Hmdb loader
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-07-25 00:11:16 UTC
Update Date2021-09-14 14:59:18 UTC
HMDB IDHMDB0012994
Secondary Accession Numbers
  • HMDB12994
Metabolite Identification
Common NameLeukotriene D5
Descriptionleukotriene D5 is coverted from 5-hydroxy-6-S-glutathionyl-7,9,11,14,17-eicosapentaenoic acid (leukotriene C5) by gamma-glutamyl transpeptidase. Leukotrienes are eicosanoids. The eicosanoids consist of the prostaglandins (PGs), thromboxanes (TXs), leukotrienes (LTs), and lipoxins (LXs). The PGs and TXs are collectively identified as prostanoids. Prostaglandins were originally shown to be synthesized in the prostate gland, thromboxanes from platelets (thrombocytes), and leukotrienes from leukocytes, hence the derivation of their names. All mammalian cells except erythrocytes synthesize eicosanoids. These molecules are extremely potent, able to cause profound physiological effects at very dilute concentrations. All eicosanoids function locally at the site of synthesis, through receptor-mediated G-protein linked signalling pathways.
Structure
Data?1582753082
Synonyms
ValueSource
LTD(,5)HMDB
Chemical FormulaC25H38N2O6S
Average Molecular Weight494.644
Monoisotopic Molecular Weight494.245057648
IUPAC Name(5R,6S,7E,9E,11Z,14Z,17Z)-6-{[(2R)-2-amino-2-[(carboxymethyl)carbamoyl]ethyl]sulfanyl}-5-hydroxyicosa-7,9,11,14,17-pentaenoic acid
Traditional Name(5R,6S,7E,9E,11Z,14Z,17Z)-6-{[(2R)-2-amino-2-(carboxymethylcarbamoyl)ethyl]sulfanyl}-5-hydroxyicosa-7,9,11,14,17-pentaenoic acid
CAS Registry NumberNot Available
SMILES
CC\C=C/C\C=C/C\C=C/C=C/C=C/[C@H](SC[C@H](N)C(=O)NCC(O)=O)[C@H](O)CCCC(O)=O
InChI Identifier
InChI=1S/C25H38N2O6S/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-22(21(28)15-14-17-23(29)30)34-19-20(26)25(33)27-18-24(31)32/h3-4,6-7,9-13,16,20-22,28H,2,5,8,14-15,17-19,26H2,1H3,(H,27,33)(H,29,30)(H,31,32)/b4-3-,7-6-,10-9-,12-11+,16-13+/t20-,21+,22-/m0/s1
InChI KeyRWLDHKGRPLNPBN-DSJHTHEWSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as hydroxyeicosapentaenoic acids. These are eicosanoic acids with an attached hydroxyl group and five CC double bonds.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassFatty Acyls
Sub ClassEicosanoids
Direct ParentHydroxyeicosapentaenoic acids
Alternative Parents
Substituents
  • Hydroxyeicosapentaenoic acid
  • Alpha-dipeptide
  • Alpha peptide
  • Long-chain fatty acid
  • N-acyl-alpha amino acid or derivatives
  • N-acyl-alpha-amino acid
  • Alpha-amino acid amide
  • Cysteine or derivatives
  • Alpha-amino acid or derivatives
  • Thia fatty acid
  • Hydroxy fatty acid
  • Unsaturated fatty acid
  • Dicarboxylic acid or derivatives
  • Fatty acid
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Secondary alcohol
  • Amino acid
  • Carboxamide group
  • Carboxylic acid derivative
  • Carboxylic acid
  • Dialkylthioether
  • Sulfenyl compound
  • Thioether
  • Amine
  • Organic oxygen compound
  • Organic nitrogen compound
  • Hydrocarbon derivative
  • Alcohol
  • Organic oxide
  • Carbonyl group
  • Organopnictogen compound
  • Primary aliphatic amine
  • Primary amine
  • Organosulfur compound
  • Organonitrogen compound
  • Organooxygen compound
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0028 g/LALOGPS
logP0.9ALOGPS
logP0.4ChemAxon
logS-5.2ALOGPS
pKa (Strongest Acidic)3.29ChemAxon
pKa (Strongest Basic)8.05ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area149.95 ŲChemAxon
Rotatable Bond Count19ChemAxon
Refractivity141.54 m³·mol⁻¹ChemAxon
Polarizability54.95 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+221.95631661259
DarkChem[M-H]-218.29531661259
DeepCCS[M+H]+221.16630932474
DeepCCS[M-H]-218.77130932474
DeepCCS[M-2H]-251.65530932474
DeepCCS[M+Na]+227.07930932474
AllCCS[M+H]+227.832859911
AllCCS[M+H-H2O]+226.032859911
AllCCS[M+NH4]+229.432859911
AllCCS[M+Na]+229.932859911
AllCCS[M-H]-220.332859911
AllCCS[M+Na-2H]-223.532859911
AllCCS[M+HCOO]-227.232859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Leukotriene D5CC\C=C/C\C=C/C\C=C/C=C/C=C/[C@H](SC[C@H](N)C(=O)NCC(O)=O)[C@H](O)CCCC(O)=O6427.2Standard polar33892256
Leukotriene D5CC\C=C/C\C=C/C\C=C/C=C/C=C/[C@H](SC[C@H](N)C(=O)NCC(O)=O)[C@H](O)CCCC(O)=O3009.8Standard non polar33892256
Leukotriene D5CC\C=C/C\C=C/C\C=C/C=C/C=C/[C@H](SC[C@H](N)C(=O)NCC(O)=O)[C@H](O)CCCC(O)=O4327.2Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Leukotriene D5,1TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C)[C@H](O)CCCC(=O)O4238.8Semi standard non polar33892256
Leukotriene D5,1TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O)O[Si](C)(C)C4285.6Semi standard non polar33892256
Leukotriene D5,1TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O[Si](C)(C)C4252.2Semi standard non polar33892256
Leukotriene D5,1TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O4367.7Semi standard non polar33892256
Leukotriene D5,1TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H](O)CCCC(=O)O4239.6Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4229.3Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4452.9Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H](O)CCCC(=O)O4318.5Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4190.4Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H](O)CCCC(=O)O4295.5Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4179.6Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4240.7Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O)O[Si](C)(C)C4350.7Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4237.0Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O[Si](C)(C)C4309.1Semi standard non polar33892256
