Structure Database (LMSD)
Common Name
Zymosterol
Systematic Name
5α-cholesta-8,24-dien-3β-ol
Synonyms
3D model of Zymosterol
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Main
Classification
Category
Main Class
Sub Class
String Representations
InChiKey (Click to copy)
CGSJXLIKVBJVRY-XTGBIJOFSA-N
InChi (Click to copy)
InChI=1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h7,19-21,23-24,28H,6,8-17H2,1-5H3/t19-,20+,21+,23-,24+,26+,27-/m1/s1
SMILES (Click to copy)
C1[C@]2(C)C3CC[C@]4(C)[C@@]([H])([C@]([H])(C)CC/C=C(\C)/C)CC[C@@]4([H])C=3CC[C@@]2([H])C[C@@H](O)C1
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Saccharomyces cerevisiae
(#4932)
Saccharomycetes
(#4891)
Studies on biosynthesis of cholesterol. IX. Zymosterol as a precursor of cholesterol.,
Arch Biochem Biophys, 1957
Arch Biochem Biophys, 1957
Pubmed ID:
13403684
Rattus norvegicus
(#10116)
Mammalia
(#40674)
Studies on biosynthesis of cholesterol. IX. Zymosterol as a precursor of cholesterol.,
Arch Biochem Biophys, 1957
Arch Biochem Biophys, 1957
Pubmed ID:
13403684
Other Databases
Wikipedia
KEGG ID
HMDB ID
CHEBI ID
LIPIDBANK ID
SST9103
PubChem CID
SwissLipids ID
Calculated Physicochemical Properties
Heavy Atoms
28
Rings
4
Aromatic Rings
0
Rotatable Bonds
4
Van der Waals Molecular Volume
429.73
Topological Polar Surface Area
20.23
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
1
logP
7.74
Molar Refractivity
119.61
Reactions
Filter by species:
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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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Admin
Created at
-
Updated at
16th Jan 2024