Literature DB >> 347050

Amino acid analogs IV:4-fluoroisoleucine.

H Gershon, L Shanks, D D Clarke.   

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.

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Year:  1978        PMID: 347050     DOI: 10.1002/jps.2600670542

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  1 in total

1.  Syntheses ofγ-fluoro-α-amino acids.

Authors:  G Haufe; S Kröger
Journal:  Amino Acids       Date:  1996-09       Impact factor: 3.520

  1 in total

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