Report for Seo SY

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References (18)

Title : Mouse Pharmacokinetics and In Vitro Metabolism of SH-11037 and SH-11008, Synthetic Homoisoflavonoids for Retinal Neovascularization - Kim_2022_Pharmaceutics_14_
Author(s) : Kim EY , Lee B , Kwon S , Corson TW , Seo SY , Lee K
Ref : Pharmaceutics , 14 : , 2022
Abstract : Kim_2022_Pharmaceutics_14_
ESTHER : Kim_2022_Pharmaceutics_14_
PubMedSearch : Kim_2022_Pharmaceutics_14_
PubMedID: 36365089

Title : Identification of Novel Natural Product Inhibitors against Matrix Metalloproteinase 9 Using Quantum Mechanical Fragment Molecular Orbital-Based Virtual Screening Methods - Lim_2022_Int.J.Mol.Sci_23_
Author(s) : Lim H , Hong H , Hwang S , Kim SJ , Seo SY , No KT
Ref : Int J Mol Sci , 23 : , 2022
Abstract : Lim_2022_Int.J.Mol.Sci_23_
ESTHER : Lim_2022_Int.J.Mol.Sci_23_
PubMedSearch : Lim_2022_Int.J.Mol.Sci_23_
PubMedID: 35457257

Title : Synthesis and biological evaluation of 1,2,4-triazolidine-3-thiones as potent acetylcholinesterase inhibitors: in vitro and in silico analysis through kinetics, chemoinformatics and computational approaches - Mahajan_2020_Mol.Divers_24_1185
Author(s) : Mahajan PG , Dige NC , Vanjare BD , Raza H , Hassan M , Seo SY , Kim CH , Lee KH
Ref : Mol Divers , 24 :1185 , 2020
Abstract : Mahajan_2020_Mol.Divers_24_1185
ESTHER : Mahajan_2020_Mol.Divers_24_1185
PubMedSearch : Mahajan_2020_Mol.Divers_24_1185
PubMedID: 31396774

Title : Drug-1,3,4-Thiadiazole Conjugates as Novel Mixed-Type Inhibitors of Acetylcholinesterase: Synthesis, Molecular Docking, Pharmacokinetics, and ADMET Evaluation - Ujan_2019_Molecules_24_
Author(s) : Ujan R , Saeed A , Channar PA , Larik FA , Abbas Q , Alajmi MF , El-Seedi HR , Rind MA , Hassan M , Raza H , Seo SY
Ref : Molecules , 24 : , 2019
Abstract : Ujan_2019_Molecules_24_
ESTHER : Ujan_2019_Molecules_24_
PubMedSearch : Ujan_2019_Molecules_24_
PubMedID: 30823444

Title : The exploration of novel Alzheimer's therapeutic agents from the pool of FDA approved medicines using drug repositioning, enzyme inhibition and kinetic mechanism approaches - Hassan_2019_Biomed.Pharmacother_109_2513
Author(s) : Hassan M , Raza H , Abbasi MA , Moustafa AA , Seo SY
Ref : Biomed Pharmacother , 109 :2513 , 2019
Abstract : Hassan_2019_Biomed.Pharmacother_109_2513
ESTHER : Hassan_2019_Biomed.Pharmacother_109_2513
PubMedSearch : Hassan_2019_Biomed.Pharmacother_109_2513
PubMedID: 30551512

Title : Designing of promising medicinal scaffolds for Alzheimer's disease through enzyme inhibition, lead optimization, molecular docking and dynamic simulation approaches - Hassan_2019_Bioorg.Chem_91_103138
Author(s) : Hassan M , Abbasi MA , Aziz Ur R , Siddiqui SZ , Shahzadi S , Raza H , Hussain G , Shah SAA , Ashraf M , Shahid M , Seo SY , Malik A
Ref : Bioorg Chem , 91 :103138 , 2019
Abstract : Hassan_2019_Bioorg.Chem_91_103138
ESTHER : Hassan_2019_Bioorg.Chem_91_103138
PubMedSearch : Hassan_2019_Bioorg.Chem_91_103138
PubMedID: 31446329

