In previous papers (Colotta, V. et al. Arch. Pharm. Pharm. Med. Chem. 1999, 332, 39. Colotta, V. et al. J. Med. Chem. 2000, 43, 1158) we reported the synthesis and binding affinity at bovine (b) A(1) and A(2A) and human
Rational substrate and enzyme engineering of transketolase for aromatics
Nature chemical biology, 5(6), 407-413 (2009-04-28)
The linking together of molecular fragments that bind to adjacent sites on an enzyme can lead to high-affinity inhibitors. Ideally, this strategy would use linkers that do not perturb the optimal binding geometries of the fragments and do not have
Synthesis of Alicyclic-lactams via the Ugi Reaction on a Solid Support.
Gedey S, et al.
Letters in Organic Chemistry, 1(3), 215-220 (2004)
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