Structure Database (LMSD)
Common Name
Ganodermaside B
Systematic Name
(22E,24R)-15β-hydroxyergosta-4,6,8(14),22-tetraen-3-one
Synonyms
LM ID
LMST01031191
Formula
Exact Mass
Calculate m/z
408.302831
Sum Composition
Status
Curated
3D model of Ganodermaside B
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Talaromyces stipitatus
(#28564)
Eurotiomycetes
(#147545)
Five undescribed steroids from Talaromyces stipitatus and their cytotoxic activities against hepatoma cell lines.,
Phytochemistry, 2021
Phytochemistry, 2021
Pubmed ID:
34087503
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
Biosci Biotechnol Biochem, 2011
Pubmed ID:
21512225
String Representations
InChiKey (Click to copy)
MMVSNLKSAHIETF-IBJCVOCSSA-N
InChi (Click to copy)
InChI=1S/C28H40O2/c1-17(2)18(3)7-8-19(4)24-16-25(30)26-22-10-9-20-15-21(29)11-13-27(20,5)23(22)12-14-28(24,26)6/h7-10,15,17-19,23-25,30H,11-14,16H2,1-6H3/b8-7+/t18-,19+,23-,24+,25+,27-,28+/m0/s1
SMILES (Click to copy)
C1CC(=O)C=C2C=CC3=C4[C@H](O)C[C@]([H])([C@]([H])(C)/C=C/[C@H](C)C(C)C)[C@@]4(C)CC[C@]3([H])[C@@]12C
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
30
Rings
4
Aromatic Rings
Rotatable Bonds
4
Van der Waals Molecular Volume
447.90
Topological Polar Surface Area
37.30
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
2
logP
6.72
Molar Refractivity
124.36
Admin
Created at
18th Jun 2021
Updated at
31st Mar 2025