2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) (YMDB11867)

Identification
YMDB IDYMDB11867
Name2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0)
SpeciesSaccharomyces cerevisiae
StrainBrewer's yeast
Description2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) is a monolysocardiolipin (MLCL). Monolysocardiolipins have three fatty acid tails, instead of the usual two. 2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) contains one chain of (9Z-tetradecenoyl) at the C1 position, one chain of (9Z-pentadecenoyl) at the C2 position, one chain of hexadecanoic acid at the C3 position, one chain of at the C4 position. MLCL is present in eukaryotes as part of the metabolic cycle of mitochondrial lipids. Removal of one acyl chain from a cardiolipin results in generation of monolysocardiolipin (MLCL). MLCL has been used as an inter­mediate in the synthesis of spin-labeled CL to study the interaction of CL with mitochondrial enzymes. Because a role for MLCL has been suggested in apoptosis, this molecule has been used to study its interaction with various enzymes involved in lipid remodeling and apoptosis. There are two species of monolysocardiolipins, 1-MLCL which is missing a fatty acid in position R1 the and 2-MLCL which is missing a fatty acid in position R4.
Structure
Thumb
MOLSDFPDBSMILESInChI
SynonymsNot Available
CAS numberNot Available
WeightAverage: 1069.342
Monoisotopic: 1068.6643112
InChI KeyKHIATNVXUDVBER-JJELMDBYSA-N
InChIInChI=1S/C54H102O16P2/c1-4-7-10-13-16-19-22-24-27-29-31-34-37-40-52(57)64-43-49(55)44-66-71(60,61)67-45-50(56)46-68-72(62,63)69-48-51(47-65-53(58)41-38-35-32-28-25-21-18-15-12-9-6-3)70-54(59)42-39-36-33-30-26-23-20-17-14-11-8-5-2/h15,17-18,20,49-51,55-56H,4-14,16,19,21-48H2,1-3H3,(H,60,61)(H,62,63)/b18-15-,20-17-/t49-,50-,51-/m1/s1
IUPAC Name[(2R)-3-({[(2R)-3-(hexadecanoyloxy)-2-hydroxypropoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy][(2R)-2-[(9Z)-pentadec-9-enoyloxy]-3-[(9Z)-tetradec-9-enoyloxy]propoxy]phosphinic acid
Traditional IUPAC Name(2R)-3-{[(2R)-3-(hexadecanoyloxy)-2-hydroxypropoxy(hydroxy)phosphoryl]oxy}-2-hydroxypropoxy((2R)-2-[(9Z)-pentadec-9-enoyloxy]-3-[(9Z)-tetradec-9-enoyloxy]propoxy)phosphinic acid
Chemical FormulaC54H102O16P2
SMILES[H][C@@](O)(COC(=O)CCCCCCCCCCCCCCC)COP(O)(=O)OC[C@@]([H])(O)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCC)OC(=O)CCCCCCC\C=C/CCCCC
Chemical Taxonomy
Physical Properties
StateSolid
Charge0
Melting pointNot Available
Experimental Properties
PropertyValueReference
Water SolubilityNot AvailablePhysProp
LogPNot AvailablePhysProp
Predicted Properties
PropertyValueSource
Water Solubility0.00042 g/LALOGPS
logP7.87ALOGPS
logP14.73ChemAxon
logS-6.4ALOGPS
pKa (Strongest Acidic)1.59ChemAxon
pKa (Strongest Basic)-3.4ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area230.88 ŲChemAxon
Rotatable Bond Count57ChemAxon
Refractivity284.94 m³·mol⁻¹ChemAxon
Polarizability123.44 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Biological Properties
Cellular Locations
  • Mitochondrion membrane
Organoleptic PropertiesNot Available
SMPDB Pathways
Cardiolipin Biosynthesis CL(14:1(9Z)/15:1(9Z)/16:0/23:1(11Z))PW010942 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(14:1(9Z)/15:1(9Z)/16:0/23:1(9Z))PW010943 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(14:1(9Z)/15:1(9Z)/16:0/25:0)PW010944 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(14:1(9Z)/15:1(9Z)/16:0/25:1(11Z))PW010945 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(14:1(9Z)/15:1(9Z)/16:0/25:1(9Z))PW010946 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG PathwaysNot Available
SMPDB Reactions
2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) → CL(14:1(9Z)/15:1(9Z)/16:0/23:1(11Z))
2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) → CL(14:1(9Z)/15:1(9Z)/16:0/23:1(9Z))
2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) → CL(14:1(9Z)/15:1(9Z)/16:0/25:0)
2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) → CL(14:1(9Z)/15:1(9Z)/16:0/25:1(11Z))
2-MLCL(14:1(9Z)/15:1(9Z)/16:0/0:0) → CL(14:1(9Z)/15:1(9Z)/16:0/25:1(9Z))
KEGG ReactionsNot Available
Concentrations
Intracellular ConcentrationsNot Available
Extracellular ConcentrationsNot Available
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0wt9-6092232050-d750b586344e4d741141JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-11bi-4193141130-01fc4f66bebc09a359c3JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-08fr-5295323110-39e64aa63b26cbee395bJSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a70-1090000010-13a3ffbe57949e2834c5JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-056r-4090000000-45fa5da629d9d592c236JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-004i-9071000000-963bb1c362e5ea64f3c7JSpectraViewer
References
References:
  • Baile MG, Lu YW, Claypool SM. (2014). "The topology and regulation of cardiolipin biosynthesis and remodeling in yeast." Chem Phys Lipids. 2014 Apr;179:25-31. doi: 10.1016/j.chemphyslip.2013.10.008. Epub 2013 Nov 1.24184646
Synthesis Reference:Not Available
External Links:
ResourceLink
CHEBI IDNot Available
HMDB IDNot Available
Pubchem Compound IDNot Available
Kegg IDNot Available
ChemSpider IDNot Available
FOODB IDNot Available
Wikipedia IDNot Available
BioCyc IDNot Available