acacetin

Acacetin (5,7-Dihydroxy-4'-methoxyflavone) is an O-methylated flavone found in various plants, exhibiting antinociceptive, anti-inflammatory, and antioxidant activities in different research models.

Acacetin-7-glucuronide is a glucuronic acid glycoside that can be isolated from the methanol leaf extract of the purple bead. It may be used in the development of nutritional health products and pharmaceutical preparations.

Acacetin 7-O-β-sophoroside, a flavonoid glycoside, has been isolated from the rhizomes and roots of valerian (Valeriana officinalis) [1].

Acacetin 7-O-β-D-xylopyranosyl-(1→2)[α-L-rhamnopyranosyl-(1→6)]-β-D-glucopyranoside (Compound 10), a flavone glycoside, is extractable from Robinia pseudoacacia leaf preparations [1].

Acacetin 7-O-β-D-glucuronopyranosyl-(1→2)[α-L-rhamnopyranosyl-(1→6)]-β-D-glucopyranoside, also known as compound 8, is a flavonoid glycoside isolated from the leaf extract of the black locust (Leguminosae) [1].

Acacetin 7-O-(6″-O-α-L-rhamnopyranosyl-β-sophoroside), a flavonoid glycoside, has been isolated from Valeriana jatamansi Jones [1].

Acacetin-7-O-beta-D-galactopyranoside is a natural product found in Chrysanthemum indicum.

Acacetin 7-[rhamnosyl-(1->2)-galacturonide] is a natural product that can be used as a reference standard. The CAS number of Acacetin 7-[rhamnosyl-(1->2)-galacturonide] is 38722-95-1.

Acacetin-7-O-(3-O-malonyl)-β-D-glucopyranoside (compound 13) is a compound extractable from the plant D. foetidum.

1. Linarin (Acacetin-7-O-rutinoside) (acacetin-7-O-β-d-rutinoside) shows selective dose dependent inhibitory effect on acetylcholinesterase. 2. Linarin alleviates GalN LPS-induced liver injury by suppressing TNF-α-mediated apoptotic pathways. 3. Linarin prevents A beta-induced neurotoxicity through the activation of PI3K Akt, which subsequently inhibits GSK-3b and up-regulates Bcl-2. 4. The piperine significantly enhanced the oral absorption of Linarin in rats by inhibiting P-glycoprotein mediated cellular efflux during the intestinal absorption and likely simultaneously by inhibiting the metabolism of Linarin.