Structure Database (LMSD)
Common Name
1-(6-[1]-ladderane-hexanoyl)-2-(8-[1]-ladderane-octanyl)-sn-glycerol
Systematic Name
1-(6-[1]-ladderane-hexanoyl)-2-(8-[1]-ladderane-octanyl)-sn-glycerol
Synonyms
3D model of 1-(6-[1]-ladderane-hexanoyl)-2-(8-[1]-ladderane-octanyl)-sn-glycerol
Please note: Where there are chiral atoms but the stereochemistry is undefined, the 3D model takes an arbitrary conformation
Classification
Category
Main Class
Sub Class
References
Taxonomy Information
Curated from
NCBI taxonomy class
Reference
Candidatus Brocadiaceae
(#1127830)
Candidatus Brocadiia
(#2517206)
Structural identification of ladderane and other membrane lipids of planctomycetes capable of anaerobic ammonium oxidation (anammox).,
FEBS J, 2005
FEBS J, 2005
Pubmed ID:
16098207
String Representations
InChiKey (Click to copy)
BRBKZFBOOOLWJO-KNVKINKTSA-N
InChi (Click to copy)
InChI=1S/C41H64O4/c42-28-32(29-45-41(43)20-8-5-7-15-31-22-24-38-34-17-10-12-19-36(34)40(38)27-31)44-25-13-4-2-1-3-6-14-30-21-23-37-33-16-9-11-18-35(33)39(37)26-30/h9,12,16,19,22,24,30-40,42H,1-8,10-11,13-15,17-18,20-21,23,25-29H2/t30?,31?,32-,33?,34?,35?,36?,37?,38?,39?,40?/m0/s1
SMILES (Click to copy)
OC[C@]([H])(OCCCCCCCCC1CC2C3CCC=CC3C2CC1)COC(=O)CCCCCC1CC2C3C=CCCC3C2C=C1
Other Databases
PubChem CID
Calculated Physicochemical Properties
Heavy Atoms
45
Rings
6
Aromatic Rings
0
Rotatable Bonds
20
Van der Waals Molecular Volume
668.30
Topological Polar Surface Area
55.76
Hydrogen Bond Donors
1
Hydrogen Bond Acceptors
4
logP
10.76
Molar Refractivity
184.43
Admin
Created at
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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.
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.