Favor DA - Search Results

1

Molecular modeling, synthesis, and structures of N-methylated 3,5-linked pyrrolin-4-ones toward the creation of a privileged nonpeptide scaffold.

Smith AB 3rd, Favor DA, Sprengeler PA, Guzman MC, Carroll PJ, Furst GT, Hirschmann R. Smith AB 3rd, et al. Among authors: favor da. Bioorg Med Chem. 1999 Jan;7(1):9-22. doi: 10.1016/s0968-0896(98)00234-x. Bioorg Med Chem. 1999. PMID: 10199652 Free article.

2

Synthesis of polypyrrolinones on solid support.

Smith AB 3rd, Liu H, Okumura H, Favor DA, Hirschmann R. Smith AB 3rd, et al. Among authors: favor da. Org Lett. 2000 Jul 13;2(14):2041-4. doi: 10.1021/ol005931u. Org Lett. 2000. PMID: 10891225

3

Azide and Cyanide Displacements via Hypervalent Silicate Intermediates.

Soli ED, Manoso AS, Patterson MC, DeShong P, Favor DA, Hirschmann R, Smith AB 3rd. Soli ED, et al. Among authors: favor da. J Org Chem. 1999 Apr 30;64(9):3171-3177. doi: 10.1021/jo982302d. J Org Chem. 1999. PMID: 11674417

4

Sulfonamides as selective oestrogen receptor β agonists.

Roberts LR, Armor D, Barker C, Bent A, Bess K, Brown A, Favor DA, Ellis D, Irving SL, MacKenny M, Phillips C, Pullen N, Stennett A, Strand L, Styles M. Roberts LR, et al. Among authors: favor da. Bioorg Med Chem Lett. 2011 Oct 1;21(19):5680-3. doi: 10.1016/j.bmcl.2011.08.041. Epub 2011 Aug 16. Bioorg Med Chem Lett. 2011. PMID: 21885279

5

Serendipity in drug-discovery: a new series of 2-(benzyloxy)benzamides as TRPM8 antagonists.

Brown A, Ellis D, Favor DA, Kirkup T, Klute W, MacKenny M, McMurray G, Stennett A. Brown A, et al. Among authors: favor da. Bioorg Med Chem Lett. 2013 Nov 15;23(22):6118-22. doi: 10.1016/j.bmcl.2013.09.016. Epub 2013 Sep 19. Bioorg Med Chem Lett. 2013. PMID: 24080460

6

Pyrrolo[2,1-f][1,2,4]triazines: From C-nucleosides to kinases and back again, the remarkable journey of a versatile nitrogen heterocycle.

Ott GR, Favor DA. Ott GR, et al. Among authors: favor da. Bioorg Med Chem Lett. 2017 Sep 15;27(18):4238-4246. doi: 10.1016/j.bmcl.2017.07.073. Epub 2017 Jul 30. Bioorg Med Chem Lett. 2017. PMID: 28801135 Review.

7

Discovery of PF-00217830: aryl piperazine napthyridinones as D2 partial agonists for schizophrenia and bipolar disorder.

Johnson DS, Choi C, Fay LK, Favor DA, Repine JT, White AD, Akunne HC, Fitzgerald L, Nicholls K, Snyder BJ, Whetzel SZ, Zhang L, Serpa KA. Johnson DS, et al. Among authors: favor da. Bioorg Med Chem Lett. 2011 May 1;21(9):2621-5. doi: 10.1016/j.bmcl.2011.01.059. Epub 2011 Jan 22. Bioorg Med Chem Lett. 2011. PMID: 21353774

8

6-Alkoxyisoindolin-1-one based dopamine D2 partial agonists as potential antipsychotics.

Favor DA, Powers JJ, White AD, Fitzgerald LW, Groppi V, Serpa KA. Favor DA, et al. Bioorg Med Chem Lett. 2010 Oct 1;20(19):5666-9. doi: 10.1016/j.bmcl.2010.08.023. Epub 2010 Aug 8. Bioorg Med Chem Lett. 2010. PMID: 20801650

9

Chemically Diverse Group I p21-Activated Kinase (PAK) Inhibitors Impart Acute Cardiovascular Toxicity with a Narrow Therapeutic Window.

Rudolph J, Murray LJ, Ndubaku CO, O'Brien T, Blackwood E, Wang W, Aliagas I, Gazzard L, Crawford JJ, Drobnick J, Lee W, Zhao X, Hoeflich KP, Favor DA, Dong P, Zhang H, Heise CE, Oh A, Ong CC, La H, Chakravarty P, Chan C, Jakubiak D, Epler J, Ramaswamy S, Vega R, Cain G, Diaz D, Zhong Y. Rudolph J, et al. Among authors: favor da. J Med Chem. 2016 Jun 9;59(11):5520-41. doi: 10.1021/acs.jmedchem.6b00638. Epub 2016 May 24. J Med Chem. 2016. PMID: 27167326

10

Total synthesis of (+)-azaspiracid-1. Part II: synthesis of the EFGHI sulfone and completion of the synthesis.

Evans DA, Dunn TB, Kvaernø L, Beauchemin A, Raymer B, Olhava EJ, Mulder JA, Juhl M, Kagechika K, Favor DA. Evans DA, et al. Among authors: favor da. Angew Chem Int Ed Engl. 2007;46(25):4698-703. doi: 10.1002/anie.200701520. Angew Chem Int Ed Engl. 2007. PMID: 17546578 No abstract available.

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