Leukotriene D5,2TMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4188.9Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4187.1Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4421.9Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4288.0Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #12CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4371.5Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #13CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4221.8Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #14CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4395.7Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4275.6Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4150.6Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4220.1Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4093.9Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4360.6Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4219.8Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4289.4Semi standard non polar33892256
Leukotriene D5,3TMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4160.6Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4188.2Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3846.4Standard non polar33892256
Leukotriene D5,4TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4854.3Standard polar33892256
Leukotriene D5,4TMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4360.5Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4001.4Standard non polar33892256
Leukotriene D5,4TMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C5015.3Standard polar33892256
Leukotriene D5,4TMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4290.8Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4042.3Standard non polar33892256
Leukotriene D5,4TMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C5048.4Standard polar33892256
Leukotriene D5,4TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4059.2Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3751.2Standard non polar33892256
Leukotriene D5,4TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C5150.4Standard polar33892256
Leukotriene D5,4TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4307.2Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C3957.9Standard non polar33892256
Leukotriene D5,4TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4973.2Standard polar33892256
Leukotriene D5,4TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4173.4Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C3912.7Standard non polar33892256
Leukotriene D5,4TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4913.9Standard polar33892256
Leukotriene D5,4TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4251.7Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C3991.5Standard non polar33892256
Leukotriene D5,4TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C5017.3Standard polar33892256
Leukotriene D5,4TMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4109.3Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C3940.7Standard non polar33892256
Leukotriene D5,4TMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4946.2Standard polar33892256
Leukotriene D5,4TMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4293.4Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O4055.8Standard non polar33892256
Leukotriene D5,4TMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O5051.4Standard polar33892256
Leukotriene D5,4TMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4328.1Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3943.8Standard non polar33892256
Leukotriene D5,4TMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4970.0Standard polar33892256
Leukotriene D5,4TMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4170.5Semi standard non polar33892256
Leukotriene D5,4TMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3901.5Standard non polar33892256
Leukotriene D5,4TMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4890.1Standard polar33892256
Leukotriene D5,5TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4206.1Semi standard non polar33892256
Leukotriene D5,5TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3944.5Standard non polar33892256
Leukotriene D5,5TMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4607.3Standard polar33892256
Leukotriene D5,5TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4080.6Semi standard non polar33892256
Leukotriene D5,5TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3908.5Standard non polar33892256
Leukotriene D5,5TMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4570.6Standard polar33892256
Leukotriene D5,5TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4264.4Semi standard non polar33892256
Leukotriene D5,5TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4002.0Standard non polar33892256
Leukotriene D5,5TMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C4695.2Standard polar33892256
Leukotriene D5,5TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4195.0Semi standard non polar33892256
Leukotriene D5,5TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4037.4Standard non polar33892256
Leukotriene D5,5TMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O[Si](C)(C)C)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C4745.2Standard polar33892256
Leukotriene D5,5TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4260.5Semi standard non polar33892256
