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Research

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POSTECH

Education

  • 2000.03 ~ 2004.02 POSTECH (박사-화학)
  • 1991.03 ~ 1993.02 한양대학교 (석사-화학)
  • 1987.03 ~ 1991.02 한양대학교 (학사-화학)

Career

  • 2008.10 ~ 2012.01 INDIANA UNIVERSITY
  • 2005.01 ~ 2008.10 UT-SOUTHWESTERN MEDICAL CENTER
  • 1993.01 ~ 2005.01 중외제약 C&C연구소

Journal Papers

International
  • Synthesis and Structural Characterization of Macrocyclic αABpeptoids and Their DNAEncoded Library, Organic Letters, , 26, 1100-1104 (2024 )
  • Aptamer and NDegron Ensemble AptaGron as a Target Protein Degradation Strategy, ACS chemical biology, , 19, 2462-2468 (2024 )
  • Evaluation of the cell permeability of bicyclic peptoids and bicyclic peptidepeptoid hybrids, Bioorganic Chemistry, , 127, - (2022 )
  • Cationic amphipathic small molecules based on a triazinepiperazinetriazine scaffold as a new class of antimicrobial agents, European Journal of Medicinal Chemistry, , 243, - (2022 )
  • Synthesis of a DNAEncoded Library of Pyrrolo23dpyrimidines, Bulletin of the Korean Chemical Society, , 42, 691-698 (2021 )
  • Hydrophobic TaggingMediated Degradation of Transcription Coactivator SRC1, INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, , 22, - (2021 )
  • Onebeadonecompound screening approach to the identification of cyclic peptoid inhibitors of cyclophilin D as neuroprotective agents from mitochondrial dysfunction, CHEMICAL COMMUNICATIONS, , 57, 2388-2391 (2021 )
  • Design and synthesis of a DNAencoded combinatorial library of bicyclic peptoids, BIOORGANIC amp MEDICINAL CHEMISTRY, , 48, - (2021 )
  • Cellpenetrating amphipathic cyclic peptoids as molecular transporters for cargo delivery, Chemical Communications, , 57, 6800-6803 (2021 )
  • Targeted Degradation of Transcription Coactivator SRC1 through the NDegron Pathway, ANGEWANDTE CHEMIEINTERNATIONAL EDITION, , 59, 17548-17555 (2020 )
  • SolidPhase Synthesis and Circular Dichroism Study of ABpeptoids, MOLECULES, , 24, - (2019 )
  • A solidphase method for synthesis of dimeric and trimeric ligands Identification of potent bivalent ligands of 1433 sigma, BIOORGANIC CHEMISTRY, , 91, - (2019 )
  • Oligomers of alphaABpeptoidbeta3peptide hybrid, BIOPOLYMERS, , 110, - (2019 )
  • DNAEncoded Combinatorial Library of Macrocyclic Peptoids, BIOCONJUGATE CHEMISTRY, , 30, 2931-2938 (2019 )
  • Bridged alphahelix mimetic small molecules, CHEMICAL COMMUNICATIONS, , 55, 13311-13314 (2019 )
  • Comparison of Cell Permeability of Cyclic Peptoids and Linear Peptoids, ACS COMBINATORIAL SCIENCE, , 20, 237-242 (2018 )
  • Submonomer Strategy toward Divergent SolidPhase Synthesis of alphaABpeptoids, ORGANIC LETTERS, , 20, 2526-2529 (2018 )
  • Colorectal Cancer Diagnosis Using EnzymeSensitive Ratiometric Fluorescence Dye and Antibody–Quantum Dot Conjugates for Multiplexed Detection, ADVANCED FUNCTIONAL MATERIALS, , 28, 1703450- (2018 )
  • A Forkhead Box ProteinC2 Inhibitor Targeting EpithelialMesenchymal Transition and Cancer Metastasis, ChemBioChem, , 19, 1359-1364 (2018 )
  • Design developments and preliminary circular dichroism spectroscopic investigations of alphabetaABpeptoids A class of betapeptoids with backbone chirality, ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, , 256, - (2018 )
  • Comparison of the Cell Permeability of Linear and Cyclic Peptoids, Journal of Peptide Science, , 24, S119-S119 (2018 )
  • Development of the Stapled Peptide Targeting the NCOA1STAT6 ProteinProtein Interaction, Journal of Peptide Science, , 24, S158-S158 (2018 )
  • Evaluation of Cell Permeability of Bicyclic Peptoids, Journal of Peptide Science, , 24, S119-S119 (2018 )
