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- W2080821707 abstract "Treatment of the macrocyclic pentapeptide cyclotheonamide A (1) with aqueous sodium carbonate or triethylamine at 23°C generated two isomeric products. X-ray analysis of a complex with α-thrombin indicates a ring-opened pentapeptide, 2, from cleavage at the α-keto amide bond. However, given the MS data for 3 and a model study in which 4 provides 5, structure 3 is suggested for the product from base treatment of 1." @default.
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- W2080821707 date "1996-05-01" @default.
- W2080821707 modified "2023-09-27" @default.
- W2080821707 title "Transformation of the marine natural product cyclotheonamide A by aqueous base. X-ray analysis of a novel ligand complexed with human α-thrombin" @default.
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- W2080821707 doi "https://doi.org/10.1016/0040-4039(96)00658-2" @default.
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