Bioorganic and Medicinal Chemistry Letters p. 1057 - 1062 (1999)
Update date:2022-07-29
Topics:
Cocuzza, Anthony J.
Hobbs, Frank W.
Arnold, Charles R.
Chidester, Dennis R.
Yarem, Jerry A.
Culp, Steven
Fitzgerald, Lawrence
Gilligan, Paul J.
A series of 4-aryl-2-(N-ethylanilino)pyrimidines has been synthesized as corticotropin-releasing hormone (CH) inhibitors. The effect of substitution on each aromatic ring on receptor binding was investigated.
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Doi:10.1007/BF00954613
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(1999)
