Katzenellenbogen JA - Search Results

1

Triarylethylene bisphenols with a novel cycle are ligands for the estrogen receptor.

Kim SH, Katzenellenbogen JA. Kim SH, et al. Among authors: katzenellenbogen ja. Bioorg Med Chem. 2000 Apr;8(4):785-93. doi: 10.1016/s0968-0896(00)00016-x. Bioorg Med Chem. 2000. PMID: 10819167

2

Guanidinophenyl-substituted enol lactones as selective, mechanism-based inhibitors of trypsin-like serine proteases.

Rai R, Katzenellenbogen JA. Rai R, et al. Among authors: katzenellenbogen ja. J Med Chem. 1992 Oct 30;35(22):4150-9. doi: 10.1021/jm00100a021. J Med Chem. 1992. PMID: 1433218

3

Effect of conformational mobility and hydrogen-bonding interactions on the selectivity of some guanidinoaryl-substituted mechanism-based inhibitors of trypsin-like serine proteases.

Rai R, Katzenellenbogen JA. Rai R, et al. Among authors: katzenellenbogen ja. J Med Chem. 1992 Nov 13;35(23):4297-305. doi: 10.1021/jm00101a006. J Med Chem. 1992. PMID: 1447734

4

Synthesis of high affinity fluorine-substituted ligands for the androgen receptor. Potential agents for imaging prostatic cancer by positron emission tomography.

Liu A, Carlson KE, Katzenellenbogen JA. Liu A, et al. Among authors: katzenellenbogen ja. J Med Chem. 1992 May 29;35(11):2113-29. doi: 10.1021/jm00089a024. J Med Chem. 1992. PMID: 1597861

5

11 beta-methoxy-, 11 beta-ethyl- and 17 alpha-ethynyl-substituted 16 alpha-fluoroestradiols: receptor-based imaging agents with enhanced uptake efficiency and selectivity.

Pomper MG, VanBrocklin H, Thieme AM, Thomas RD, Kiesewetter DO, Carlson KE, Mathias CJ, Welch MJ, Katzenellenbogen JA. Pomper MG, et al. Among authors: katzenellenbogen ja. J Med Chem. 1990 Dec;33(12):3143-55. doi: 10.1021/jm00174a009. J Med Chem. 1990. PMID: 1701833

6

Efficient and selective photoaffinity labeling of the estrogen receptor using two nonsteroidal ligands that embody aryl azide or tetrafluoroaryl azide photoreactive functions.

Pinney KG, Carlson KE, Katzenellenbogen BS, Katzenellenbogen JA. Pinney KG, et al. Among authors: katzenellenbogen bs, katzenellenbogen ja. Biochemistry. 1991 Mar 5;30(9):2421-31. doi: 10.1021/bi00223a018. Biochemistry. 1991. PMID: 2001370

7

Beta-substituted beta-phenylpropionyl chymotrypsins. Structural and stereochemical features in stable acyl enzymes.

Reed PE, Katzenellenbogen JA. Reed PE, et al. Among authors: katzenellenbogen ja. J Med Chem. 1991 Mar;34(3):1162-76. doi: 10.1021/jm00107a041. J Med Chem. 1991. PMID: 2002457

8

Torsionally and hydrophobically modified 2,3-diarylindenes as estrogen receptor ligands.

Anstead GM, Peterson CS, Pinney KG, Wilson SR, Katzenellenbogen JA. Anstead GM, et al. Among authors: katzenellenbogen ja. J Med Chem. 1990 Oct;33(10):2726-34. doi: 10.1021/jm00172a008. J Med Chem. 1990. PMID: 2213825

9

Hydroxylated 2,3-diarylindenes: synthesis, estrogen receptor binding affinity, and binding orientation considerations.

Anstead GM, Peterson CS, Katzenellenbogen JA. Anstead GM, et al. Among authors: katzenellenbogen ja. J Steroid Biochem. 1989 Nov;33(5):877-87. doi: 10.1016/0022-4731(89)90235-5. J Steroid Biochem. 1989. PMID: 2601332

10

2-Arylindenes and 2-arylindenones: molecular structures and considerations in the binding orientation of unsymmetrical nonsteroidal ligands to the estrogen receptor.

Anstead GM, Wilson SR, Katzenellenbogen JA. Anstead GM, et al. Among authors: katzenellenbogen ja. J Med Chem. 1989 Sep;32(9):2163-71. doi: 10.1021/jm00129a024. J Med Chem. 1989. PMID: 2769689

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