Evaluation of thioamides, thiolactams and thioureas as hydrogen sulfide (H2S) donors for lowering blood pressure

被引:20
作者
Zaorska, Ewelina [1 ]
Hutsch, Tomasz [1 ]
Gawrys-Kopczynska, Marta [1 ]
Ostaszewski, Ryszard [2 ]
Ufnal, Marcin [1 ]
Koszelewski, Dominik [2 ]
机构
[1] Med Univ Warsaw, Lab Ctr Preclin Res, Dept Expt Physiol & Pathophysiol, Pawinskiego 3c, PL-02106 Warsaw, Poland
[2] Polish Acad Sci, Inst Organ Chem, Kasprzaka 44-52, PL-01224 Warsaw, Poland
关键词
Hydrogen sulfide; Thioamides; Thiolactams; Thiourea; Cardiovascular; FLUORESCENT-PROBE; IN-VITRO; ORGANOPHOSPHORUS COMPOUNDS; PHARMACOLOGICAL EVALUATION; PHOSPHORUS PENTASULFIDE; REAGENT COMBINATION; EFFICIENT SYNTHESIS; ELEMENTAL SULFUR; KINDLER REACTION; RATIONAL DESIGN;
D O I
10.1016/j.bioorg.2019.102941
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogen sulfide (H2S) is a biologically important gaseous molecule that exhibits promising protective effects against a variety of pathological processes. For example, it was recognized as a blood pressure lowering agent. Aligned with the need for easily modifiable platforms for the H2S supply, we report here the preparation and the H2S release kinetics from a series of structurally diversified thioamides, thiolactams and thioureas. Three different thionation methods based on the usage of a phosphorus pentasulfide and Lawesson reagent were applied to prepare the target thioamides and thiolactams. Furthermore, obtained H2S donors were evaluated both in in vivo and in vitro studies. The kinetic parameters of the liberating H2S was determined and compared with NaHS and GYY4137 using two different detection technics i.e.; fluorescence labeling 7-azido-4-methyl-2H-chromen-2-one and 5,5'-dithiobis (2-nitrobenzoic acid), sulfhydryl probe, also known as the Ellman's reagent. We have proved that the amount of releasing H2S from these compounds is controllable through structural modifications. Finally, the present study shows a hypotensive response to an intravenous administration of the developed donors in the anesthetized rats.
引用
收藏
页数:11
相关论文
共 156 条
[1]  
Abe K, 1996, J NEUROSCI, V16, P1066
[2]  
Albert A., 1988, BIOORGAN MED CHEM, V8, P2203
[3]   Regulation of vascular nitric oxide in vitro and in vivo; a new role for endogenous hydrogen sulphide? [J].
Ali, M. Y. ;
Ping, C. Y. ;
Mok, Y-Y P. ;
Ling, L. ;
Whiteman, M. ;
Bhatia, M. ;
Moore, P. K. .
BRITISH JOURNAL OF PHARMACOLOGY, 2006, 149 (06) :625-634
[4]  
Amagase H, 2006, J NUTR, V136, p716S, DOI 10.1093/jn/136.3.716S
[5]   A New DNA Gyrase Inhibitor Subclass of the Cyclothialidine Family Based on a Bicyclic Dilactam-Lactone Scaffold. Synthesis and Antibacterial Properties [J].
Angehrn, Peter ;
Goetschi, Erwin ;
Gmuender, Hans ;
Hebeisen, Paul ;
Hennig, Michael ;
Kuhn, Bernd ;
Luebbers, Thomas ;
Reindl, Peter ;
Ricklin, Fabienne ;
Schmitt-Hoffmann, Anne .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (07) :2207-2224
[6]   Cell-Permeable and Plasma-Stable Peptidomimetic Inhibitors of the Postsynaptic Density-95/N-Methyl-D-Aspartate Receptor Interaction [J].
Bach, Anders ;
Eildal, Jonas N. N. ;
Stuhr-Hansen, Nicolai ;
Deeskamp, Rasmus ;
Gottschalk, Marie ;
Pedersen, Soren W. ;
Kristensen, Anders S. ;
Stromgaard, Kristian .
JOURNAL OF MEDICINAL CHEMISTRY, 2011, 54 (05) :1333-1346
[7]   Thioamides in Nature: In Search of Secondary Metabolites in Anaerobic Microorganisms [J].
Banala, Srinivas ;
Suessmuth, Roderich D. .
CHEMBIOCHEM, 2010, 11 (10) :1335-1337
[8]   Catalytic promiscuity and heme-dependent redox regulation of H2S synthesis [J].
Banerjee, Ruma .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2017, 37 :115-121
[9]   Iminothioethers as Hydrogen Sulfide Donors: From the Gasotransmitter Release to the Vascular Effects [J].
Barresi, Elisabetta ;
Nesi, Giulia ;
Citi, Valentina ;
Piragine, Eugenia ;
Piano, Ilaria ;
Taliani, Sabrina ;
Da Settimo, Federico ;
Rapposelli, Simona ;
Testai, Lara ;
Breschi, Maria Cristina ;
Gargini, Claudia ;
Calderone, Vincenzo ;
Martelli, Alma .
JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (17) :7512-7523
[10]   A THIOAMIDE SUBSTRATE OF CARBOXYPEPTIDASE-A [J].
BARTLETT, PA ;
SPEAR, KL ;
JACOBSEN, NE .
BIOCHEMISTRY, 1982, 21 (07) :1608-1611