Chrysoeriol

Chemical Information
4',5,7-trihydroxy-3'-methoxyflavone is the 3'-O-methyl derivative of luteolin. It has a role as an antioxidant, a metabolite and an antineoplastic agent. It is a monomethoxyflavone and a trihydroxyflavone. It is functionally related to a luteolin. It is a conjugate acid of a 4',5-dihydroxy-3'-methoxyflavon-7-olate(1-).
| CAS Number | 491-71-4 |
| PubChem CID | 5280666 |
| IUPAC Name | 5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one |
| Molecular Formula | C16H12O6 |
| Molecular Weight | 300.26 |
| XLogP | 1.7 |
| Topological Polar Surface Area | 96.2 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 2 |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 462 |
| Property | Value |
|---|---|
| Molecular Weight | 300.26 |
| XLogP3 | 1.7 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 2 |
| Exact Mass | 300.06338810 |
| Monoisotopic Mass | 300.06338810 |
| Topological Polar Surface Area | 96.2 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 462 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| 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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