Title : 2-Furoic piperazide derivatives as promising drug candidates of type 2 diabetes and Alzheimer's diseases: In vitro and in silico studies - Abbasi_2018_Comput.Biol.Chem_77_72
Author(s) : Abbasi MA , Hassan M , Ur-Rehman A , Siddiqui SZ , Hussain G , Shah SAA , Ashraf M , Shahid M , Seo SY
Ref : Comput Biol Chem , 77 :72 , 2018
Abstract : Abbasi_2018_Comput.Biol.Chem_77_72
ESTHER : Abbasi_2018_Comput.Biol.Chem_77_72
PubMedSearch : Abbasi_2018_Comput.Biol.Chem_77_72
PubMedID: 30245349

Title : One-pot four-component synthesis of thiazolidin-2-imines using Cu(I)\/Zn(II) dual catalysis: A new class of acetylcholinesterase inhibitors - Shehzadi_2018_Bioorg.Chem_84_518
Author(s) : Shehzadi SA , Khan I , Saeed A , Larik FA , Channar PA , Hassan M , Raza H , Abbas Q , Seo SY
Ref : Bioorg Chem , 84 :518 , 2018
Abstract : Shehzadi_2018_Bioorg.Chem_84_518
ESTHER : Shehzadi_2018_Bioorg.Chem_84_518
PubMedSearch : Shehzadi_2018_Bioorg.Chem_84_518
PubMedID: 30610971

Title : Chemical Proteomics Reveals Soluble Epoxide Hydrolase as a Therapeutic Target for Ocular Neovascularization - Sulaiman_2018_ACS.Chem.Biol_13_45
Author(s) : Sulaiman RS , Park B , Sheik Pran Babu SP , Si Y , Kharwadkar R , Mitter SK , Lee B , Sun W , Qi X , Boulton ME , Meroueh SO , Fei X , Seo SY , Corson TW
Ref : ACS Chemical Biology , 13 :45 , 2018
Abstract : Sulaiman_2018_ACS.Chem.Biol_13_45
ESTHER : Sulaiman_2018_ACS.Chem.Biol_13_45
PubMedSearch : Sulaiman_2018_ACS.Chem.Biol_13_45
PubMedID: 29193961

Title : Synthesis, enzyme inhibitory kinetics mechanism and computational study of N-(4-methoxyphenethyl)-N-(substituted)-4-methylbenzenesulfonamides as novel therapeutic agents for Alzheimer's disease - Abbasi_2018_PeerJ_6_e4962
Author(s) : Abbasi MA , Hassan M , Aziz Ur R , Siddiqui SZ , Shah SAA , Raza H , Seo SY
Ref : PeerJ , 6 :e4962 , 2018
Abstract : Abbasi_2018_PeerJ_6_e4962
ESTHER : Abbasi_2018_PeerJ_6_e4962
PubMedSearch : Abbasi_2018_PeerJ_6_e4962
PubMedID: 29967717

Title : Facile Synthesis, Crystal Structure, DFT Calculation and Biological Activities of 4-(2-fluorophenyl)-3-(3-methoxybenzyl)-1H-1,2,4-triazol-5 (4H)-one (5) - Saleem_2018_Med.Chem_14_451
Author(s) : Saleem M , Rafiq M , Jeong YK , Cho DW , Kim CH , Seo SY , Choi CS , Hong SK , Lee KH
Ref : Med Chem , 14 :451 , 2018
Abstract : Saleem_2018_Med.Chem_14_451
ESTHER : Saleem_2018_Med.Chem_14_451
PubMedSearch : Saleem_2018_Med.Chem_14_451
PubMedID: 29332593

