817166-98-6Relevant academic research and scientific papers
Development of a solid-phase approach to the natural product class of Ahp-containing cyclodepsipeptides
Stolze, Sara C.,Meltzer, Michael,Ehrmann, Michael,Kaiser, Markus
experimental part, p. 1616 - 1625 (2012/05/04)
The 3-amino-6-hydroxy-2-piperidone (Ahp) containing cyclodepsipeptides are an interesting class of natural products that inhibit S1 (trypsin and chymotrypsin-like) serine protease in a reversible, noncovalent manner, turning them into potential chemical t
Solid phase total synthesis of the 3-amino-6-hydroxy-2-piperidone (Ahp) cyclodepsipeptide and protease inhibitor Symplocamide A
Stolze, Sara C.,Meltzer, Michael,Ehrmann, Michael,Kaiser, Markus
supporting information; experimental part, p. 8857 - 8859 (2011/02/23)
The solid phase total synthesis of the marine cyanobacterial Ahp-cyclodepsipeptide Symplocamide A is reported as a model for a general route for the synthesis of tailor-made non-covalent serine protease inhibitors. The Royal Society of Chemistry 2010.
A general strategy for the synthesis of azapeptidomimetic lactams
Broadrup, Robert L.,Wang, Bei,Malachowski, William P.
, p. 10277 - 10284 (2007/10/03)
A selection of azapeptidomimetics containing constraining lactam rings have been prepared by Mitsunobu cyclization of serine/homologated serine-azaalanine derivatives. These include sterically-congested β-lactams, as well as γ-butyrolactam and δ-valerolac
Synthesis of a Gln-Phe hydroxy-ethylene dipeptide isostere
Haug, Bengt Erik,Rich, Daniel H.
, p. 4783 - 4786 (2007/10/03)
(Chemical Equation Presented) The protected Gln-Phe hydroxyethylene dipeptide isostere 1 was synthesized as a precursor for preparation of potential inhibitors of Botulinum neurotoxin B metalloprotease. The method allows for the synthesis of additional hydroxyethylene dipeptide isosteres such as 2 with functionalized P1 side chains. The isosteres prepared were coupled with a dipeptide to produce protected pseudotetrapeptide derivatives.