  • Triazinebridged cyclic peptoids as molecular transporters Applications in drug delivery, ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, , 256, - (2018 )
  • Intracellular and transdermal protein delivery mediated by noncovalent interactions with a synthetic guanidinerich molecular carrier, International Journal of Pharmaceutics, , 528, 646-654 (2017 )
  • Targeted Inhibition of the NCOA1STAT6 ProteinProtein Interaction, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, , 139, 16056-16059 (2017 )
  • Screening methods for identifying pharmacological chaperones, Molecular BioSystems, , 13, 638-647 (2017 )
  • A chemical inhibitor of the Skp2p300 interaction that promotes p53mediated apoptosis, ANGEWANDTE CHEMIEINTERNATIONAL EDITION, , 55, 602-606 (2016 )
  • Converting OneFace αHelix Mimetics into Amphiphilic αHelix Mimetics as Potent Inhibitors of ProteinProtein Interactions, ACS Combinatorial Science, , 18, 36-42 (2016 )
  • Oligomers of NSubstituted β2Homoalanines Peptoids with Backbone Chirality, Organic Letters, , 18, 3878-3681 (2016 )
  • Skp2 Inhibitors Novel Anticancer Strategies, Current Medicinal Chemistry, , 23, 2363-2379 (2016 )
  • Chemical inhibitor of the Skp2p300 interaction that promotes p53mediated apoptosis, ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, , 251, - (2016 )
  • Synthesis and screening of smallmolecule alphahelix mimetic libraries targeting proteinprotein interactions, CURRENT OPINION IN CHEMICAL BIOLOGY, , 24, 38-47 (2015 )
  • Design SolidPhase Synthesis and Evaluation of a PhenylPiperazineTriazine Scaffold as alphaHelix Mimetics, ACS COMBINATORIAL SCIENCE, , 16, 695-701 (2014 )
  • Facile Method To Sequence Cyclic PeptidesPeptoids via OnePot RingOpeningCleavage Reaction, ORGANIC LETTERS, , 16, 5710-5713 (2014 )
  • Potential pharmacological chaperones targeting cancerassociated MCL1 and Parkinson diseaseassociated alphasynuclein, PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, , 111, 11007-11012 (2014 )
  • Solidphase synthesis of tetrasubstituted pyrrolo23dpyrimidines, ORGANIC BIOMOLECULAR CHEMISTRY, , 10, 4229-4235 (2012 )
  • Design and Facile SolidPhase Synthesis of Conformationally Constrained Bicyclic Peptoids, ORGANIC LETTERS, , 13, 5012-5015 (2011 )
  • Novel PyrrolopyrimidineBased alphaHelix Mimetics CellPermeable Inhibitors of ProteinProtein Interactions, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, , 133, 676-679 (2011 )
  • A simple strategy for the construction of combinatorial cyclic peptoid libraries, CHEMICAL COMMUNICATIONS, , 46, 8615-8617 (2010 )
  • Potent and selective photoinactivation of proteins with peptoidruthenium conjugates, NATURE CHEMICAL BIOLOGY, , 6, 258-260 (2010 )
  • Nonproteolytic Regulation of p53mediated Transcription through Destabilization of the ActivatorPromoter Complex by the Proteasomal ATPases, JOURNAL OF BIOLOGICAL CHEMISTRY, , 284, 34522-34530 (2009 )
  • Rapid identification of the pharmacophore in a peptoid inhibitor of the proteasome regulatory particle, CHEMICAL COMMUNICATIONS, , , 1064-1066 (2008 )
  • Periodatetriggered crosslinking reveals Sug2Rpt4 as the molecular target of a peptoid inhibitor of the 19S proteasome regulatory particle, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, , 129, 12936- (2007 )
  • Identification of a peptoid inhibitor of the proteasome 19S regulatory particle, JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, , 129, 7750- (2007 )
  • Design and synthesis of a cellpermeable synthetic transcription factor mimic, JOURNAL OF COMBINATORIAL CHEMISTRY, , 9, 592-600 (2007 )
  • A cellpermeable synthetic transcription factor mimic, ANGEWANDTE CHEMIEINTERNATIONAL EDITION, , 46, 2865-2868 (2007 )

