Jiyoun Nam

发表

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

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

Discovery of 3,4-dihydropyrimidin-2(1H)-ones with inhibitory activity against HIV-1 replication.

Sung-Jun Han, Wonyoung So, Peter Sommer, 2012, Bioorganic & medicinal chemistry letters.

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.

High-Content Screening of Raw Actinomycete Extracts for the Identification of Antituberculosis Activities

J. Suh, David Shum, Hanki Lee, 2017, SLAS discovery : advancing life sciences R & D.

Antimicrobial and anti-inflammatory activities of chemokine CXCL14-derived antimicrobial peptide and its analogs.

S. Shin, Dasom Jeon, Yangmee Kim, 2019, Biochimica et biophysica acta. Biomembranes.

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.

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.

Discovery and characterization of a novel 7-aminopyrazolo[1,5-a]pyrimidine analog as a potent hepatitis C virus inhibitor.

J. Cechetto, Hee-Young Kim, Junwon Kim, 2012, Bioorganic & medicinal chemistry letters.

Dynamic thermodynamic resolution of N-methylpseudoephedrine α-bromo esters for asymmetric syntheses of α-hydroxy carboxylic acid derivatives

Jiyoun Nam, Y. Park, Sang-kuk Lee, 2003 .

para-Aminosalicylic Acid Is a Prodrug Targeting Dihydrofolate Reductase in Mycobacterium tuberculosis♦

Jichan Jang, Thomas Dick, Eric J. Rubin, 2013, The Journal of Biological Chemistry.

Asymmetric nucleophilic substitution of α-bromo amides via dynamic kinetic resolution for the preparation of dipeptide analogues

S. Jang, Yangmee Kim, Ji-yeon Chang, 2004 .

Antileishmanial High-Throughput Drug Screening Reveals Drug Candidates with New Scaffolds

Auguste Genovesio, Jiyeon Jang, Jair L. Siqueira-Neto, 2010, PLoS neglected tropical diseases.

Anti‐staphylococcal activity of a cyclic lipopeptide, C15‐bacillomycin D, produced by Bacillus velezensis NST6

Jaeyoung Choi, M. Seo, Jiyoun Nam, 2020, Journal of applied microbiology.

Dynamic kinetic resolution of α-bromo amides for asymmetric syntheses of di- and tripeptide analogues

K. Hahm, Ji-yeon Chang, Jiyoun Nam, 2003 .

Structural characterization and temperature-dependent production of C17-fengycin B derived from Bacillus amyloliquefaciens subsp. plantarum BC32-1

H. Lee, S. Kim, C. Lee, 2015, Biotechnology and Bioprocess Engineering.

Complete genome sequence of Bacillus velezensis NST6 and comparison with the species belonging to operational group B. amyloliquefaciens.

Jaeyoung Choi, M. Seo, Jiyoun Nam, 2020, Genomics.

Structure and Mechanism of Surfactin Peptide from Bacillus velezensis Antagonistic to Fungi Plant Pathogens

C. Lee, Jiyoun Nam, Jaekyeong Song, 2019, Bulletin of the Korean Chemical Society.

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.

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.

Structural and Functional Assessment of mBjAMP1, an Antimicrobial Peptide from Branchiostoma japonicum, Revealed a Novel α-Hairpinin-like Scaffold with Membrane Permeable and DNA Binding Activity.

J. Kim, Srinivasan Dinesh Kumar, S. Shin, 2018, Journal of medicinal chemistry.

Analysis of two quorum sensing-deficient isolates of Pseudomonas aeruginosa.

D. J. Lee, Jiyoun Nam, Youn-Tae Chi, 2018, Microbial pathogenesis.