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Bioorg Med Chem. 2004 Sep 1;12(17):4749-59.

Isoform-specific phosphoinositide 3-kinase inhibitors from an arylmorpholine scaffold.

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1
Program in Chemistry and Chemical Biology, University of California-San Francisco, San Francisco, CA 94143, USA.

Abstract

Phosphoinositide 3-kinases (PI3-Ks) are an ubiquitous class of signaling enzymes that regulate diverse cellular processes including growth, differentiation, and motility. Physiological roles of PI3-Ks have traditionally been assigned using two pharmacological inhibitors, LY294002 and wortmannin. Although these compounds are broadly specific for the PI3-K family, they show little selectivity among family members, and the development of isoform-specific inhibitors of these enzymes has been long anticipated. Herein, we prepare compounds from two classes of arylmorpholine PI3-K inhibitors and characterize their specificity against a comprehensive panel of targets within the PI3-K family. We identify multiplex inhibitors that potently inhibit distinct subsets of PI3-K isoforms, including the first selective inhibitor of p110beta/p110delta (IC(50) p110beta=0.13 microM, p110delta=0.63 microM). We also identify trends that suggest certain PI3-K isoforms may be more sensitive to potent inhibition by arylmorpholines, thereby guiding future drug design based on this pharmacophore.

PMID:
15358300
DOI:
10.1016/j.bmc.2004.06.022
[Indexed for MEDLINE]
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