IP

  • 임현석,박준형,김정연,서창덕, 비천연 올리고뉴클레오타이드-암호화 라이브러리 및 이의 스크리닝 방법, -, PCT/KR2024/0085 (P202)
  • 임현석,이영주, 신규한 프로탁 키메라 화합물, 이를 포함하는 표적 단백질 분해를 통한 질환의 예방, 개선 또는 치료용 약학적 조성물, USA, 18/148,653 (P202)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, USA, 15/326,422 (P201)
  • 임현석,왕희명, 유비퀴틴 리가아제의 리간드 화합물 및 이를 포함하는 PROTAC 분자, 한국, 10-2024-0055604 (IP24)
  • 임현석,왕희명, 유비퀴틴 리가아제의 리간드 화합물 및 이를 포함하는 PROTAC 분자, 한국, 10-2024-0055455 (IP24)
  • 임현석,박준형,김현수, 트리아진-피페라진-트리아진 골격을 기반으로 한 저분자 화합물 및 이를 포함하는 항균 또는 항염용 조성물, 한국, 10-2023-0110628 (2023)
  • 임현석,박준형,김정연,서창덕, 비천연 올리고뉴클레오타이드-암호화 라이브러리 및 이의 스크리닝 방법, 한국, 10-2024-0080515 (2023)
  • 임현석,박준형,김정연,서창덕, 비천연 올리고뉴클레오타이드-암호화 라이브러리 및 이의 스크리닝 방법, 한국, 10-2023-0079211 (2023)
  • 임현석,이영주, 신규한 프로탁 키메라 화합물, 이를 포함하는 표적 단백질 분해를 통한 질환의 예방, 개선 또는 치료용 약학적 조성물, USA, 18/148,653 (2022)
  • 임현석,박준형,김현수, 새로운 종류의 항균제로서 트리아진-피페라진-트리아진 골격을 기반으로 한 양이온성 및 양친매성 저분자 화합물 및 이의 용도, 한국, 10-2022-0107018 (2022)
  • 임현석,이영주, 신규한 프로탁 키메라 화합물, 이를 포함하는 표적 단백질 분해를 통한 질환의 예방, 개선 또는 치료용 약학적 조성물, -, PCT/KR2021/0084 (2021)
  • 임현석,김현수,신민현,이영주, 세포-투과 및 양친매성의 신규 고리형 펩토이드 및 이의 용도, 한국, 10-2022-0068170 (2021)
  • 임현석,이영주, 신규한 프로탁 키메라 화합물, 이를 포함하는 표적 단백질 분해를 통한 질환의 예방, 개선 또는 치료용 약학적 조성물, 한국, 10-2020-0081373 (2020)
  • 임현석,이영주, 신규한 프로탁 키메라 화합물, 이를 포함하는 표적 단백질 분해를 통한 질환의 예방, 개선 또는 치료용 약학적 조성물, 한국, 10-2020-0081373 (2020)
  • 임현석,이강주, 나노구조체, 나노구조체를 포함하는 바이오센서, 및 스크리닝 방법, USA, 16/803,731 (2020)
  • 임현석,이강주, 나노구조체, 나노구조체를 포함하는 바이오센서, 및 스크리닝 방법, USA, 16/803,731 (2020)
  • 임현석,이강주, 나노구조체, 나노구조체를 포함하는 바이오센서, 및 스크리닝 방법, 한국, 10-2020-0023925 (2020)
  • 임현석,이강주, 나노구조체, 나노구조체를 포함하는 바이오센서, 및 스크리닝 방법, 한국, 10-2020-0023925 (2020)
  • 임현석,이영주, NCOA1/STAT6 단백질-단백질 상호작용을 저해하는 신규 스테이플 펩타이드 및 이의 용도, 한국, 10-2017-0139637 (2017)
  • 임현석,이영주, NCOA1/STAT6 단백질-단백질 상호작용을 저해하는 신규 스테이플 펩타이드 및 이의 용도, 한국, 10-2017-0139637 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 중국, 201480081313.2 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 중국, 201480081313.2 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 일본, 2017-502630 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 일본, 2017-502630 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, USA, 15/326,422 (2017)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, USA, 15/326,422 (2017)
  • 임현석, 신규한 항암제로서 Skp2 저해제, 한국, 10-2015-0156519 (2015)
  • 임현석, 신규한 항암제로서 Skp2 저해제, 한국, 10-2015-0156519 (2015)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, -, PCT/KR2014/0127 (2014)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 한국, 10-2014-0088669 (2012)
  • 임현석,오미숙, 트리아진-피페라진 골격을 갖는 알파-헬릭스 유사체 및 이의 제조방법, 한국, 10-2014-0088669 (2012)
  • 정성기,임현석, 신규한 스핑고신-1-포스페이트의 유도체 및 이의 제조방법, 한국, 10-2002-0042857 (1992)
  • 정성기,박규환,임현석, β-D-만노피라노시드의 입체선택적 제조방법, 한국, 10-2000-0086281 (1992)

