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857134C

Avanti

18:1 Hemi BMP (S,R)

sn-(3-oleoyl-2-hydroxy)-glycerol-1-phospho-sn-3′-(1′,2′-dioleoyl)-glycerol (ammonium salt), chloroform

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Synonym(s):
110734
Empirical Formula (Hill Notation):
C60H114NO11P
CAS Number:
474943-36-7
Molecular Weight:
1056.52
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

liquid

packaging

pkg of 1 × 1 mL (857134C-5mg)

manufacturer/tradename

Avanti Polar Lipids 857134C

concentration

5 mg/mL (857134C-5mg)

lipid type

cardiolipins
phospholipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP(OC[C@@]([H])(O)COC(CCCCCCC/C=C\CCCCCCCC)=O)([O-])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCC/C=C\CCCCCCCC)=O.[NH4+]

General description

18:1 Hemi BMP (S,R) is also called as acyl phosphatidylglycerol or hemi-bis (diacylglycero) phosphate. It has acyl chains at the sn-3 and sn-1′ positions, along with an additional acyl chain at position sn-2.

Application

18:1 Hemi BMP (S,R) is suitable to study its interfacial physical properties using Langmuir monomolecular films.

Biochem/physiol Actions

18:1 Hemi BMP (S,R) can acts as putative precursors of bis(monoacylglycero)phosphate (BMP).

Packaging

5 mL Clear Glass Sealed Ampule (857134C-5mg)

Pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

Signal Word

Danger

Hazard Classifications

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

Target Organs

Central nervous system

WGK

WGK 3

Flash Point(F)

does not flash

Flash Point(C)

does not flash

Regulatory Information

新产品

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Bis (monoacylglycero) phosphate interfacial properties and lipolysis by pancreatic lipase-related protein 2, an enzyme present in THP-1 human monocytes
Record M, et al.
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1811(7-8), 419-430 (2011)
Qiang Cheng et al.
Nature nanotechnology, 15(4), 313-320 (2020-04-07)
CRISPR-Cas gene editing and messenger RNA-based protein replacement therapy hold tremendous potential to effectively treat disease-causing mutations with diverse cellular origin. However, it is currently impossible to rationally design nanoparticles that selectively target specific tissues. Here, we report a strategy

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