Cyclomulberrin

Chemical Information
Cyclomulberrin is a extended flavonoid that is 6H,7H-chromeno[4,3-b]chromen-7-one which is substituted by a 2-methylprop-1-en-1-yl group at position 6, a 3-methylbut-2-en-1-yl group at position 11, and hydroxy groups at positions 3, 8, and 10. It is found in the bark of Morus species and has been reported to protect human neuronal cells derived from the human neuroblastoma SH-SY5Y cell line. It has a role as a protective agent and a plant metabolite. It is a chromenochromene, a polyphenol, an organic heterotetracyclic compound, a cyclic ketone and an extended flavonoid.
| CAS Number | 19275-51-5 |
| PubChem CID | 11742872 |
| IUPAC Name | 3,8,10-trihydroxy-11-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one |
| Molecular Formula | C25H24O6 |
| Molecular Weight | 420.5 |
| XLogP | 5.8 |
| Topological Polar Surface Area | 96.2 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 803 |
| Property | Value |
|---|---|
| Molecular Weight | 420.5 |
| XLogP3 | 5.8 |
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 3 |
| Exact Mass | 420.15728848 |
| Monoisotopic Mass | 420.15728848 |
| Topological Polar Surface Area | 96.2 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 803 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 1 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Alternative Products
| Catalog | Name |
|---|---|
| HY-N12514 | Cyclomulberrin |
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