Invited Talk or Presentations

  • Design Synthesis and Circular Dichrosism Studies of a New Class of Heterogeneous Foldamers β3PeptideαABpeptoid Hybrid Oligomers , , 0, 0, - (2018)
  • Targeted Protein Degradation Using NEnd Rule Pathway , , 0, 0, - (2018)
  • Identification of potential mETV5 modulator via a DNAencoded Cyclic PeptidePeptoid Hybrid Library , , 0, 0, - (2018)
  • Development of the Inhibitor Targeting NCOA1STAT6 Interaction Based on the StructureActivity Relationship SAR study , , 0, 0, - (2018)
  • Identification of Cyclic Peptoid Inhibitors of Skp2 Using a Vast DNAEncoded OneBead OneCompound Library , , 0, 0, - (2018)
  • Comparison of Cell Permeability of Bicyclic Peptoids and Linear Peptoids , , 0, 0, - (2018)
  • Synthesis of a Vast DNAEncoded Cyclic Peptoid Library to Identification of Skp2 Inhibitors , , 0, 0, - (2018)
  • Conformational Study of Cyclic αABpeptoids , , 0, 0, - (2018)
  • Development of Novel Proteolysis Targeting Chimeras Using NEnd Rule Pathway , , 0, 0, - (2018)
  • Evaluation of Cell Permeability of Bicyclic Peptoids , , 0, 0, - (2018)
  • Comparison of the Cell Permeability of Linear and Cyclic Peptoids , , 0, 0, - (2018)
  • Development of the Stapled Peptide Targeting the NCOA1STAT6 ProteinProtein Interaction , , 0, 0, - (2018)
  • Triazinebridged cyclic peptoids as molecular transporters Applications in drug delivery , , 0, 0, - (2018)
  • Targeted Inhibition of the NCOA1STAT6 ProteinProtein Interaction , , 0, 0, - (2018)
  • Comparison of Cell Permeability between Linear Peptoids and Cyclic Peptoids , , 0, 0, - (2018)
  • Triazinebridged cyclic peptoids as molecular transporters , , 0, 0, - (2017)
  • Stapled αHelix Mimetic SmallMolecules Targeting Mcl1 , , 0, 0, - (2017)
  • Design Synthesis and CD Spectroscopy Investigation of αAbpeptoidsβpeptides Hybrid Oligomers , , 0, 0, - (2017)
  • Identification of Skp2 Inhibitors using a DNAEncoded Cyclic Peptoid Library , , 0, 0, - (2017)
  • Oligomers of NSubstituted β2 and β3 Homoalanines A Novel Class of BetaPeptoids with Backbond Chirality , , 0, 0, - (2017)
  • Synthesis and Circular Dichroism Studies of ABpeptoidsβpeptides Hybrid Oligomers , , 0, 0, - (2017)
  • OnePot Synthesis of Novel Bivalent Phosphopeptide Targeting 1433σ , , 0, 0, - (2017)
  • Identification of Peptidomimetic Inhibitors of Skp2 using a Vast OneBead OneCompound Library , , 0, 0, - (2017)
  • Design Synthesis and Circular Dichroism Studies of Novel Hybrid Oligomers with Backbone Chirality , , 0, 0, - (2017)
  • Development of Molecular Transporter Based on Cyclic Poly Peptoids , , 0, 0, - (2017)
  • Synthesis and CD Spectroscopic Studies of a New Class of PeptoidBased Foldamers Nsubstituted β2 or β3Homoalanines , , 0, 0, - (2017)
  • Identification of Peptidomimetic Inhibitors of Skp2 , , 0, 0, - (2017)
  • Assessment of Cell Permeability of Cyclic Peptoids and Linear Peptoids , , 0, 0, - (2017)
  • Development of a Stapled Peptide Inhibitor Targeting NCoA1STAT6 Interaction , , 0, 0, - (2017)
  • Oligomers of NSubstituted β2Homoalanines as Antimicrobial Agents , , 0, 0, - (2017)
  • Design triazine assisted potent bivalent phosphopeptide for targeting 1433σ , , 0, 0, - (2017)
  • New class of hybrid oligomers with backbone chirality , , 0, 0, - (2017)
  • Construction and highthroughput screen of an ultralarge bead library for rapid discovery of potent protein binding ligands , , 0, 0, - (2016)
