Wheelock CE - Search Results

1

Comparison of benzil and trifluoromethyl ketone (TFK)-mediated carboxylesterase inhibition using classical and 3D-quantitative structure-activity relationship analysis.

Harada T, Nakagawa Y, Wadkins RM, Potter PM, Wheelock CE. Harada T, et al. Among authors: wheelock ce. Bioorg Med Chem. 2009 Jan 1;17(1):149-64. doi: 10.1016/j.bmc.2008.11.008. Epub 2008 Nov 9. Bioorg Med Chem. 2009. PMID: 19062296 Free PMC article.

2

3-D QSAR analysis of inhibition of murine soluble epoxide hydrolase (MsEH) by benzoylureas, arylureas, and their analogues.

Nakagawa Y, Wheelock CE, Morisseau C, Goodrow MH, Hammock BG, Hammock BD. Nakagawa Y, et al. Among authors: wheelock ce. Bioorg Med Chem. 2000 Nov;8(11):2663-73. doi: 10.1016/s0968-0896(00)00198-x. Bioorg Med Chem. 2000. PMID: 11092551

3

Use of ab initio calculations to predict the biological potency of carboxylesterase inhibitors.

Wheelock CE, Colvin ME, Uemura I, Olmstead MM, Sanborn JR, Nakagawa Y, Jones AD, Hammock BD. Wheelock CE, et al. J Med Chem. 2002 Dec 5;45(25):5576-93. doi: 10.1021/jm020072w. J Med Chem. 2002. PMID: 12459025

4

Use of classical and 3-D QSAR to examine the hydration state of juvenile hormone esterase inhibitors.

Wheelock CE, Nakagawa Y, Akamatsu M, Hammock BD. Wheelock CE, et al. Bioorg Med Chem. 2003 Nov 17;11(23):5101-16. doi: 10.1016/j.bmc.2003.08.023. Bioorg Med Chem. 2003. PMID: 14604674

5

High-throughput screening of ecdysone agonists using a reporter gene assay followed by 3-D QSAR analysis of the molting hormonal activity.

Wheelock CE, Nakagawa Y, Harada T, Oikawa N, Akamatsu M, Smagghe G, Stefanou D, Iatrou K, Swevers L. Wheelock CE, et al. Bioorg Med Chem. 2006 Feb 15;14(4):1143-59. doi: 10.1016/j.bmc.2005.09.034. Epub 2005 Oct 24. Bioorg Med Chem. 2006. PMID: 16249087

6

Analysis of mammalian carboxylesterase inhibition by trifluoromethylketone-containing compounds.

Wadkins RM, Hyatt JL, Edwards CC, Tsurkan L, Redinbo MR, Wheelock CE, Jones PD, Hammock BD, Potter PM. Wadkins RM, et al. Among authors: wheelock ce. Mol Pharmacol. 2007 Mar;71(3):713-23. doi: 10.1124/mol.105.021683. Epub 2006 Dec 13. Mol Pharmacol. 2007. PMID: 17167034

7

Influence of sulfur oxidation state and steric bulk upon trifluoromethyl ketone (TFK) binding kinetics to carboxylesterases and fatty acid amide hydrolase (FAAH).

Wheelock CE, Nishi K, Ying A, Jones PD, Colvin ME, Olmstead MM, Hammock BD. Wheelock CE, et al. Bioorg Med Chem. 2008 Feb 15;16(4):2114-30. doi: 10.1016/j.bmc.2007.10.081. Epub 2007 Nov 26. Bioorg Med Chem. 2008. PMID: 18023188 Free PMC article.

8

Identification of endocrine disruptor biodegradation by integration of structure-activity relationship with pathway analysis.

Kadowaki T, Wheelock CE, Adachi T, Kudo T, Okamoto S, Tanaka N, Tonomura K, Tsujimoto G, Mamitsuka H, Goto S, Kanehisa M. Kadowaki T, et al. Among authors: wheelock ce. Environ Sci Technol. 2007 Dec 1;41(23):7997-8003. doi: 10.1021/es062751s. Environ Sci Technol. 2007. PMID: 18186328

9

Synthesis of new carboxylesterase inhibitors and evaluation of potency and water solubility.

Wheelock CE, Severson TF, Hammock BD. Wheelock CE, et al. Chem Res Toxicol. 2001 Dec;14(12):1563-72. doi: 10.1021/tx015508+. Chem Res Toxicol. 2001. PMID: 11743738

10

Identification, expression, and purification of a pyrethroid-hydrolyzing carboxylesterase from mouse liver microsomes.

Stok JE, Huang H, Jones PD, Wheelock CE, Morisseau C, Hammock BD. Stok JE, et al. Among authors: wheelock ce. J Biol Chem. 2004 Jul 9;279(28):29863-9. doi: 10.1074/jbc.M403673200. Epub 2004 Apr 30. J Biol Chem. 2004. PMID: 15123619 Free article.

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