The preparation of [14C]-labelled 16-aryloxy prostaglandin f2α analogues. [I.C.I. 81,008 and I.C.I. 80,996]
Author:
Publisher
Wiley
Subject
Organic Chemistry,Spectroscopy,Drug Discovery,Radiology, Nuclear Medicine and imaging,Biochemistry,Analytical Chemistry
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1. Synthesis of [phenyl-2-3H]-travoprost: isopropyl ester prodrug of a selective prostaglandin FP receptor agonist;Journal of Labelled Compounds and Radiopharmaceuticals;2001
2. A general method for the preparation of 14C-labeled metabolically stable prostaglandins;Journal of Labelled Compounds and Radiopharmaceuticals;1985-02
3. Synthesis of [3H]- and -[14C]-labelled sulprostone (CP-34,089/ZK-57,671);Prostaglandins;1982-09
4. The metabolic fate of the synthetic prostaglandin cloprostenol (‘Estrumate’) in the cow: Use of ion cluster techniques to facilitate metabolite identification;Biological Mass Spectrometry;1980-05
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