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63371

Sigma-Aldrich

2-Oleoyl-1-palmitoyl-sn-glycero-3-phospho-rac-(1-glycerol) sodium salt

≥98.0% (TLC)

Sinonimo/i:

(9Z)-9-Octadecenoic acid (1R)-1-[[[(2,3-dihydroxypropoxy)hydroxyphosphinyl]oxy]methyl]-2-[(1-oxohexadecyl)oxy]ethyl ester monosodium salt, 1-Palmitoyl-2-oleoyl-sn-glycero-3-phospho-(1′-rac-glycerol) sodium salt, 1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoglycerol sodium salt, 1-hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phospho-(1′-rac-glycerol) sodium salt, L-α-Phosphatidyl-DL-glycerol, β-oleoyl-γ-palmitoyl sodium salt, PG(16:0/18:1(9Z)), POPG, POPG-Na

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About This Item

Formula empirica (notazione di Hill):
C40H76NaO10P
Numero CAS:
268550-95-4
Peso molecolare:
770.99
Numero MDL:
MFCD00674290
Codice UNSPSC:
12352211
ID PubChem:
329759846
NACRES:
NA.85

Origine biologica

synthetic

Saggio

≥98.0% (TLC)

Forma fisica

powder

Gruppo funzionale

ester

Tipo di lipide

phosphoglycerides

Temperatura di conservazione

−20°C

Stringa SMILE

[H][C@@](COP([O-])(OCC(O)CO)=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C40H77O10P.Na/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-40(44)50-38(36-49-51(45,46)48-34-37(42)33-41)35-47-39(43)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2;/h17-18,37-38,41-42H,3-16,19-36H2,1-2H3,(H,45,46);/q;+1/p-1/b18-17-;/t37?,38-;/m1./s1
FJXDNGDRHUDFST-XQYKCTAGSA-M

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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L-α-Phosphatidyl-DL-glycerol sodium salt from egg yolk lecithin ≥99% (TLC), lyophilized powder

Sigma-Aldrich

P8318

L-α-Phosphatidyl-DL-glycerol sodium salt from egg yolk lecithin

MAPCHO™-12 Avanti Research™ - A Croda Brand

Avanti

850336P

MAPCHO™-12

16:0-18:1 DG 1-palmitoyl-2-oleoyl-sn-glycerol, chloroform

Avanti

800815C

16:0-18:1 DG

16:0-18:1 PE Avanti Research™ - A Croda Brand

Avanti

850757P

16:0-18:1 PE

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Scientific reports, 10(1), 11652-11652 (2020-07-17)
Magainin 2 and PGLa are cationic, amphipathic antimicrobial peptides which when added as equimolar mixture exhibit a pronounced synergism in both their antibacterial and pore-forming activities. Here we show for the first time that the peptides assemble into defined supramolecular
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PloS one, 13(10), e0205727-e0205727 (2018-10-17)
The occurrence of nosocomial infections has been on the rise for the past twenty years. Notably, infections caused by the Gram-positive bacteria Staphylococcus aureus represent a major clinical problem, as an increase in antibiotic multi-resistant strains has accompanied this rise.
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Cyclic nucleotide-gated (CNG) ion channels are non-selective cation channels key to signal transduction. The free energy difference of cyclic-nucleotide (cAMP/cGMP) binding/unbinding is translated into mechanical work to modulate the open/closed probability of the pore, i.e., gating. Despite the recent advances
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