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L6629

1-Myristoyl-sn-glycero-3-phosphocholine

Name: 1-Myristoyl-<I>sn</I>-glycero-3-phosphocholine
Brand: SIGMA

synthetic, ~99%

别名:

3-sn-Lysophosphatidylcholine, 1-myristoyl, L-γ-Myristoyl-α-lysolecithin, Lysolecithin, tetradecanoyl, Myristoyl L-α-lysophosphatidylcholine

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关于此项目

经验公式（希尔记法）:

C₂₂H₄₆NO₇P

化学文摘社编号:

20559-16-4

分子量:

467.58

PubChem Substance ID:

24896439

UNSPSC Code:

12352211

MDL number:

MFCD00036902

Beilstein/REAXYS Number:

5776231

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biological source

synthetic

assay

~99%

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCC(=O)OC[C@@H](O)COP([O-])(=O)OCC[N+](C)(C)C

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

129F8461

067F8360

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Lipid metabolism in Trypanosoma brucei: utilization of myristate and myristoyllysophosphatidylcholine for myristoylation of glycosyl phosphatidylinositols.

K A Werbovetz et al.

The Biochemical journal, 318 ( Pt 2), 575-581 (1996-09-01)

Myristate is the exclusive fatty acid species in the glycosyl phosphatidylinositol (GPI) anchor of the Trypanosoma brucei variant surface glycoprotein (VSG). [3H]Myristate can be incorporated into T. brucei GPIs by two distinct processes known as fatty acid remodelling and myristate

From elicitins to lipid-transfer proteins: a new insight in cell signalling involved in plant defence mechanisms.

Jean-Pierre Blein et al.

Trends in plant science, 7(7), 293-296 (2002-07-18)

Elicitins and lipid-transfer proteins are small cysteine-rich lipid-binding proteins secreted by oomycetes and plant cells, respectively, that share some structural and functional properties. In spite of intensive work on their structure and diversity at the protein and genetic levels, the

Photolabelling of D-beta-hydroxybutyrate apodehydrogenase with azidoaryl phospholipids.

M S el Kebbaj et al.

FEBS letters, 182(1), 176-180 (1985-03-11)

Two synthetic photoactive azidoarylphosphatidylcholines were used to investigate the level of interaction between D-beta-hydroxybutyrate apodehydrogenase (apoBDH), an amphipathic membrane protein, with the hydrophobic domain of phospholipids. The two synthetic lecithins, PL I (1-myristoyl-2-12-N-(4-azido-2-nitrophenyl) aminododecanoyl-sn-glycero-3-phosphocholine) and PL II (1-myristoyl-2-(2-azido-4-nitrobenzoyl)-sn-glycero-3-phosphocholine), are able

Lipid-protein interactions. Effect of apolipoprotein A-I on phosphatidylcholine polar group conformation as studied by proton nuclear magnetic resonance.

D J Reijngoud et al.

Biochemistry, 21(12), 2977-2983 (1982-06-08)

Spin-spin coupling constants derived from high-resolution 1H NMR spectra of pure 1-myristoyl-sn-glycero-3-phosphocholine (MLPC) micelles and 60:1 mol/mol been analyzed in order to determine the effects of apoprotein on phosphatidylcholine (PC) polar group conformation. The shift ratios of the polar group

State of aggregation of detergent-solubilized sarcoplasmic reticulum adenosine triphosphatase investigated by high-performance liquid chromatography.

H Lüdi et al.

Journal of chromatography, 297, 111-117 (1984-08-03)

The state of aggregation of purified sarcoplasmic reticulum adenosine triphosphatase (ATPase) was investigated by high-performance liquid chromatography (LKB TSK-G 4000 SW column) in the presence of various detergents: sodium dodecylsulphate, dodecyl octaethylene glycol monoether (C12E8), sodium deoxycholate, Triton X-100 and

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