U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C34H66O10P.Na
Molecular Weight 688.8454
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

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

SMILES

[Na+].CCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OC[C@@H](O)CO)OC(=O)CCCCCCCCCCCCC

InChI

InChIKey=QLNOOKSBAYIHQI-XJEPUKKESA-M
InChI=1S/C34H67O10P.Na/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);/q;+1/p-1/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-(PHOSPHO-S-(1-GLYCEROL)), SODIUM SALT
Preferred Name English
SODIUM 1,2-DIMYRISTOYL-SN-GLYCERO-3-(PHOSPHO-S-(1-GLYCEROL))
Common Name English
TETRADECANOIC ACID, 1-((((2,3-DIHYDROXYPROPOXY)HYDROXYPHOSPHINYL)OXY)METHYL)-1,2-ETHANEDIYL ESTER, MONOSODIUM SALT, (R-(R*,S*))-
Systematic Name English
Code System Code Type Description
PUBCHEM
72941659
Created by admin on Mon Mar 31 18:03:45 GMT 2025 , Edited by admin on Mon Mar 31 18:03:45 GMT 2025
PRIMARY
FDA UNII
P17P4C999T
Created by admin on Mon Mar 31 18:03:45 GMT 2025 , Edited by admin on Mon Mar 31 18:03:45 GMT 2025
PRIMARY
CAS
116870-30-5
Created by admin on Mon Mar 31 18:03:45 GMT 2025 , Edited by admin on Mon Mar 31 18:03:45 GMT 2025
PRIMARY
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966