Structure via PubChem · Public domain (PubChem)
ononin
Sign in to saveAlso known as Formononetin glucoside, 4'-methoxyisoflavone-7-O-beta-D-glucopyranoside, formononetin 7-O-beta-D-glucopyranoside, Formononetin 7-O-glucoside
Ononin is an isoflavone glycoside, the 7-O-β-D-glucopyranoside of formononetin, which in turn is the 4'-O-methyl (4'-methoxy) derivative of the parent isoflavone daidzein.
Chemical data
- Formula
- C22H22O9
- Molecular weight
- 430.4 g/mol
- IUPAC name
- 3-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
- SMILES
- COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
- InChIKey
- MGJLSBDCWOSMHL-MIUGBVLSSA-N
- XLogP
- 1
- Polar surface area
- 135 Ų
- H-bond donors
- 4
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- isoflavone
- Mass
- 430.126382
Show 4 more facts
- canonical SMILES
- COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O
- chemical formula
- C₂₂H₂₂O₉
- found in taxon
- Deguelia scandens
- isomeric SMILES
- COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Natural sources
- Pharmacokinetics
- Pharmacodynamics
- References
{{Chembox | Verifiedfields = changed | Watchedfields = changed | verifiedrevid = 414762729 | Name = Ononin | Reference = | ImageFile = Ononin.svg | IUPACName = 7-(β-D-Glucopyranosyloxy)-4′-methoxyisoflavone | SystematicName = 3-(4-Methoxyphenyl)-7-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-1-benzopyran-4-one | OtherNames = Formononetin glucosideFormononetin-7-glucosideFormononetin 7-O-glucoside |Section1= |Section2= |Section7= }}
Ononin is an isoflavone glycoside, the 7-O-β-D-glucopyranoside of formononetin, which in turn is the 4'-O-methyl (4'-methoxy) derivative of the parent isoflavone daidzein.
Excerpted from Wikipedia’s “ononin” article, available under the CC BY-SA 4.0 licence.