Literature DB >> 4451380

Microbial transformation of methyl 5(6)-butyl-2-benzimidazolecarbamate.

J R Valenta, C J DiCuollo, L R Fare, J F Pagano.   

Abstract

The anthelmintic agent methyl 5(6)-butyl-2-benzimidazolecarbamate (Parbendazole) was transformed to two of its animal metabolites, methyl 5(6)-(4-hydroxybutyl)-2-benzimidazolecarbamate and methyl 5(6)-3-(carboxypropyl)-2-benzimidazolecarbamate, by the filamentous fungus Cunninghamella bainieri ATCC 9244. The transformation pathway was shown to be through the 4-hydroxybutyl product to the 3-carboxypropyl product. The reaction favored accumulation of the latter product.

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Year:  1974        PMID: 4451380      PMCID: PMC186870          DOI: 10.1128/am.28.6.995-998.1974

Source DB:  PubMed          Journal:  Appl Microbiol        ISSN: 0003-6919


  2 in total

1.  Metabolites of methyl 5(6)-butyl-2-benzimidazolecarbamate (parbendazole). Structure and synthesis.

Authors:  G L Dunn; G Gallagher; L D Davis; J R Hoover; R J Stedman
Journal:  J Med Chem       Date:  1973-09       Impact factor: 7.446

2.  New broad spectrum anthelmintic, methyl 5(6)-butyl-2-benzimidazolecarbamate.

Authors:  P Actor; E L Anderson; C J DiCuollo; R J Ferlauto; J R Hoover; J F Pagano; L R Ravin; S F Scheidy; R J Stedman; V J Theodorides
Journal:  Nature       Date:  1967-07-15       Impact factor: 49.962

  2 in total
  1 in total

1.  Bacterial breakdown of benomyl. I. Pure cultures.

Authors:  A Fuchs; F W de Vries
Journal:  Antonie Van Leeuwenhoek       Date:  1978       Impact factor: 2.271

  1 in total

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