Page last updated: 2024-12-08

dimyristoylphosphatidylsulfocholine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth

Description

1,2-di-O-myristoyl-sn-glycero-3-phosphosulfocholine : A 1,2-diacyl-sn-glycero-3-phosphosulfocholine where the two phosphatidyl acyl groups are specified as tetradecanoyl (myristoyl). [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID42607418
CHEBI ID63031
MeSH IDM0178249

Synonyms (13)

Synonym
1,2-ditetradecanoyl-sn-glycero-3-phosphosulfocholine
LMGP00000051
dmpsc
dimyristoylphosphatidylsulfocholine
(2r)-2,3-bis(tetradecanoyloxy)propyl 2-(dimethylsulfonio)ethyl phosphate
1,2-di-o-tetradecanoyl-sn-glycero-3-phosphosulfocholine
CHEBI:63031 ,
dimyristoylphosphatidyl sulfocholine
dimyristoyl-sn-glycero-3-phosphosulfocholine
1,2-di-o-myristoyl-sn-glycero-3-phosphosulfocholine
ditetradecanoyl-sn-glycero-3-phosphosulfocholine
EPITOPE ID:156815
Q27132348
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
antigenAny substance that stimulates an immune response in the body, such as through antibody production or by presentation to a T-cell receptor after binding to a major histocompability complex (MHC).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (2)

ClassDescription
1,2-diacyl-sn-glycero-3-phosphosulfocholineA phosphatidylsulfocholine in which the hydroxyl group of sulfocholine is esterified to the phosphate group of phosphatidic acid.
tetradecanoate esterA fatty acid ester obtained by condensation of the carboxy group of tetradecanoic acid (also known as myristic acid) with a hydroxy group of an alcohol or phenol.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (16.67)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]