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. 2015 Jun 10;6(8):4889–4896. doi: 10.1039/c5sc01774b

Table 2. Results of the cyclic peptide library synthesis by protected cyclization in solution (method A) and by KAHA cyclization (method B).

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aHighlighted residues indicate the distinctive position of similar sequences with and without a turn inducing template. The last position indicates the α-ketoacid used for cyclization (Leu or Phe). The peptide concentration for cyclization was 6.25 mM for both methods. [T§ = (S)-homoserine].

bIsolated yields on 50 μmol scale after RP-HPLC purification.

cDetermined by HPLC as relative area% at 220 nm.

dGypsophin B25 analogue.

ePseudostellarin G25 analogue.

fSegetalin F25 analogue.