183508-58-9Relevant academic research and scientific papers
Novel, potent non-covalent thrombin inhibitors incorporating P3-lactam scaffolds
Ho, Jonathan Z.,Gibson, Tony S.,Semple
, p. 743 - 748 (2007/10/03)
Evolution of P1-argininal inhibitor prototypes led to a series of non-covalent P3-7-membered lactam inhibitors 1a-w, featuring novel peptidomimetic units that probe each of the S1, S2, and S3 specificity pockets of thrombin. Rigid P1-arginine surrogates possessing a wide range of basicity (calcd pKa's~neutral-14) were surveyed. The design, synthesis, and biological activity of these targets are presented.
Phosphonic acid-substituted benzazepinone-n-acetic acid derivatives process for their preparation and pharmaceutical compositions comprising them
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, (2008/06/13)
Compounds having NEP-inhibitory activity, corresponding to the formula I in whichR 1 is hydrogen or a group forming a biolabile phosphonic acid ester,R 2 is hydrogen or a group forming a biolabile phosphonic acid ester and R. sup.3 is hydrogen or a group forming a biolabile carboxylic acid esterand physiologically acceptable salts of acids of formula I, and pharmaceutical compositions comprising these compounds.