  • Construction of a Vast OneBead OneCompound Library of Cyclic Peptoids , , 0, 0, - (2016)
  • Identification of a Chemical Inhibitor of the Skp2p300 Interaction , , 0, 0, - (2016)
  • A Cyclic Peptoid Inhibitor of the Skp2p300 Interaction, , 0, 0, - (2016)
  • Development of firstinclass NCoA1STAT6 inhibitor using stapled peptide , , 0, 0, - (2016)
  • Design Synthesis and Cricular Dichroism Studies of Nsubstituted β2Homoalanines as a New Class of Peptoid Foldamers , , 0, 0, - (2016)
  • Development of Amphiphilic Twoface αHelix Mimetics as Specific Modulators of ProteinProtein Interactions , , 0, 0, - (2016)
  • Development of firstinclass NCoA1STAT6 inhibitor using stapled peptide , , 0, 0, - (2016)
  • TwoFace Amphiphilic αHelix Mimetics as Potent Inhibitors of ProteinProtein Interactions , , 0, 0, - (2016)
  • Identification of an Inhibitor of the Skp2p300 interaction that promotes p53mediated apoptosis , , 0, 0, - (2016)
  • Converting OneFace aHelix Mimetics into Amphiphilic aHelix Mimetics as potent Inhibitors of ProteinProtein Interactions, , 0, 0, - (2016)
  • Simple sequencing strategy for bicyclic peptoidspeptides via onepot ringopening and cleavage reaction , , 0, 0, - (2016)
  • Stapled aHelix Mimetic SmallMolecules, , 0, 0, - (2016)
  • A novel stabilization strategy of αhelix mimetic small molecules using hydrocarbon bridge, , 0, 0, - (2015)
  • Cellular Uptake Evaluation of TriazineBridged Cyclic Peptoids, , 0, 0, - (2015)
  • Design Synthesis and Antimicrobial Activities of a Facile Amphiphlic Peptidomimetics, , 0, 0, - (2015)
  • SolidPhase Synthesis and Sequence Analysis of Small Molecule alphaHelix Mimetic Oligobenzamides, , 0, 0, - (2015)
  • A OnePot RingOpening and Cleavage Strategy for Constructing a Combinatorial Library of Bicyclic Peptoids, , 0, 0, - (2015)
  • Oligomers of NSubstituted β2Homoalanines New Peptoid Foldamers, , 0, 0, - (2015)
  • A OnePot RingOpeningCleavage Reaction for Constructing Combinatorial Cyclic Peptoid Libraries, , 0, 0, - (2015)
  • OnResin Protection for Efficient Sequence Determination of Cyclic Peptoids, , 0, 0, - (2015)
  • A OnePot RingOpening and Cleavage Strategy for a Combinatorial Library of Bicyclic Peptoids, , 0, 0, - (2015)
  • Synthetic Antimicrobial Peptidomimetics Using Facile Amphiphilic Helical Scaffold, , 0, 0, - (2015)
  • A Facile Method for Sequence Determination of Cyclic PeptidesPeptoids via CNBrMediated OnePot RingOpeningCleavage Reaction, , 0, 0, - (2015)
  • Design synthesis and evaluation of phenylpiperazinetriazinebased alhpahelix mimetics as protein capture reagents, , 0, 0, - (2015)
  • Targeting ProteinProtein Interactions Using alphaHelix Mimetics with Easy Synthetic Manipulation, , 0, 0, - (2015)
  • Onbead screening method for Rapid and Efficient Identification of αHelix Mimetics Targeting ProteinProtein Interactions, , 0, 0, - (2015)
  • A Simple RingOpening Strategy for Cyclic Peptide and Cyclic Peptoid Libraries, , 0, 0, - (2015)
  • StructureActivity Relationship Study of alphaHelix Mimetics Targeting ProteinProtein Interactions, , 0, 0, - (2015)
  • A Simple Strategy for Sequence Determination of Cyclic PeptidesPeptoids via CNBrMediated OnePot RingOpeningCleavage Reaction, , 0, 0, - (2015)
  • A Combinatorial Library Approach for Rapid and Efficient Identification of αHelix Mimetics Targeting ProteinProtein Interactions, , 0, 0, - (2015)

