Fluorescent probes for adenosine receptors: Synthesis and biology of N-6-dansylaminoalkyl-substituted NECA derivatives

Citation
M. Macchia et al., Fluorescent probes for adenosine receptors: Synthesis and biology of N-6-dansylaminoalkyl-substituted NECA derivatives, BIOORG MED, 8(22), 1998, pp. 3223-3228
Citations number
9
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
ISSN journal
0960894X → ACNP
Volume
8
Issue
22
Year of publication
1998
Pages
3223 - 3228
Database
ISI
SICI code
0960-894X(19981117)8:22<3223:FPFARS>2.0.ZU;2-1
Abstract
New fluorescent ligands for adenosine receptors are described; these compou nds were obtained by the insertion, in the N-6 position of NECA (a potent a denosine agonist), of dansylaminoalkyl moieties with alkyl spacers of incre asing carbon chain length (from 3 to 12). Among them, the compound with a C 6 alkyl spacer proved to be the most interesting one, showing a marked sele ctivity for the A(1) receptor subtype; furthermore, in fluorescence microsc opy assays it proved to be able to visualize and localize this receptor sub type at the level of the molecular layer of the rat cerebellar cortex. (C) 1998 Elsevier Science Ltd. All rights reserved.