Biologically Active Small Molecules

A selective PI3K inhibitor that targets the &beta isoform more potently than PI3K&delta, PI3K&gamma, or PI3K&alpha (IC₅₀s = 0.69, 13.

A selective PI3K inhibitor that targets the &beta isoform more potently than PI3K&delta, PI3K&gamma, or PI3K&alpha (IC₅₀s = 0.69, 13.

A selective PI3K inhibitor that targets the &beta isoform more potently than PI3K&delta, PI3K&gamma, or PI3K&alpha (IC₅₀s = 0.69, 13.

A selective PI3K inhibitor that targets the &beta isoform more potently than PI3K&delta, PI3K&gamma, or PI3K&alpha (IC₅₀s = 0.69, 13.

Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPAR&gamma. One of these substances was recently isolated and purified from oxLDL, and

Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPAR&gamma. One of these substances was recently isolated and purified from oxLDL, and

Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPAR&gamma. One of these substances was recently isolated and purified from oxLDL, and

Oxidized low-density lipoprotein (oxLDL) particles contain low molecular weight species which promote the differentiation of monocytes via the nuclear receptor PPAR&gamma. One of these substances was recently isolated and purified from oxLDL, and

azido-FTY720 is a highly photoreactive analog of FTY720 that can be used to identify receptor binding sites for this ligand.

azido-FTY720 is a highly photoreactive analog of FTY720 that can be used to identify receptor binding sites for this ligand.

azido-FTY720 is a highly photoreactive analog of FTY720 that can be used to identify receptor binding sites for this ligand.

azido-FTY720 is a highly photoreactive analog of FTY720 that can be used to identify receptor binding sites for this ligand.