Burris K - Search Results

1

Novel inhibitors of fatty acid amide hydrolase.

Sit SY, Conway C, Bertekap R, Xie K, Bourin C, Burris K, Deng H. Sit SY, et al. Among authors: burris k. Bioorg Med Chem Lett. 2007 Jun 15;17(12):3287-91. doi: 10.1016/j.bmcl.2007.04.009. Epub 2007 Apr 10. Bioorg Med Chem Lett. 2007. PMID: 17459705

2

Oxime carbamate--discovery of a series of novel FAAH inhibitors.

Sit SY, Conway CM, Xie K, Bertekap R, Bourin C, Burris KD. Sit SY, et al. Among authors: burris kd. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1272-7. doi: 10.1016/j.bmcl.2009.11.080. Epub 2009 Nov 24. Bioorg Med Chem Lett. 2010. PMID: 20036536

3

(+)-Dinapsoline: an efficient synthesis and pharmacological profile of a novel dopamine agonist.

Sit SY, Xie K, Jacutin-Porte S, Taber MT, Gulwadi AG, Korpinen CD, Burris KD, Molski TF, Ryan E, Xu C, Wong H, Zhu J, Krishnananthan S, Gao Q, Verdoorn T, Johnson G. Sit SY, et al. Among authors: burris kd. J Med Chem. 2002 Aug 15;45(17):3660-8. doi: 10.1021/jm0101545. J Med Chem. 2002. PMID: 12166939

4

Synthesis and SAR exploration of dinapsoline analogues.

Sit SY, Xie K, Jacutin-Porte S, Boy KM, Seanz J, Taber MT, Gulwadi AG, Korpinen CD, Burris KD, Molski TF, Ryan E, Xu C, Verdoorn T, Johnson G, Nichols DE, Mailman RB. Sit SY, et al. Among authors: burris kd. Bioorg Med Chem. 2004 Feb 15;12(4):715-34. doi: 10.1016/j.bmc.2003.11.015. Bioorg Med Chem. 2004. PMID: 14759732

5

Interaction of the novel antipsychotic aripiprazole with 5-HT1A and 5-HT 2A receptors: functional receptor-binding and in vivo electrophysiological studies.

Stark AD, Jordan S, Allers KA, Bertekap RL, Chen R, Mistry Kannan T, Molski TF, Yocca FD, Sharp T, Kikuchi T, Burris KD. Stark AD, et al. Psychopharmacology (Berl). 2007 Feb;190(3):373-82. doi: 10.1007/s00213-006-0621-y. Epub 2006 Nov 25. Psychopharmacology (Berl). 2007. PMID: 17242925

6

An orally active corticotropin releasing factor 1 receptor antagonist from 8-aryl-1,3a,7,8-tetraaza-cyclopenta[a]indenes.

Han X, Civiello R, Pin SS, Burris K, Balanda LA, Knipe J, Ren S, Fiedler T, Browman KE, Macci R, Taber MT, Zhang J, Dubowchik GM. Han X, et al. Among authors: burris k. Bioorg Med Chem Lett. 2007 Apr 1;17(7):2026-30. doi: 10.1016/j.bmcl.2007.01.008. Epub 2007 Jan 13. Bioorg Med Chem Lett. 2007. PMID: 17258456

7

Synthesis and structure-activity relationship of imidazo[1,2-a]benzimidazoles as corticotropin-releasing factor 1 receptor antagonists.

Han X, Pin SS, Burris K, Fung LK, Huang S, Taber MT, Zhang J, Dubowchik GM. Han X, et al. Among authors: burris k. Bioorg Med Chem Lett. 2005 Sep 15;15(18):4029-32. doi: 10.1016/j.bmcl.2005.06.028. Bioorg Med Chem Lett. 2005. PMID: 15982881

8

2-arylaminothiazoles as high-affinity corticotropin-releasing factor 1 receptor (CRF1R) antagonists: synthesis, binding studies and behavioral efficacy.

Dubowchik GM, Michne JA, Zuev D, Schwartz W, Scola PM, James CA, Ruediger EH, Pin SS, Burris KD, Balanda LA, Gao Q, Wu D, Fung L, Fiedler T, Browman KE, Taber MT, Zhang J. Dubowchik GM, et al. Bioorg Med Chem Lett. 2003 Nov 17;13(22):3997-4000. doi: 10.1016/j.bmcl.2003.08.055. Bioorg Med Chem Lett. 2003. PMID: 14592493

9

Synthesis, structure-activity relationships, and anxiolytic activity of 7-aryl-6,7-dihydroimidazoimidazole corticotropin-releasing factor 1 receptor antagonists.

Han X, Michne JA, Pin SS, Burris KD, Balanda LA, Fung LK, Fiedler T, Browman KE, Taber MT, Zhang J, Dubowchik GM. Han X, et al. Among authors: burris kd. Bioorg Med Chem Lett. 2005 Sep 1;15(17):3870-3. doi: 10.1016/j.bmcl.2005.05.117. Bioorg Med Chem Lett. 2005. PMID: 15990298

10

Design, synthesis and evaluation of constrained tetrahydroimidazopyrimidine derivatives as antagonists of corticotropin-releasing factor type 1 receptor (CRF1R).

Vrudhula VM, Dasgupta B, Pin SS, Burris KD, Balanda LA, Fung LK, Fiedler T, Browman KE, Taber MT, Zhang J, Macor JE, Dubowchik GM. Vrudhula VM, et al. Among authors: burris kd. Bioorg Med Chem Lett. 2010 Mar 15;20(6):1905-9. doi: 10.1016/j.bmcl.2010.01.127. Epub 2010 Feb 4. Bioorg Med Chem Lett. 2010. PMID: 20185312

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