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Identification
YMDB IDYMDB11472
Name1-MLCL(0:0/12:0/14:1(9Z)/16:0)
SpeciesSaccharomyces cerevisiae
StrainBrewer's yeast
Description1-MLCL(0:0/12:0/14:1(9Z)/16:0) is a monolysocardiolipin (MLCL). Monolysocardiolipins have three fatty acid tails, instead of the usual two. 1-MLCL(0:0/12:0/14:1(9Z)/16:0) contains one chain of at the C1 position, one chain of dodecanoic acid at the C2 position, one chain of (9Z-tetradecenoyl) at the C3 position, one chain of hexadecanoic acid 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
SynonymsNot Available
CAS numberNot Available
WeightAverage: 1029.277
Monoisotopic: 1028.633011072
InChI KeyALNMIASPQSJKTR-MCWYSYFTSA-N
InChIInChI=1S/C51H98O16P2/c1-4-7-10-13-16-19-21-22-24-27-30-33-36-39-51(56)67-48(43-61-49(54)37-34-31-28-26-23-20-17-14-11-8-5-2)45-65-69(59,60)63-42-46(53)41-62-68(57,58)64-44-47(40-52)66-50(55)38-35-32-29-25-18-15-12-9-6-3/h14,17,46-48,52-53H,4-13,15-16,18-45H2,1-3H3,(H,57,58)(H,59,60)/b17-14-/t46-,47+,48+/m0/s1
IUPAC Name[(2S)-3-({[(2R)-2-(dodecanoyloxy)-3-hydroxypropoxy](hydroxy)phosphoryl}oxy)-2-hydroxypropoxy][(2R)-2-(hexadecanoyloxy)-3-[(9Z)-tetradec-9-enoyloxy]propoxy]phosphinic acid
Traditional IUPAC Name(2S)-3-{[(2R)-2-(dodecanoyloxy)-3-hydroxypropoxy(hydroxy)phosphoryl]oxy}-2-hydroxypropoxy((2R)-2-(hexadecanoyloxy)-3-[(9Z)-tetradec-9-enoyloxy]propoxy)phosphinic acid
Chemical FormulaC51H98O16P2
SMILES[H][C@](O)(COP(O)(=O)OC[C@@]([H])(CO)OC(=O)CCCCCCCCCCC)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCC)OC(=O)CCCCCCCCCCCCCCC
Chemical Taxonomy
Physical Properties
StateSolid
Charge0
Melting pointNot Available
Experimental Properties
PropertyValueReference
Water SolubilityNot AvailablePhysProp
LogPNot AvailablePhysProp
Predicted Properties
PropertyValueSource
Water Solubility0.0006 g/LALOGPS
logP7.56ALOGPS
logP13.76ChemAxon
logS-6.2ALOGPS
pKa (Strongest Acidic)1.59ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-2ChemAxon
Hydrogen Acceptor Count9ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area230.88 ŲChemAxon
Rotatable Bond Count55ChemAxon
Refractivity270.02 m³·mol⁻¹ChemAxon
Polarizability117.92 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(12:0/14:1(9Z)/16:0/18:0)PW006639 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(12:0/14:1(9Z)/16:0/18:1(11Z))PW006640 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(12:0/14:1(9Z)/16:0/18:1(9Z))PW006641 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(12:0/14:1(9Z)/16:0/20:0)PW006642 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(12:0/14:1(9Z)/16:0/20:1(11Z))PW006643 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG PathwaysNot Available
SMPDB Reactions
CL(12:0/14:1(9Z)/16:0/18:0)1-MLCL(0:0/12:0/14:1(9Z)/16:0)
CL(12:0/14:1(9Z)/16:0/18:1(11Z))1-MLCL(0:0/12:0/14:1(9Z)/16:0)
CL(12:0/14:1(9Z)/16:0/18:1(9Z))1-MLCL(0:0/12:0/14:1(9Z)/16:0)
CL(12:0/14:1(9Z)/16:0/20:0)1-MLCL(0:0/12:0/14:1(9Z)/16:0)
CL(12:0/14:1(9Z)/16:0/20:1(11Z))1-MLCL(0:0/12:0/14:1(9Z)/16:0)
KEGG ReactionsNot Available
Concentrations
Intracellular ConcentrationsNot Available
Extracellular ConcentrationsNot Available
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-08i0-7490142330-0045ff80c37ec32da9f8JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0bt9-5790213420-32b1f1deecf62d98cf30JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a4i-5590123000-5576a85a066665de1d3eJSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a6r-3391010220-b0f37d63f042253762c1JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-004i-9283011100-a1b005a950305cbaaab4JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-004j-9151000000-ea6f4101f4972ce763cdJSpectraViewer
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