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ChemicalBook--->CAS DataBase List--->154436-48-3

154436-48-3

154436-48-3 Structure

154436-48-3 Structure
IdentificationBack Directory
[Name]

1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC
[CAS]

154436-48-3
[Synonyms]

1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC
[Molecular Formula]

C46H84NO10P
[MOL File]

154436-48-3.mol
[Molecular Weight]

842.15
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

Ethanol: 30 mg/mL; Ethanol:PBS (pH 7.2)(1:2): 0.3 mg/mL
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319
[Precautionary statements ]

P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
Hazard InformationBack Directory
[Description]

1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC is a phospholipid that contains stearic acid at the sn-1 position and 15(S)-HpETE at the sn-2 position. It is produced via oxidation of 1-stearoyl-2-arachidonoyl-sn-glycero-3-PC (SAPC; ) by 15-lipoxygenase (15-LO).1 1-Stearoyl-2-15(S)-HpETE-sn-glycero-3-PC is toxic to human umbilical vein endothelial cells (HUVECs) when used at a concentration of 100 μM.2
[storage]

Store at -20°C
[References]

1. Morgan, A.H., Hammond, V.J., Morgan, L., et al. Quantitative assays for esterified oxylipins generated by immune cells Nat. Protoc. 5(12),1919-1931(2010).
2. Kaneko, T., Baba, N., and Matsuo, M. Cytotoxicity of phosphatidylcholine hydroperoxides is exerted through decomposition of fatty acid hydroperoxide moiety Curr. Opin. Struct. Biol. 21(2),173-179(1996).
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