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  • Title: Isolation and Synthetic Diversification of Jadomycin 4-Amino-l-phenylalanine.
    Author: Martinez-Farina CF, Robertson AW, Yin H, Monro S, McFarland SA, Syvitski RT, Jakeman DL.
    Journal: J Nat Prod; 2015 Jun 26; 78(6):1208-14. PubMed ID: 26035093.
    Abstract:
    Streptomyces venezuelae ISP5230 was grown in the presence of phenylalanine analogues to observe whether they could be incorporated into novel jadomycin structures. It was found that the bacteria successfully produced jadomycins incorporating 4-aminophenylalanine enantiomers. Upon isolation and characterization of jadomycin 4-amino-l-phenylalanine (1), it was synthetically derivatized, using activated succinimidyl esters, to yield a small jadomycin amide library. These are the first examples of oxazolone-ring-containing jadomycins that have incorporated an amino functionality subsequently used for derivatization.
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