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LM1502

Avanti

17:0-20:4 PI

Avanti Research™ - A Croda Brand LM1502, methanol solution

Synonym(s):

1-heptadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phospho-(1′-myo-inositol) (ammonium salt)

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About This Item

Empirical Formula (Hill Notation):
C46H84NO13P
CAS Number:
1246304-59-5
Molecular Weight:
890.13
UNSPSC Code:
12352211
NACRES:
NA.25

form

methanol solution

packaging

pkg of 1 × 1 mL (LM1502-1EA)

manufacturer/tradename

Avanti Research™ - A Croda Brand LM1502

concentration

~10 μg/mL (Refer to C of A for lot specific concentration. )

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](O)[C@H]1O)=O)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(CCCCCCCCCCCCCCCC)=O.[NH4+]

General description

Phosphatidylinositol (PI) is soluble in water and chloroform/methanol. It is commonly found in animal tissues and bacteria.

Application

17:0-20:4 PI has been used as an internal standard for:
  • lipid extraction from isolated pure mitochondria by modified Bligh and Dyer method
  • lipid quantitation using liquid chromatography-mass spectrometry (LC-MS)
  • the analysis of phosphatidylinositol (PI) and phosphatidylinositol bisphosphates (PI(3,4)P2 and PI(4,5)P2) by high performance liquid chromatography-mass spectrometry (HPLC-MS)

Packaging

2 mL Amber Glass Sealed Ampule (LM1502-1EA)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

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Ulrike Bruning et al.
Cell metabolism, 28(6), 866-880 (2018-08-28)
The role of fatty acid synthesis in endothelial cells (ECs) remains incompletely characterized. We report that fatty acid synthase knockdown (FASNKD) in ECs impedes vessel sprouting by reducing proliferation. Endothelial loss of FASN impaired angiogenesis in vivo, while FASN blockade reduced
Milena Vukotic et al.
Molecular cell, 67(3), 471-483 (2017-07-18)
Mutations in mitochondrial acylglycerol kinase (AGK) cause Sengers syndrome, which is characterized by cataracts, hypertrophic cardiomyopathy, and skeletal myopathy. AGK generates phosphatidic acid and lysophosphatidic acid, bioactive phospholipids involved in lipid signaling and the regulation of tumor progression. However, the

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