Ju C, Lee YJ, Yoon HS, Kim BH, Kim IH (2022) <br />Efficient Synthesis of Stearidonic Acid Enriched Triacylglycerol from Ahiflower Seed Oil via a Two-Step Enzyme Reaction<br /><i>J Oleo Sci</i> <b>71</b>: 1679<br /><br />Roh S, Lee S, Kim IH, Hee Kim B (2022) <br />Enzymatic structural modification of monogalactosyldiacylglycerols for potential modulation of hydrophile-lipophile balance<br /><i>Food Chem</i> <b>385</b>: 132705<br /><br />Kim NH, Kim H, Choi N, Kim Y, Kim BH, Kim IH (2019) <br />Production of stearidonic acid-rich triacylglycerol via a two-step enzymatic esterification<br /><i>Food Chem</i> <b>270</b>: 332<br /><br />Kim H, Choi N, Kim HR, Lee J, Kim IH (2018) <br />Preparation of High Purity delta5-Olefinic Acids from Pine Nut Oil via Repeated Lipase-Catalyzed Esterification<br /><i>J Oleo Sci</i> <b>67</b>: 1435<br /><br />Ryu J, Choi N, Kim H, Kim BH, Kim HR, Kim IH (2018) <br />Synthesis of Fatty Acid Methyl Esters Using Mixed Enzyme in a Packed Bed Reactor<br /><i>J Oleo Sci</i> <b>67</b>: 321<br /><br />Ha S, Lee M, Seo HO, Song SG, Kim KS, Park CH, Kim IH, Kim YD, Song C (2017) <br />Structural Effect of Thioureas on the Detection of Chemical Warfare Agent Simulants<br /><i>ACS Sens</i> <b>2</b>: 1146<br /><br />Kim H, Choi N, Oh SW, Kim Y, Hee Kim B, Kim IH (2017) <br />Synthesis of alpha-linolenic acid-rich triacylglycerol using a newly prepared immobilized lipase<br /><i>Food Chem</i> <b>237</b>: 654<br /><br />Choi N, Lee JS, Kwak J, Lee J, Kim IH (2016) <br />Production of Biodiesel from Acid Oil via a Two-Step Enzymatic Transesterification<br /><i>J Oleo Sci</i> <b>65</b>: 913<br /><br />Singh SK, Stogsdill JA, Pulimood NS, Dingsdale H, Kim YH, Pilaz LJ, Kim IH, Manhaes AC, Rodrigues WS, Jr., Pamukcu A, Enustun E, Ertuz Z, Scheiffele P, Soderling SH, Silver DL, Ji RR, Medina AE, Eroglu C (2016) <br />Astrocytes Assemble Thalamocortical Synapses by Bridging NRX1alpha and NL1 via Hevin<br /><i>Cell</i> <b>164</b>: 183<br /><br />Baik JY, Kim NH, Oh SW, Kim IH (2015) <br />Preparation of Highly Purified Stearidonic Acid from Echium Oil via an Enzymatic Method Combined with Preparative High Performance Liquid Chromatography<br /><i>J Oleo Sci</i> <b>64</b>: 729<br /><br />Kim IH, Park YK, Nishiwaki H, Hammock BD, Nishi K (2015) <br />Structure-activity relationships of amide-phosphonate derivatives as inhibitors of the human soluble epoxide hydrolase<br /><i>Bioorganic & Medicinal Chemistry</i> <b>23</b>: 7199<br /><br />Liu JY, Tsai HJ, Morisseau C, Lango J, Hwang SH, Watanabe T, Kim IH, Hammock BD (2015) <br />In vitro and in vivo metabolism of N-adamantyl substituted urea-based soluble epoxide hydrolase inhibitors<br /><i>Biochemical Pharmacology</i> <b>98</b>: 718<br /><br />Kim IH, Lee IH, Nishiwaki H, Hammock BD, Nishi K (2014) <br />Structure-activity relationships of substituted oxyoxalamides as inhibitors of the human soluble epoxide hydrolase<br /><i>Bioorganic & Medicinal Chemistry</i> <b>22</b>: 1163<br /><br />Choi JH, Kim BH, Hong SI, Kim CT, Kim CJ, Kim Y, Kim IH (2012) <br />Lipase-catalysed production of triacylglycerols enriched in pinolenic acid at the sn-2 position from pine nut oil<br /><i>J Sci Food Agric</i> <b>92</b>: 870<br /><br />Scherman MS, North EJ, Jones V, Hess TN, Grzegorzewicz AE, Kasagami T, Kim IH, Merzlikin O, Lenaerts AJ, Lee RE, Jackson M, Morisseau C, McNeil MR (2012) <br />Screening a library of 1600 adamantyl ureas for anti-Mycobacterium tuberculosis activity in vitro and for better physical chemical properties for bioavailability<br /><i>Bioorganic & Medicinal Chemistry</i> <b>20</b>: 3255<br /><br />Chae MH, Park HK, Kwon KI, Kim JW, Hong SI, Kim Y, Kim BH, Kim IH (2011) <br />Lipase-catalyzed interesterification in packed bed reactor using 2 different temperatures<br /><i>J Food Sci</i> <b>76</b>: C555<br /><br />Kim IH, Park YK, Hammock BD, Nishi K (2011) <br />Structure-activity relationships of cycloalkylamide derivatives as inhibitors of the soluble epoxide hydrolase<br /><i>Journal of Medicinal Chemistry</i> <b>54</b>: 1752<br /><br />Kim HR, Kim IH, Hou CT, Kwon KI, Shin BS (2010) <br />Production of a novel cold-active lipase from Pichia lynferdii Y-7723<br /><i>Journal of Agricultural and Food Chemistry</i> <b>58</b>: 1322<br /><br />Tsai HJ, Hwang SH, Morisseau C, Yang J, Jones PD, Kasagami T, Kim IH, Hammock BD (2010) <br />Pharmacokinetic screening of soluble epoxide hydrolase inhibitors in dogs<br /><i>Eur J Pharm Sci</i> <b>40</b>: 222<br /><br />Oh JE, Lee KW, Park HK, Kim JY, Kwon KI, Kim JW, Kim HR, Kim IH (2009) <br />Lipase-catalyzed acidolysis of olive oil with capric acid: effect of water activity on incorporation and acyl migration<br /><i>Journal of Agricultural and Food Chemistry</i> <b>57</b>: 9280<br /><br />Fife KL, Liu Y, Schmelzer KR, Tsai HJ, Kim IH, Morisseau C, Hammock BD, Kroetz DL (2008) <br />Inhibition of soluble epoxide hydrolase does not protect against endotoxin-mediated hepatic inflammation<br /><i>Journal of Pharmacology & Experimental Therapeutics</i> <b>327</b>: 707<br /><br />Ulu A, Davis BB, Tsai HJ, Kim IH, Morisseau C, Inceoglu B, Fiehn O, Hammock BD, Weiss RH (2008) <br />Soluble epoxide hydrolase inhibitors reduce the development of atherosclerosis in apolipoprotein e-knockout mouse model<br /><i>J Cardiovasc Pharmacol</i> <b>52</b>: 314<br /><br />Kim IH, Tsai HJ, Nishi K, Kasagami T, Morisseau C, Hammock BD (2007) <br />1,3-disubstituted ureas functionalized with ether groups are potent inhibitors of the soluble epoxide hydrolase with improved pharmacokinetic properties<br /><i>Journal of Medicinal Chemistry</i> <b>50</b>: 5217<br /><br />Kim IH, Nishi K, Tsai HJ, Bradford T, Koda Y, Watanabe T, Morisseau C, Blanchfield J, Toth I, Hammock BD (2007) <br />Design of bioavailable derivatives of 12-(3-adamantan-1-yl-ureido)dodecanoic acid, a potent inhibitor of the soluble epoxide hydrolase<br /><i>Bioorganic & Medicinal Chemistry</i> <b>15</b>: 312<br /><br />Lee GH, Bae JH, Suh MJ, Kim IH, Hou CT, Kim HR (2007) <br />New finding and optimal production of a novel extracellular alkaline lipase from Yarrowia lipolytica NRRL Y-2178<br /><i>J Microbiol Biotechnol</i> <b>17</b>: 1054<br /><br />Nishi K, Huang H, Kamita SG, Kim IH, Morisseau C, Hammock BD (2006) <br />Characterization of pyrethroid hydrolysis by the human liver carboxylesterases hCE-1 and hCE-2<br /><i>Archives of Biochemistry & Biophysics</i> <b>445</b>: 115<br /><br />Olearczyk JJ, Field MB, Kim IH, Morisseau C, Hammock BD, Imig JD (2006) <br />Substituted adamantyl-urea inhibitors of the soluble epoxide hydrolase dilate mesenteric resistance vessels<br /><i>Journal of Pharmacology & Experimental Therapeutics</i> <b>318</b>: 1307<br /><br />Schmelzer KR, Inceoglu B, Kubala L, Kim IH, Jinks SL, Eiserich JP, Hammock BD (2006) <br />Enhancement of antinociception by coadministration of nonsteroidal anti-inflammatory drugs and soluble epoxide hydrolase inhibitors<br /><i>Proc Natl Acad Sci U S A</i> <b>103</b>: 13646<br /><br />Jung O, Brandes RP, Kim IH, Schweda F, Schmidt R, Hammock BD, Busse R, Fleming I (2005) <br />Soluble epoxide hydrolase is a main effector of angiotensin II-induced hypertension<br /><i>Hypertension</i> <b>45</b>: 759<br /><br />Kim IH, Heirtzler FR, Morisseau C, Nishi K, Tsai HJ, Hammock BD (2005) <br />Optimization of amide-based inhibitors of soluble epoxide hydrolase with improved water solubility<br /><i>Journal of Medicinal Chemistry</i> <b>48</b>: 3621<br /><br />Schmelzer KR, Kubala L, Newman JW, Kim IH, Eiserich JP, Hammock BD (2005) <br />Soluble epoxide hydrolase is a therapeutic target for acute inflammation<br /><i>Proc Natl Acad Sci U S A</i> <b>102</b>: 9772<br /><br />Kim IH, Morisseau C, Watanabe T, Hammock BD (2004) <br />Design, synthesis, and biological activity of 1,3-disubstituted ureas as potent inhibitors of the soluble epoxide hydrolase of increased water solubility<br /><i>Journal of Medicinal Chemistry</i> <b>47</b>: 2110<br /><br />Zhao X, Yamamoto T, Newman JW, Kim IH, Watanabe T, Hammock BD, Stewart J, Pollock JS, Pollock DM, Imig JD (2004) <br />Soluble epoxide hydrolase inhibition protects the kidney from hypertension-induced damage<br /><i>J Am Soc Nephrol</i> <b>15</b>: 1244<br /><br />