ScholarWorks@SUNGKYUNKWAN UNIVERSITY: KIM, IN SU

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KIM, IN SU (김인수)

Pharmacy (Pharmacy)

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Rhodium:11||CH functionalization:11||CH activation:10||Amination:9||Chlorosulfonyl isocyanate:8||chlorosulfonyl isocyanate:6||rhodium:6||Indolines:5||apoptosis:4||Azobenzenes:4||Apoptosis:4||amination:4||Nitrogen heterocycles:4||alkylation:4||Autophagy:3||Heterocycles:3||Alkylation:3||indoles:3||autophagy:3||Azaindoles:3||CH Activation:3||indolines:3||Indoles:3||acylation:3||diabetic nephropathy:2||Prostate cancer:2||Inhalation:2||Catalytic:2||Cyclization:2||Reactive oxygen species:2||Nitration:2||Regioselectivity:2||vinylene carbonate:2||Cytotoxicity:2||glycolysis:2||transition metal:2||aminocyclopentitol:2||Olefins:2||Ruthenium:2||Isocyanates:2||Amidation:2||inflammation:2||Dendropanax morbifera:2||Asymmetric:2||HDAC inhibitor:2||Anticancer:2||methylation:2||MHY2256:2||catalytic:2||Dioxazolones:2||Allylation:2||oxidative stress:2||Palladium:2||p53:2||TRAIL:2||phthalazinones:2||Cancer:2||Nbenzyltriflamides:2||Nheterocycles:2||Cellular respiration:1||Chalcogenation:1||Chemotherapy:1||Chitosan hydrogels:1||Chlorosulfonyl isocyan:1||Chromanol:1||Cisplatin:1||Codonopsinine:1||Collagen I:1||Computeraided drug design:1||Conduramine:1||Conjugate addition:1||Copper:1||Cromakalim:1||Crosscoupling:1||Crotylati:1||DPPIV:1||Decanoic acid:1||Deoxyfagomine:1||Diastereoselectivity:1||Diazo compounds:1||Doxorubicin:1||Drugresistance:1||EGFR:1||EPO:1||EX527:1||Enols:1||Enones:1||Esterification:1||Estrogen deficiency:1||Ethyl glyoxalate:1||Exendin4:1||FAP inhibitor:1||Fagomine:1||Fatty acid modification:1||Fibroblast activation protein:1||Fibroblast growth factor 21:1||H functionalization:1||HDAC6 selective inhibitor:1||HIFPHs (PHDs):1||Heterocyclic scaffolds:1||Histamine receptor antagonists:1||Homogeneous catalysis:1||Human serum albumin:1||Hydrogel:1||Imines:1||In situ formation:1||Indatraline:1||Indole:1||Indoline:1||Inhibitor:1||Inhibitors:1||Internal olefins:1||Iridium:1||Ishikawa:1||Ketoesters:1||Lipid metabolism:1||Liver fibrosis:1||Loratadine:1||Lu:1||MDM2:1||MHY4381:1||Manufacturing process:1||Metathesis:1||Metathesis reaction:1||Mitochondrial dynamics:1||Mitophagy:1||Mitsunobu etherification:1||Molineria recurvata:1||MoritaBaylisHillman adducts:1||Multicomponent Reaction:1||NHeterocycles:1||NOxides:1||NSCLC:1||Nanoparticles:1||Natural product:1||Nepenthes alata:1||Neplanocin:1||Nucleoside:1||Olefination:1||OnePot Synthesis:1||Oxindoles:1||P:1||Pgp:1||P53:1||PEGylation:1||PI3K/Akt/mTOR:1||PKA:1||PKM2 inhibitors:1||PLGA nanoparticles:1||PREP:1||Pancreatic cancer:1||Paraformaldehyde:1||Pharmacokinetics:1||Phthalides:1||Phytosphingosine:1||Plumbagin:1||Poly(D,Llacticcoglycolic acid):1||Polyethylene glycol:1||Polyhydroxyindolizidine alkaloids:1||Porous microparticles:1||Potassiumcompetitive acid blocker:1||Pyruvate kinase M2:1||Quinazoline:1||Quinazolinoes:1||Quinazolinones:1||Quinoxaline:1||Redox homeostasis:1||Renoprotective effect:1||Repositioning drug:1||Resistant lung cancer:1||Rutaceae:1||SIRT inhibitor:1||SIRT1/3 dual inhibitor:1||SIRT4:1||SPC180002:1||Selenium:1||Selfassembly:1||Sharpless asymmetric dihydroxylation:1||Stabilizer:1||Structureactivity relationship:1||Sulfonyl azides:1||Synthesis:1||Synthesis