Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Drug, Enzyme Inhibitors"'
Autor:
Rossen Radkov, Solange Kharoubi-Hess, Danièle Schaer, Käthi Geering, Jean-Daniel Horisberger, Nikolai N. Modyanov
Publikováno v:
Biochemical and Biophysical Research Communications, vol. 356, no. 1, pp. 142-6
Cardiac steroids inhibit Na,K-ATPase and the related non-gastric H,K-ATPase, while they do not interact with gastric H,K-ATPase. Introducing an arginine, the residue present in the gastric H,K-ATPase, in the second extracellular loop at the correspon
Autor:
Jorge Alejandro Palermo, Marie Gompel, Lydia Puricelli, Laurent Meijer, Maryse Leost, Elisa Bal de Kier Joffé, Laura Hernandez Franco
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2004, 14, pp.1703-1707
Bioorganic and Medicinal Chemistry Letters, 2004, 14, pp.1703-1707
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2004, 14, pp.1703-1707
Bioorganic and Medicinal Chemistry Letters, 2004, 14, pp.1703-1707
Meridianins are brominated 3-(2-aminopyrimidine)-indoles which are purified from Aplidium meridianum, an Ascidian from the South Atlantic (South Georgia Islands). We here show that meridianins inhibit various protein kinases such as cyclin-dependent
Autor:
Giuliana Decorti, Alessandra Pontillo, Alberto Tommasini, Luigina De Leo, Sergio Crovella, Annalisa Marcuzzi
Publikováno v:
Pediatric research. 70(1)
The shortage of geranylgeranyl-pyrophosphate (GGPP) was associated to an increased IL-1β release in the autoinflammatory syndrome mevalonate kinase deficiency (MKD), a rare inherited disease that has no specific therapy. Farnesyltransferase inhibito
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2004, 11, pp.413-416
Bioorganic and Medicinal Chemistry Letters, 2004, 11, pp.413-416
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2004, 11, pp.413-416
Bioorganic and Medicinal Chemistry Letters, 2004, 11, pp.413-416
Kenpaullone derivatives with a modified parent ring system were synthesized in order to develop kinase inhibitors with enhanced selectivity. Among the novel structures, 1-azakenpaullone was found to act as a selective GSK-3beta versus CDK1 inhibitor.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::884c3e2eff0f8de3485cc434e53cac27
https://hal.archives-ouvertes.fr/hal-00020128
https://hal.archives-ouvertes.fr/hal-00020128