Structure Database (LMSD)

Common Name
2-O-(beta-D-galactopyranosyl-(1->6)-beta-D-galactopyranosyl) 2S-hydroxyundecanoic acid
Systematic Name
2-O-(β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl) 2S-hydroxyundecanoic acid
Synonyms
LM ID
LMFA13010047
Formula
Exact Mass
Calculate m/z
526.262545
Status
Curated

Classification

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Lichtheimia corymbifera (#42458)
Mucoromycetes (#2212703)
Astonishing diversity of natural surfactants: 1. Glycosides of fatty acids and alcohols.,
Lipids, 2004
Pubmed ID: 15691016

String Representations

InChiKey (Click to copy)
LMSCLROPNINDDT-NBEBUOOJSA-N
InChi (Click to copy)
InChI=1S/C23H42O13/c1-2-3-4-5-6-7-8-9-12(21(31)32)34-23-20(30)18(28)16(26)14(36-23)11-33-22-19(29)17(27)15(25)13(10-24)35-22/h12-20,22-30H,2-11H2,1H3,(H,31,32)/t12-,13+,14+,15-,16-,17-,18-,19+,20+,22+,23+/m0/s1
SMILES (Click to copy)
CCCCCCCCC[C@H](O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO[C@H]2[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O2)O1)C(=O)O

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 36
Rings 2
Aromatic Rings 0
Rotatable Bonds 15
Van der Waals Molecular Volume 493.37
Topological Polar Surface Area 219.97
Hydrogen Bond Donors 8
Hydrogen Bond Acceptors 13
logP 1.94
Molar Refractivity 128.13

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Created at
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Updated at
11th May 2021