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Fluorescent probes for adenosine receptors: synthesis and biology of N6-dansylaminoalkyl-substituted NECA derivatives
- Source :
- Scopus-Elsevier
- Publication Year :
- 1999
-
Abstract
- New fluorescent ligands for adenosine receptors are described; these compounds were obtained by the insertion, in the N 6 position of NECA (a potent adenosine agonist), of dansylaminoalkyl moieties with alkyl spacers of increasing carbon chain length (from 3 to 12). Among them, the compound with a C6 alkyl spacer proved to be the most interesting one, showing a marked selectivity for the A 1 receptor subtype; furthermore, in fluorescence microscopy assays it proved to be able to visualize and localize this receptor subtype at the level of the molecular layer of the rat cerebellar cortex.
- Subjects :
- Agonist
Stereochemistry
medicine.drug_class
Clinical Biochemistry
Pharmaceutical Science
Adenosine-5'-(N-ethylcarboxamide)
Biochemistry
Chemical synthesis
Radioligand Assay
Structure-Activity Relationship
Drug Discovery
Fluorescence microscope
medicine
Animals
Molecular Biology
Alkyl
Fluorescent Dyes
chemistry.chemical_classification
Dansyl Compounds
Chemistry
Organic Chemistry
Receptors, Purinergic P1
Adenosine receptor
Fluorescence
Adenosine
Rats
Cerebellar cortex
Molecular Medicine
medicine.drug
Subjects
Details
- ISSN :
- 0960894X
- Volume :
- 8
- Issue :
- 22
- Database :
- OpenAIRE
- Journal :
- Bioorganicmedicinal chemistry letters
- Accession number :
- edsair.doi.dedup.....5448e4b78d196567f98eac1f8b500931