2,3-Dihydroxypropyl oleate

2,3-Dihydroxypropyl oleate is a lipid of Glycerolipids (GL) class. The involved functions are known as enzyme activity and acyltransferase activity. 2,3-dihydroxypropyl oleate often locates in soluble fraction.

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Introduction

To understand associated biological information of 2,3-Dihydroxypropyl oleate, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with 2,3-Dihydroxypropyl oleate?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with 2,3-Dihydroxypropyl oleate

PubChem Associated disorders and diseases

What pathways are associated with 2,3-Dihydroxypropyl oleate

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with 2,3-Dihydroxypropyl oleate?

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What functions are associated with 2,3-Dihydroxypropyl oleate?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with 2,3-Dihydroxypropyl oleate?

There are no associated biomedical information in the current reference collection.

What genes are associated with 2,3-Dihydroxypropyl oleate?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with 2,3-Dihydroxypropyl oleate?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with 2,3-Dihydroxypropyl oleate

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Authors Title Published Journal PubMed Link
Efrat R et al. Solubilization of hydrophobic guest molecules in the monoolein discontinuous QL cubic mesophase and its soft nanoparticles. 2009 Langmuir pmid:18781793
Nonomura Y et al. Phase behavior of bile acid/lipid/water systems containing model dietary lipids. 2009 J Colloid Interface Sci pmid:19682701
Ericsson EM et al. Glycerol monooleate-blood interactions. 2009 Colloids Surf B Biointerfaces pmid:18996684
Biradar SV et al. Preparation of multiparticulate vaginal tablet using glyceryl monooleate for sustained progesterone delivery. 2009 Pharm Dev Technol pmid:18802845
Ahmed AR and Bodmeier R Preparation of preformed porous PLGA microparticles and antisense oligonucleotides loading. 2009 Eur J Pharm Biopharm pmid:18840521
Lee KW et al. Nanostructure of liquid crystalline matrix determines in vitro sustained release and in vivo oral absorption kinetics for hydrophilic model drugs. 2009 Int J Pharm pmid:18790030
Libster D et al. Molecular interactions in reverse hexagonal mesophase in the presence of Cyclosporin A. 2009 Int J Pharm pmid:18977286
Pichot R et al. Mixed-emulsifier stabilised emulsions: Investigation of the effect of monoolein and hydrophilic silica particle mixtures on the stability against coalescence. 2009 J Colloid Interface Sci pmid:18977494
Uyama M et al. Useful modified cellulose polymers as new emulsifiers of cubosomes. 2009 Langmuir pmid:19296640
Fong WK et al. Stimuli responsive liquid crystals provide 'on-demand' drug delivery in vitro and in vivo. 2009 J Control Release pmid:19331865