ChemInform Abstract: Synthesis and in vitro and in vivo Evaluation of the 2-(6′Methoxy-3′,4′-dihydro-1′-naphthyl)-4H-3,1-benzoxazin-4-one as a New Potent Substrate Inhibitor of Human Leukocyte Elastase.
✍ Scribed by Antonio Arcadi; Cinzia Asti; Laura Brandolini; Gianfranco Caselli; Fabio Marinelli; Viviana Ruggieri
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 29 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
Synthesis of Novel Succinamide Derivatives Having a 5,11-Dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one Skeleton as Potent and Selective M 2 Muscarinic Receptor Antagonists. Part 2. -Among the screened compounds derivative (IIIe) exhibits the highest affinity for M 2 muscarinic receptors and (III
Synthesis and Dimroth Rearrangement of 6-Cyano-1,2,4-triazolo[4,3a]pyrimidin-5-and 7-ones. A Novel Alkylation with Orthoesters and a New Participation of the Cyano Group in the Rearrangement. -Formic acid and triethyl orthoformate react with 2-hydrazinopyrimidin-4-ones (I) and (VI) to furnish triazo