Yoonae Ko

发表

Identification of (beta-carboxyethyl)-rhodanine derivatives exhibiting peroxisome proliferator-activated receptor gamma activity.

Sukjoon Yoon, Jiwon Choi, Hui-Sun Lee, 2010, European journal of medicinal chemistry.

Discovery of Q203, a potent clinical candidate for the treatment of tuberculosis

Se Yeon Kim, R. Wintjens, J. Cechetto, 2013, Nature Medicine.

Benzothiazepinecarboxamides: Novel hepatitis C virus inhibitors that interfere with viral entry and the generation of infectious virions.

Hee-Young Kim, Rita Song, Yoonae Ko, 2016, Antiviral research.

Lead optimization of a novel series of imidazo[1,2-a]pyridine amides leading to a clinical candidate (Q203) as a multi- and extensively-drug-resistant anti-tuberculosis agent.

H. J. Kim, Inhee Choi, Yoonae Ko, 2014, Journal of medicinal chemistry.

The ThiL enzyme is a valid antibacterial target essential for both thiamine biosynthesis and salvage pathways in Pseudomonas aeruginosa

Soojin Jang, H. J. Kim, Inhee Choi, 2020, The Journal of Biological Chemistry.

ThiL is a valid antibacterial target that is essential for both thiamine biosynthesis and salvage pathway in Pseudomonas aeruginosa

Soojin Jang, H. J. Kim, Inhee Choi, 2020, bioRxiv.

Cyanobacterial glucokinase complements the glucose sensing role of Arabidopsis thaliana hexokinase 1.

Sang-Bong Choi, Sukjoon Yoon, Yoonae Ko, 2008, Biochemical and biophysical research communications.

A novel 3,4-dihydropyrimidin-2(1H)-one: HIV-1 replication inhibitors with improved metabolic stability.

Doohyun Lee, Sung-Jun Han, Wonyoung So, 2012, Bioorganic & medicinal chemistry letters.

Synthesis and evaluation of hexahydropyrimidines and diamines as novel hepatitis C virus inhibitors.

J. Cechetto, Inhee Choi, Eunjung Park, 2013, European journal of medicinal chemistry.

Discovery of Phenylaminopyridine Derivatives as Novel HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors.

Doohyun Lee, Sung-Jun Han, Wonyoung So, 2012, ACS medicinal chemistry letters.

Pharmacological perturbation of thiamine metabolism sensitizes Pseudomonas aeruginosa to multiple antibacterial agents.

U. Sauer, J. Cechetto, Soojin Jang, 2022, Cell chemical biology.

Kinome-Wide RNA Interference Screening Identifies Mitogen-Activated Protein Kinases and Phosphatidylinositol Metabolism as Key Factors for Rabies Virus Infection

Seonhee Kim, Jihwan Song, R. Grailhe, 2019, mSphere.

Putative 3D Structure of QcrB from Mycobacterium tuberculosis Cytochrome bc1 Complex, a Novel Drug-Target for New Series of Antituberculosis Agent Q203

Inhee Choi, Yoonae Ko, 2016 .

Serendipitous discovery of 2-((phenylsulfonyl)methyl)-thieno[3,2-d]pyrimidine derivatives as novel HIV-1 replication inhibitors.

J. Cechetto, Sung-jun Han, Inhee Choi, 2014, Bioorganic & medicinal chemistry letters.

Identification of a Novel Sulfonamide Non-Nucleoside Reverse Transcriptase Inhibitor by a Phenotypic HIV-1 Full Replication Assay

Sung-Jun Han, Peter Sommer, Ho Jeong Kwon, 2013, PloS one.

Synthesis and biological evaluation of triazolothienopyrimidine derivatives as novel HIV-1 replication inhibitors.

J. Cechetto, Sung-jun Han, Inhee Choi, 2013, Bioorganic & medicinal chemistry letters.

High‐throughput drug screening using the Ebola virus transcription‐ and replication‐competent virus‐like particle system

David Shum, J. Min, C. Radu, 2018, Antiviral research.

Targeting HMG-CoA synthase 2 suppresses tamoxifen-resistant breast cancer growth by augmenting mitochondrial oxidative stress-mediated cell death.

Seungsu Kim, Y. Shin, Mi-Ock Lee, 2023, Life sciences.

Identification of pyrrolo[3,2-c]pyridin-4-amine compounds as a new class of entry inhibitors against influenza viruses in vitro.

So Young Chang, J. Min, Yoonae Ko, 2016, Biochemical and biophysical research communications.

Anti-Obesity Phenotypic Screening Looking to Increase OBR Cell Surface Expression

H. Kwon, Dong-Hwa Choi, R. Jockers, 2014, Journal of biomolecular screening.