Kaempferitrin

Chemical Information
Kaempferol 3,7-di-O-alpha-L-rhamnoside is a glycosyloxyflavone that is kaempferol attached to alpha-L-rhamnopyranosyl residues at positions 3 and 7 respectively via glycosidic linkages. It has been isolated from the aerial parts of Vicia faba and Lotus edulis. It has a role as an antidepressant, a hypoglycemic agent, an antineoplastic agent, a bone density conservation agent, an immunomodulator, an anti-inflammatory agent, an apoptosis inducer and a plant metabolite. It is a polyphenol, an alpha-L-rhamnoside, a dihydroxyflavone, a glycosyloxyflavone and a monosaccharide derivative. It is functionally related to a kaempferol.
| CAS Number | 482-38-2 |
| PubChem CID | 5486199 |
| IUPAC Name | 5-hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]chromen-4-one |
| Molecular Formula | C27H30O14 |
| Molecular Weight | 578.5 |
| XLogP | -0.1 |
| Topological Polar Surface Area | 225 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 5 |
| Heavy Atom Count | 41 |
| Formal Charge | 0 |
| Complexity | 968 |
| Property | Value |
|---|---|
| Molecular Weight | 578.5 |
| XLogP3 | -0.1 |
| Hydrogen Bond Donor Count | 8 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 5 |
| Exact Mass | 578.16355563 |
| Monoisotopic Mass | 578.16355563 |
| Topological Polar Surface Area | 225 Ų |
| Heavy Atom Count | 41 |
| Formal Charge | 0 |
| Complexity | 968 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 10 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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