Discovery of Q203, a potent clinical candidate for the treatment of tuberculosis von Pethe, Kevin, Bifani, Pablo, Jang, Jichan, Kang, Sunhee, Park, Seijin, Ahn, Sujin, Jiricek, Jan, Jung, Juyoung, Jeon, Hee Kyoung, Cechetto, Jonathan, Christophe, Thierry, Lee, Honggun, Kempf, Marie, Jackson, Mary, Lenaerts, Anne J, Pham, Ha, Jones, Victoria, Seo, Min Jung, Kim, Young Mi, Seo, Mooyoung, Seo, Jeong Jea, Park, Dongsik, Ko, Yoonae, Choi, Inhee, Kim, Ryangyeo, Kim, Se Yeon, Lim, SeungBin, Yim, Seung-Ae, Nam, Jiyoun, Kang, Hwankyu, Kwon, Haejin, Oh, Chun-Taek, Cho, Yoojin, Jang, Yunhee, Kim, Junghwan, Chua, Adeline, Tan, Bee Huat, Nanjundappa, Mahesh B, Rao, Srinivasa P S, Barnes, Whitney S, Wintjens, René, Walker, John R, Alonso, Sylvie, Lee, Saeyeon, Kim, Jungjun, Oh, Soohyun, Oh, Taegwon, Nehrbass, Ulf, Han, Sung-Jun, No, Zaesung, Lee, Jinhwa, Brodin, Priscille, Cho, Sang-Nae, Nam, Kiyean, Kim, Jaeseung

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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 von Kang, Sunhee, Kim, Ryang Yeo, Seo, Min Jung, Lee, Saeyeon, Kim, Young Mi, Seo, Mooyoung, Seo, Jeong Jea, Ko, Yoonae, Choi, Inhee, Jang, Jichan, Nam, Jiyoun, Park, Seijin, Kang, Hwankyu, Kim, Hyung Jun, Kim, Jungjun, Ahn, Sujin, Pethe, Kevin, Nam, Kiyean, No, Zaesung, Kim, Jaeseung

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High content screening identifies decaprenyl-phosphoribose 2' epimerase as a target for intracellular antimycobacterial inhibitors von Christophe, Thierry, Jackson, Mary, Jeon, Hee Kyoung, Fenistein, Denis, Contreras-Dominguez, Monica, Kim, Jaeseung, Genovesio, Auguste, Carralot, Jean-Philippe, Ewann, Fanny, Kim, Eun Hye, Lee, Sae Yeon, Kang, Sunhee, Seo, Min Jung, Park, Eun Jung, Skovierová, Henrieta, Pham, Ha, Riccardi, Giovanna, Nam, Ji Youn, Marsollier, Laurent, Kempf, Marie, Joly-Guillou, Marie-Laure, Oh, Taegwon, Shin, Won Kyung, No, Zaesung, Nehrbass, Ulf, Brosch, Roland, Cole, Stewart T, Brodin, Priscille

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Discovery and characterization of a novel 7-aminopyrazolo[1,5-a]pyrimidine analog as a potent hepatitis C virus inhibitor von Hwang, Jong Yeon, Windisch, Marc Peter, Jo, Suyeon, Kim, Keumhyun, Kong, Sunju, Kim, Hyoung Cheul, Kim, Soohyun, Kim, Heeyoung, Lee, Myung Eun, Kim, Youngmi, Choi, Jihyun, Park, Dong-Sik, Park, Eunjung, Kwon, Jeongjin, Nam, Jiyoun, Ahn, Sujin, Cechetto, Jonathan, Kim, Junwon, Liuzzi, Michel, No, Zaesung, Lee, Jinhwa

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Discovery of 3,4-dihydropyrimidin-2(1H)-ones with inhibitory activity against HIV-1 replication von Kim, Junwon, Park, Changmin, Ok, Taedong, So, Wonyoung, Jo, Mina, Seo, Minjung, Kim, Youngmi, Sohn, Jeong-Hun, Park, Youngsam, Ju, Moon Kyeong, Kim, Junghwan, Han, Sung-Jun, Kim, Tae-Hee, Cechetto, Jonathan, Nam, Jiyoun, Sommer, Peter, No, Zaesung

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Synthesis and evaluation of hexahydropyrimidines and diamines as novel hepatitis C virus inhibitors von Hwang, Jong Yeon, Kim, Hee-Young, Jo, Suyeon, Park, Eunjung, Choi, Jihyun, Kong, Sunju, Park, Dong-Sik, Heo, Ja Myung, Lee, Jong Seok, Ko, Yoonae, Choi, Inhee, Cechetto, Jonathan, Kim, Jaeseung, Lee, Jinhwa, No, Zaesung, Windisch, Marc Peter

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Synthesis and structure-activity studies of side chain analogues of the anti-tubercular agent, Q203 von Kang, Sunhee, Kim, Young Mi, Kim, Ryang Yeo, Seo, Min Jung, No, Zaesung, Nam, Kiyean, Kim, Sanghee, Kim, Jaeseung

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Automated HTS/HCS for antivirals using visual HIV full replication assays von Carralot, Jean-Philippe, Kim, Mi-Ri, Kieffer-Kwon, Philippe, Corre, Sandra, Kim, Hwa Pyung, Kim, Junwon, Lenseigne, Boris, Lee, Changbok, Fenistein, Denis, Dorval, Thierry, Oh, Hyunrim, Han, Sungjun, No, Zaesung, Brodin, Priscille, Cechetto, Jonathan, Boese, Annette, Christophe, Thierry, Sommer, Peter