Research Activities

  • , 포항공과대학교 (2012-2013)
  • DEVELOPMENT OF CHEMICAL MODULATORS OF PROTEIN-PROTEIN INTERACTIONS, 포항공과대학교 (2012-2013)
  • , 포항공과대학교 (2012-2013)
  • DEVELOPMENT OF MCL-1 INHIBITORS USING Α-HELIX MIMETIC SMALL MOLECULES, 재단법인한국연구재단 (2012-2013)
  • DEVELOPMENT OF IMPROVED INHIBITORS OF MCL1/BH3 PROTEIN-PRO, 포항공대산학협력단 (2013-2013)
  • DEVELOPMENT OF CHEMICAL MODULATORS OF PROTEIN-PROTEIN INTERACTIONS, 포항공과대학교 (2013-2014)
  • (학생)인건비풀링과제, 포항공대산학협력단 (2013-2040)
  • DEVELOPMENT OF MCL-1 INHIBITORS USING Α-HELIX MIMETIC SMALL MOLECULES, 재단법인한국연구재단 (2013-2014)
  • , 재단법인한국연구재단 (2013-2014)
  • , 포항공대산학협력단 (2014-2014)
  • , 포항공과대학교 (2014-2015)
  • , 포항공과대학교 (2014-2015)
  • , 포항공과대학교 (2014-2015)
  • DEVELOPMENT OF MCL-1 INHIBITORS USING Α-HELIX MIMETIC SMALL MOLECULES, 재단법인한국연구재단 (2014-2015)
  • , 재단법인한국연구재단 (2014-2015)
  • TECHNOLOGY FOR FACILITATED DISCOVERY OF DRUG CANDIDATES BY AFFINITY-BASED HIGH THROUGHPUT SCREENING OF ULTRA LARGE COMBINATORIAL LIBRARIES, 대구경북첨단의료산업진흥재단 (2014-2015)
  • DEVELOPMENT OF “ANTIBODY SURROGATE MOLECULES” FOR TARGETING PROTEIN-PROTEIN INTERACTIONS, 재단법인 삼성미래기술육성재단 (2014-2020)
  • , 포항공과대학교 (2015-2021)
  • , 포항공과대학교 (2015-2016)
  • TECHNOLOGY FOR FACILITATED DISCOVERY OF DRUG CANDIDATES BY AFFINITY-BASED HIGH THROUGHPUT SCREENING OF ULTRA LARGE COMBINATORIAL LIBRARIES, 대구경북첨단의료산업진흥재단 (2015-2016)
  • TECHNOLOGY FOR FACILITATED DISCOVERY OF DRUG CANDIDATES BY AFFINITY-BASED HIGH THROUGHPUT SCREENING OF ULTRA LARGE COMBINATORIAL LIBRARIES, 대구경북첨단의료산업진흥재단 (2016-2017)
  • , 포항공과대학교 (2016-2017)
  • , 포항공과대학교 (2016-2016)
  • , 포항공과대학교 (2017-2017)
  • , 재단법인한국연구재단 (2017-2018)
  • FAP(FIBROBLAST ACTIVATION PROTEIN) 저해제 개발, 보령제약(주)안산공장 (2017-2017)
  • DEVELOPMENT OF PEPTIDO-MIMETIC POTENTIATORS FOR REPOSITIONING DRUGS AGAINST DRUG-RESISTANT BACTERIA, 서울대학교 산학협력단 (2017-2018)
  • A NOVEL FORWARD CHEMICAL GENETIC APPROACH USING AFFINITY-BASED SCREENING, 재단법인한국연구재단 (2018-2019)
  • , 재단법인한국연구재단 (2018-2019)
  • Development of peptido-mimetic potentiators for repositioning drugs against drug-resistant bacteria, 서울대학교 산학협력단 (2018-2019)
  • DEVELOPMENT OF PEPTIDO-MIMETIC POTENTIATORS FOR REPOSITIONING DRUGS AGAINST DRUG-RESISTANT BACTERIA, 서울대학교 산학협력단 (2018-2019)
