Z)–Leu–Y–Pro–ONSu (X=Val or D-Val, and Y=Phe or D-Phe)] related to gramicidin S were allowed to cyclize in pyridine. The peptides with a L-Phe residue preceding Pro tend to form various cyclic polymers, while ones with a D-Phe residue exclusively yielded a cyclic monomer or cyclic dimer. Peptides with a D-Val residue at the N-terminal produced monomerization products. The observed tendencies were similar for cyclization of four hexapeptide N-hydroxysuccinimide esters [X–Val–Orn(Z)–Leu–Y–Pro–ONSu (X=Tyr(Bzl) or D-Tyr(BzlCl2), and Y= Phe or D-Phe)] related to gratisin." @default.
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- W2029897481 date "1989-02-01" @default.
- W2029897481 modified "2023-09-25" @default.
- W2029897481 title "Cyclization of Penta- and Hexapeptide Active Esters Related to Gramicidin S and Gratisin" @default.
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- W2029897481 doi "https://doi.org/10.1246/bcsj.62.594" @default.
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