800 results on '"Moon, Hyung Ryong"'
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152. Benzylidene-linked thiohydantoin derivatives as inhibitors of tyrosinase and melanogenesis: importance of the β-phenyl-α,β-unsaturated carbonyl functionality
153. A novel oxiranylchromenone derivative, MHY336, induces apoptosis and cell cycle arrest via a p53- and p21-dependent pathway in HCT116 human colon cancer cells
154. Potent Anti-Diabetic Effects of MHY908, a Newly Synthesized PPAR α/γ Dual Agonist in db/db Mice
155. Corrigendum to “De novo tyrosinase inhibitor: 4-(6,7-Dihydro-5H-indeno[5,6-d]thiazol-2-yl)benzene-1,3-diol (MHY1556)” [Bioorg. Med. Chem. Lett. 23 (2013) 4172–4176]
156. A novel hydroxamic acid derivative, MHY218, induces apoptosis and cell cycle arrest through downregulation of NF-κB in HCT116 human colon cancer cells
157. A novel anthracene derivative, MHY412, induces apoptosis in doxorubicin-resistant MCF-7/Adr human breast cancer cells through cell cycle arrest and downregulation of P-glycoprotein expression
158. The Novel PPAR α/γ Dual Agonist MHY 966 Modulates UVB–Induced Skin Inflammation by Inhibiting NF-κB Activity
159. Characterization of a small molecule inhibitor of melanogenesis that inhibits tyrosinase activity and scavenges nitric oxide (NO)
160. A novel histone deacetylase (HDAC) inhibitor MHY219 induces apoptosis via up-regulation of androgen receptor expression in human prostate cancer cells
161. Synthesis of Novel N-(2-Hydroxyphenyl)arylsulfonamides as Selective HDAC Inhibitory and Cytotoxic Agents
162. Development of Akt-activated GSK3β inhibitory peptide
163. Correction: Inhibitory Effect of mTOR Activator MHY1485 on Autophagy: Suppression of Lysosomal Fusion
164. A Novel Synthesized Tyrosinase Inhibitor: (E)-2-((2,4-Dihydroxyphenyl)diazenyl)phenyl 4-Methylbenzenesulfonate as an Azo-Resveratrol Analog
165. Molecular Docking Studies of (1E,3E,5E)-1,6-Bis(substituted phenyl)hexa-1,3,5-triene and 1,4-Bis(substituted trans-styryl)benzene Analogs as Novel Tyrosinase Inhibitors
166. Suppression of melanogenesis by a newly synthesized compound, MHY966 via the nitric oxide/protein kinase G signaling pathway in murine skin
167. Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X 7 receptor
168. Preparative Synthesis of the Key Intermediate, (4R,5R)-3-Benzyloxymethyl-4,5-isopropylidenedioxycyclopent-2-enone for Carbocyclic Nucleosides
169. Inhibitory Effect of mTOR Activator MHY1485 on Autophagy: Suppression of Lysosomal Fusion
170. Pulmonary administered palmitic-acid modified exendin-4 peptide prolongs hypoglycemia in type 2 diabetic db/db mice
171. 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)
172. Characterization of a novel tyrosinase inhibitor, (2RS,4R)-2-(2,4-dihydroxyphenyl)thiazolidine-4-carboxylic acid (MHY384)
173. ChemInform Abstract: Design, Synthesis and Anticancer Activity of Novel Dihydrobenzofuro[4,5-b][1,8]naphthyridin-6-one Derivatives.
174. Design, synthesis and biological evaluation of 2-(substituted phenyl)thiazolidine-4-carboxylic acid derivatives as novel tyrosinase inhibitors
175. Novel dihydrobenzofuro[4,5-b][1,8]naphthyridin-6-one derivative, MHY-449, induces apoptosis and cell cycle arrest in HCT116 human colon cancer cells
176. Crystallization and preliminary X-ray crystallographic analysis of the β-N-acetylglucosaminidase CbsA fromThermotoga neapolitana
177. A new synthetic HDAC inhibitor, MHY218, induces apoptosis or autophagy-related cell death in tamoxifen-resistant MCF-7 breast cancer cells
178. ChemInform Abstract: Synthesis and Importance of Bulky Aromatic Cap of Novel SAHA Analogues for HDAC Inhibition and Anticancer Activity.
179. Synthesis and Importance of Bulky Aromatic Cap of Novel SAHA Analogs for HDAC Inhibition and Anticancer Activity
180. Analogs of 5-(substituted benzylidene)hydantoin as inhibitors of tyrosinase and melanin formation
181. Crystallization and preliminary X-ray crystallographic analysis ofSalmonellaTyphimurium CueP
182. Synthesis and biological activity of hydroxy substituted phenyl-benzo[d]thiazole analogues for antityrosinase activity in B16 cells
183. Synthesis and biological activity of hydroxybenzylidenyl pyrrolidine-2,5-dione derivatives as new potent inhibitors of tyrosinase
184. Using conformationally locked nucleosides to calibrate the anomeric effect: implications for glycosyl bond stability
185. ChemInform Abstract: Synthesis and Antiviral Activity of L-2′-Deoxy-2′-up-fluoro-4′-thionucleosides
186. ChemInform Abstract: Synthesis of Cyclopropyl-Fused Carbocyclic Nucleosides via the Regioselective Opening of Cyclic Sulfites.
187. ChemInform Abstract: Synthesis and Biological Evaluation of Novel Thioapio Dideoxynucleosides.
188. ChemInform Abstract: Synthesis and Biological Evaluation of Novel D-2′-Azido-2′,3′-dideoxyarabinofuranosyl-4′-thiopyrimidines and Purines.
189. ChemInform Abstract: Highly Concise Synthesis of 3′-“Up”-ethynyl-5′-methylbicyclo[3.1.0]hexyl Purine and Pyrimidine Nucleoside Derivatives Using Rhodium(II) Carbenoid Cycloaddition and Highly Diastereoselective Grignard Reaction.
190. ChemInform Abstract: Synthesis of Neplanocin A Analogue with 2′-“up”-C-Methyl Substituent as Potential anti-HCV Agent.
191. First synthesis of 2′-oxabicyclo[3.1.0]hexyl nucleosides with a north conformation
192. Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase
193. ChemInform Abstract: Design, Synthesis, Antitumor Activity and Mode of Action of Novel Oxiranyl and Thiiranyl Phenol Derivatives.
194. Highly Concise Synthesis of 3'-"Up"-ethynyl-5'-methylbicyclo- [3.1.0]hexyl Purine and Pyrimidine Nucleoside Derivatives Using Rhodium(II) Carbenoid Cycloaddition and Highly Diastereoselective Grignard Reaction
195. Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists
196. ChemInform Abstract: Synthesis of Methyl-Substituted Bicyclic Carbanucleoside Analogues as Potential Antiherpetic Agents.
197. Corrigendum to “Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X7 receptor” [Bioorg. Med. Chem. Lett. 18 (2008) 571–575]
198. Structure−Activity Relationships of Truncatedd- andl-4′-Thioadenosine Derivatives as Species-Independent A3Adenosine Receptor Antagonists(1)
199. ChemInform Abstract: Asymmetric Synthesis and Biological Activity of L-Bicyclocarba-d4T
200. ChemInform Abstract: Synthesis and anti-HCV Activity of 2′-β-Hydroxymethylated Nucleosides
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