Structure Database (LMSD)

Common Name
Calditoglycerocaldachaeol
Systematic Name
Synonyms
LM ID
LMGL02060006
Status
Active
Exact Mass
Calculate m/z
1463.368215
Formula


Download as...
MDLMOL SDF CSV TSV
MDLMOL files can be opened in various drawing programs. In ChemDraw, open as filetype "MDL Molfile".

Main

Classification

String Representations

InChiKey (Click to copy)
IJPWROQOANOMJA-YXOGYJPTSA-N
InChi (Click to copy)
InChI=1S/C92H182O11/c1-70-29-17-33-74(5)41-25-49-82(13)57-61-99-66-86(65-93)101-63-59-84(15)51-27-43-76(7)35-19-31-72(3)39-23-47-80(11)55-53-79(10)46-22-38-71(2)30-18-34-75(6)42-26-50-83(14)58-62-100-67-87(68-103-91-89(96)88(95)90(97)92(91,98)69-94)102-64-60-85(16)52-28-44-77(8)36-20-32-73(4)40-24-48-81(12)56-54-78(9)45-21-37-70/h70-91,93-98H,17-69H2,1-16H3/t70-,71-,72-,73-,74+,75+,76+,77+,78-,79-,80-,81-,82+,83+,84+,85+,86+,87-,88+,89?,90-,91+,92?/m0/s1
SMILES (Click to copy)
C([C@]1(OCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@@H](CC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCOC[C@@](OCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CCC[C@H](C)CC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCC[C@@H](C)CCOC1)([H])CO)C)[H])O[C@@H]1C(O)[C@@H](O)[C@H](O)C1(O)CO

References

Reference
PubMed ID: 16306681
Comments
Submitted by Henry Boumann, Netherlands

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Sulfolobus acidocaldarius (#2285)
Thermoprotei (#183924)
Recent advances in structural research on ether lipids from archaea including comparative and physiological aspects.,
Biosci Biotechnol Biochem, 2005
Pubmed ID: 16306681

Other Databases

PubChem CID

Calculated Physicochemical Properties

Heavy Atoms 103
Rings 2
Aromatic Rings 0
Rotatable Bonds 5
Van der Waals Molecular Volume 1672.13
Topological Polar Surface Area 175.81
Hydrogen Bond Donors 6
Hydrogen Bond Acceptors 11
logP 27.91
Molar Refractivity 445.77

Admin

Created at
-
Updated at
-
LIPID MAPS® abbreviations for glycerolipids (GL)

The LIPID MAPS® glycerolipid abbreviations (MG,DG,TG) are used here to refer to species with one, two or three radyl side-chains, respectively, where the structures of the side chains are indicated within parentheses in the 'Prefix(sn1/sn2/sn3)' format (e.g. TG(16:0/18:1(9Z)/18:0). Acyl chains are assumed by default. The alkyl ether linkage is represented by the 'O-' prefix, e.g. DG(O-16:0/18:1(9Z)/0:0), whereas the 1Z-alkenyl ether (Plasmalogen) linkage is represented by the 'P-' prefix, e.g. and DG(P-14:0/18:1(9Z)/0:0).

For Diradylglycerols and Triradylglycerols, it is not always possible to experimentally determine the exact position of radyl groups on the glycerol group. For Diradylglycerols with two different radyl groups, two different structural isomers exist. For Triradylglycerols with three different radyl groups, six different isomers exist.

Instead of drawing all possible structural isomers explicitly for Diradylglycerols and Triradylglycerols, the LIPID MAPS® abbreviation scheme supports the isomeric specification. A suffix containing 'iso' along with the number of possible isomers is appended to the abbreviation (e.g. [iso2],[iso6]) and a single unique LM_ID is assigned. The structure assigned to the LM_ID corresponds to the radyl substitution shown in the abbreviation. An option is provided to display the other isomers in the group.

The [rac] designation refers to racemic mixtures due to substitution at the sn1 and sn3 positions of glycerol.