Structure Database (LMSD)

Common Name
Ganodermaside C
Systematic Name
9α-hydroxyergosta-4,6,8(14),22-tetraene-3,15-dione
Synonyms
LM ID
LMST01031371
Formula
C28H38O3
Exact Mass
Calculate m/z
422.282096
Sum Composition
ST 28:6;O3
Status
Curated
Show lipids differing only in stereochemistry/bond geometry

Classification

Category
Main Class
Sub Class
Sterol Lipids [ST]
Sterols [ST01]
Ergosterols and C24-methyl derivatives [ST0103]

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Ganoderma lucidum (#5315)
Agaricomycetes (#155619)
Ganodermasides C and D, two new anti-aging ergosterols from spores of the medicinal mushroom Ganoderma lucidum.,
Biosci Biotechnol Biochem, 2011
Pubmed ID: 21512225

String Representations

InChiKey (Click to copy)
PUAPOLUQVUHYJA-VKDITDTOSA-N
InChi (Click to copy)
InChI=1S/C28H38O3/c1-17(2)18(3)7-8-19(4)23-16-24(30)25-22-10-9-20-15-21(29)11-12-27(20,6)28(22,31)14-13-26(23,25)5/h7-10,15,17-19,23,31H,11-14,16H2,1-6H3/b8-7+/t18-,19+,23+,26+,27-,28+/m0/s1
SMILES (Click to copy)
C1CC(=O)C=C2C=CC3=C4C(=O)C[C@]([H])([C@H](C)/C=C/[C@H](C)C(C)C)[C@@]4(C)CC[C@]3(O)[C@@]12C

Other Databases

PubChem CID
101789954

Calculated Physicochemical Properties

Heavy Atoms 31
Rings 4
Aromatic Rings
Rotatable Bonds 4
Van der Waals Molecular Volume 454.05
Topological Polar Surface Area 54.37
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 3
logP 6.04
Molar Refractivity 124.82

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Created at
31st Mar 2025
Updated at
31st Mar 2025