## Abstract ^14^C‐Labeled E4010, [4‐(3‐chloro‐4‐methoxybenzyl)amino‐1‐(4‐hydroxy) ‐piperidino]‐6‐[4‐^14^C]phthalazinecarbonitrile monohydrochloride was synthesized for drug metabolism and pharmacokinetic studies using [1‐chloro‐4‐(3‐chloro‐4‐methoxybenzyl)amino]‐6‐[4‐^14^C]phthalazinecarbonitrile a
Synthesis of 14C-labelled sodium pariprazole (E3810)
✍ Scribed by Katsuya Tagami; Shigeru Chiku; Shigeru Sohda
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 206 KB
- Volume
- 33
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Sodium pariprazole (E3810), an inhibitory of H^+^,K^+^‐ATPase, was synthesized labelled with carbon‐14, starting from 2‐mercapto[2‐^14^C]‐benzimidazole 1 with a specific activity of 888 MBq/mmol. It was obtained in 49.3% radiochemical yield with a radiochemical purity of more than 98%.
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## Abstract Cefclidin (E1040), a new injectable cephalosporin with potent antipseudomonal activity, was synthesized labelled with carbon‐14, starting from bromo[1‐^14^C]acetic acid according to the method illustrated in Scheme 1, 2. [^14^C] Cefclidin, having a specific activity of 3.43 MBq/mg (wate
## Abstract Sodium 6‐[ (R)‐2‐(4‐hydroxy‐1,5‐naphthyridine‐4‐^14^C‐3‐carboxy‐^14^C‐amido)‐2‐phenylacetamido]penicillanate (apalcillin‐^14^C sodium) (**1**) was synthesized for use in metabolic studies. Reaction of ethyl malonate‐1‐^14^C (**2**) with ethyl orthoformate in the presence of zinc chlorid
14C-Labelled satigrel, or 4-cyano-5-(4'-methoxy tring-U-14CI phenyl)-5-(4"methoxyphenyl)-4-pentenoic acid was synthesized for drug metabolism and pharmacokinetic studies using 4,4'-diniethoxy [ring-U-W ] benzophenone as the starting material. The radiochemical yield was 10.0%. The specific radioacti