Pioglitazone hydrochloride

General description The protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation,

General description Peroxisome proliferators include hypolipidemic drugs, herbicides, leukotriene antagonists, and plasticizers: this term arises because they induce an increase in the size and number of peroxisomes. Peroxisomes are subcellular

MP07-66, a FTY720 analogue, is devoid of immunosuppressive effects and shows promising antitumor effects in chronic lymphocytic leukemia by disruption of the SET-PP2A complex leading to PP2A reactivation.Form:Oil.

MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.

MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.

MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.

MPEP is a selective mGlu5 receptor antagonist with IC50 of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.

InformationMPEP is a selectivemGlu5receptor antagonist withIC50of 36 nM, exhibits no appreciable activity at mGlu1b/2/3/4a/7b/8a/6 receptors.In vitroMPEP has no appreciable agonist or antagonist activity at the closely related recombinant human

A potent, highly selective, and centrally active antagonist at the mGlu5a receptor subtype (IC₅₀ = 36 nM) also has been reported as a positive allosteric modulator of mGluR4 at higher concentrations.

A potent, highly selective, and centrally active antagonist at the mGlu5a receptor subtype (IC₅₀ = 36 nM) also has been reported as a positive allosteric modulator of mGluR4 at higher concentrations.

A potent, highly selective, and centrally active antagonist at the mGlu5a receptor subtype (IC₅₀ = 36 nM) also has been reported as a positive allosteric modulator of mGluR4 at higher concentrations.

A potent, highly selective, and centrally active antagonist at the mGlu5a receptor subtype (IC₅₀ = 36 nM) also has been reported as a positive allosteric modulator of mGluR4 at higher concentrations.