17 articles for RG Smith
The following articles (labelled with PubMed ID or TBD) are for your review
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The design and synthesis of orally active short duration spiroindane growth hormone secretagogues

TBA
Modeling directed design and biological evaluation of quinazolinones as non-peptidic growth hormone secretagogues.

Merck Research Laboratories
Heterocyclic derivatives of 2-(3,5-dimethylphenyl)tryptamine as GnRH receptor antagonists.

Merck Research Laboratories
2-(3,5-Dimethylphenyl)tryptamine derivatives that bind to the GnRH receptor.

Merck Research Laboratories
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor.

Merck Research Laboratories
SAR studies of novel 5-substituted 2-arylindoles as nonpeptidyl GnRH receptor antagonists.

Merck Research Laboratories
Initial structure-activity relationship of a novel class of nonpeptidyl GnRH receptor antagonists: 2-arylindoles.

Merck Research Laboratories
Quinolones as gonadotropin releasing hormone (GnRH) antagonists: simultaneous optimization of the C(3)-aryl and C(6)-substituents.

Merck Research Laboratories
Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides.

Merck Research Laboratories
Investigation of the 4-O-alkylamine substituent of non-peptide quinolone GnRH receptor antagonists.

Merck Research Laboratories
Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist.

Merck Research Laboratories
Potent 3-spiropiperidine growth hormone secretagogues.

Merck Research Laboratories
Peptidomimetic growth hormone secretagogues. Design considerations and therapeutic potential.

Merck Research Laboratories
Development of a high specific activity sulfur-35-labeled sulfonamide radioligand that allowed the identification of a new growth hormone secretagogue receptor.

Merck Research Laboratories
Synthesis and anxiolytic activity of a series of pyrazino[1,2-a][1,4]benzodiazepine derivatives.

TBA
Terphenyl-Based Bak BH3 alpha-helical proteomimetics as low-molecular-weight antagonists of Bcl-xL.

Yale University
Synthesis and in vitro evaluation of sulfonamide isatin Michael acceptors as small molecule inhibitors of caspase-6.

Washington University