| Identification | Back Directory | [Name]
1,2-dipalMitoyl-sn-glycero-3-[phospho-rac-(3-lysyl(1-glycerol))] (chloride salt) | [CAS]
1246303-06-9 | [Synonyms]
16:0 Lysyl PG
1,2-dipalmitoyl-sn-glycero-3-[phospho-rac-(3-lysyl(1-glycerol))] (chloride salt)
1,2-DIPALMITOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(3-LYSYL(1-GLYCEROL))] (CHLORIDE SALT);16:0 LYSYL PG
1,2-dipalMitoyl-sn-glycero-3-[phospho-rac-(3-lysyl(1-glycerol))] (chloride salt)
1,2-DIPALMITOYL-SN-GLYCERO-3-[PHOSPHO-RAC-(3-LYSYL(1-GLYCEROL))] (CHLORIDE SALT);16:0 LYSYL PG | [Molecular Formula]
C44H88ClN2O11P | [MDL Number]
MFCD22416793 | [MOL File]
1246303-06-9.mol | [Molecular Weight]
887.61 |
| Hazard Information | Back Directory | [Uses]
16:0 Lysyl PG is suitable for use:
- as a standard for lipidomics analysis by using three-dimensional hydrophilic interaction liquid chromatography-ion mobility-mass spectrometry (HILIC-IM-MS)
- to analyse the influence of peptides on the phase transition behavior of lipids by fourier transform infrared spectroscopy
- in the preparation of artificial vesicles modelled on the lipid composition of Staphylococcal membranes to study the effect of galloyl catechins
| [Biological Activity]
Lysyl phosphatidylglycerol (Lysyl-PG) is formed by lysinylation of PG in the presence of multiprotein resistance factor (MprF). MprF flips lysyl-PG from inner to outer membrane leafletincreasing the positive charge on the membrane. Lysyl PG is essential for domain formation and antibiotic resistance. |
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Merck KGaA
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Creative Enzymes
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