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790146P

Avanti

16:0-23:2 Diyne PC

1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine, powder

Synonym(e):

PTPC

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25 MG
€ 161,00

€ 161,00


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25 MG
€ 161,00

About This Item

Empirische Formel (Hill-System):
C47H86NO8P
CAS-Nummer:
Molekulargewicht:
824.16
MDL-Nummer:
UNSPSC-Code:
12352211
NACRES:
NA.25

€ 161,00


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Assay

>99% (TLC)

Form

powder

Verpackung

pkg of 1 × 25 mg (790146P-25mg)

Hersteller/Markenname

Avanti Research - A Croda Brand 790146P

Versandbedingung

dry ice

Lagertemp.

−20°C

Anwendung

16:0-23:2 Diyne PC or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine has been used in lipid-monolayer interface of nanoparticles (NPs) to modify the drug diffusion across the layer.[1]

Biochem./physiol. Wirkung

16:0-23:2 Diyne PC or 1-palmitoyl-2-(10,12-tricosadiynoyl)-sn-glycero-3-phosphocholine (PTPC) is a polymerizable lipid that can cross-link with adjacent PTPC molecules under ultraviolet light (UV)-irradiation.[1]

Verpackung

5 mL Amber Glass Screw Cap Vial (790146P-25mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids


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Esther Shohami et al.
British journal of pharmacology, 163(7), 1402-1410 (2011-03-23)
Traumatic brain injury (TBI) represents the leading cause of death in young individuals. It triggers the accumulation of harmful mediators, leading to secondary damage, yet protective mechanisms are also set in motion. The endocannabinoid (eCB) system consists of ligands, such
S Punnamaraju et al.
Langmuir : the ACS journal of surfaces and colloids, 28(20), 7657-7664 (2012-05-03)
A combination of nonpolymerizable phospholipids (DPPC or DPhPC) and a smaller amount of cross-linking photopolymerizable phospholipids (23:2 DiynePC) is incorporated in an unsupported artificial lipid bilayer formed using the droplet interface bilayer (DIB) approach. The DIB is formed by contacting
Manish Sethi et al.
Nanoscale, 6(4), 2321-2327 (2014-01-15)
The effects of nanoparticle (NP) properties, such as size, shape and surface charge, on their efficacy and toxicity have been studied extensively. However, the effect of controlled drug release on NP efficacy and toxicity has not been thoroughly evaluated in

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