design:1||TGFβ1:1||TNFrelated apoptosisinducing ligand:1||Tegoprazan:1||Tenovin1:1||Thioacetamide:1||Total synthesis:1||Transition metal catalysts:1||Transition metals:1||Transitionmetalfree:1||Triple mutation:1||Triterpene saponin:1||Type 2 diabetes:1||Valienamine:1||Weinheim acylation:1||Wittig reaction:1||Wittig reagents:1||Xenograft model:1||Zanthoxylum piperitum:1||aldehydes:1||aldimines:1||alkyl halides:1||allyl surrogates:1||allylation:1||allylic acetal:1||ammation:1||annulation:1||anthranils:1||antiinflammatory:1||antiinfluenza activity:1||benzazepines:1||benzylamines:1||breast cancer:1||cMet inhibitors:1||cMet kinase:1||catalysis:1||cell cycle:1||cell metabolism:1||chitosancoating:1||chlorosulfony isocyanate:1||cinnoline:1||cinnolines:1||cobalt:1||controlled release:1||cyanation:1||cytotoxicity:1||decarboxylative:1||deoxoprosophylline:1||deoxyallonojirimycin:1||deoxymannojirimycin:1||deoxynojirimycin:1||dihydropyridine:1||dihydroxylation:1||dimethylformamide:1||dipolar cycloaddition:1||diradicals:1||divergent synthesis:1||eliglustat:1||endometrial cancer:1||enones:1||ether:1||etherification:1||fatty liver:1||flavonol glycoside:1||glass infiltration:1||hepatic fibrosis:1||heterocycles:1||highfat diet:1||histone deacetylase inhibitor:1||indazolones:1||indenes:1||indenopyrazolopyrazolone:1||inhalation:1||intermolecular olefination:1||intramolecular cyclization:1||liver fibrosis:1||mTOR:1||maleimides:1||mannostatin:1||multilayer:1||neuraminidase inhibitor:1||nitrogen ylides:1||nonshrinkable ceramics:1||oxidative:1||oxindole derivative:1||pa:1||palladium:1||pancreatic cancer:1||passive radiative cooling:1||polyoxamic acid:1||polyoxin:1||prostate cancer:1||pyridine Noxides:1||pyridinium salts:1||radical reaction:1||regioselectivity:1||renal fibrosis:1||ruthenium:1||sodium hydride:1||succinimides:1||sugar:1||sulfur ylides:1||symmetrical and unsymmetrical ethers:1||synthetic methods:1||tButyl nitrite:1||tandem reaction:1||thermal management:1||thioacetamide:1||total synthesis:1||tumor xenograft:1||urinary biomarkers:1||α1CPropyl3,6diepinojirimycin:1||αGlucosidase inhibitor:1||αSMA:1||#8722:1||αsmooth muscle actin:1||(2H)Indazoles:1||oxocarboxylic acids:1||2Arylbenzothiazole:1||2Hydroxymethylpiperidin3ol:1||3Hydroxypipecolic acid:1||3β,6βdihydroxyurs12en27oic acid:1||4hydroxyatomoxetine:1||Acridines:1||Acylcontaining molecules:1||Acylation:1||Adipocyte:1||Adipogenesis:1||Aerangis lactone:1||Afrocyclamin A:1||Albumin:1||Alcohols:1||Aldehydes:1||Alkaloids:1||Alkenes:1||Alkynes:1||Allylic phosphonate:1||Amidomercuration:1||Aminoindanes:1||Annulation:1||Anthranilic acids:1||Anthranils:1||Antiinflammatory:1||Antisepsis:1||Antioxidants:1||Aroylureas:1||Aryl benzoate:1||Astilbe chinensis:1||Asymmetric hydrogenation:1||Atomoxetine:1||Azelastine:1||Azo compounds:1||Benzamides:1||Benzoic acids:1||Biological activities:1||Bisazaindoles:1||C–H activation:1||C–H functionalization:1||C−H functionalization:1||C&:1||CH Functionalization:1||Ch activation:1||C7position:1||C797S:1||CBS reduction:1||CF3Allylated indole:1||CH acti:1||CH activation:1||CYP2D6*10:1||Cancer metabolism:1||Carbasugar:1||Carbonylation:1||Carboxamide:1||CatalystFree:1||

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(03063) 25-2, SUNGKYUNKWAN-RO, JONGNO-GU, SEOUL, KOREAsamsunglib@skku.edu

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