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Pd-catalyzed ortho-arylation of 3,4-dihydroisoquinolones via C–H bond activation: synthesis of 8-aryl-1,2,3,4-tetrahydroisoquinolines von Kim, Junwon, Jo, Mina, So, Wonyoung, No, Zaesung

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A novel 3,4-dihydropyrimidin-2(1H)-one: HIV-1 replication inhibitors with improved metabolic stability von Kim, Junwon, Ok, Taedong, Park, Changmin, So, Wonyoung, Jo, Mina, Kim, Youngmi, Seo, Minjung, Lee, Doohyun, Jo, Suyeon, Ko, Yoonae, Choi, Inhee, Park, Youngsam, Yoon, Jaewan, Ju, Moon Kyeong, Ahn, JiYe, Kim, Junghwan, Han, Sung-Jun, Kim, Tae-Hee, Cechetto, Jonathan, Nam, Jiyoun, Liuzzi, Michel, Sommer, Peter, No, Zaesung

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Design, synthesis, and evaluation of 2-aryl-7-(3′,4′-dialkoxyphenyl)-pyrazolo[1,5- a]pyrimidines as novel PDE-4 inhibitors von Kim, Ikyon, Song, Jong Hwan, Park, Chang Min, Jeong, Joon Won, Kim, Hyung Rae, Ha, Jin Ryul, No, Zaesung, Hyun, Young-Lan, Cho, Young Sik, Sook Kang, Nam, Jeon, Dong Ju

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Discovery of a novel orally active PDE-4 inhibitor effective in an ovalbumin-induced asthma murine model von Kwak, Hyun Jeong, Nam, Ji Yeon, Song, Jin Sook, No, Zaesung, Yang, Sung Don, Cheon, Hyae Gyeong

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Discovery of 2-iminobenzimidazoles as potent hepatitis C virus inhibitors with a novel mechanism of action von Windisch, Marc Peter, Jo, Suyeon, Kim, Hee-Young, Kim, Soo-Hyun, Kim, Keumhyun, Kong, Sunju, Jeong, Hyangsuk, Ahn, Sujin, No, Zaesung, Hwang, Jong Yeon

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Synthesis and biological evaluation of triazolothienopyrimidine derivatives as novel HIV-1 replication inhibitors von Kim, Junwon, Kwon, Jeongjin, Lee, Doohyun, Jo, Suyeon, Park, Dong-Sik, Choi, Jihyun, Park, Eunjung, Hwang, Jong Yeon, Ko, Yoonae, Choi, Inhee, Ju, Moon Kyeong, Ahn, JiYe, Kim, Junghwan, Han, Sung-Jun, Kim, Tae-Hee, Cechetto, Jonathan, Nam, Jiyoun, Ahn, Sujin, Sommer, Peter, Liuzzi, Michel, No, Zaesung, Lee, Jinhwa

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Novel Synthesis of Chiral 5-Cyanomethyl-3,4-dihydroxy-2-iodomethyltetrahydrofuran from 3-Diphenylmethyl-5-(1,2-dihydroxy-3-butenyl)isoxazolines via Iodoetheration Reaction von 김형래, Bum Suk Son, Bok Ju Song, Ji Young Kim, Hak Do Kim, Min Jung Seo, Bo Gan Song, Sang Dae Lee, Zaesung No

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A Substrate Mimetic Approach for Influenza Neuraminidase Inhibitors von 정준원, Jae Kuk Kim, 우병영, 송복주, 하덕찬, Zaesung No

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Discovery of Phenylaminopyridine Derivatives as Novel HIV-1 Non-nucleoside Reverse Transcriptase Inhibitors von Kim, Junwon, Lee, Doohyun, Park, Changmin, So, Wonyoung, Jo, Mina, Ok, Taedong, Kwon, Jeongjin, Kong, Sunju, Jo, Suyeon, Kim, Youngmi, Choi, Jihyun, Kim, Hyoung Cheul, Ko, Yoonae, Choi, Inhee, Park, Youngsam, Yoon, Jaewan, Ju, Moon Kyeong, Kim, Junghwan, Han, Sung-Jun, Kim, Tae-Hee, Cechetto, Jonathan, Nam, Jiyoun, Sommer, Peter, Liuzzi, Michel, Lee, Jinhwa, No, Zaesung

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Identification of two HIV inhibitors that also inhibit human RNaseH2 von Kim, J.H., Institut Pasteur Korea, Seongnam, Republic of korea, Yoon, J.W., Institut Pasteur Korea, Seongnam, Republic of korea, Ju, M.K., Institut Pasteur Korea, Seongnam, Republic of korea, Lee, Y.M., Institut Pasteur Korea, Seongnam, Republic of korea, Kim, T.H., Yonsei University, Seoul, Republic of Korea, Kim, J.W., Institut Pasteur Korea, Seongnam, Republic of korea, Sommer, P., Institut Pasteur Korea, Seongnam, Republic of korea, No, Z.S., Institut Pasteur Korea, Seongnam, Republic of korea, Cechetto, J., Institut Pasteur Korea, Seongnam, Republic of korea, Han, S.J., Konkuk University, Seoul, Republic of Korea

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EK-6136 (3-methyl-4-( O-methyl-oximino)-1-phenylpyrazolin-5-one): A novel Cdc25B inhibitor with antiproliferative activity von Kim, Kwang-Rok, Kwon, Ju-Lee, Kim, Ji-Sun, No, Zaesung, Kim, Hyoung Rae, Cheon, Hyae Gyeong

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Synthesis of 3′-C-substituted thymidine derivatives by free-radical techniques: scope and limitations von Horton, Derek, Chen, Kuangmin, No, Zaesung, Lee, Howard C.

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