
Bioorganic and Medicinal Chemistry Letters p. 1431 - 1436 (1998)
Update date:2022-07-29
Topics:
Barakat, Khaled J.
Cheng, Kang
Chan, Wanda W.-S
Butler, Bridget S.
Jacks, Thomas M.
Schleim, Klaus D.
Hora Jr., Donald F.
Hickey, Gerard J.
Smith, Roy G.
Patchett, Arthur A.
Nargund, Ravi P.
A new class of potent, orally active phenyl piperazine-based GH secretagogues have been discovered from attempts to mimic the arrangement of the phenyl substitutent in the spiroindanyl piperidine and spiroindoline sulfonamide privileged structures of 4 and 1, respectively. The best of these compounds, 18 (EC50 = 2.8 nM) is nearly as potent as MK-0677 for releasing GH from rat pituitary cells.
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