3123-73-7

Usage

Uses

Used in Pharmaceutical Industry:
1-Palmitoyl-2-oleoyl-sn-glycerol is used as a bioactive compound for increasing the activity of the ARF1 GTPase-activating protein on membrane-bound ARF1GTP. This enhancement in activity can have potential implications in the development of new therapeutic strategies and drug targets.
Used in Research Applications:
In the field of research, 1-palmitoyl-2-oleoyl-sn-glycerol serves as an important tool for studying the role of diacylglycerols in cellular signaling pathways and membrane dynamics. Its unique structure allows scientists to investigate the specific interactions and effects of this molecule on various cellular processes.
Used in Cosmetics Industry:
Due to its lipid nature and ability to interact with cellular membranes, 1-palmitoyl-2-oleoyl-sn-glycerol may also find applications in the cosmetics industry, potentially being used as an ingredient in skincare products to improve skin barrier function and overall skin health.
Used in Food Industry:
In the food industry, 1-palmitoyl-2-oleoyl-sn-glycerol could be utilized as an additive to improve the texture and stability of certain food products, taking advantage of its properties as a diacylglycerol.

InChI:InChI=1/C37H70O5/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-37(40)42-35(33-38)34-41-36(39)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,35,38H,3-16,19-34H2,1-2H3/b18-17-

Upstream product

• 1587-92-4 DL-β-(9,10-Dibromstearoyl)-α-palmitoyl-glycerin 
• 3443-84-3 2-Oleoylglycerol 
• 112-67-4 n-hexadecanoyl chloride 
• 64-17-5 ethanol 
• 2190-25-2 2-Oleodipalmitin 
• 10564-36-0 cis-5-oleoyloxy-2-phenyl-[1,3]dioxane 
• 1487-54-3 DL-α-Benzyl-β-(9,10-dibrom-stearoyl)-2'-palmitoyl-glycerin 
• 1487-53-2 DL-α-Benzyl-β-oleoyl-α'-palmitoyl-glycerin 
• 1487-51-0 1-O-benzyl-3-O-palmitoyl-rac-glycerol 
• 277749-20-9 (Z)-Octadec-9-enoic acid [1,3]dioxan-5-yl ester 
• 112-80-1 cis-Octadecenoic acid 
• 122-32-7 trioleoylglycerol 

Downstream Products

• 2190-27-4 1-palmitoyl-2-oleoyl-3-stearoylglycerol 

Relevant academic research and scientific papers

A new strategy to synthesize pure mixed diglycerides

The acylolytic cleavage of glycerol methylene acetals with fatty acids provides a new synthetic strategy that leads to pure mixed 1,2-diglycerides.

Conversion of a carboxylesterase into a triacylglycerol lipase by a random mutation

A true convert: The carboxylesterase enzyme R.34 (see picture) can be converted into a triacylglycerol lipase without modification of the shape, size, or hydrophobicity of the substrate binding site. The substitution of Asn33 by Asp results in a salt bridge between the Asp33 and Arg49, which causes a distortion of the enzyme structure that makes the catalytic site more accessible to larger substrates but also more labile. (Figure Presented).

Parasitic wasp, Dinarmus basalis, utilizes oviposition-marking pheromone of host azuki bean weevils as host-recognizing kairomone

A host-recognizing kairomone responsible for the stinging behavior of the parasitic wasp, Dinarmus basalis, was studied. Fresh azuki beans coated with an acetone extract of the azuki beans, from which both emerged wasps and their host weevils were removed, elicited stinging behavior from female wasps. The kairomone is a mixture of saturated hydrocarbons and diacylglycerols, both of which are required for activity. The kairomone is composed of normal and methyl-branched hydrocarbons with carbon numbers ranging from 25 to 35, most of which are known as the hydrocarbon constituents of an oviposition-marking pheromone of the host azuki bean weevils, Callosobruchus chinensis. This indicates that D. basalis utilizes the oviposition-marking pheromone of its host weevils as a host-recognizing kairomone.