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P5693

1,2-Dimyristoyl-sn-glycero-3-phosphoethanolamine

Name: 1,2-Dimyristoyl-<I>sn</I>-glycero-3-phosphoethanolamine
Brand: SIGMA

synthetic, ≥99%

Synonym(s):

1,2-Ditetradecanoyl-sn-glycero-3-phosphoethanolamine, 3-sn-Phosphatidylethanolamine, 1,2-dimyristoyl, L-β,γ-Dimyristoyl-α-cephalin, DMPE, Dimyristoyl-L-α-phosphatidylethanolamine, PE(14:0/14:0), Tetradecanoic acid (1R)-1-[[[(2-aminoethoxy)hydroxyphosphinyl]oxy]methyl]-1,2-ethanediyl ester

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About This Item

Empirical Formula (Hill Notation):

C₃₃H₆₆NO₈P

CAS Number:

998-07-2

Molecular Weight:

635.85

UNSPSC Code:

51191904

NACRES:

NA.25

PubChem Substance ID:

24898693

MDL number:

MFCD00036775

Beilstein/REAXYS Number:

1730529

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Properties

biological source

synthetic

Quality Level

200

assay

≥99%

form

powder

functional group

amine, ester

lipid type

phosphoglycerides

shipped in

ambient

storage temp.

−20°C

SMILES string

CCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OCCN)OC(=O)CCCCCCCCCCCCC

InChI

1S/C33H66NO8P/c1-3-5-7-9-11-13-15-17-19-21-23-25-32(35)39-29-31(30-41-43(37,38)40-28-27-34)42-33(36)26-24-22-20-18-16-14-12-10-8-6-4-2/h31H,3-30,34H2,1-2H3,(H,37,38)/t31-/m1/s1

InChI key

NEZDNQCXEZDCBI-WJOKGBTCSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Continuous Uptake or Saturation-Investigation of Concentration and Surface-Packing-Specific Hemin Interaction with Lipid Membranes.

R P Giri et al.

The journal of physical chemistry. B, 122(30), 7547-7554 (2018-07-10)

Drug design and targeted delivery in cells serve as a flourishing area not only for scientific inquiry, owing to numerous clinical applications, but also for understanding cell interaction with exogenous materials. The membrane localization of heme and its analog hemin

Obese mother offspring have hepatic lipidic modulation that contributes to sex-dependent metabolic adaptation later in life.

Christina Savva et al.

Communications biology, 4(1), 14-14 (2021-01-06)

With the increasing prevalence of obesity in women of reproductive age, there is an urgent need to understand the metabolic impact on the fetus. Sex-related susceptibility to liver diseases has been demonstrated but the underlying mechanism remains unclear. Here we

Disturbed phospholipid homeostasis in endoplasmic reticulum initiates tri-o-cresyl phosphate-induced delayed neurotoxicity.

Li Zhu et al.

Scientific reports, 6, 37574-37574 (2016-11-25)

Tri-o-cresyl phosphate (TOCP) is a widely used organophosphorus compound, which can cause a neurodegenerative disorder, i.e., organophosphate-induced delayed neurotoxicity (OPIDN). The biochemical events in the initiation of OPIDN were not fully understood except for the essential inhibition of neuropathy target

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Global Trade Item Number

SKU	GTIN
P5693-100MG	04061835547906
P5693-1G	04061835507146
P5693-250MG	04061835513963