Structure Database (LMSD)
Common Name
16:2 Stigmasterol ester
Systematic Name
Stigmast-5,22E-dien-3β-yl (7Z,10Z-hexadecadienoate)
Synonyms
No other lipid differing only in stereochemistry/bond geometry found
3D model of 16:2 Stigmasterol ester
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
Arabidopsis thaliana
(#3702)
Magnoliopsida
(#3398)
Quantification of sterol lipids in plants by quadrupole time-of-flight mass spectrometry.,
J Lipid Res, 2011
J Lipid Res, 2011
Pubmed ID:
21382968
DOI:
10.1194/jlr.D013987
String Representations
InChiKey (Click to copy)
FGVPRDISXWKMPO-QGSJLZPCSA-N
InChi (Click to copy)
InChI=1S/C45H74O2/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/h13-14,16-17,23-25,34-36,38-42H,8-12,15,18-22,26-33H2,1-7H3/b14-13-,17-16-,24-23+/t35-,36-,38+,39+,40-,41+,42+,44+,45-/m1/s1
SMILES (Click to copy)
C1[C@H](OC(=O)CCCCC/C=C\C/C=C\CCCCC)CC2=CC[C@@]3([H])[C@]4([H])CC[C@]([H])([C@]([H])(C)/C=C/[C@@H](CC)C(C)C)[C@@]4(C)CC[C@]3([H])[C@@]2(C)C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
47
Rings
4
Aromatic Rings
0
Rotatable Bonds
19
Van der Waals Molecular Volume
742.00
Topological Polar Surface Area
26.30
Hydrogen Bond Donors
0
Hydrogen Bond Acceptors
2
logP
13.67
Molar Refractivity
202.63
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Updated at
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