Structure Database (LMSD)
Common Name
Sitostanyl-16:0
Systematic Name
Stigmast-3β-yl-hexadecanoate
Synonyms
3D model of Sitostanyl-16:0
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Viridiplantae
(#33090)
An approach based on ultrahigh performance liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry allowing the quantification of both individual phytosteryl and phytostanyl fatty acid esters in complex mixtures.,
J Chromatogr A, 2016
J Chromatogr A, 2016
Pubmed ID:
26718186
String Representations
InChiKey (Click to copy)
QXDOCEWFNOQOEP-HQVNQYTDSA-N
InChi (Click to copy)
InChI=1S/C45H82O2/c1-8-10-11-12-13-14-15-16-17-18-19-20-21-22-43(46)47-38-29-31-44(6)37(33-38)25-26-39-41-28-27-40(45(41,7)32-30-42(39)44)35(5)23-24-36(9-2)34(3)4/h34-42H,8-33H2,1-7H3/t35-,36-,37+,38+,39+,40-,41+,42+,44+,45-/m1/s1
SMILES (Click to copy)
C1[C@]2(C)[C@@]3([H])CC[C@]4(C)[C@@]([H])([C@]([H])(C)CC[C@@H](CC)C(C)C)CC[C@@]4([H])[C@]3([H])CC[C@@]2([H])C[C@@H](OC(CCCCCCCCCCCCCCC)=O)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
47
Rings
4
Aromatic Rings
0
Rotatable Bonds
22
Van der Waals Molecular Volume
752.56
Topological Polar Surface Area
26.30
Hydrogen Bond Donors
0
Hydrogen Bond Acceptors
2
logP
14.42
Molar Refractivity
202.94
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Updated at
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