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Biomedical subjects

C J Dutton

Publications and source records attributed to C J Dutton.

8 recordsLinked to original sources
PubMed2001

A modified protocol for sex identification of in ovo avian embryos and its application as a management tool for endangered species conservation programs.

A simple, reliable, and safe protocol was developed for the collection of small amounts of blood from avian eggs of variable size and at early stages of development. Fifty eggs were used in the study; 40 were common chicken (Gallus domesticus) eggs, six were homing pigeon (Columba livia domestica) eggs, and four were burrowing owl (Athene cunicularia) eggs. Collection was attempted approximately halfway through incubation. The success rate for collection of blood or blood-tinged fluid from eggs was high, averaging 68% in the chicken eggs, 100% in the homing pigeon eggs, and 75% in the burrowing owl eggs. Collection did not affect subsequent hatchability. This blood could then be used to determine the sex of the embryo by utilizing a DNA probe or restriction fragment length polymorphism technique. Sex identification in ovo allowed the demographic management of small populations of birds within our institution.

Animals↗
PubMed1999

8-aminoquinolines as anticoccidials - Part III.

Analogues of the antimalarial pentaquine, 1, in which the nature of the side-chain on the 8-amino position was varied, were prepared and evaluated for anticoccidial activity both in vitro and in vivo. Specifically, both the inter-nitrogen distance and the nature of the terminal amino group were investigated. Novel analogues of equal or improved efficacy in vitro and in vivo to pentaquine were discovered.

Aminoquinolines↗
PubMed1998

8-Aminoquinolines as anticoccidials--II.

During a chemistry program aimed at finding a novel analogue of pentaquine with improved in vivo activity, a number of hypotheses concerning the way this drug acts in the chicken were investigated. Consideration of the products of monoamine oxidase metabolism of pentaquine suggested that pentaquine aldehyde is the likely active metabolite. Although isolation of this unstable compound was not possible, oxime and cyclic acetal and ketal derivatives were obtained and shown to possess in vitro anticoccidial activity.

Aminoquinolines↗
PubMed1998

Carbocyclic frenolicin analogues: novel anticoccidial agents.

Carbocyclic analogues of the antibacterial natural product frenolicin B have been synthesised. These analogues were active against parasitic protozoa of the genus Eimeria and represent a new series of anticoccidial agents. The synthesis of simplified analogues helped to define a possible pharmacophore for frenolicin.

Animals↗
PubMed1991

Novel avermectins produced by mutational biosynthesis.

Avermectins with a wide range of novel C-25 substituents have been prepared by feeding carboxylic acids or their biosynthetic precursors to a Streptomyces avermitilis mutant strain ATCC 53568. This organism lacks the ability to form isobutyric and S-2-methylbutyric acids from their 2-oxo acid precursors and thus is unable to produce natural avermectins unless supplied with these acids. The novel avermectins produced by mutational biosynthesis possess broad-spectrum antiparasitic activity.

Animals↗