Katzenellenbogen JA - Search Results

1

Synthesis, antitubulin and antimitotic activity, and cytotoxicity of analogs of 2-methoxyestradiol, an endogenous mammalian metabolite of estradiol that inhibits tubulin polymerization by binding to the colchicine binding site.

Cushman M, He HM, Katzenellenbogen JA, Lin CM, Hamel E. Cushman M, et al. Among authors: katzenellenbogen ja. J Med Chem. 1995 Jun 9;38(12):2041-9. doi: 10.1021/jm00012a003. J Med Chem. 1995. PMID: 7783135

2

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

3

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

4

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

5

Preparation, receptor binding, and fluorescence properties of hexestrol-fluorophore conjugates: evaluation of site of attachment, fluorophore structure, and fluorophore-ligand spacing.

Fevig TL, Lloyd JE, Zablocki JA, Katzenellenbogen JA. Fevig TL, et al. Among authors: katzenellenbogen ja. J Med Chem. 1987 Jan;30(1):156-65. doi: 10.1021/jm00384a026. J Med Chem. 1987. PMID: 3027331

6

Bis(4-hydroxyphenyl)[2-(phenoxysulfonyl)phenyl]methane: isolation and structure elucidation of a novel estrogen from commercial preparations of phenol red (phenolsulfonphthalein).

Bindal RD, Katzenellenbogen JA. Bindal RD, et al. Among authors: katzenellenbogen ja. J Med Chem. 1988 Oct;31(10):1978-83. doi: 10.1021/jm00118a020. J Med Chem. 1988. PMID: 3172132

7

2,3-Diarylindenes and 2,3-diarylindenones: synthesis, molecular structure, photochemistry, estrogen receptor binding affinity, and comparisons with related triarylethylenes.

Anstead GM, Altenbach RJ, Wilson SR, Katzenellenbogen JA. Anstead GM, et al. Among authors: katzenellenbogen ja. J Med Chem. 1988 Jul;31(7):1316-26. doi: 10.1021/jm00402a011. J Med Chem. 1988. PMID: 3385728

8

11 beta-substituted estradiol derivatives. 2. Potential carbon-11- and iodine-labeled probes for the estrogen receptor.

Napolitano E, Fiaschi R, Carlson KE, Katzenellenbogen JA. Napolitano E, et al. Among authors: katzenellenbogen ja. J Med Chem. 1995 Jul 7;38(14):2774-9. doi: 10.1021/jm00014a028. J Med Chem. 1995. PMID: 7629815

9

Fluorine-18-labeled progestin 16 alpha, 17 alpha-dioxolanes: development of high-affinity ligands for the progesterone receptor with high in vivo target site selectivity.

Buckman BO, Bonasera TA, Kirschbaum KS, Welch MJ, Katzenellenbogen JA. Buckman BO, et al. Among authors: katzenellenbogen ja. J Med Chem. 1995 Jan 20;38(2):328-37. doi: 10.1021/jm00002a014. J Med Chem. 1995. PMID: 7830275

10

11 beta-Substituted estradiol derivatives, potential high-affinity carbon-11-labeled probes for the estrogen receptor: a structure-affinity relationship study.

Napolitano E, Fiaschi R, Carlson KE, Katzenellenbogen JA. Napolitano E, et al. Among authors: katzenellenbogen ja. J Med Chem. 1995 Feb 3;38(3):429-34. doi: 10.1021/jm00003a005. J Med Chem. 1995. PMID: 7853335

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