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Citation: Wt. Ashton et al., Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activity, BIOORG MED, 11(19), 2001, pp. 2597-2602

Authors: Ashton, WT Sisco, RM Yang, YT Lo, JL Yudkovitz, JB Cheng, K Goulet, MT

Citation: Wt. Ashton et al., Substituted indole-5-carboxamides and -acetamides as potent nonpeptide GnRH receptor antagonists, BIOORG MED, 11(13), 2001, pp. 1723-1726

Authors: Ashton, WT Sisco, RM Yang, YT Lo, JL Yudkovitz, JB Gibbons, PH Mount, GR Ren, RN Butler, BS Cheng, K Goulet, MT

Citation: Wt. Ashton et al., Potent nonpeptide GnRH receptor antagonists derived from substituted indole-5-carboxamides and -acetamides bearing a pyridine side-chain terminus, BIOORG MED, 11(13), 2001, pp. 1727-1731

Authors: Toney, JH Cleary, KA Hammond, GG Yuan, XL May, WJ Hutchins, SM Ashton, WT Vanderwall, DE

Citation: Jh. Toney et al., Structure-activity relationships of biphenyl tetrazoles as metallo-beta-lactamase inhibitors, BIOORG MED, 9(18), 1999, pp. 2741-2746