Synthesis and anticonvulsant properties of BW A78U structurally-related compounds
✍ Scribed by Laurent Désaubry; Camille G. Wermuth; Annie Boehrer; Christian Marescaux; Jean-Jacques Bourguignon
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 234 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0960-894X
No coin nor oath required. For personal study only.
✦ Synopsis
Several analogues of the anticonvulsant BW A78U 1 have been synthesized and tested for their anticonvulsant properties, providing preliminary data concerning the structural requirements for this family of drugs.
Currently marketed antiepileptic drugs do not often provide complete control of seizures and are associated with a wide range of side effects ~. Due to the need for better antiepileptic drugs, a program was initiated to discover and develop improved antiepileptic agents. The potent anticonvulsant purine BW A78U
📜 SIMILAR VOLUMES
## Abstract 1‐(3,6,6‐Trimethyl‐1,3‐cyclohexadien‐1‐yl)‐2‐buten‐1‐one (**1**), a β‐damascenone isomer, was synthesized from 3,6,6‐trimethyl‐2‐cyclohexenone (**14**). This starting ketone **14** was obtained in good yield from 3‐methyl‐2‐butanone (**11**) and 3‐buten‐2‐one (**12**). Ethynylation of *
The chemical synthesis of cytidine-5'-alkyl-and cytidine-5'-alkyl(acyl)deoxyglycerophosphonophosphates is reported. The compounds obtained represent a novel class of cytostatically active agents based on phospholipids, which inhibit the growth of various tumor cell lines in vitro. They are phosphono