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Chemistry (Weinheim an Der Bergstrasse, Germany)|May 13, 2003
Diastereoselective solution and multipin-based combinatorial array synthesis of a novel class of potent phosphinic metalloprotease inhibitorsAnastasios Makaritis, Dimitris Georgiadis, Vincent Dive, et al.
Organic Letters|September 25, 2009
A modular rearrangement approach toward medicinally relevant phosphinic structuresVassilis Rogakos, Dimitris Georgiadis, Vincent Dive, et al.
ACS Omega|October 10, 2022
Design, Synthesis, and Study of a Novel RXPA380-Proline Hybrid (RXPA380-P) as an Antihypertensive AgentMoaz M Abdou, Dewen Dong, Paul M O'Neill, et al.
Plos One|April 4, 2018
Functional examination of novel kisspeptin phosphinic peptidesXiaoyang Zhang, Magdalini Matziari, Yixin Xie, 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.
ACS Omega|January 1, 2026
Highly Potent Phosphinic HIV‑1 Protease Inhibitors: Synthesis, In Vitro Evaluation, and Docking StudiesKomal Hayat, Danwen Qiu, Yuanyuan Wang, 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.
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