Title of article :
Synthesis and SAR of a novel, potent and structurally simple LTD4 antagonist of the quinoline class
Author/Authors :
Andreas von Sprecher، نويسنده , , Marc Gerspacher، نويسنده , , Andreas Beck، نويسنده , , Sabine Kimmel، نويسنده , , Hansruedi Wiestner، نويسنده , , Gary P. Anderson، نويسنده , , Ulrich Niederhauser، نويسنده , , Natarajan Subramanian، نويسنده , , Michael A. Bray، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1998
Pages :
6
From page :
965
To page :
970
Abstract :
The two geminal ethyl groups in the succinic acid moiety of CGP57698 (4-[3-(7-fluoro-2-quinolinyl-methoxy)phenyl-amino]-2,2-diethyl-4-oxo-butanoic acid) are responsible for the high in vitro and in vivo potency of this peptidoleukotriene antagonist of the quinoline type. The synthesis and structure activity relationships of CGP57698 and its analogs are described.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1998
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
789357
Link To Document :
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