Edwards JP - Search Results

1

Preparation, resolution, and biological evaluation of 5-aryl-1, 2-dihydro-5H-chromeno[3,4-f]quinolines: potent, orally active, nonsteroidal progesterone receptor agonists.

Edwards JP, Zhi L, Pooley CL, Tegley CM, West SJ, Wang MW, Gottardis MM, Pathirana C, Schrader WT, Jones TK. Edwards JP, et al. J Med Chem. 1998 Jul 16;41(15):2779-85. doi: 10.1021/jm980190c. J Med Chem. 1998. PMID: 9667968

2

5-Aryl-1,2-dihydro-5H-chromeno[3,4-f]quinolines as potent, orally active, nonsteroidal progesterone receptor agonists: the effect of D-ring substituents.

Edwards JP, West SJ, Marschke KB, Mais DE, Gottardis MM, Jones TK. Edwards JP, et al. J Med Chem. 1998 Jan 29;41(3):303-10. doi: 10.1021/jm9705770. J Med Chem. 1998. PMID: 9464361

3

Synthesis and biological activity of a novel series of nonsteroidal, peripherally selective androgen receptor antagonists derived from 1,2-dihydropyridono[5,6-g]quinolines.

Hamann LG, Higuchi RI, Zhi L, Edwards JP, Wang XN, Marschke KB, Kong JW, Farmer LJ, Jones TK. Hamann LG, et al. Among authors: edwards jp. J Med Chem. 1998 Feb 12;41(4):623-39. doi: 10.1021/jm970699s. J Med Chem. 1998. PMID: 9484511

4

Discovery and preliminary SAR studies of a novel, nonsteroidal progesterone receptor antagonist pharmacophore.

Pooley CL, Edwards JP, Goldman ME, Wang MW, Marschke KB, Crombie DL, Jones TK. Pooley CL, et al. Among authors: edwards jp. J Med Chem. 1998 Aug 27;41(18):3461-6. doi: 10.1021/jm9801915. J Med Chem. 1998. PMID: 9719599

5

New nonsteroidal androgen receptor modulators based on 4-(trifluoromethyl)-2(1H)-pyrrolidino[3,2-g] quinolinone.

Edwards JP, West SJ, Pooley CL, Marschke KB, Farmer LJ, Jones TK. Edwards JP, et al. Bioorg Med Chem Lett. 1998 Apr 7;8(7):745-50. doi: 10.1016/s0960-894x(98)00107-3. Bioorg Med Chem Lett. 1998. PMID: 9871534

6

Nonsteroidal progesterone receptor antagonists based on a conformationally-restricted subseries of 6-aryl-1,2-dihydro-2,2,4-trimethylquinolines.

Hamann LG, Winn DT, Pooley CL, Tegley CM, West SJ, Farmer LJ, Zhi L, Edwards JP, Marschke KB, Mais DE, Goldman ME, Jones TK. Hamann LG, et al. Among authors: edwards jp. Bioorg Med Chem Lett. 1998 Oct 6;8(19):2731-6. doi: 10.1016/s0960-894x(98)00482-x. Bioorg Med Chem Lett. 1998. PMID: 9873612

7

5-Alkyl 1,2-dihydrochromeno[3,4-f]quinolines: a novel class of nonsteroidal progesterone receptor modulators.

Zhi L, Tegley CM, Edwards JP, West SJ, Marschke KB, Gottardis MM, Mais DE, Jones TK. Zhi L, et al. Among authors: edwards jp. Bioorg Med Chem Lett. 1998 Dec 1;8(23):3365-70. doi: 10.1016/s0960-894x(98)00608-8. Bioorg Med Chem Lett. 1998. PMID: 9873735

8

Nonsteroidal androgen receptor agonists based on 4-(trifluoromethyl)-2H-pyrano[3,2-g]quinolin-2-one.

Edwards JP, Higuchi RI, Winn DT, Pooley CL, Caferro TR, Hamann LG, Zhi L, Marschke KB, Goldman ME, Jones TK. Edwards JP, et al. Bioorg Med Chem Lett. 1999 Apr 5;9(7):1003-8. doi: 10.1016/s0960-894x(99)00118-3. Bioorg Med Chem Lett. 1999. PMID: 10230628

9

4-Alkyl- and 3,4-dialkyl-1,2,3,4-tetrahydro-8-pyridono[5,6-g]quinolines: potent, nonsteroidal androgen receptor agonists.

Higuchi RI, Edwards JP, Caferro TR, Ringgenberg JD, Kong JW, Hamann LG, Arienti KL, Marschke KB, Davis RL, Farmer LJ, Jones TK. Higuchi RI, et al. Among authors: edwards jp. Bioorg Med Chem Lett. 1999 May 3;9(9):1335-40. doi: 10.1016/s0960-894x(99)00186-9. Bioorg Med Chem Lett. 1999. PMID: 10340624

10

Effects of isosteric pyridone replacements in androgen receptor antagonists based on 1,2-dihydro- and 1,2,3,4-tetrahydro-2,2-dimethyl-6-trifluoromethyl-8-pyridono[5,6-g]quin olines.

Kong JW, Hamann LG, Ruppar DA, Edwards JP, Marschke KB, Jones TK. Kong JW, et al. Among authors: edwards jp. Bioorg Med Chem Lett. 2000 Mar 6;10(5):411-4. doi: 10.1016/s0960-894x(00)00010-x. Bioorg Med Chem Lett. 2000. PMID: 10743937

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