Glimepiride/pioglitazone

(±)5-HETrE is an essential fatty acid analogue of arachidonic acid that is readily converted to leukotriene A3 via the 5-lipoxygenase-leukotriene pathway. Studies suggest that (±)5-HETrE has depressive effects on osteoblast activity. In addition,

A pyroglutamylated form of apelin-13, in that the N-terminal glutamine residue is cyclized to pyroglutamic acid a potent APJ receptor agonist (EC₅₀ = 0.30 nM) the major apelin isoform in the plasma of healthy human subjects.

A member of the 2-aryl propionic acid group of NSAIDs that reduces inflammation through inhibition of NF-&kappaB and AP-1 activation decreases survival of prostate tumor cells by inducing p75NTR protein expression inhibits the enzyme

A member of the 2-aryl propionic acid group of NSAIDs that reduces inflammation through inhibition of NF-&kappaB and AP-1 activation decreases survival of prostate tumor cells by inducing p75NTR protein expression inhibits the enzyme

A member of the 2-aryl propionic acid group of NSAIDs that reduces inflammation through inhibition of NF-&kappaB and AP-1 activation decreases survival of prostate tumor cells by inducing p75NTR protein expression inhibits the enzyme

Selective group II mGlu antagonist.

Selective group II mGlu antagonist.

DescriptionAs the Pd G3 complex, this ligand from the Buchwald group offers best-in-class performance in the arylation of sterically hindered primary amines.

An analog of the PKC-activating second messenger diacylglycerol activates PKC 15% at 25 &microM.

An analog of the PKC-activating second messenger diacylglycerol activates PKC 15% at 25 &microM.

An analog of the PKC-activating second messenger diacylglycerol activates PKC 15% at 25 &microM.

An analog of the PKC-activating second messenger diacylglycerol activates PKC 15% at 25 &microM.