Phelan KM - Search Results

1

Synthesis and antibacterial activity of novel bifunctional macrolides.

Akritopoulou-Zanze I, Phelan KM, Marron TG, Yong H, Ma Z, Stone GG, Daly MM, Hensey DM, Nilius AM, Djuric SW. Akritopoulou-Zanze I, et al. Among authors: phelan km. Bioorg Med Chem Lett. 2004 Jul 16;14(14):3809-13. doi: 10.1016/j.bmcl.2004.04.077. Bioorg Med Chem Lett. 2004. PMID: 15203167

2

Scaffold oriented synthesis. Part 1: Design, preparation, and biological evaluation of thienopyrazoles as kinase inhibitors.

Akritopoulou-Zanze I, Darczak D, Sarris K, Phelan KM, Huth JR, Song D, Johnson EF, Jia Y, Djuric SW. Akritopoulou-Zanze I, et al. Among authors: phelan km. Bioorg Med Chem Lett. 2006 Jan 1;16(1):96-9. doi: 10.1016/j.bmcl.2005.09.042. Epub 2005 Oct 10. Bioorg Med Chem Lett. 2006. PMID: 16216502

3

Hit-to-lead optimization of 1,4-dihydroindeno[1,2-c]pyrazoles as a novel class of KDR kinase inhibitors.

Dinges J, Akritopoulou-Zanze I, Arnold LD, Barlozzari T, Bousquet PF, Cunha GA, Ericsson AM, Iwasaki N, Michaelides MR, Ogawa N, Phelan KM, Rafferty P, Sowin TJ, Stewart KD, Tokuyama R, Xia Z, Zhang HQ. Dinges J, et al. Among authors: phelan km. Bioorg Med Chem Lett. 2006 Aug 15;16(16):4371-5. doi: 10.1016/j.bmcl.2006.05.052. Epub 2006 Jun 5. Bioorg Med Chem Lett. 2006. PMID: 16750628

4

Structure-activity relationships of non-imidazole H(3) receptor ligands. Part 1.

Faghih R, Dwight W, Gentles R, Phelan K, Esbenshade TA, Ireland L, Miller TR, Kang CH, Fox GB, Gopalakrishnan SM, Hancock AA, Bennani YL. Faghih R, et al. Bioorg Med Chem Lett. 2002 Aug 5;12(15):2031-4. doi: 10.1016/s0960-894x(02)00309-8. Bioorg Med Chem Lett. 2002. PMID: 12113835

5

Structure-activity relationships of non-imidazole H(3) receptor ligands. Part 2: binding preference for D-amino acids motifs.

Faghih R, Dwight W, Black L, Liu H, Gentles R, Phelan K, Esbenshade TA, Ireland L, Miller TR, Kang CH, Krueger KM, Fox GB, Hancock AA, Bennani YL. Faghih R, et al. Among authors: phelan k. Bioorg Med Chem Lett. 2002 Aug 5;12(15):2035-7. doi: 10.1016/s0960-894x(02)00310-4. Bioorg Med Chem Lett. 2002. PMID: 12113836

6

Optimization of the 4-aryl group of 4-aryl-pyridine glucagon antagonists: development of an efficient, alternative synthesis.

Smith RA, Hertzog DL, Osterhout MH, Ladouceur GH, Korpusik M, Bobko MA, Jones JH, Phelan K, Romero RH, Hundertmark T, MacDougall ML, Livingston JN, Schoen WR. Smith RA, et al. Bioorg Med Chem Lett. 2002 May 6;12(9):1303-6. doi: 10.1016/s0960-894x(02)00143-9. Bioorg Med Chem Lett. 2002. PMID: 11965376

7

Microwave-assisted synthesis utilizing supported reagents: a rapid and efficient acylation procedure.

Sauer DR, Kalvin D, Phelan KM. Sauer DR, et al. Among authors: phelan km. Org Lett. 2003 Nov 27;5(24):4721-4. doi: 10.1021/ol0358915. Org Lett. 2003. PMID: 14627424

8

D-alanine piperazine-amides: novel non-imidazole antagonists of the histamine H3 receptor.

Faghih R, Phelan K, Esbenshade TA, Miller TR, Kang CH, Krueger KM, Yao BB, Fox GB, Bennani YL, Hancock AA. Faghih R, et al. Among authors: phelan k. Inflamm Res. 2003 Apr;52 Suppl 1:S47-8. doi: 10.1007/s000110300049. Inflamm Res. 2003. PMID: 12755406 No abstract available.

9

Integration of optimized substituent patterns to produce highly potent 4-aryl-pyridine glucagon receptor antagonists.

Ladouceur GH, Cook JH, Hertzog DL, Jones JH, Hundertmark T, Korpusik M, Lease TG, Livingston JN, MacDougall ML, Osterhout MH, Phelan K, Romero RH, Schoen WR, Shao C, Smith RA. Ladouceur GH, et al. Bioorg Med Chem Lett. 2002 Dec 2;12(23):3421-4. doi: 10.1016/s0960-894x(02)00736-9. Bioorg Med Chem Lett. 2002. PMID: 12419375

10

Lithium interaction with the cyclooxygenase 2 inhibitors rofecoxib and celecoxib and other nonsteroidal anti-inflammatory drugs.

Phelan KM, Mosholder AD, Lu S. Phelan KM, et al. J Clin Psychiatry. 2003 Nov;64(11):1328-34. doi: 10.4088/jcp.v64n1108. J Clin Psychiatry. 2003. PMID: 14658947 Review.

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