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Synthesis and applications of cyclopeptides and depsipeptides
Authors:John S. Davies  Joanne Howe  Janitha Jayatilake  Tony Riley
Affiliation:(1) Chemistry Department, University of Wales, Singleton Park, SA2 8PP Swansea, U.K.;(2) Amersham International plc, Amersham, Bucks, U.K.
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.
Keywords:Solid phase  Depside synthesis   t-Butyldimethylsilyl protection  HATU/PyBrop couplings  Dolastatin D analogues  Cyclic RGD pentapeptides  DTPA derivatisation
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