Fry D - Search Results

1

Characterizing the mu-conotoxin binding site on voltage-sensitive sodium channels with toxin analogs and channel mutations.

Chahine M, Chen LQ, Fotouhi N, Walsky R, Fry D, Santarelli V, Horn R, Kallen RG. Chahine M, et al. Among authors: fry d. Recept Channels. 1995;3(3):161-74. Recept Channels. 1995. PMID: 8821790

2

The design and synthesis of potent cyclic peptide VCAM-VLA-4 antagonists incorporating an achiral Asp-Pro mimetic.

Fotouhi N, Joshi P, Fry D, Cook C, Tilley JW, Kaplan G, Hanglow A, Rowan K, Schwinge V, Wolitzky B. Fotouhi N, et al. Among authors: fry d. Bioorg Med Chem Lett. 2000 Jun 5;10(11):1171-3. doi: 10.1016/s0960-894x(00)00174-8. Bioorg Med Chem Lett. 2000. PMID: 10866374

3

A predictive pharmacophore model of human melanocortin-4 receptor as derived from the solution structures of cyclic peptides.

Sun H, Greeley DN, Chu XJ, Cheung A, Danho W, Swistok J, Wang Y, Zhao C, Chen L, Fry DC. Sun H, et al. Bioorg Med Chem. 2004 May 15;12(10):2671-7. doi: 10.1016/j.bmc.2004.03.017. Bioorg Med Chem. 2004. PMID: 15110848

4

N-acyl-L-phenylalanine derivatives as potent VLA-4 antagonists that mimic a cyclic peptide conformation.

Chen L, Tilley J, Trilles RV, Yun W, Fry D, Cook C, Rowan K, Schwinge V, Campbell R. Chen L, et al. Among authors: fry d. Bioorg Med Chem Lett. 2002 Jan 21;12(2):137-40. doi: 10.1016/s0960-894x(01)00711-9. Bioorg Med Chem Lett. 2002. PMID: 11755339

5

A selective phosphatase of regenerating liver phosphatase inhibitor suppresses tumor cell anchorage-independent growth by a novel mechanism involving p130Cas cleavage.

Daouti S, Li WH, Qian H, Huang KS, Holmgren J, Levin W, Reik L, McGady DL, Gillespie P, Perrotta A, Bian H, Reidhaar-Olson JF, Bliss SA, Olivier AR, Sergi JA, Fry D, Danho W, Ritland S, Fotouhi N, Heimbrook D, Niu H. Daouti S, et al. Among authors: fry d. Cancer Res. 2008 Feb 15;68(4):1162-9. doi: 10.1158/0008-5472.CAN-07-2349. Cancer Res. 2008. PMID: 18281492

6

Focused library approach for identification of new N-acylphenylalanines as VCAM/VLA-4 antagonists.

Chen L, Trilles R, Miklowski D, Huang TN, Fry D, Campbell R, Rowan K, Schwinge V, Tilley JW. Chen L, et al. Among authors: fry d. Bioorg Med Chem Lett. 2002 Jun 17;12(12):1679-82. doi: 10.1016/s0960-894x(02)00201-9. Bioorg Med Chem Lett. 2002. PMID: 12039589

7

Concepts and progress in the development of peptide mimetics.

Olson GL, Bolin DR, Bonner MP, Bös M, Cook CM, Fry DC, Graves BJ, Hatada M, Hill DE, Kahn M, et al. Olson GL, et al. Among authors: fry dc. J Med Chem. 1993 Oct 15;36(21):3039-49. doi: 10.1021/jm00073a001. J Med Chem. 1993. PMID: 8230089 Review. No abstract available.

8

Analogs of CCK incorporating conformationally constrained replacements for Asp32.

Tilley JW, Danho W, Madison V, Fry D, Swistok J, Makofske R, Michalewsky J, Schwartz A, Weatherford S, Triscari J, et al. Tilley JW, et al. Among authors: fry d. J Med Chem. 1992 Oct 30;35(22):4249-52. doi: 10.1021/jm00100a033. J Med Chem. 1992. PMID: 1433225 No abstract available.

9

NMR characterization of interleukin-2 in complexes with the IL-2Ralpha receptor component, and with low molecular weight compounds that inhibit the IL-2/IL-Ralpha interaction.

Emerson SD, Palermo R, Liu CM, Tilley JW, Chen L, Danho W, Madison VS, Greeley DN, Ju G, Fry DC. Emerson SD, et al. Protein Sci. 2003 Apr;12(4):811-22. doi: 10.1110/ps.0232803. Protein Sci. 2003. PMID: 12649439 Free PMC article.

10

Structure-Based Design and Synthesis of Potent Cyclic Peptides Inhibiting the YAP-TEAD Protein-Protein Interaction.

Zhang Z, Lin Z, Zhou Z, Shen HC, Yan SF, Mayweg AV, Xu Z, Qin N, Wong JC, Zhang Z, Rong Y, Fry DC, Hu T. Zhang Z, et al. ACS Med Chem Lett. 2014 Jul 14;5(9):993-8. doi: 10.1021/ml500160m. eCollection 2014 Sep 11. ACS Med Chem Lett. 2014. PMID: 25221655 Free PMC article.

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