Katzenellenbogen JA - Search Results

1

Molecular structures, conformational analysis, and preferential modes of binding of 3-aroyl-2-arylbenzo[b]thiophene estrogen receptor ligands: LY117018 and aryl azide photoaffinity labeling analogs.

Kym PR, Anstead GM, Pinney KG, Wilson SR, Katzenellenbogen JA. Kym PR, et al. Among authors: katzenellenbogen ja. J Med Chem. 1993 Nov 26;36(24):3910-22. doi: 10.1021/jm00076a020. J Med Chem. 1993. PMID: 8254621

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

Donor-acceptor tetrahydrochrysenes, inherently fluorescent, high-affinity ligands for the estrogen receptor: binding and fluorescence characteristics and fluorometric assay of receptor.

Hwang KJ, Carlson KE, Anstead GM, Katzenellenbogen JA. Hwang KJ, et al. Among authors: katzenellenbogen ja. Biochemistry. 1992 Nov 24;31(46):11536-45. doi: 10.1021/bi00161a035. Biochemistry. 1992. PMID: 1445887

4

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

5

Nonsteroidal estrogens bearing acyl azide functions: potential electrophilic and photoaffinity labeling agents for the estrogen receptor.

Pinney KG, Carlson KE, Katzenellenbogen JA. Pinney KG, et al. Among authors: katzenellenbogen ja. Steroids. 1992 May;57(5):222-32. doi: 10.1016/0039-128x(92)90106-j. Steroids. 1992. PMID: 1488784

6

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

7

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

8

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

9

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

10

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

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