Amino acid analogs IV:4-fluoroisoleucine.

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 Sci

authors

Gershon H,Shanks L,Clarke DD

doi

10.1002/jps.2600670542

subject

Has Abstract

pub_date

1978-05-01 00:00:00

pages

715-7

issue

5

eissn

0022-3549

issn

1520-6017

pii

S0022-3549(15)42013-1

journal_volume

67

pub_type

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