
Narirutin
Narirutin is a disaccharide derivative that is (S)-naringenin substituted by a 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. It has a role as an antioxidant, a metabolite and an anti-inflammatory agent. It is a member of 4'-hydroxyflavanones, a (2S)-flavan-4-one, a rutinoside, a dihydroxyflavanone and a disaccharide derivative. It is functionally related to a (S)-naringenin. — ChEBI
- IUPAC name
- (2S)-5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-one
- Molecular formula
- C27H32O14
- Molecular weight
- 580.5 g/mol
- Exact mass
- 580.17920569 Da
- XLogP3
- -1.1
- Topological polar surface area
- 225.0 Ų
- Hydrogen-bond donors
- 8
- Hydrogen-bond acceptors
- 14
- Covalent units
- 1
- Defined stereocentres
- 11
Also known as
16 more reported names
External database identifiers
- ChEBI:CHEBI:28705
- ChEMBL:CHEMBL446246
- EPA DTXSID:DTXSID30931535
- PubMed:22957912
- PubMed:22953908
- PubMed:22888512
- PubMed:22813871
- PubMed:22454671
- PubMed:22254014
- PubMed:22194772
- PubMed:22125675
- PubMed:21837249
- PubMed:21802267
- PubMed:21799684
- PubMed:21779843
Retrieved from NIH PubChem on 2026-08-31 by checksum-valid CAS matching. Chemical properties do not replace the regulatory decision on this page.