Abstract:
:4-Fluoroisoleucine was produced by ammonolysis of 2-bromo-4-fluoro-3-methylpentanoic acid, which resulted from the bromofluorination of 4-methyl-2-pentenoic acid. It did not inhibit Plasmodium berghei in mice at 640 mg/kg and was not toxic to the animals. The fluoroamino acid inhibited Aspergillus niger, Trichoderma viride, Myrothecium verrucaria, Trichophyton mentagrophytes, and Mucor mucedo in Czapek solution agar at a concentration between 10(4) and 10(3) microgram/ml. Growth of Escherichia coli was inhibited 25% at 900 microgram/ml in a defined medium.
journal_name
J Pharm Scijournal_title
Journal of pharmaceutical sciencesauthors
Gershon H,Shanks L,Clarke DDdoi
10.1002/jps.2600670542subject
Has Abstractpub_date
1978-05-01 00:00:00pages
715-7issue
5eissn
0022-3549issn
1520-6017pii
S0022-3549(15)42013-1journal_volume
67pub_type
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