Show simple item record

dc.creatorPerlin,David S.
dc.date1998-08-01
dc.date.accessioned2020-02-17T15:30:09Z
dc.date.available2020-02-17T15:30:09Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0717-34581998000200002
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/128912
dc.descriptionThe development of an effective target for therapeutic intervention remains a critical part of the drug discovery process. One such target class is the P-type ion translocating ATPases, which include the Na+,K+-ATPase of cardiac cells and the H+,K+-ATPase of gastric parietal cells. These enzymes serve as selective targets for digoxin and omeprazole, which are used to treat heart disease and gastrointestinal ulcers, and are two of the leading prescribed therapeutics worldwide. It is the exquisite selectivity that can be achieved between family members that continues to make the P-type enzymes desirable targets for developing new therapeutics including a new generation of antiulcer therapeutic and a new class of antifungal therapeutic.
dc.formattext/html
dc.languageen
dc.publisherPontificia Universidad Católica de Valparaíso
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceElectronic Journal of Biotechnology v.1 n.2 1998
dc.titleIon pumps as targets for therapeutic intervention: Old and new paradigms


This item appears in the following Collection(s)

Show simple item record