Chiodini Dr. Giuseppe Ph. D.


  • Master degree in Chemical and Pharmaceutical technology University of MIlan 2009.
  • Research Fellowship at Chemistry and Biochemistry for Medicine University of Milan 2010.
  • Ph.D. studies about Chemical Sciences, Medicinal Chemistry Course, From 2011 to 2013.

Work Expirience

  • 2014 – 2016 Freelance Professional in Chemical and Pharmaceutical Areas
  • 2017 – CCF Project supervisor.


  1. C. Bolchi, M. Pallavicini, S. K. Bernini, G. Chiodini, A. Corsini, N. Ferri, L. Fumagalli, V.Straniero and E. Valoti Thiazole- and imidazole-containing peptidomimetic inhibitors of protein Farnesyltransferase; Bioorg. and Med. Chem. Letts, 2011, Volume 21, Issue 18, 5408-5412
  2. L. Fumagalli, M. Pallavicini, R. Budriesi, M. Gobbi, V. Straniero, M. Zagami, G. Chiodini, C. Bolchi and E. Valoti Affinity and Activity profiling of unchiral 8-substitued 1,4-benzodioxane analogues of WB4101 reveals a potent and selective α1B-adrenoceptor antagonist; Eur. J. Med. Chem. 2012, Volume 58, 184-191
  3. L. Fumagalli, M. Pallavicini, R. Budriesi, C. Bolchi, M. Canovi, A. Chiarini, G. Chiodini, M. Gobbi, P. Laurino and E. Valoti 6-Methoxy-7-benzofuranoxy and 6-Methoxy-7-indolyloxy Analogues of 2-[2-(2,6-Dimethoxyphenoxy)ethyl]aminomethyl-1,4-benzodioxane (WB4101): Discovery of a Potent and Selective α1D-Adrenoceptor Antagonist; J. Med. Chem. Volume 56, Issue 16, 6402-6412
  4. V.Straniero · M. Pallavicini · G. Chiodini L. Fumagalli · C. Bolchi · A. Corsini  E. Valoti · Farnesyltransferase inhibitors: CAAX mimetics based on different biaryl scaffolds  Bioorg. and Med. Chem. Letts, 2014, Volume 24, Issue 13, 2924-2927
  5. G. Chiodini· M. Pallavicini · C. Zanotto C. Bolchi · L. Fumagalli · C. De Giuli Morghen · E. Valoti · Benzodioxane–benzamides as new bacterial cell division inhibitors Eur. J. Med. Chem. 2015, Volume 89, 252-265
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