Literature DB >> 15864721

Synthesis of modular dipeptide mimetics on the basis of diazabicycloalkanes and derivatives thereof with sulphur containing side chains.

D C Grohs1, W Maison.   

Abstract

We present the synthesis of new modular dipeptide mimetics based on diazabicycloalkane backbones. These diazabicycloalkanes are ligands for the prostate specific membrane antigen (PSMA), a well known tumor marker. Our previously described synthetic route to enantiomerically pure diazabicycloalkanes is extended to yield polyfunctional diazabicycloalkanes with a modular character using a new ring closing methodology. This, finally, allows us to attach linker moieties to different positions of the diazabicycloalkane scaffold providing conjugation sites to other functional molecules such as markers or cytostatic compounds. Furthermore, successful synthesis of sulphur-containing dipeptide analogues as for example CysX(AA)- or HCysX(AA)-mimetics on the basis of diazabicycloalkanes is described.

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Year:  2005        PMID: 15864721     DOI: 10.1007/s00726-005-0182-0

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  2 in total

Review 1.  Translational molecular imaging for cancer.

Authors:  Martin G Pomper
Journal:  Cancer Imaging       Date:  2005-11-23       Impact factor: 3.909

2.  Desymmetrization of 7-azabicycloalkenes by tandem olefin metathesis for the preparation of natural product scaffolds.

Authors:  Wolfgang Maison; Marina Büchert; Nina Deppermann
Journal:  Beilstein J Org Chem       Date:  2007-12-18       Impact factor: 2.883

  2 in total

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