Ononin

CAS: 486-62-4

Ref. 3D-FO65770

Produktinformation

• Name: Ononin
• Synonyme: Glucosyl-7-O-Formononetin, 3-(4-methoxyphenyl)-4-oxo-4H-chromen-7-yl beta-D-glucopyranoside, 4'-Methoxyisoflavone-7-O-beta-D-glucopyranoside, 4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-methoxyphenyl)-, 4H-1-Benzopyran-4-one, 7-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3-(4-methoxyphenyl)-, 7-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one, 7-(β-Glucosyloxy)-3-(4-methoxyphenyl)isoflavone, 7-Hydroxy-4′-methoxyisoflavone-7-O-β-<span class="text-smallcaps">D</span>-glucoside, Formononetin 7-O-glucoside, Formononetin 7-O-β-<span class="text-smallcaps">D</span>-glucopyranoside, Formononetin 7-O-β-<span class="text-smallcaps">D</span>-glucoside, Formononetin 7-glucoside, Formononetin 7β-<span class="text-smallcaps">D</span>-glucopyranoside, Formononetin glucoside, Formononetin-7-O-beta-D-glucopyranoside, Formononetin-7-O-β-<span class="text-smallcaps">D</span>-glycoside, Ononoside

Beschreibung

Ononin is a furocoumarin that has been shown to have significant cytotoxicity in vitro. It also has the ability to modulate the response of cells to various stimuli by binding to DNA and activating transcription. Ononin can be found in pueraria lobata, which is a plant that is native to Japan and China, as well as in other plants such as kidney beans, ligustrum fruit, and fructus quinquefolii. The chemical structure of ononin has similarities with biochanin A, a compound found in black cohosh, which has been used for centuries for its purported anti-inflammatory properties.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 430.4 g/mol
• Formel: C₂₂H₂₂O₉
• Reinheit: Min. 95%
• Farbe/Form: White Powder
• InChl: InChI=1S/C22H22O9/c1-28-12-4-2-11(3-5-12)15-10-29-16-8-13(6-7-14(16)18(15)24)30-22-21(27)20(26)19(25)17(9-23)31-22/h2-8,10,17,19-23,25-27H,9H2,1H3/t17-,19-,20+,21-,22-/m1/s1
• InChI Key: InChIKey=MGJLSBDCWOSMHL-MIUGBVLSSA-N
• SMILES: COc1ccc(-c2coc3cc(O[C@@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)ccc3c2=O)cc1