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Merck

810857P

Avanti

14:0 NPS PC

1-myristoyl-2-(4-nitrophenylsuccinyl)-sn-glycero-3-phosphocholine, powder

Synonym(e):

1-tetradecanoyl-2-(4-nitrophenylsuccinyl)-sn-glycero-3-phosphocholine

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise


About This Item

Empirische Formel (Hill-System):
C32H53N2O12P
CAS-Nummer:
Molekulargewicht:
688.74
UNSPSC-Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

Form

powder

Verpackung

pkg of 1 × 100 mg (810857P-100mg)
pkg of 2 × 100 mg (810857P-200mg)
pkg of 1 × 25 mg (810857P-25mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 810857P

Versandbedingung

dry ice

Lagertemp.

−20°C

Verpackung

5 mL Clear Glass Sealed Ampule (810857P-100mg)
5 mL Clear Glass Sealed Ampule (810857P-200mg)
5 mL Clear Glass Sealed Ampule (810857P-25mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids


Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

M Serban et al.
Journal of cellular and molecular medicine, 6(4), 643-647 (2003-03-04)
Non-insulin dependent diabetes mellitus (NIDDM) represents an independent risk factor for cardiovascular diseases (CVD), being characterized by a continuous low-grade inflammation and endothelial activation state. Plasma platelet - activating factor - acetylhydrolases (PAF-AHs) are a subgroup of Ca(2+)-independent phospholipase A(2)
T Kosaka et al.
Clinica chimica acta; international journal of clinical chemistry, 296(1-2), 151-161 (2000-05-16)
We developed a spectrophotometric assay for serum platelet-activating factor acetylhydrolase (PAF-AH, EC 3.1.1.47.) activity using a platelet-activating factor (PAF) analogue with a 4-nitrophenyl group as substrate. PAF-AH hydrolyzes the sn-2 position of the substrate ¿1-myristoyl-2-(p-nitrophenylsuccinyl)phosphatidylcholine, producing p-nitrophenyl succinate. This liberation
Karl Winkler et al.
Circulation, 111(8), 980-987 (2005-02-16)
Platelet-activating factor acetylhydrolase (PAF-AH), also denoted as lipoprotein-associated phospholipase A2, is a lipoprotein-bound enzyme that is possibly involved in inflammation and atherosclerosis. This study investigates the relationship of PAF-AH activity to angiographic coronary artery disease (CAD), the use of cardiovascular
T Kosaka et al.
Clinica chimica acta; international journal of clinical chemistry, 312(1-2), 179-183 (2001-10-03)
A spectrophotometric assay for platelet-activating factor acetylhydrolase (PAF-AH) activity differs from the radioisotopic assay in its value because of a difference in substrate specificity. The spectrophotometric assay is more precise than the radioisotopic assay, providing information that is not clear

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