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Results: 1-7 |
Results: 7
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor
Authors: DeVita, RJ Walsh, TF Young, JR Jiang, JL Ujjainwalla, F Toupence, RB Parikh, M Huang, SX Fair, JA Goulet, MT Wyvratt, MJ Lo, JL Ren, N Yudkovitz, JB Yang, YT Cheng, K Cui, JS Mount, G Rohrer, SP Schaeffer, JM Rhodes, L Drisko, JE McGowan, E MacIntyre, DE Vincent, S Carlin, JR Cameron, J Smith, RG
Citation: Rj. Devita et al., A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor, J MED CHEM, 44(6), 2001, pp. 917-922
Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides
Authors: Walsh, TF Toupence, RB Young, JR Huang, SX Ujjainwalla, F DeVita, RJ Goulet, MT Wyvratt, MJ Fisher, MH Lo, JL Ren, N Yudkovitz, JB Yang, YT Cheng, K Smith, RG
Citation: Tf. Walsh et al., Potent antagonists of gonadotropin releasing hormone receptors derived from quinolone-6-carboxamides, BIOORG MED, 10(5), 2000, pp. 443-447
Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents
Authors: Young, JR Huang, SX Chen, I Walsh, TF DeVita, RJ Wyvratt, MJ Goulet, MT Ren, N Lo, J Yang, YT Yudkovitz, JB Cheng, K Smith, RG
Citation: Jr. Young et al., Quinolones as gonadotropin releasing hormone (GnRH) antagonists: Simultaneous optimization of the C(3)-aryl and C(6)-substituents, BIOORG MED, 10(15), 2000, pp. 1723-1727
Identification of Phe(313) of the gonadotropin-releasing hormone (GnRH) receptor as a site critical for the binding of nonpeptide GnRH antagonists
Authors: Cui, JS Smith, RG Mount, GR Lo, JL Yu, JH Walsh, TF Singh, SB DeVita, RJ Goulet, MT Schaeffer, JM Cheng, K
Citation: Js. Cui et al., Identification of Phe(313) of the gonadotropin-releasing hormone (GnRH) receptor as a site critical for the binding of nonpeptide GnRH antagonists, MOL ENDOCR, 14(5), 2000, pp. 671-681
Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist
Authors: DeVita, RJ Hollings, DD Goulet, MT Wyvratt, MJ Fisher, MH Lo, JL Yang, YT Cheng, K Smith, RG
Citation: Rj. Devita et al., Identification and initial structure-activity relationships of a novel non-peptide quinolone GnRH receptor antagonist, BIOORG MED, 9(17), 1999, pp. 2615-2620
Investigation of the 4-O-alkylamine substituent of non-peptide quinolone GnRH receptor antagonists
Authors: DeVita, RJ Goulet, MT Wyvratt, MJ Fisher, MH Lo, JL Yang, YT Cheng, K Smith, RG
Citation: Rj. Devita et al., Investigation of the 4-O-alkylamine substituent of non-peptide quinolone GnRH receptor antagonists, BIOORG MED, 9(17), 1999, pp. 2621-2624
Asymmetric synthesis of chiral, nonracemic trifluoromethyl-substituted piperidines and decahydroquinolines
Authors: Jiang, JL DeVita, RJ Doss, GA Goulet, MT Wyvratt, MJ
Citation: Jl. Jiang et al., Asymmetric synthesis of chiral, nonracemic trifluoromethyl-substituted piperidines and decahydroquinolines, J AM CHEM S, 121(3), 1999, pp. 593-594
Risultati: 1-7 |