Title : Novel PI analogues selectively block activation of the pro-survival serine/threonine kinase Akt.

Pub. Date : 2003 Feb 5

PMID : 12553797






1 Functional Relationships(s)
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1 The synthesis from l-quebrachitol of a series of 3-deoxygenated ether lipid-type phosphatidylinositol (PI) analogues is reported, that selectively block activation of Akt and downstream substrates without affecting activation of the upstream kinase, PDK-1, or other kinases downstream of ras such as MAPK in H157 and H1703 lung cancer cells that have high levels of constitutively active Akt. quebrachitol pyruvate dehydrogenase kinase 1 Homo sapiens