810857P
Avanti
14:0 NPS PC
1-myristoyl-2-(4-nitrophenylsuccinyl)-sn-glycero-3-phosphocholine, powder
Synonim(y):
1-tetradecanoyl-2-(4-nitrophenylsuccinyl)-sn-glycero-3-phosphocholine
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About This Item
Wzór empiryczny (zapis Hilla):
C32H53N2O12P
Numer CAS:
Masa cząsteczkowa:
688.74
Kod UNSPSC:
12352211
NACRES:
NA.25
Polecane produkty
Próba
>99% (TLC)
Postać
powder
opakowanie
pkg of 1 × 100 mg (810857P-100mg)
pkg of 2 × 100 mg (810857P-200mg)
pkg of 1 × 25 mg (810857P-25mg)
producent / nazwa handlowa
Avanti Research™ - A Croda Brand 810857P
Warunki transportu
dry ice
temp. przechowywania
−20°C
Opakowanie
5 mL Clear Glass Sealed Ampule (810857P-100mg)
5 mL Clear Glass Sealed Ampule (810857P-200mg)
5 mL Clear Glass Sealed Ampule (810857P-25mg)
Informacje prawne
Avanti Research is a trademark of Avanti Polar Lipids, LLC
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Kod klasy składowania
11 - Combustible Solids
Certyfikaty analizy (CoA)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
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
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
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)
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