  • , 서울대학교 산학협력단 (2018-2019)
  • , 포항공과대학교 (2018-2035)
  • A NOVEL FORWARD CHEMICAL GENETIC APPROACH USING AFFINITY-BASED SCREENING, 재단법인한국연구재단 (2019-2020)
  • , 재단법인한국연구재단 (2019-2020)
  • DEVELOPMENT OF PEPTIDO-MIMETIC POTENTIATORS FOR REPOSITIONING DRUGS AGAINST DRUG-RESISTANT BACTERIA, 서울대학교 산학협력단 (2019-2020)
  • , 포항공대산학협력단 (2019-2040)
  • , 주식회사 유빅스테라퓨틱스 (2019-2020)
  • , 재단법인한국연구재단 (2020-2021)
  • , 재단법인한국연구재단 (2020-2021)
  • , (주)테라젠이텍스 (2020-2021)
  • DEVELOPMENT OF A NANO-BASED ENCODED LIBRARY TECHNOLOGY, 재단법인한국연구재단 (2021-2021)
  • , 재단법인한국연구재단 (2022-2023)
  • , 재단법인한국연구재단 (2022-2022)
  • , 재단법인한국연구재단 (2022-2023)
  • DEVELOPMENT OF NDTACS AS AN INNOVATIVE PLATFORM TECHNOLOGY FOR TARGETED PROTEIN DEGRADATION, 재단법인한국연구재단 (2023-2023)
  • , 포항공대산학협력단 (2023-2040)
  • , 재단법인한국연구재단 (2023-2023)
  • , 재단법인한국연구재단 (2023-2024)
  • , 재단법인한국연구재단 (2023-2024)
  • , 재단법인한국연구재단 (2023-2023)
  • DISCOVERY OF LONG-ACTING TARGETED ANTI-CANCER DRUG CANDIDATES BY DEVELOPING A NOVEL PEPTIDE-BASED THERAPEUTIC PLATFORM, 재단법인한국연구재단 (2023-2024)
  • , 재단법인한국연구재단 (2023-2023)
  • , 재단법인한국연구재단 (2024-2024)
  • REVOLUTIONIZING DEL SCREENING METHODS FOR PROTEIN INTERACTION MODULATORS, 재단법인한국연구재단 (2024-2024)
  • DISCOVERY OF LONG-ACTING TARGETED ANTI-CANCER DRUG CANDIDATES BY DEVELOPING A NOVEL PEPTIDE-BASED THERAPEUTIC PLATFORM, 재단법인한국연구재단 (2024-2024)
  • , 재단법인한국연구재단 (2024-2024)
  • , 재단법인한국연구재단 (2024-2024)
  • DEVELOPMENT OF NDTACS AS AN INNOVATIVE PLATFORM TECHNOLOGY FOR TARGETED PROTEIN DEGRADATION, 재단법인한국연구재단 (2024-2025)
  • , 재단법인한국연구재단 (2024-2025)
  • , 재단법인한국연구재단 (2024-2025)
  • NOVEL INTERFACIAL REACTION DYNAMICS THEORY COVERING ENTIRE PERIODIC TABLE FOR MATERIALS SYNTHESIS AT DIMENSIONAL BOUNDARY, 재단법인한국연구재단 (2024-2025)
  • DISCOVERY OF LONG-ACTING TARGETED ANTI-CANCER DRUG CANDIDATES BY DEVELOPING A NOVEL PEPTIDE-BASED THERAPEUTIC PLATFORM, 재단법인한국연구재단 (2025-2025)
  • DEVELOPMENT OF NDTACS AS AN INNOVATIVE PLATFORM TECHNOLOGY FOR TARGETED PROTEIN DEGRADATION, 재단법인한국연구재단 (2025-2025)
  • REVOLUTIONIZING DEL SCREENING METHODS FOR PROTEIN INTERACTION MODULATORS, 재단법인한국연구재단 (2025-2025)

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