Lucidal

Chemical Information
Lucialdehyde C is a tetracyclic triterpenoid that is lanosta-8,24-dien-26-al substituted by a beta-hydroxy group at position 3 and an oxo group at position 7. Isolated from Ganoderma lucidum and Ganoderma pfeifferi, it exhibits cytotoxic activity. It has a role as a metabolite and an antineoplastic agent. It is an aldehyde, a tetracyclic triterpenoid, a secondary alcohol and a cyclic terpene ketone. It derives from a hydride of a lanostane.
| CAS Number | 252351-96-5 |
| PubChem CID | 10366713 |
| IUPAC Name | (E,6R)-6-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-7-oxo-1,2,3,5,6,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enal |
| Molecular Formula | C30H46O3 |
| Molecular Weight | 454.7 |
| XLogP | 6.6 |
| Topological Polar Surface Area | 54.4 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 894 |
| Property | Value |
|---|---|
| Molecular Weight | 454.7 |
| XLogP3 | 6.6 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 5 |
| Exact Mass | 454.34469533 |
| Monoisotopic Mass | 454.34469533 |
| Topological Polar Surface Area | 54.4 Ų |
| Heavy Atom Count | 33 |
| Formal Charge | 0 |
| Complexity | 894 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 7 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
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