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
Mengesha AE et al. Binary blend of glyceryl monooleate and glyceryl monostearate for magnetically induced thermo-responsive local drug delivery system. 2013 Pharm. Res. pmid:24158728
Swarnakar NK et al. Enhanced oromucosal delivery of progesterone via hexosomes. 2007 Pharm. Res. pmid:17828445
Kararli TT et al. Enhancement of nasal delivery of a renin inhibitor in the rat using emulsion formulations. 1992 Pharm. Res. pmid:1409372
Kararli TT et al. Oral delivery of a renin inhibitor compound using emulsion formulations. 1992 Pharm. Res. pmid:1438002
Lopes LB et al. Reverse hexagonal phase nanodispersion of monoolein and oleic acid for topical delivery of peptides: in vitro and in vivo skin penetration of cyclosporin A. 2006 Pharm. Res. pmid:16715364
Geraghty PB et al. The in vitro release of some antimuscarinic drugs from monoolein/water lyotropic liquid crystalline gels. 1996 Pharm. Res. pmid:8865324
Patil SS et al. Mapping ion-induced mesophasic transformation in lyotropic in situ gelling system and its correlation with pharmaceutical performance. 2013 Pharm. Res. pmid:23595880
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Kulkarni CV et al. Monoolein: a magic lipid? 2011 Phys Chem Chem Phys pmid:21183976
Angelov B et al. SAXS investigation of a cubic to a sponge (L3) phase transition in self-assembled lipid nanocarriers. 2011 Phys Chem Chem Phys pmid:21079857