Unknown

Dataset Information

0

6-N,N-dimethylamino-2,3-naphthalimide: a new environment-sensitive fluorescent probe in delta- and mu-selective opioid peptides.


ABSTRACT: A new environment-sensitive fluorophore, 6-N,N-(dimethylamino)-2,3-naphthalimide (6DMN) was introduced in the delta-selective opioid peptide agonist H-Dmt-Tic-Glu-NH(2) and in the mu-selective opioid peptide agonist endomorphin-2 (H-Tyr-Pro-Phe-Phe-NH(2)). Environment-sensitive fluorophores are a special class of chromophores that generally exhibit a low quantum yield in aqueous solution but become highly fluorescent in nonpolar solvents or when bound to hydrophobic sites in proteins or membranes. New fluorescent delta-selective irreversible antagonists (H-Dmt-Tic-Glu-NH-(CH(2))(5)-CO-Dap(6DMN)-NH(2) (1) and H-Dmt-Tic-Glu-Dap(6DMN)-NH(2) (2)) were identified as potential fluorescent probes showing good properties for use in studies of distribution and internalization of delta receptors by confocal laser scanning microscopy.

SUBMITTER: Vazquez ME 

PROVIDER: S-EPMC1994907 | biostudies-literature | 2006 Jun

REPOSITORIES: biostudies-literature

altmetric image

Publications

6-N,N-dimethylamino-2,3-naphthalimide: a new environment-sensitive fluorescent probe in delta- and mu-selective opioid peptides.

Vázquez M Eugenio ME   Blanco Juan B JB   Salvadori Severo S   Trapella Claudio C   Argazzi Roberto R   Bryant Sharon D SD   Jinsmaa Yunden Y   Lazarus Lawrence H LH   Negri Lucia L   Giannini Elisa E   Lattanzi Roberta R   Colucci Mariantonella M   Balboni Gianfranco G  

Journal of medicinal chemistry 20060601 12


A new environment-sensitive fluorophore, 6-N,N-(dimethylamino)-2,3-naphthalimide (6DMN) was introduced in the delta-selective opioid peptide agonist H-Dmt-Tic-Glu-NH(2) and in the mu-selective opioid peptide agonist endomorphin-2 (H-Tyr-Pro-Phe-Phe-NH(2)). Environment-sensitive fluorophores are a special class of chromophores that generally exhibit a low quantum yield in aqueous solution but become highly fluorescent in nonpolar solvents or when bound to hydrophobic sites in proteins or membrane  ...[more]

Similar Datasets

| S-EPMC4698909 | biostudies-literature
| S-EPMC8190919 | biostudies-literature
| S-EPMC2919913 | biostudies-literature
| S-EPMC2572960 | biostudies-literature
2023-03-10 | PXD022106 | Pride