New furin inhibitors based on weakly basic amidinohydrazones
作者:Frank Sielaff、Manuel E. Than、Dorian Bevec、Iris Lindberg、Torsten Steinmetzer
DOI:10.1016/j.bmcl.2010.11.092
日期:2011.1
A novel series of amidinohydrazone-derived furin inhibitors was prepared; the most potent compounds 17 and 21 inhibit furin with K-i values of 0.46 and 0.59 mu M, respectively. In contrast to inhibitor 17, which still contains a guanidino residue, compound 21 possesses only weakly basic amidinohydrazone groups. (C) 2010 Elsevier Ltd. All rights reserved.
Studies on Methylglyoxal Bis(guanylhydrazone)<sup>1</sup> Analogs. II. Structural Variations on Methylglyoxal Bis(guanylhydrazone)<sup>2</sup>
作者:Fred Baiocchi、C. C. Cheng、W. J. Haggerty、Leland R. Lewis、T. K. Liao、Wayne H. Nyberg、Darrell E. O'Brien、Eugene G. Podrebarac
DOI:10.1021/jm00340a020
日期:1963.7
Antibacterial Agents. Some New Guanyhydrazone Derivatives
decontamination of chromate anions from the wastewater by this cationic ligand was resulted from an instantaneous crystallization. The produced guanidium chromate salts have an extremely low solubility (Ksp,BBIG = 8.19 × 10−9). Such superior removal performance of these materials was attributed to the charge-assisted hydrogen bonding between the cationic ligand and chromate-water hydrate anions, which was revealed