|Improved and alternative synthesis of D-and L-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides|
HR Moon, WJ Choi, HO Kim, LS Jeong
Tetrahedron: Asymmetry 13 (11), 1189-1193, 2002
|Inhibitory effect of mTOR activator MHY1485 on autophagy: suppression of lysosomal fusion|
YJ Choi, YJ Park, JY Park, HO Jeong, DH Kim, YM Ha, JM Kim, YM Song, ...
Public Library of Science 7 (8), e43418, 2012
|Preparative and stereoselective synthesis of the versatile intermediate for carbocyclic nucleosides: effects of the bulky protecting groups to enforce facial selectivity|
WJ Choi, HR Moon, HO Kim, BN Yoo, JA Lee, DH Shin, LS Jeong
The Journal Of Organic Chemistry 69 (7), 2634-2636, 2004
|N6-Substituted D-4‘-Thioadenosine-5‘-methyluronamides: Potent and Selective Agonists at the Human A3 Adenosine Receptor|
LS Jeong, DZ Jin, HO Kim, DH Shin, HR Moon, P Gunaga, MW Chun, ...
Journal of medicinal chemistry 46 (18), 3775-3777, 2003
|Design, Synthesis, and Biological Evaluation of Fluoroneplanocin A as the Novel Mechanism-Based Inhibitor of S-Adenosylhomocysteine Hydrolase|
LS Jeong, SJ Yoo, KM Lee, MJ Koo, WJ Choi, HO Kim, HR Moon, MY Lee, ...
Journal of Medicinal Chemistry 46 (2), 201-203, 2003
|Syntheses of d- and l-Cyclopentenone Derivatives Using Ring-Closing Metathesis: Versatile Intermediates for the Synthesis of d- and l-Carbocyclic Nucleosides|
WJ Choi, JG Park, SJ Yoo, HO Kim, HR Moon, MW Chun, YH Jung, ...
The Journal of Organic Chemistry 66 (19), 6490-6494, 2001
|Colon-targeted delivery of budesonide using dual pH-and time-dependent polymeric nanoparticles for colitis therapy|
M Naeem, M Choi, J Cao, Y Lee, M Ikram, S Yoon, J Lee, HR Moon, ...
Drug design, development and therapy 9, 3789, 2015
|Design and synthesis of 5-(substituted benzylidene) thiazolidine-2, 4-dione derivatives as novel tyrosinase inhibitors|
YM Ha, YJ Park, JA Kim, D Park, JY Park, HJ Lee, JY Lee, HR Moon, ...
European journal of medicinal chemistry 49, 245-252, 2012
|Discovery of a New Nucleoside Template for Human A3 Adenosine Receptor Ligands: d-4‘-Thioadenosine Derivatives without 4‘-Hydroxymethyl Group asá…|
LS Jeong, SA Choe, P Gunaga, HO Kim, HW Lee, SK Lee, DK Tosh, ...
Journal of medicinal chemistry 50 (14), 3159-3162, 2007
|Colon-targeted delivery of cyclosporine A using dual-functional Eudragit« FS30D/PLGA nanoparticles ameliorates murine experimental colitis|
M Naeem, J Bae, MA Oshi, MS Kim, HR Moon, BL Lee, E Im, Y Jung, ...
International journal of nanomedicine 13, 1225, 2018
|Structure−Activity Relationships of 2-Chloro-N6-substituted-4‘-thioadenosine-5‘-uronamides as Highly Potent and Selective Agonists at the Human A3 Adenosineá…|
LS Jeong, HW Lee, KA Jacobson, HO Kim, DH Shin, JA Lee, ZG Gao, ...
Journal of medicinal chemistry 49 (1), 273-281, 2006
|Tyrosinase inhibitors: a patent review (2011-2015)|
S Ullah, S Son, HY Yun, DH Kim, P Chun, HR Moon
Expert Opinion on Therapeutic Patents 26 (3), 347-362, 2016
|Construction of the bicyclo [3.1. 0] hexane template of a conformationally locked carbocyclic adenosine via an olefin keto-carbene cycloaddition|
KJ Shin, HR Moon, C George, VE Marquez
The Journal of Organic Chemistry 65 (7), 2172-2178, 2000
|A highly efficient synthesis of unnatural L-sugars from D-ribose|
M Yun, HR Moon, HO Kim, WJ Choi, YC Kim, CS Park, LS Jeong
Tetrahedron Letters 46 (35), 5903-5905, 2005
|Analogs of 5-(substituted benzylidene) hydantoin as inhibitors of tyrosinase and melanin formation|
YM Ha, JA Kim, YJ Park, D Park, JM Kim, KW Chung, EK Lee, JY Park, ...
Biochimica et Biophysica Acta (BBA)-General Subjects 1810 (6), 612-619, 2011
|Synthesis of Novel d-2‘-Deoxy-2‘- C-difluoromethylene-4‘-thiocytidine as a Potential Antitumor Agent|
MH Lim, HO Kim, HR Moon, MW Chun, LS Jeong
Organic Letters 4 (4), 529-531, 2002
|Design, synthesis and biological evaluation of 2-(substituted phenyl) thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors|
YM Ha, YJ Park, JY Lee, D Park, YJ Choi, EK Lee, JM Kim, JA Kim, ...
Biochimie 94 (2), 533-540, 2012
|Synthesis of cyclopropyl-fused carbocyclic nucleosides via the regioselective opening of cyclic sulfites|
HR Moon, HO Kim, MW Chun, LS Jeong, VE Marquez
The Journal of Organic Chemistry 64 (13), 4733-4741, 1999
|Evaluation of in vitro and in vivo anti-melanogenic activity of a newly synthesized strong tyrosinase inhibitor (E)-3-(2, 4 dihydroxybenzylidene) pyrrolidine-2, 5-dione (3-DBP)|
KW Chung, YJ Park, YJ Choi, MH Park, YM Ha, Y Uehara, JH Yoon, ...
Biochimica et Biophysica Acta (BBA)-General Subjects 1820 (7), 962-969, 2012
|Synthesis of novel azo-resveratrol, azo-oxyresveratrol and their derivatives as potent tyrosinase inhibitors|
YM Song, YM Ha, JA Kim, KW Chung, Y Uehara, KJ Lee, P Chun, Y Byun, ...
Bioorganic & medicinal chemistry letters 22 (24), 7451-7455, 2012