Frangulin A

CAS : 521-62-0

Ref. 3D-FF65554

Informations sur le produit

• Nom: Frangulin A
• Synonymes: Emodin-L-rhamnosideRhamnoxanthin, 3-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-1,8-dihydroxy-6-methyl-9,10-anthracenedione, 3-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-1,8-dihydroxy-6-methylanthraquinone, 3-[(6-Deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-1,8-dihydroxy-6-methyl-9,10-anthracenedione, 4,5-dihydroxy-7-methyl-9,10-dioxo-9,10-dihydroanthracen-2-yl 6-deoxy-alpha-L-mannopyranoside, 9,10-Anthracenedione, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-1,8-dihydroxy-6-methyl-, 9,10-Anthracenedione, 3-[(6-deoxy-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-1,8-dihydroxy-6-methyl-, Anthraquinone, 3-((6-deoxy-alpha-L-mannopyranosyl)oxy)-1,8-dihydroxy-6-methyl-, Brn 0059993, Emodin-<span class="text-smallcaps">L</span>-rhamnoside, Frangulin A (8CI), Franguloside, Rhamnoxanthin
• CAS: 521-62-0

Description

Frangulin A is an acetate extract of the fungus Frangula alnus. It has been shown to have insulin-sensitizing effects and may be useful in the treatment of diabetes mellitus and hepatitis. The mechanism of action of Frangulin A is not known, but it has been shown to inhibit bacterial enzymes such as glycoside hydrolase and esterase, which are involved in fatty acid synthesis. Frangulin A has been shown to increase glucose uptake in liver cells by inhibiting the activity of phosphofructokinase-1, which is a key enzyme in glycolysis. This product also has antiviral properties that may be due to its ability to inhibit RNA polymerases and reverse transcriptases found in viruses such as HIV-1.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 416.38 g/mol
• Formule: C₂₁H₂₀O₉
• Degré de pureté: Min. 95%
• Couleur/Forme: Solid
• InChI: InChI=1S/C21H20O9/c1-7-3-10-14(12(22)4-7)18(26)15-11(17(10)25)5-9(6-13(15)23)30-21-20(28)19(27)16(24)8(2)29-21/h3-6,8,16,19-24,27-28H,1-2H3/t8-,16-,19+,20+,21-/m0/s1
• Code InChI: InChIKey=DTTVUKLWJFJOHO-FUCRAMRQSA-N
• SMILES: Cc1cc(O)c2c(c1)C(=O)c1cc(O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](O)[C@H]3O)cc(O)c1C2=O