Literature DB >> 9871779

Synthesis and biological activities of phenyl piperazine-based peptidomimetic growth hormone secretagogues.

K J Barakat1, K Cheng, W W Chan, B S Butler, T M Jacks, K D Schleim, D F Hora, G J Hickey, R G Smith, A A Patchett, R P Nargund.   

Abstract

A new class of potent, orally active phenyl piperazine-based GH secretagogues have been discovered from attempts to mimic the arrangement of the phenyl substituent 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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Year:  1998        PMID: 9871779     DOI: 10.1016/s0960-894x(98)00238-8

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  An efficient synthesis of a spirocyclic oxindole analogue.

Authors:  Dawei Teng; Hongxing Zhang; A Mendonca
Journal:  Molecules       Date:  2006-09-14       Impact factor: 4.411

  1 in total

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