Selective inhibition of human erythrocyte Na+/K+ ATPase by cardiac glycosides and by a mammalian digitalis like factor

Life Sciences

Volumn 67, Issue 16, 2000, Pages 1921-1928

  Balzan, Silvana ^a   D'Urso, Giuseppina ^b   Ghione, Sergio ^a   Martinelli, Adriano ^b   Montali, Umberto ^b  

^a CNR   (Italy)

^b UNIVERSITY OF PISA   (Italy)

Author keywords

Cardiac glycosides; Endogenous digitalis like factor; Human red blood cells; Na+ K+ATPase

Indexed keywords

ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CARDIAC GLYCOSIDE; DIGITALIS LIKE FACTOR; DIGITOXIGENIN; DIGITOXIN; DIGOXIGENIN; DIGOXIN; OUABAGENIN; OUABAIN; PROSCILLARIDIN; STROPHANTHIDIN;

ARTICLE; BINDING AFFINITY; BINDING SITE; CONTROLLED STUDY; DOSE RESPONSE; DRUG RECEPTOR BINDING; DRUG SELECTIVITY; DRUG STRUCTURE; ENZYME INHIBITION; HUMAN; HUMAN CELL; NEWBORN; STRUCTURE ACTIVITY RELATION;

CARDIAC GLYCOSIDES; CARDIOTONIC AGENTS; DOSE-RESPONSE RELATIONSHIP, DRUG; ENZYME INHIBITORS; ERYTHROCYTES; FETAL BLOOD; HUMANS; INHIBITORY CONCENTRATION 50; NA(+)-K(+)-EXCHANGING ATPASE; RUBIDIUM RADIOISOTOPES; SAPONINS; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 0034622950     PISSN: 00243205     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0024-3205(00)00779-7     Document Type: Article

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