857131P

14:0 BMP (S,R)

bis(monomyristoylglycero)phosphate (S,R Isomer) (ammonium salt), powder

• Synonym(s): Bis(monoacylglycerol)phosphate, sn-(3-tetradecanoyl-2-hydroxy)-glycerol-1-phospho-sn-3′-(1′-tetradecanoyl-2′-hydroxy)-glycerol (ammonium salt); lysobisphosphatidic acid; LBPA; 110857
• Empirical Formula (Hill Notation): C₃₄H₇₀NO₁₀P
• CAS Number: 325466-03-3
• Molecular Weight: 683.89
• UNSPSC Code: 51191904
• NACRES: NA.25

Properties

• Assay: >99% (BMP (contains 30% positional isomers), TLC)
• form: powder
• packaging: pkg of 1 × 10 mg (857131P-10mg); pkg of 1 × 5 mg (857131P-5mg)
• manufacturer/tradename: Avanti Research^™ - A Croda Brand 857131P
• lipid type: cardiolipins; phospholipids
• shipped in: dry ice
• storage temp.: −20°C
• SMILES string: [H][C@@](COP(OC[C@@]([H])(O)COC(CCCCCCCCCCCCC)=O)([O-])=O)(O)COC(CCCCCCCCCCCCC)=O.[NH4+]

Description

General description

Bis(monoacylglycerol)phosphate (BMP)/lysobisphosphatidic acid is a phospholipid, that has two phosphate-linked glycerol molecules. This phosphate-linked glycerol molecules are present in an unusual sn-1 glycerophospho-sn-1′ glycerol stereo conformation, and each glycerol molecule esterified with fattyacid. It is usually seen in the intraluminal vesicles (ILVs) of late endosomes and lysosomes.

Biochem/physiol Actions

Bis(monoacylglycerol)phosphate (BMP)/lysobisphosphatidic acid actively participates in cargo sorting by inducing the degradation and sorting of lipids. It also plays a major role in polyunsaturated fatty acid (PUFA) sorting in acidic organelles.

Packaging

5 mL Amber Glass Screw Cap Vial (857131P-10mg)

5 mL Amber Glass Screw Cap Vial (857131P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3