Literature DB >> 836023

Microbial transformation of 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine by fungi.

J Jiu, S Mizuba, J Hribar.   

Abstract

The microbial transformation of 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine (compound I) was undertaken to obtain new derivatives. Compound I was transformed by Hormodendrum sp. (NRRL 8133) to 8-chloro-10,11-dihydrodibenz(b,f)(1,4)oxazepine-11-one (compound II) and 2-(2-amino-4-chlorophenoxy)benzyl alcohol (compound IV). Microbial cleavage of the nonaromatic ring to form compound IV was accomplished by several other fungi. Compound I was transformed to 8-chlorodibenz(b,f)(1,4)oxazepine (compound III) by Hormodendrum cladosporioides (NRRL 8132).

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Year:  1977        PMID: 836023      PMCID: PMC170569          DOI: 10.1128/aem.33.1.26-30.1977

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  5 in total

1.  Endogenous prostaglandins modulate lipolytic processes in adipose tissue.

Authors:  G Illiano; P Cuatrecasas
Journal:  Nat New Biol       Date:  1971-11-17

2.  Anticonvulsant semicarbazides.

Authors:  W E Coyne; J W Cusic
Journal:  J Med Chem       Date:  1968-11       Impact factor: 7.446

3.  Reversal of the antilipolytic effect of prostaglandin E 2 by an oxazepine derivative (SC-19220).

Authors:  F M Radzialowski; L Novak
Journal:  Life Sci I       Date:  1971-11-15

4.  Antiinflammatory dialkylaminoalkylureas.

Authors:  W E Coyne; J W Cusic
Journal:  J Med Chem       Date:  1967-07       Impact factor: 7.446

5.  Studies on prostaglandin antagonists.

Authors:  A Bennett; J Posner
Journal:  Br J Pharmacol       Date:  1971-08       Impact factor: 8.739

  5 in total

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