Ring-substituted 4-Hydroxy-1H-quinolin-2-ones: Preparation and Biological Activity
✍ Scribed by Jampilek, Josef; Musiol, Robert; Pesko, Matus; Kralova, Katarina; Vejsova, Marcela; Carroll, James; Coffey, Aidan; Finster, Jacek; Tabak, Dominik; Niedbala, Halina; Kozik, Violetta; Polanski, Jaroslaw; Csollei, Jozef; Dohnal, Jiri
- Book ID
- 121370430
- Publisher
- Molecular Diversity Preservation International
- Year
- 2009
- Tongue
- English
- Weight
- 180 KB
- Volume
- 14
- Category
- Article
- ISSN
- 1420-3049
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## Abstract For Abstract see ChemInform Abstract in Full Text.
## Abstract A variety of 4‐substituted quinolin‐2(1__H__)‐ones were prepared and evaluated for __N__‐methyl‐D‐aspar‐tate (NMDA) receptor binding site activity and their abilities to inhibit neurotoxicity. The 4‐(2‐car‐bethoxyethanamino)‐7‐chloro‐3‐nitroquinolin‐2(1__H__)‐one (**9b**) exhibited favo