𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of high specific activity tritium-labelled chloroethylcyclohexylnitrosourea and its application to the study of dna modification

✍ Scribed by Ernest L. Siew; Yvette Habraken; David B. Ludlum


Publisher
John Wiley and Sons
Year
1991
Tongue
French
Weight
286 KB
Volume
29
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


A small-scale synthesis of high specific activity, N-(2-chloro-2-[3H]-ethyl)-N'-cyclohexyl-N-nitrosourea ([3H]-CCNU) has been accomplished from tritium-labelled ethanolamine. The product is pure by TLC and HPLC analysis and has been used successfully to modify DNA. The overall yield on radioactivity including losses in HPLC purification is approximately 4 percent. The availability of this tritiumlabelled compound makes studies of DNA repair and of cellular resistance to N-(2-chloroethyl)-N'-cyclohexyl-N-nitrosourea possible.


📜 SIMILAR VOLUMES


The synthesis of betaxolol labelled with
✍ John Allen; André Tizot 📂 Article 📅 1988 🏛 John Wiley and Sons 🌐 French ⚖ 204 KB

## Department of Chemistry Labelled Compounds and Metabolite Synthesis Group 31, avenue Paul Vaillant-Couturier 92220 BAGNEUX (FRANCE) SmOuRY The synthesis of betaxolol, a new 8-blocking agent. labelled with tritium in high specific activity ('19 Ci/mmol) is described. The tritium was incorporated

Super high specific activity tritium lab
✍ Leyi Gong; Howard Parnes 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 French ⚖ 406 KB 👁 2 views

We describe herein the synthesis of polybromodiphenylacetic acid (&), a fragment common to the tritiation substrates (a) and (JJ) of the sodium channel blocker, PD-85639 (1) and the angiotensin II inhibitor EXP-655 (2) respectively. Preparation of (a) and (11) followed by reductive debromonation wit

Synthesis of high specific activity 80mB
✍ Rc Mease; Sj Gatley; Am Friedman 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 French ⚖ 458 KB

## Abstract Convenient preparations of ^80m^Br and ^123^I‐labeled 5‐halodeoxyuridines, required for basic investigations of Auger electron radiotoxicity, are described. These radioactive thymidine analogs were synthesized from deoxyuridine, radiohalide and N‐chlorosuccinimide in dilute sulfuric aci

An expedient synthesis of high specific
✍ Neile A. Grayson; Brian R. de Costa; Joannes T. M. Linders; Kenner C. Rice 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 French ⚖ 319 KB 👁 1 views

## Abstract [^18^F]4‐Fluoro‐1‐[1‐(2‐thienyl)cyclohexyl)]piperidine is a ligand potentially useful for positron emission tomography of the PCP/NMDA receptor complex in the mammalian brain. The tritium‐labelled title compound was synthesized in 5 steps starting with cyclohexanone. Catalytic tritiolys