Anstead GM - Search Results

1

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. J Med Chem. 1988 Jul;31(7):1316-26. doi: 10.1021/jm00402a011. J Med Chem. 1988. PMID: 3385728

2

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: anstead gm. Biochemistry. 1992 Nov 24;31(46):11536-45. doi: 10.1021/bi00161a035. Biochemistry. 1992. PMID: 1445887

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. J Med Chem. 1990 Oct;33(10):2726-34. doi: 10.1021/jm00172a008. J Med Chem. 1990. PMID: 2213825

4

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

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

5

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. J Med Chem. 1989 Sep;32(9):2163-71. doi: 10.1021/jm00129a024. J Med Chem. 1989. PMID: 2769689

6

Optimizing of 2,3-diarylindenes as fluorescent estrogens: variation of the acceptor group, ortho substitution of the 2-ring, and C-1 methylation.

Anstead GM, Katzenellenbogen JA. Anstead GM, et al. J Med Chem. 1988 Sep;31(9):1754-61. doi: 10.1021/jm00117a014. J Med Chem. 1988. PMID: 3411601

7

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: anstead gm. J Med Chem. 1993 Nov 26;36(24):3910-22. doi: 10.1021/jm00076a020. J Med Chem. 1993. PMID: 8254621

8

Characterization of the spectroscopic properties of a tetrahydrochrysene system containing a rigidified hydroxynitrostilbene chromophore: an inherently fluorescent ligand designed for the estrogen receptor.

Anstead GM, Hwang KJ, Katzenellenbogen JA. Anstead GM, et al. Photochem Photobiol. 1993 Apr;57(4):616-28. doi: 10.1111/j.1751-1097.1993.tb02927.x. Photochem Photobiol. 1993. PMID: 8506389

9

The estradiol pharmacophore: ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site.

Anstead GM, Carlson KE, Katzenellenbogen JA. Anstead GM, et al. Steroids. 1997 Mar;62(3):268-303. doi: 10.1016/s0039-128x(96)00242-5. Steroids. 1997. PMID: 9071738 Review.

10

The effect of acceptor group variation on the solvatochromism of donor-acceptor fluorophores.

Anstead GM, Carlson KE, Kym PR, Hwang KJ, Katzenellenbogen JA. Anstead GM, et al. Photochem Photobiol. 1993 Dec;58(6):785-94. doi: 10.1111/j.1751-1097.1993.tb04971.x. Photochem Photobiol. 1993. PMID: 8309998

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