Basic information
- CAS
35682-55-4- Standard SMILES
COc1c(O[C@@H]2O[C@@H](C)[C@H](O)[C@@H](O)[C@H]2O)cc2oc(-c3ccc(O)c(O)c3)cc(=O)c2c1O- InChIKey
UXCXDWDJBSJZOU-CKPDRDNLSA-N- Molecular formula
- C22H22O11
- Average molar mass
- 462.4 g/mol
- Monoisotopic mass
- 462.11621151
Overview
6-methoxyluteolin 7-alpha-L-rhamnoside is a glycosyloxyflavone that is luteolin substituted by a methoxy group at position 6 and an alpha-L-rhamnosyl moiety at position 7 via a glycosidic linkage. It is a monomethoxyflavone, a trihydroxyflavone, an alpha-L-rhamnoside, a glycosyloxyflavone and a monosaccharide derivative. It is functionally related to a luteolin.
Names & identifiers
- Preferred name
- 7-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4H-1-benzopyran-4-one
- IUPAC
- 2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one
Names & synonyms
6-Methoxyluteolin 7-rhamnoside35682-55-4DTXSID60331882RefChem:1074300DTXCID102829762-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-((2S,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one7-((6-Deoxy-alpha-L-mannopyranosyl)oxy)-2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4H-1-benzopyran-4-one6-methoxyluteolin 7-alpha-L-rhamnoside2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one2-(3,4-dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-chromen-7-yl 6-deoxy-alpha-L-mannopyranosideCHEBI:28314LMPK12111174
Show more names
Q271036312-(3,4-Dihydroxyphenyl)-5-hydroxy-6-methoxy-4-oxo-4H-1-benzopyran-7-yl 6-deoxy-alpha-L-mannopyranoside
Database identifiers
- CAS
35682-55-4
Properties
Computed structural properties
- XLogP
- 1
- Topological polar surface area
- 175 Ų
- Hydrogen bond donors
- 6
- Hydrogen bond acceptors
- 11
- Rotatable bonds
- 4
- Heavy atoms
- 33
- Formal charge
- 0
- Complexity
- 744
Experimental & physicochemical properties
LipidsPolyketides [PK] -> Flavonoids [PK12] -> Flavones and Flavonols [PK1211]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
Loading…