Abstract |
Despite intense efforts to increase vaccine coverage, measles virus (MV) still causes significant morbidity and mortality in the world sometimes as a results of severe, chronic and lethal diseases. In an effort to develop therapies to supplement immunization strategies a number of 1-oxo-2-[[(1E)-phenylmethylene]amino]-1,2- dihydroisoquinoline-4- carboxylic acid derivatives were synthesized and evaluated for anti- measles activity. The substituents on the aromatic ring were chosen in order to evaluate the influence of electron-withdrawing or electron-donating effects on the electronic density of the aromatic moiety. We also evaluated the introduction of a vinyl chain between the exocyclic nitrogen and phenyl moiety. The biological results allow to outline some preliminary considerations on structure-activity relationship.
|
Authors | N A Santagati, E Bousquet, A Garozzo, O Prezzavento, A Spadaro, G Ronsisvalle |
Journal | Farmaco (Societa chimica italiana : 1989)
(Farmaco)
Vol. 58
Issue 12
Pg. 1217-25
(Dec 2003)
ISSN: 0014-827X [Print] France |
PMID | 14630231
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Antiviral Agents
- Isoquinolines
- isoquinoline
|
Topics |
- Antiviral Agents
(chemical synthesis, pharmacology)
- Isoquinolines
(chemical synthesis, pharmacology)
- Measles virus
(drug effects, growth & development)
- Structure-Activity Relationship
|