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The Journal of Organic Chemistry|December 2, 2006
Chemoselective protection of solid-phase compatible Fmoc-phosphinic building blocksMagdalini Nasopoulou, Magdalini Matziari, Vincent Dive, et al.
The Journal of Organic Chemistry|August 25, 2007
A versatile annulation protocol toward novel constrained phosphinic peptidomimeticsMagdalini Nasopoulou, Dimitris Georgiadis, Magdalini Matziari, et al.
Journal of Medicinal Chemistry|January 9, 2004
Evaluation of P1'-diversified phosphinic peptides leads to the development of highly selective inhibitors of MMP-11Magdalini Matziari, Fabrice Beau, Philippe Cuniasse, et al.
Biochemistry|June 24, 2004
Structural determinants of RXPA380, a potent and highly selective inhibitor of the angiotensin-converting enzyme C-domainDimitris Georgiadis, Philippe Cuniasse, Jöel Cotton, et al.
Current Pharmaceutical Design|November 21, 2009
Inhibition of zinc metallopeptidases in cardiovascular disease--from unity to trinity, or duality?Vincent Dive, Cheng-Fu Chang, Athanasios Yiotakis, et al.
The FEBS Journal|April 21, 2006
Combined use of selective inhibitors and fluorogenic substrates to study the specificity of somatic wild-type angiotensin-converting enzymeNicolas D Jullien, Philippe Cuniasse, Dimitris Georgiadis, et al.
Journal of Medicinal Chemistry|November 11, 2009
Phosphinic tripeptides as dual angiotensin-converting enzyme C-domain and endothelin-converting enzyme-1 inhibitorsNicolas Jullien, Anastasios Makritis, Dimitris Georgiadis, et al.
Journal of Medicinal Chemistry|March 8, 2008
Development of potent and selective phosphinic peptide inhibitors of angiotensin-converting enzyme 2Andreas Mores, Magdalini Matziari, Fabrice Beau, et al.
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