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Synthesis and cannabinoid receptor binding activity of conjugated triene anandamide, a novel eicosanoid

Overview of attention for article published in Experientia, January 1996
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Article details
Title
Synthesis and cannabinoid receptor binding activity of conjugated triene anandamide, a novel eicosanoid
Published in
Experientia, January 1996
DOI 10.1007/bf01922423
Pubmed ID
Authors
Abstract

A polyenoic fatty-acid isomerase (PFI) from a red marine alga was used to convert anandamide (5Z,8Z,11Z,14Z-eicosatetraenoyl-N-ethan olamide) to the 5Z,7E,9E,14Z-eicosatetraenoyl-N-ethanol amide isomer. This novel eicosanoid, termed conjugated triene anandamide (CTA), was assessed for its ability to bind to the cannabinoid receptor in rat brain membrane preparations. CTA is a high affinity cannabimimetic substance whose novel structure provides new insight into structure-activity relationships of cannabinoid receptor ligands. These experiments illustrate the utility of enzymes isolated from marine organisms in the development of pharmacological probes.

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Mendeley demographics

Mendeley demographics

The data shown below were compiled from readership statistics for 14 Mendeley readers of this research output. Click here to see the associated Mendeley record.
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Geographical breakdown

Geographical breakdown
Country Count As %
United States 1 7%
Unknown 13 93%

Demographic breakdown

Readers by professional status
Readers by professional status Count As %
Researcher 4 29%
Student > Bachelor 2 14%
Professor 2 14%
Student > Ph. D. Student 2 14%
Lecturer > Senior Lecturer 1 7%
Other 2 14%
Unknown 1 7%
Readers by discipline
Readers by discipline Count As %
Medicine and Dentistry 4 29%
Pharmacology, Toxicology and Pharmaceutical Science 3 21%
Agricultural and Biological Sciences 3 21%
Social Sciences 2 14%
Engineering 1 7%
Other 0 0%
Unknown 1 7%