2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) (YMDB11870)

Identification
YMDB IDYMDB11870
Name2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0)
SpeciesSaccharomyces cerevisiae
StrainBrewer's yeast
Description2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) is a monolysocardiolipin (MLCL). Monolysocardiolipins have three fatty acid tails, instead of the usual two. 2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) contains three chains of (9Z-pentadecenoyl) at the C1, C2 and C3 positions, 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: 1067.326
Monoisotopic: 1066.648661136
InChI KeyWLEMABZRJGEJQH-YFMBIHRKSA-N
InChIInChI=1S/C54H100O16P2/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-52(57)64-43-49(55)44-66-71(60,61)67-45-50(56)46-68-72(62,63)69-48-51(70-54(59)42-39-36-33-30-27-24-21-18-15-12-9-6-3)47-65-53(58)41-38-35-32-29-26-23-20-17-14-11-8-5-2/h16-21,49-51,55-56H,4-15,22-48H2,1-3H3,(H,60,61)(H,62,63)/b19-16-,20-17-,21-18-/t49-,50-,51-/m1/s1
IUPAC Name[(2R)-2,3-bis[(9Z)-pentadec-9-enoyloxy]propoxy][(2R)-2-hydroxy-3-({hydroxy[(2R)-2-hydroxy-3-[(9Z)-pentadec-9-enoyloxy]propoxy]phosphoryl}oxy)propoxy]phosphinic acid
Traditional IUPAC Name(2R)-2,3-bis[(9Z)-pentadec-9-enoyloxy]propoxy((2R)-2-hydroxy-3-{[hydroxy((2R)-2-hydroxy-3-[(9Z)-pentadec-9-enoyloxy]propoxy)phosphoryl]oxy}propoxy)phosphinic acid
Chemical FormulaC54H100O16P2
SMILES[H][C@@](O)(COC(=O)CCCCCCC\C=C/CCCCC)COP(O)(=O)OC[C@@]([H])(O)COP(O)(=O)OC[C@@]([H])(COC(=O)CCCCCCC\C=C/CCCCC)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 Solubility0.00037 g/LALOGPS
logP7.84ALOGPS
logP14.37ChemAxon
logS-6.5ALOGPS
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 Count56ChemAxon
Refractivity286.06 m³·mol⁻¹ChemAxon
Polarizability121.19 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(15:0/15:1(9Z)/15:1(9Z)/15:1(9Z))PW011626 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(15:1(11Z)/15:1(9Z)/15:1(9Z)/15:1(9Z))PW011923 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/15:1(11Z))PW012219 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/15:1(9Z))PW012220 ThumbThumb?image type=greyscaleThumb?image type=simple
Cardiolipin Biosynthesis CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/23:1(11Z))PW012221 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG PathwaysNot Available
SMPDB Reactions
2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) → CL(15:0/15:1(9Z)/15:1(9Z)/15:1(9Z))
2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) → CL(15:1(11Z)/15:1(9Z)/15:1(9Z)/15:1(9Z))
2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) → CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/15:1(11Z))
2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) → CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/15:1(9Z))
2-MLCL(15:1(9Z)/15:1(9Z)/15:1(9Z)/0:0) → CL(15:1(9Z)/15:1(9Z)/15:1(9Z)/23:1(11Z))
KEGG ReactionsNot Available
Concentrations
Intracellular ConcentrationsNot Available
Extracellular ConcentrationsNot Available
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-002b-8080353190-1df918b18ae8ebe94ed4JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-5191252240-77b3623a728ae0962264JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-052b-5190312111-5edc8cf01fcf4fe7f3b6JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-009i-4091010040-0b2338eae8dbb09bf4e4JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-004r-7193020020-b7eb36619daaf421eadcJSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-004j-9052010000-54acf1457e2ee0c4aefcJSpectraViewer
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