Pinney KG - Search Results

1

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. Biochemistry. 1991 Mar 5;30(9):2421-31. doi: 10.1021/bi00223a018. Biochemistry. 1991. PMID: 2001370

2

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. Steroids. 1992 May;57(5):222-32. doi: 10.1016/0039-128x(92)90106-j. Steroids. 1992. PMID: 1488784

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

4

[3H]DU41165: a high affinity ligand and novel photoaffinity labeling reagent for the progesterone receptor.

Pinney KG, Carlson KE, Katzenellenbogen JA. Pinney KG, et al. J Steroid Biochem. 1990 Feb;35(2):179-89. doi: 10.1016/0022-4731(90)90272-t. J Steroid Biochem. 1990. PMID: 2308335

5

Target tissue uptake selectivity of three fluorine-substituted progestins: potential imaging agents for receptor-positive breast tumors.

Pomper MG, Pinney KG, Carlson KE, van Brocklin H, Mathias CJ, Welch MJ, Katzenellenbogen JA. Pomper MG, et al. Among authors: pinney kg. Int J Rad Appl Instrum B. 1990;17(3):309-19. doi: 10.1016/0883-2897(90)90058-9. Int J Rad Appl Instrum B. 1990. PMID: 2341287

6

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

7

Synthesis and biological evaluation of aryl azide derivatives of combretastatin A-4 as molecular probes for tubulin.

Pinney KG, Mejia MP, Villalobos VM, Rosenquist BE, Pettit GR, Verdier-Pinard P, Hamel E. Pinney KG, et al. Bioorg Med Chem. 2000 Oct;8(10):2417-25. doi: 10.1016/s0968-0896(00)00176-0. Bioorg Med Chem. 2000. PMID: 11058036

8

A new anti-tubulin agent containing the benzo[b]thiophene ring system.

Pinney KG, Bounds AD, Dingeman KM, Mocharla VP, Pettit GR, Bai R, Hamel E. Pinney KG, et al. Bioorg Med Chem Lett. 1999 Apr 19;9(8):1081-6. doi: 10.1016/s0960-894x(99)00143-2. Bioorg Med Chem Lett. 1999. PMID: 10328289

9

Preparation of new anti-tubulin ligands through a dual-mode, addition-elimination reaction to a bromo-substituted alpha, beta-unsaturated sulfoxide.

Chen Z, Mocharla VP, Farmer JM, Pettit GR, Hamel E, Pinney KG. Chen Z, et al. Among authors: pinney kg. J Org Chem. 2000 Dec 15;65(25):8811-5. doi: 10.1021/jo0004761. J Org Chem. 2000. PMID: 11112609 No abstract available.

10

Oxi4503, a novel vascular targeting agent: effects on blood flow and antitumor activity in comparison to combretastatin A-4 phosphate.

Hua J, Sheng Y, Pinney KG, Garner CM, Kane RR, Prezioso JA, Pettit GR, Chaplin DJ, Edvardsen K. Hua J, et al. Among authors: pinney kg. Anticancer Res. 2003 Mar-Apr;23(2B):1433-40. Anticancer Res. 2003. PMID: 12820406

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