Title of article :
8-Aminoquinolines as anticoccidials — II
Author/Authors :
Richard E. Armer، نويسنده , , Jacqueline S. Barlow، نويسنده , , Christopher J. Dutton، نويسنده , , David H. J. Greenway، نويسنده , , Sean D. W. Greenwood، نويسنده , , Nita Lad، نويسنده , , Adrian P. Thompson، نويسنده , , Kam-Wah Thong، نويسنده , , Ivan Tommasini، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1998
Pages :
6
From page :
1487
To page :
1492
Abstract :
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
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1998
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
789457
Link To Document :
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