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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 Cellular Biochemistry|March 21, 2003
Vascular smooth muscle cells efficiently activate a new proteinase cascade involving plasminogen and fibronectinXavier Houard, Catherine Monnot, Vincent Dive, 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.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 6, 2013
Crystal structure of full-length human collagenase 3 (MMP-13) with peptides in the active site defines exosites in the catalytic domainEnrico A Stura, Robert Visse, Philippe Cuniasse, et al.
Biochimie|August 11, 2010
Third generation of matrix metalloprotease inhibitors: Gain in selectivity by targeting the depth of the S1' cavityLaurent Devel, Bertrand Czarny, Fabrice Beau, 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.
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