MW 298.4 Da, Purity >98%. Activates PPARα and PPARγ. Inhibits acyl-CoA:cholesterol acyl transferase (ACAT). Modulates estrogen receptors and disrupts ERK1/2-mediated phosphorylation of 4EBP1 and eIF4B. Chemopreventive properties. Active in vivo and in vitro.
MEL-1A-R, MR, MT-1, MTNR 1A, MTR1A_HUMAN, Mel1a melatonin receptor, Mel1a receptor, MelR, Melatonin receptor 1A, Melatonin receptor type 1A
MW 298.4 Da, Purity >98%. Activates PPARα and PPARγ. Inhibits acyl-CoA:cholesterol acyl transferase (ACAT). Modulates estrogen receptors and disrupts ERK1/2-mediated phosphorylation of 4EBP1 and eIF4B. Chemopreventive properties. Active in vivo and in vitro.
Soluble in DMSO to 50 mM.
Activates PPARα and PPARγ. Inhibits acyl-CoA:cholesterol acyl transferase (ACAT). Modulates estrogen receptors and disrupts ERK1/2-mediated phosphorylation of 4EBP1 and eIF4B. Chemopreventive properties. Active in vivo and in vitro.
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2D chemical structure image of ab141907, Auraptene, Activates PPARalpha and PPARgamma
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