Structure Database (LMSD)

Common Name
(10S,13S,16S)-d14-9-PhytoF[9R,12S]
Systematic Name
8-((2R,3S,5S)-5-((1S,4S,E)-1,4-dihydroxyhex-2-en-1-yl)-3-hydroxytetrahydrofuran-2-yl)octanoic acid
Synonyms
LM ID
LMFA02040099
Formula
C18H32O6
Exact Mass
Calculate m/z
344.21989
Sum Composition
FA 18:2;O4
Status
Active (generated by computational methods)
Show lipids differing only in stereochemistry/bond geometry

Classification

Category
Main Class
Sub Class
Fatty Acyls [FA]
Octadecanoids [FA02]
Phytofurans [FA0204]

String Representations

InChiKey (Click to copy)
XSSRKBRTVPNAMX-PBPVBRRBSA-N
InChi (Click to copy)
InChI=1S/C18H32O6/c1-2-13(19)10-11-14(20)17-12-15(21)16(24-17)8-6-4-3-5-7-9-18(22)23/h10-11,13-17,19-21H,2-9,12H2,1H3,(H,22,23)/b11-10+/t13-,14-,15-,16+,17-/m0/s1
SMILES (Click to copy)
C(CCCCCCC[C@@]1([H])O[C@]([H])([C@@H](O)/C=C/[C@@H](O)CC)C[C@@H]1O)(=O)O

Other Databases

PubChem CID
134812174

Calculated Physicochemical Properties

Heavy Atoms 24
Rings 1
Aromatic Rings 0
Rotatable Bonds 12
Van der Waals Molecular Volume 355.06
Topological Polar Surface Area 109.29
Hydrogen Bond Donors 4
Hydrogen Bond Acceptors 6
logP 3.44
Molar Refractivity 93.24

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Created at
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Updated at
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