Fasiglifam 50 mg | Purity Not Available
TargetMol

Fasiglifam (TAK875) is a potent, selective and orally bioavailable GPR40 agonist.
More Information Supplier PageFasiglifam (TAK875) is a potent, selective and orally bioavailable GPR40 agonist.
More Information Supplier PageFasiglifam (TAK875) is a potent, selective and orally bioavailable GPR40 agonist.
More Information Supplier PageFasiglifam (TAK875) is a potent, selective and orally bioavailable GPR40 agonist.
More Information Supplier PageEnasidenib is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
More Information Supplier PageEnasidenib is an orally available inhibitor of specific mutant forms of the mitochondrial enzyme isocitrate dehydrogenase type 2 (IDH2), with potential antineoplastic activity.
More Information Supplier PageCarbinoxamine Maleate Salt (Lergefin) is an ethanolamine class of H1 antihistamines with mild antimuscarinic and sedative properties.
More Information Supplier Page2-Methoxyestradiol is an orally bioavailable estradiol metabolite with potential antineoplastic activity. 2-Methoxyestradiol inhibits angiogenesis by reducing endothelial cell proliferation and inducing endothelial cell apoptosis. This agent also inhibits tumor cell growth by binding to tubulin, resulting in antimitotic activity, and by inducing caspase activation, resulting in cell cycle arrest in the G2 phase, DNA fragmentation, […]
More Information Supplier PageEntacapone is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).
More Information Supplier PageEntacapone is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).
More Information Supplier PageEntacapone is a selective and reversible inhibitor of catechol-O-methyltransferase (COMT).
More Information Supplier Page