Structure Database (LMSD)
Common Name
32-hydroxylanosterol
Systematic Name
4,4-dimethyl-14α-hydroxymethyl-5α-cholesta-8,24-dien-3β-ol
Synonyms
- lanosta-8,24-dien-3beta,30-diol
LM ID
LMST01010124
Formula
Exact Mass
Calculate m/z
442.38108
Sum Composition
Status
Active
No other lipid differing only in stereochemistry/bond geometry found
3D model of 32-hydroxylanosterol
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
Reactions
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Reactions are shown if the E.C. number of the enzyme catalysing it is annotated in the UniProt database for a species belonging to the selected taxonomic class.
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References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Saccharomyces cerevisiae
(#4932)
Saccharomycetes
(#4891)
Mechanistic studies of lanosterol C-32 demethylation. Conditions which promote oxysterol intermediate accumulation during the demethylation process.,
J Biol Chem, 1986
J Biol Chem, 1986
Pubmed ID:
3782148
Rattus norvegicus
(#10116)
Mammalia
(#40674)
Mechanistic studies of lanosterol C-32 demethylation. Conditions which promote oxysterol intermediate accumulation during the demethylation process.,
J Biol Chem, 1986
J Biol Chem, 1986
Pubmed ID:
3782148
String Representations
InChiKey (Click to copy)
DWVYYKFZEDMMPU-PUXRVUTHSA-N
InChi (Click to copy)
InChI=1S/C30H50O2/c1-20(2)9-8-10-21(3)22-14-18-30(19-31)24-11-12-25-27(4,5)26(32)15-16-28(25,6)23(24)13-17-29(22,30)7/h9,21-22,25-26,31-32H,8,10-19H2,1-7H3/t21-,22-,25+,26+,28-,29-,30-/m1/s1
SMILES (Click to copy)
C12CC[C@@]3([H])C(C)(C)[C@@H](O)CC[C@]3(C)C=1CC[C@]1(C)[C@@]([H])([C@@](C)([H])CC/C=C(\C)/C)CC[C@@]21CO
Other Databases
Calculated Physicochemical Properties
Heavy Atoms
32
Rings
4
Aromatic Rings
0
Rotatable Bonds
5
Van der Waals Molecular Volume
490.42
Topological Polar Surface Area
40.46
Hydrogen Bond Donors
2
Hydrogen Bond Acceptors
2
logP
8.02
Molar Refractivity
135.29
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Updated at
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