Title : Exploration of synthetic multifunctional amides as new therapeutic agents for Alzheimer's disease through enzyme inhibition, chemoinformatic properties, molecular docking and dynamic simulation insights - Hassan_2018_J.Theor.Biol_458_169
Author(s) : Hassan M , Abbasi MA , Aziz Ur R , Siddiqui SZ , Hussain G , Shah SAA , Shahid M , Seo SY
Ref : Journal of Theoretical Biology , 458 :169 , 2018
Abstract : Hassan_2018_J.Theor.Biol_458_169
ESTHER : Hassan_2018_J.Theor.Biol_458_169
PubMedSearch : Hassan_2018_J.Theor.Biol_458_169
PubMedID: 30243565

Title : Kinetics and Molecular Docking Studies of 6-Formyl Umbelliferone Isolated from Angelica decursiva as an Inhibitor of Cholinesterase and BACE1 - Ali_2017_Molecules_22_
Author(s) : Ali MY , Seong SH , Reddy MR , Seo SY , Choi JS , Jung HA
Ref : Molecules , 22 : , 2017
Abstract : Ali_2017_Molecules_22_
ESTHER : Ali_2017_Molecules_22_
PubMedSearch : Ali_2017_Molecules_22_
PubMedID: 28946641

Title : Acetylcholinesterase immobilization and characterization, and comparison of the activity of the porous silicon-immobilized enzyme with its free counterpart - Saleem_2016_Biosci.Rep_36_
Author(s) : Saleem M , Rafiq M , Seo SY , Lee KH
Ref : Bioscience Reports , 36 : , 2016
Abstract : Saleem_2016_Biosci.Rep_36_
ESTHER : Saleem_2016_Biosci.Rep_36_
PubMedSearch : Saleem_2016_Biosci.Rep_36_
PubMedID: 26839417

Title : ACETYLCHOLINESTERASE INHIBITION ACTIVITY OF SOME QUINOLINYL SUBSTITUTED TRIAZOLOTHIADIAZOLE DERIVATIVES - Rafiq_2015_Bioorg.Khim_41_195
Author(s) : Rafiq M , Abbas Q , Saleem M , Hanif M , Lee KH , Seo SY
Ref : Bioorganicheskaia Khimiia , 41 :195 , 2015
Abstract : Rafiq_2015_Bioorg.Khim_41_195
ESTHER : Rafiq_2015_Bioorg.Khim_41_195
PubMedSearch : Rafiq_2015_Bioorg.Khim_41_195
PubMedID: 26165126

Title : Antidiabetic and antiacetylcholinesterase effects of ethyl acetate fraction of Chaenomeles sinensis (Thouin) Koehne fruits in streptozotocin-induced diabetic rats - Sancheti_2013_Exp.Toxicol.Pathol_65_55
Author(s) : Sancheti S , Seo SY
Ref : Exp Toxicol Pathol , 65 :55 , 2013
Abstract : Sancheti_2013_Exp.Toxicol.Pathol_65_55
ESTHER : Sancheti_2013_Exp.Toxicol.Pathol_65_55
PubMedSearch : Sancheti_2013_Exp.Toxicol.Pathol_65_55
PubMedID: 21764274

Title : Evaluation of antiglycosidase and anticholinesterase activities of Boehmeria nivea - Sancheti_2010_Pak.J.Pharm.Sci_23_236
Author(s) : Sancheti S , Seo SY
Ref : Pak J Pharm Sci , 23 :236 , 2010
Abstract : Sancheti_2010_Pak.J.Pharm.Sci_23_236
ESTHER : Sancheti_2010_Pak.J.Pharm.Sci_23_236
PubMedSearch : Sancheti_2010_Pak.J.Pharm.Sci_23_236
PubMedID: 20363706

Title : Mechanism for increased bioavailability of tacrine in fasted rats - Sung_2006_J.Pharm.Pharmacol_58_643
Author(s) : Sung JH , Hong SS , Ahn SH , Li H , Seo SY , Park CH , Park BS , Chung SJ
Ref : J Pharm Pharmacol , 58 :643 , 2006
Abstract : Sung_2006_J.Pharm.Pharmacol_58_643
ESTHER : Sung_2006_J.Pharm.Pharmacol_58_643
PubMedSearch : Sung_2006_J.Pharm.Pharmacol_58_643
PubMedID: 16640833