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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
139594
PubMed

PubMed

TitleDatePubMed
Thermal transitions in the bilayer assembly of dimyristoylphosphatidylglycerol sodium salt dispersion in water: a new phase transition through an intermediate state.
2000 Dec 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 Jun 1
Enhanced bactericidal potency of nanoliposomes by modification of the fusion activity between liposomes and bacterium.
2013
Name Type Language
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
1,2-DIMYRISTOYL SN-GLYCERO-3-PHOSPHATIDYL-1'-SN-GLYCEROL
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 Fri Dec 15 18:37:19 GMT 2023 , Edited by admin on Fri Dec 15 18:37:19 GMT 2023
PRIMARY
FDA UNII
L34S99KZCX
Created by admin on Fri Dec 15 18:37:19 GMT 2023 , Edited by admin on Fri Dec 15 18:37:19 GMT 2023
PRIMARY
PUBCHEM
3246995
Created by admin on Fri Dec 15 18:37:19 GMT 2023 , Edited by admin on Fri Dec 15 18:37:19 GMT 2023
PRIMARY
NIH
NCATS
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