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840061C

Avanti

16:0-20:4 PS

1-palmitoyl-2-arachidonoyl-sn-glycero-3-phospho-L-serine (sodium salt), chloroform

Synonym(e):

1-hexadecanoyl-2-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-sn-glycero-3-phospho-L-serine (sodium salt); PAPS; PS(16:0/20:4(5Z,8Z,11Z,14Z)); 110670

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About This Item

Empirische Formel (Hill-System):
C42H73NO10PNa
CAS-Nummer:
Molekulargewicht:
805.99
UNSPSC-Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

Form

liquid

Verpackung

pkg of 1 × 1 mL (840061C-10mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 840061C

Konzentration

10 mg/mL (840061C-10mg)

Lipid-Typ

phospholipids

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

[H][C@@](COP([O-])(OC[C@](C([O-])=O)([H])[NH3+])=O)(OC(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI

1S/C42H74NO10P.Na/c1-3-5-7-9-11-13-15-17-18-19-20-22-24-26-28-30-32-34-41(45)53-38(36-51-54(48,49)52-37-39(43)42(46)47)35-50-40(44)33-31-29-27-25-23-21-16-14-12-10-8-6-4-2;/h11,13,17-18,20,22,26,28,38-39H,3-10,12,14-16,19,21,23-25,27,29-37,43H2,1-2H3,(H,46,47)(H,48,49);/q;+1/p-1/b13-11-,18-17-,22-20-,28-26-;/t38-,39+;/m1./s1

InChIKey

MMDGTLYKZWZGJV-ANGKXMAJSA-M

Verwandte Kategorien

Allgemeine Beschreibung

16:0-20:4 PS or 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phospho-L-serine is a glycerophospholipid having, palmitic acid and arachidonic acid attached to the sn-1 and sn-2 positions of the glycerol backbone. The phospholipid in this compound is phosphoserine, a negatively charged lipid.

Anwendung

16:0-20:4 PS or 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phospho-L-serine has been used as a calibration standard for lipidomic analysis.

Verpackung

5 mL Clear Glass Sealed Ampule (840061C-10mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Piktogramme

Skull and crossbonesHealth hazard

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

Zielorgane

Central nervous system

WGK

WGK 3


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Die Dokumentenbibliothek aufrufen

Ségolène Hescot et al.
Oncotarget, 8(66), 109924-109940 (2018-01-05)
Mitotane (o,p'DDD), the most effective drug in adrenocortical carcinoma, concentrates into the mitochondria and impacts mitochondrial functions. To address the molecular mechanisms of mitotane action and to identify its potential target, metabolomic and lipidomic approaches as well as imaging analyses
Marco M Manni et al.
eLife, 7 (2018-03-16)
Phospholipid membranes form cellular barriers but need to be flexible enough to divide by fission. Phospholipids generally contain a saturated fatty acid (FA) at position sn1 whereas the sn2-FA is saturated, monounsaturated or polyunsaturated. Our understanding of the impact of
Peter A Leventis et al.
Annual review of biophysics, 39, 407-427 (2010-03-03)
Phosphatidylserine (PS) is the most abundant negatively charged phospholipid in eukaryotic membranes. PS directs the binding of proteins that bear C2 or gamma-carboxyglutamic domains and contributes to the electrostatic association of polycationic ligands with cellular membranes. Rather than being evenly

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