l-Methyl-2-nitro-1K-imidazolea carrying d i f f e r e n t 5-side chain. (iaopropyl, hydroxymethylethyl, ethenyl) have been syn- t h e b e d l a b e l l e d with I 4 C a t C2 of t h e imidazole nucleua.
Synthesis of 1-(2,3-dihydroxypropyl)-2-nitro-1H-imidazole-2-14C and N-(2-hydroxyethyl)-2-(2-nitro-1H-imidazol-1-YL-2-14C) acetamide
β Scribed by Mary T. Fong; Morris A. Leaffer
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- French
- Weight
- 227 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
β¦ Synopsis
We have prepared the 14C-labeled analogs of NSC 261036, 1-(2,3-dIhydroxypropy1)-2-ni t r0-1H-imIda~ole-2-~~C, and NSC 301467, N-(2-hydroxyethyl)-2-(2-nitro-lH-imldazol-l-yl-2-14C) acetamide, for pharmacological, drug distribution, and mechanisms of action studies. The latter is an analog designed for lower toxicity and improved properties. The former is a metabolite of, and appears to be less toxic than, misonidazole.
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