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Details

Stereochemistry ABSOLUTE
Molecular Formula C34H67O10P
Molecular Weight 666.8635
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-DIMYRISTOYL-SN-GLYCERO-3-(PHOSPHO-S-(1-GLYCEROL))

SMILES

CCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@@H](O)CO)OC(=O)CCCCCCCCCCCCC

InChI

InChIKey=BPHQZTVXXXJVHI-AJQTZOPKSA-N
InChI=1S/C34H67O10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-33(37)41-29-32(30-43-45(39,40)42-28-31(36)27-35)44-34(38)26-24-22-20-18-16-14-12-10-8-6-4-2/h31-32,35-36H,3-30H2,1-2H3,(H,39,40)/t31-,32+/m0/s1

HIDE SMILES / InChI

Description

1,2-DIMYRISTOYL-SN-GLYCERO-3-(PHOSPHO-S-(1-GLYCEROL)), SODIUM SALT is a prototype for the preparation of liposomes with negatively charged hydrophilic head groups. It can be used in the generation of different types of artificial membranes.

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Enhanced bactericidal potency of nanoliposomes by modification of the fusion activity between liposomes and bacterium.
2013
Thermal transitions in the bilayer assembly of dimyristoylphosphatidylglycerol sodium salt dispersion in water: a new phase transition through an intermediate state.
2000-12-11
A Fourier transform infrared spectroscopic study of the interaction of alkaline earth cations with the negatively charged phospholipid 1, 2-dimyristoyl-sn-glycero-3-phosphoglycerol.
2000-06-01
Name Type Language
1,2-DIMYRISTOYL SN-GLYCERO-3-PHOSPHATIDYL-1'-SN-GLYCEROL
Preferred Name English
1,2-DIMYRISTOYL-SN-GLYCERO-3-(PHOSPHO-S-(1-GLYCEROL))
II  
Common Name English
1,2-DIMYRISTOYL-SN-GLYCERO-3-(PHOSPHO-S-(1-GLYCEROL)) [II]
Common Name English
TETRADECANOIC ACID, 1,1'-((1R)-1-(((((2S)-2,3-DIHYDROXYPROPOXY)HYDROXYPHOSPHINYL)OXY)METHYL)-1,2-ETHANEDIYL) ESTER
Common Name English
TETRADECANOIC ACID, (1R)-1-(((((2S)-2,3-DIHYDROXYPROPOXY)HYDROXYPHOSPHINYL)OXY)METHYL)-1,2-ETHANEDIYL ESTER
Common Name English
Code System Code Type Description
CAS
57618-28-7
Created by admin on Mon Mar 31 19:17:11 GMT 2025 , Edited by admin on Mon Mar 31 19:17:11 GMT 2025
PRIMARY
FDA UNII
L34S99KZCX
Created by admin on Mon Mar 31 19:17:11 GMT 2025 , Edited by admin on Mon Mar 31 19:17:11 GMT 2025
PRIMARY
PUBCHEM
3246995
Created by admin on Mon Mar 31 19:17:11 GMT 2025 , Edited by admin on Mon Mar 31 19:17:11 GMT 2025
PRIMARY
NIH
NCATS
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