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1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC

CAS No.
1872379-72-0
Chemical Name:
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC
Synonyms
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC;1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC MaxSpec Standard;(7R)-4,7-dihydroxy-N,N,N-trimethyl-10-oxo-3,5,9-trioxa-4-phosphapentacosan-22,22,23,23,24,24,25,25,25-d9-1-aminium, 4-oxide, inner salt
CBNumber:
CB16197572
Molecular Formula:
C24H50NO7P
Molecular Weight:
495.64
MDL Number:
MOL File:
1872379-72-0.mol
Last updated:2023-05-21 10:59:17

1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC Properties

storage temp. Store at -20°C
solubility DMF: 10 mg/ml; DMSO: 10 mg/ml; Ethanol: 10 mg/ml; PBS (pH 7.2): 10 mg/ml
form A crystalline solid

1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC Chemical Properties,Uses,Production

Description

1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC is intended for use as an internal standard for the quantification of 1-palmitoyl-2-hydroxy-sn-glycero-3-PC by GC- or LC-MS. 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC is the ubiquitous lipid species generated following phospholipase A2 (PLA2) hydrolysis of phosphatidylcholine.1 It increases the production of reactive oxygen species (ROS) and decreases superoxide dismutase (SOD) and endothelial nitric oxide synthase (eNOS) protein levels and phosphorylation of ERK1/2 in human umbilical vein endothelial cells (HUVECs) when used at a concentration of 125 μM.2 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC potentiates the secretion of IL-6, IL-1β, IL-12, and TNF-α in LPS-stimulated M1 macrophages, but has no effect on CD163, CD206, CD36, or IL-10 in LPS-stimulated M2 macrophages when used at concentrations of 0.3 and 1.0 μM.3 It increases TGF-β1 production and enhances Foxp3 protein levels in Treg cells in isolated human peripheral blood when used at a concentration of 10 μM.4 1-Palmitoyl-2-hydroxy-sn-glycero-3-PC enhances neutrophil function, bacterial clearance, and survival in mouse models of sepsis when administered at a dose of 10 mg/kg.5

References

1. Balsinde, J., Winstead, M.V., and Dennis, E.A. Phospholipase A2 regulation of arachidonic acid mobilization FEBS Lett. 531(1),2-6(2002).
2. Choi, S., Park, S., Liang, G.H., et al. Superoxide generated by lysophosphatidylcholine induces endothelial nitric oxide synthase downregulation in human endothelial cells Cell Physiol. Biochem. 25(2-3),233-240(2010).
3. Qin, X., Qiu, C., and Zhao, L. Lysophosphatidylcholine perpetuates macrophage polarization toward classically activated phenotype in inflammation Cell. Immunol. 289(1-2),185-190(2014).
4. Hasegawa, H., Lei, J., Matsumoto, T., et al. Lysophosphatidylcholine enhances the suppressive function of human naturally occurring regulatory T cells through TGF-β production Biochem. Biophys. Res. Commun. 415(3),526-531(2011).
5. Yan, J.-J., Jung, J.-S., Lee, J.-E., et al. Therapeutic effects of lysophosphatidylcholine in experimental sepsis Nat. Med. 10(2),161-167(2004).

1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC Preparation Products And Raw materials

Raw materials

Preparation Products

1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC Suppliers

Global( 5)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Hongye Biotechnology Co. Ltd 400-9205774 sales@glpbio.cn China 6870 58
ChemeGen(Shanghai) Biotechnology Co.,Ltd. 18818260767 sales@chemegen.com China 11289 58
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 8740 58
Jilin Chinese Academy of Sciences-yanshen Technology 18143011203 ET-market@chemextension.com China 40885 58
1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC 1-Palmitoyl-d9-2-hydroxy-sn-glycero-3-PC MaxSpec Standard (7R)-4,7-dihydroxy-N,N,N-trimethyl-10-oxo-3,5,9-trioxa-4-phosphapentacosan-22,22,23,23,24,24,25,25,25-d9-1-aminium, 4-oxide, inner salt 1872379-72-0