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63371

Sigma-Aldrich

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

≥98.0% (TLC)

Sinônimo(s):

(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

Fórmula empírica (Notação de Hill):
C40H76NaO10P
Número CAS:
Peso molecular:
770.99
Número MDL:
Código UNSPSC:
12352211
ID de substância PubChem:
NACRES:
NA.85

fonte biológica

synthetic

Ensaio

≥98.0% (TLC)

Formulário

powder

grupo funcional

ester

tipo de lipídio

phosphoglycerides

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[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

chave InChI

FJXDNGDRHUDFST-XQYKCTAGSA-M

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Christopher Aisenbrey et al.
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
Yutaro Shiraishi et al.
Nature communications, 9(1), 194-194 (2018-01-18)
The C-terminal region of G-protein-coupled receptors (GPCRs), stimulated by agonist binding, is phosphorylated by GPCR kinases, and the phosphorylated GPCRs bind to arrestin, leading to the cellular responses. To understand the mechanism underlying the formation of the phosphorylated GPCR-arrestin complex
Keiichi Inoue et al.
Nature communications, 10(1), 1993-1993 (2019-05-02)
Microbial rhodopsins are photoreceptive membrane proteins that transport various ions using light energy. While they are widely used in optogenetics to optically control neuronal activity, rhodopsins that function with longer-wavelength light are highly demanded because of their low phototoxicity and
Arin Marchesi et al.
Nature communications, 9(1), 3978-3978 (2018-09-30)
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
Vivian Montero-Alejo et al.
Developmental and comparative immunology, 67, 310-321 (2016-09-13)
Beta_defensin have been solely found in vertebrates until β-defensin-like peptides were described as transcript isoforms in two species of Panulirus genus. They were considered as putative antimicrobials since their biological activity have not been demonstrated. Here we purified and characterized

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