A preliminary pharmacological study of a thiophenic isoster of propranolol and related compounds with a tert. butylamino or homoveratrylamino group instead of the isopropylamino group is described. The synthesis and some pharmacological properties of derivatives in which the benzene ring is replaced
Synthesis and Antiplatelet Activity of 1-tert-Butylamino-3-(3-thienyloxy)-2-propanols
✍ Scribed by Susana Abdallah; Victoriano Darias; Rosa Donoso; Pilar Jordán de Urríes; Jaime Lissavetzky
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 600 KB
- Volume
- 329
- Category
- Article
- ISSN
- 0365-6233
No coin nor oath required. For personal study only.
✦ Synopsis
The synthesis of new l-terf-butylamino-3-(3-thienyloxy)-2propanols by two alternative methods is described. Their initial antiplatelet activity evaluation against ADP, adrenaline, and collagen is reported, and the preliminary structure-activity relationships are established. The appropriateness of further pharmacological investigations, especially for the best compound of the series lf, is indicated.
📜 SIMILAR VOLUMES
S-2-(3-tert-Butylamino-2-hydroxypropoxy)-3-cyanopyridine was recovered (approximately 90%) from human plasma and detected by conversion to a diheptafluorobutyryl derivative for electron-capture GLC. A homolog served as an internal standard. The method measures plasma drug concentrations at the 5-ng/
## Microwave-Promoted Synthesis of 1-Aryloxy-3-alkylamino-2propanols. -Microwave heating is found to accelerate significantly both steps of the known synthesis of the title compounds (V) from epichlorohydrin. -(PCHELKA, B.;