Katzenellenbogen JA - Search Results

1

Selective and potent agonists for estrogen receptor beta derived from molecular refinements of salicylaldoximes.

Bertini S, De Cupertinis A, Granchi C, Bargagli B, Tuccinardi T, Martinelli A, Macchia M, Gunther JR, Carlson KE, Katzenellenbogen JA, Minutolo F. Bertini S, et al. Among authors: katzenellenbogen ja. Eur J Med Chem. 2011 Jun;46(6):2453-62. doi: 10.1016/j.ejmech.2011.03.030. Epub 2011 Mar 23. Eur J Med Chem. 2011. PMID: 21481497 Free PMC article.

2

Antiestrogens and antiestrogen metabolites: preparation of tritium-labeled (+/-)-cis-3-[p-(1,2,3,4-tetrahydro-6-methoxy-2-phenyl-1-naphthyl)phenoxyl]-1,2-propanediol (U-23469) and characterization and synthesis of a biologically important metabolite.

Tatee T, Carlson KE, Katzenellenbogen JA, Robertson DW, Katzenellenbogen BS. Tatee T, et al. Among authors: katzenellenbogen bs, katzenellenbogen ja. J Med Chem. 1979 Dec;22(12):1509-17. doi: 10.1021/jm00198a015. J Med Chem. 1979. PMID: 536996

3

Characterization of trypsin-treated forms of the estrogen receptor from rat and lamb uterus.

Carlson KE, Sun LH, Katzenellenbogen JA. Carlson KE, et al. Among authors: katzenellenbogen ja. Biochemistry. 1977 Sep 20;16(19):4288-96. doi: 10.1021/bi00638a025. Biochemistry. 1977. PMID: 901772 No abstract available.

4

Chemical probes of estrogen action: affinity labeling.

Katzenellenbogen JA, Carlson KE, Johnson HJ Jr, Myers HN. Katzenellenbogen JA, et al. J Toxicol Environ Health Suppl. 1976;1:205-30. J Toxicol Environ Health Suppl. 1976. PMID: 1033295

5

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

6

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

7

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

8

Preparation and evaluation of 17-ethynyl-substituted 16 alpha-[18F]fluoroestradiols: selective receptor-based PET imaging agents.

VanBrocklin HF, Pomper MG, Carlson KE, Welch MJ, Katzenellenbogen JA. VanBrocklin HF, et al. Among authors: katzenellenbogen ja. Int J Rad Appl Instrum B. 1992 Apr;19(3):363-74. doi: 10.1016/0883-2897(92)90122-f. Int J Rad Appl Instrum B. 1992. PMID: 1629026

9

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

10

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

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