产品名称
16:0 Dimethyl PE, 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine-N,N-dimethyl, powder
SMILES string
[H][C@@](COP([O-])(OCC[N+](C)(C)[H])=O)(OC(CCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O
InChI
1S/C39H78NO8P/c1-5-7-9-11-13-15-17-19-21-23-25-27-29-31-38(41)45-35-37(36-47-49(43,44)46-34-33-40(3)4)48-39(42)32-30-28-26-24-22-20-18-16-14-12-10-8-6-2/h37H,5-36H2,1-4H3,(H,43,44)
InChI key
SKWDCOTXHWCSGS-UHFFFAOYSA-N
assay
>99% (TLC)
form
powder
packaging
pkg of 1 × 25 mg (850854P-25mg)
manufacturer/tradename
Avanti Research™ - A Croda Brand 850854P
shipped in
dry ice
storage temp.
−20°C
Application
16:0 Dimethyl PE or phosphatidyl-N,N-dimethylethanolamine (PDME) has been used as a substrate for phosphatidylethanolamine (PE) N-methyl transferase.
Biochem/physiol Actions
16:0 Dimethyl PE or phosphatidyl-N,N-dimethylethanolamine (PDME) acts as an intermediate for the synthesis of phosphatidylcholine (PC).
Packaging
5 mL Amber Glass Screw Cap Vial (850854P-25mg)
Legal Information
Avanti Research is a trademark of Avanti Polar Lipids, LLC
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Purification of phosphatidylethanolamine N-methyltransferase from rat liver.
Ridgway N, et al.
Test, 262(35), 17231-17239 (1987)
Rat brain phosphatidyl-N, N-dimethylethanolamine is rich in polyunsaturated fatty acids
Tacconi M, et al.
Journal of Neurochemistry, 45(3), 805-809 (1985)
Kinetic mechanism of phosphatidylethanolamine N-methyltransferase.
Ridgway N, et al.
The Journal of Biological Chemistry, 263(32), 16864-16871 (1988)
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