Synthesis and applications of cyclopeptides and depsipeptides |
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Authors: | John S. Davies Joanne Howe Janitha Jayatilake Tony Riley |
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Affiliation: | (1) Chemistry Department, University of Wales, Singleton Park, SA2 8PP Swansea, U.K.;(2) Amersham International plc, Amersham, Bucks, U.K. |
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Abstract: | Summary A solid phase protocol has been devised for the synthesis of linear precursors to cyclic depsipeptide analogues of dolastatin D.t-Butyldimethylsilyl groups were used for hydroxy group protection, with deprotection being carried out byt-butyl ammonium fluoride. HATU and PyBrop were successful in coupling highly hindered residues and in depside bond formation. Cyclic peptide analogues, cyclo[Arg-Gly-Asp-d-Phe-Lys(or Tyr)] have been synthesised and modified for use as carrier molecules for the transport of radio isotopes (111In and125I) into blood platelets as prototypes for medical imaging. |
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Keywords: | Solid phase Depside synthesis t-Butyldimethylsilyl protection HATU/PyBrop couplings Dolastatin D analogues Cyclic RGD pentapeptides DTPA derivatisation |
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