Traditional GnRH receptor antagonists are often peptide-based, but nonpeptide antagonists are usually preferred for drug development because they tend to have better oral bioavailability, stability, and lower immunogenicity.
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3-Pyridineethanol,6-methoxy-(9CI)
t-butyl 3-bromo-4-[[(2-phenylethyl)amino]methyl]-benzoate
Carbamic acid, [(5-methyl-1H-imidazo[4,5-b]pyridin-2-yl)methyl]-, phenylmethyl ester
ethyl 7-chloro-5-oxo-1-p-toluenesulfonyl-2,3,4,5-tetrahydro-1H-1-benzazepine-4-carboxylate
2-[5-(4-nitro-benzoyl)-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl]-acetamide
2-[2-(3-tert-butyl-ureido)-ethyl]-1-(2-chloro-benzyl)-1H-benzoimidazole-5-sulfonyl chloride
1H-1-Benzazepine, 1-(4-aminobenzoyl)-2,3,4,5-tetrahydro-
