## Abstract 5‐Methoxy‐2‐methyl‐1‐(3,4‐methylenedioxybenzoyl)indole‐3‐acetic acid (ID‐955)(I), a new anti‐inflammatory agent, was labelled with carbon‐14 at C‐2 position of indole nucleus for the use of metabolic studies. The procedure used is shown in Fig. 1 and 2. Levulinic‐4‐^14^C acid was synthe
Synthesis of labeled anti-inflammatory agents
✍ Scribed by W. Hafferl; A. Hary
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- French
- Weight
- 237 KB
- Volume
- 9
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The synthesis of the anti‐ inflammatory agents d‐2‐(6′‐methoxy‐2′‐naphthyl)‐propionic acid and 1‐2‐(6′‐methoxy‐2′‐naphthyl)‐propanol labeled with ^14^C and ^3^H is described.
📜 SIMILAR VOLUMES
## Abstract The marijuana plant (__Cannabis sativa__) and preparations derived from it have been used for medicinal purposes for thousands of years. It is likely that the therapeutic benefits of smoked marijuana are due to some combination of its more than 60 cannabinoids and 200–250 non‐cannabinoi
## Abstract magnified image N‐Benzoylamino‐1,2,3,6‐tetrahydropyridines **9a‐q** were synthesized from 4‐substituted pyridines in four steps. Amination of pyridines was carried out to prepare intermediate N‐aminopyridinium mesylates using mesytelenesulfonyl hydroxmate (MSH) as aminating agent. N‐am