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Key Documents

850757C

Avanti

16:0-18:1 PE

Avanti Research - A Croda Brand

Sinonimo/i:

1-hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine; POPE; PE(16:0/18:1(9Z)); 110637

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About This Item

Formula empirica (notazione di Hill):
C39H76NO8P
Numero CAS:
Peso molecolare:
718.00
Codice UNSPSC:
51191904
NACRES:
NA.25

Descrizione

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine, chloroform

Saggio

>99% (TLC)

Forma fisica

liquid

Confezionamento

pkg of 1 × 2.5 mL (850757C-25mg)
pkg of 2 × 20 mL (850757C-1g)
pkg of 2 × 4 mL (850757C-200mg)
pkg of 5 × 4 mL (850757C-500mg)

Produttore/marchio commerciale

Avanti Research - A Croda Brand

Concentrazione

10 mg/mL (850757C-25mg)
25 mg/mL (850757C-1g)
25 mg/mL (850757C-200mg)
25 mg/mL (850757C-500mg)

Tipo di lipide

cardiolipins
phospholipids

Condizioni di spedizione

dry ice

Temperatura di conservazione

−20°C

Stringa SMILE

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C39H76NO8P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-39(42)48-37(36-47-49(43,44)46-34-33-40)35-45-38(41)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,37H,3-16,19-36,40H2,1-2H3,(H,43,44)/b18-17-
FHQVHHIBKUMWTI-ZCXUNETKSA-N

Applicazioni

16:0-18:1 PE has been used as a synthetic lipid for the preparation of liposomes.

Confezionamento

30 mL Amber Narrow Mouth Glass Bottle with Screw Cap (850757C-1g)
5 mL Clear Glass Sealed Ampule (850757C-200mg)
5 mL Clear Glass Sealed Ampule (850757C-25mg)
5 mL Clear Glass Sealed Ampule (850757C-500mg)

Note legali

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pittogrammi

Skull and crossbonesHealth hazard

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Central nervous system, Liver,Kidney

Codice della classe di stoccaggio

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Sathappa M and Alder NN
Bio-protocol, 6(22) (2016)
Mitochondria: Practical Protocols (2018)
Tânia Silva et al.
Langmuir : the ACS journal of surfaces and colloids, 34(5), 2158-2170 (2018-01-07)
An understanding of the mechanism of action of antimicrobial peptides is fundamental to the development of new and more active antibiotics. In the present work, we use a wide range of techniques (SANS, SAXD, DSC, ITC, CD, and confocal and
Sónia Troeira Henriques et al.
Journal of the American Chemical Society, 141(51), 20460-20469 (2019-11-26)
Peptides with pharmaceutical activities are attractive drug leads, and knowledge of their mode-of-action is essential for translation into the clinic. Comparison of native and enantiomeric peptides has long been used as a powerful approach to discriminate membrane- or receptor-mediated modes-of-action
Charles G Cranfield et al.
Langmuir : the ACS journal of surfaces and colloids, 33(26), 6630-6637 (2017-06-14)
Cyclotides are cyclic disulfide-rich peptides that are chemically and thermally stable and possess pharmaceutical and insecticidal properties. The activities reported for cyclotides correlate with their ability to target phosphatidylethanolamine (PE)-phospholipids and disrupt cell membranes. However, the mechanism by which this

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