Structure Database (LMSD)
Systematic Name
5α,9α-epidioxy-3β-hydroxy-ergosta-7-en-6-one
Synonyms
- 6-Oxo-5,9-epidioxy-5alpha-ergosta-7-en-3beta-ol
LM ID
LMST01031335
Formula
Exact Mass
Calculate m/z
444.32396
Sum Composition
Status
Active
3D model of
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
Hypsizygus marmoreus
(#39966)
Agaricomycetes
(#155619)
Sterol constituents from five edible mushrooms,
Chem Pharm Bull, 1998
Chem Pharm Bull, 1998
DOI:
10.1248/cpb.46.944
String Representations
InChiKey (Click to copy)
FZOPHVRKJMCTDV-ZFZPKPCHSA-N
InChi (Click to copy)
InChI=1S/C28H44O4/c1-17(2)18(3)7-8-19(4)21-9-10-22-23-15-24(30)28-16-20(29)11-12-26(28,6)27(23,31-32-28)14-13-25(21,22)5/h15,17-22,29H,7-14,16H2,1-6H3/t18-,19+,20-,21+,22-,25+,26+,27+,28-/m0/s1
SMILES (Click to copy)
C12=CC(=O)[C@]34OO[C@@]1(CC[C@@]1(C)[C@@]2([H])CC[C@@]1([C@H](C)CC[C@H](C)C(C)C)[H])[C@@]3(C)CC[C@H](O)C4
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
32
Rings
5
Aromatic Rings
Rotatable Bonds
5
Van der Waals Molecular Volume
461.04
Topological Polar Surface Area
59.90
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
4
logP
6.88
Molar Refractivity
126.18
Admin
Created at
5th Oct 2023
Updated at
5th Oct 2023