Literature DB >> 16742464

The preparation and biological activity of methyl 5,6-epoxy-retinoate.

B Morgan1, J N Thompson.   

Abstract

1. Oxidation of methyl retinoate with monoperphthalic acid gave methyl 5,6-epoxyretinoate, obtained as pale-yellow crystals, m.p. 89 degrees . 2. The structure of the epoxide was confirmed by its ultraviolet, infrared, nuclear-magnetic-resonance and mass spectra. 3. The biological properties of the epoxide were investigated in male and female rats, and were found to be qualitatively similar to those of retinoic acid and methyl retinoate. 4. When administered to male rats reared on a vitamin A-free diet, the epoxide permitted growth although it did not maintain good general health. 5. Rats given a vitamin A-free diet and supplements of the epoxide had degenerate testes. 6. Female rats, maintained on a vitamin A-free diet containing retinoic acid and given supplements of the epoxide during pregnancy, resorbed their foetuses and failed to deliver litters. 7. The threshold of the electroretinogram response in male rats reared on a vitamin A-free diet with supplements of the epoxide was elevated above normal and was similar to that of rats maintained with methyl retinoate. 8. The oral administration of the epoxy acid to rats did not result in the accumulation of the corresponding epoxy alcohol in their livers.

Entities:  

Year:  1966        PMID: 16742464      PMCID: PMC1270192          DOI: 10.1042/bj1010835

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  7 in total

1.  VITAMIN A AND REPRODUCTION IN RATS.

Authors:  J N THOMPSON; J M HOWELL; G A PITT
Journal:  Proc R Soc Lond B Biol Sci       Date:  1964-02-18

2.  Vitamin A and mucopolysaccharide biosynthesis by cell-free particle suspensions.

Authors:  G WOLF; J G BERGAN; P R SUNDARESAN
Journal:  Biochim Biophys Acta       Date:  1963-03-05

3.  Studies on metabolism of vitamin A. 1. The biological activity of vitamin A acid in rats.

Authors:  P MALATHI; K S RAO; P S SASTRY; J GANGULY
Journal:  Biochem J       Date:  1963-05       Impact factor: 3.857

4.  THE BIOLOGICAL FUNCTION OF VITAMIN A ACID.

Authors:  J E Dowling; G Wald
Journal:  Proc Natl Acad Sci U S A       Date:  1960-05       Impact factor: 11.205

5.  Salt mixtures for purified-type diets. III. An improved salt mixtures for chicks.

Authors:  M R Fox; G M Briggs
Journal:  J Nutr       Date:  1960-10       Impact factor: 4.798

6.  METABOLISM AND BIOLOGICAL POTENCY OF 5,6-MONOEPOXYVITAMIN A ALDEHYDE IN THE RAT.

Authors:  M R LAKSHMANAN; F B JUNGALWALA; H R CAMA
Journal:  Biochem J       Date:  1965-04       Impact factor: 3.857

7.  PREPARATION AND PROPERTIES OF 5,6-MONOEPOXYVITAMIN A ACETATE, 5,6-MONOEPOXYVITAMIN A ALCOHOL, 5,6-MONOEPOXYVITAMIN A ALDEHYDE AND THEIR CORRESPONDING 5,8-MONOEPOXY (FURANOID) COMPOUNDS.

Authors:  F B JUNGALWALA; H R CAMA
Journal:  Biochem J       Date:  1965-04       Impact factor: 3.857

  7 in total
  5 in total

1.  Identification of 5,8-oxyretinoic acid isolated from small intestine of vitamin A-deficient rats dosed with retinoic acid.

Authors:  J L Napoli; A M McCormick; H K Schnoes; H F DeLuca
Journal:  Proc Natl Acad Sci U S A       Date:  1978-06       Impact factor: 11.205

2.  5,6-epoxyretinoic acid is a physiological metabolite of retinoic acid in the rat.

Authors:  A M McCormick; J L Napoli; S Yoshizawa; H F DeLuca
Journal:  Biochem J       Date:  1980-02-15       Impact factor: 3.857

3.  Preparation, properties and metabolism of 5,6-monoepoxy-3-dehydroretinal.

Authors:  A K Mallia; M R Lakshmanan; K V John; H R Cama
Journal:  Biochem J       Date:  1969-01       Impact factor: 3.857

4.  Synthesis and metabolism of all-trans-[11-3H]retinyl beta-glucuronide in rats in vivo.

Authors:  A B Barua; R O Batres; J A Olson
Journal:  Biochem J       Date:  1988-06-01       Impact factor: 3.857

5.  Haemoglobin-catalysed retinoic acid 5,6-epoxidation.

Authors:  H Iwahashi; A Ikeda; R Kido
Journal:  Biochem J       Date:  1985-12-01       Impact factor: 3.857

  5 in total

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