Leukotriene D5,5TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C3989.9Standard non polar33892256
Leukotriene D5,5TMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C)O[Si](C)(C)C4683.8Standard polar33892256
Leukotriene D5,1TBDMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4497.0Semi standard non polar33892256
Leukotriene D5,1TBDMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4537.7Semi standard non polar33892256
Leukotriene D5,1TBDMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4512.4Semi standard non polar33892256
Leukotriene D5,1TBDMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O4567.6Semi standard non polar33892256
Leukotriene D5,1TBDMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4491.0Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4740.7Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4882.3Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4749.2Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4685.8Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4741.0Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4669.6Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4758.7Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4795.9Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4731.8Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4746.2Semi standard non polar33892256
Leukotriene D5,2TBDMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4677.7Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #1CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4905.6Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #10CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C5108.3Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #11CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4936.9Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #12CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C5065.5Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #13CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4870.1Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #14CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O5036.8Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #2CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4931.2Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #3CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O)O[Si](C)(C)C(C)(C)C4890.5Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #4CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4871.7Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #5CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O[Si](C)(C)C(C)(C)C4830.5Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #6CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@@H](C(=O)NCC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O5051.7Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #7CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)N(CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)CCCC(=O)O4870.1Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #8CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N[Si](C)(C)C(C)(C)C)C(=O)NCC(=O)O)[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4942.8Semi standard non polar33892256
Leukotriene D5,3TBDMS,isomer #9CC/C=C\C/C=C\C/C=C\C=C\C=C\[C@H](SC[C@H](N)C(=O)N(CC(=O)O)[Si](C)(C)C(C)(C)C)[C@@H](CCCC(=O)O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4894.2Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Leukotriene D5 GC-MS (Non-derivatized) - 70eV, Positivesplash10-002f-7409700000-83e939c62a0ea02275302017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Leukotriene D5 GC-MS (2 TMS) - 70eV, Positivesplash10-00dl-9201413000-27f134b031ca64a41d5c2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Leukotriene D5 GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 10V, Positive-QTOFsplash10-004j-1102900000-277c515a8d3daefa8a032017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 20V, Positive-QTOFsplash10-0553-8629400000-0dec09bc040f66c326df2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 40V, Positive-QTOFsplash10-00b9-9135000000-2e83d6d8222c372a562a2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 10V, Negative-QTOFsplash10-002g-0203900000-907d2e0aa49d3c007bb72017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 20V, Negative-QTOFsplash10-003r-2439100000-4ebe077961b7db2fa6552017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 40V, Negative-QTOFsplash10-00di-6911000000-4fa82eb1763f102d27602017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 10V, Negative-QTOFsplash10-002f-0900800000-f53c678447ec8200f8da2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 20V, Negative-QTOFsplash10-054n-4902100000-d4d9b128bdbc46a0f8ed2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 40V, Negative-QTOFsplash10-0007-9310000000-a9ac521af7b8f2b37c8d2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 10V, Positive-QTOFsplash10-00kk-3944500000-a380ce16e2876ad8790d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 20V, Positive-QTOFsplash10-00ku-2900000000-4268e484dedf07ab514a2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Leukotriene D5 40V, Positive-QTOFsplash10-0apl-2900000000-d1b3bac1a61d90e4a36a2021-09-23Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB029238
KNApSAcK IDNot Available
Chemspider ID30776673
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53481571
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.