Individual and common inhibitors of coronavirus and picornavirus main proteases von Kuo, Chih-Jung, Liu, Hun-Ge, Lo, Yueh-Kuei, Seong, Churl-Min, Lee, Kee-In, Jung, Young-Sik, Liang, Po-Huang

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Discovery of 3-aryl-3-methyl-1H-quinoline-2,4-diones as a new class of selective 5-HT6 receptor antagonists von Seong, Churl Min, Park, Woo Kyu, Park, Chul Min, Kong, Jae Yang, Park, No Sang

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An efficient base-mediated intramolecular condensation of 2-(disubstituted amino)-benzonitriles to 3-aminoindoles von Seong, Churl Min, Park, Chul Min, Choi, Jinil, Park, No Sang

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Synthesis and Evaluation of 4-Hydroxyphenylacetic Acid Amides and 4-Hydroxycinnamamides as Antioxidants von Jung, Young-Sik, Kang, Tae-Souk, Yoon, Joong-Ho, Joe, Bo-Young, Lim, Hee-Jong, Seong, Churl-Min, Park, Woo-Kyu, Kong, Jae-Yang, Cho, Jungsook, Park, No-Sang

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Synthesis and structure-activity relationship of 1H-indole-3-carboxylic acid pyridine-3-ylamides : A novel series of 5-HT2C receptor antagonists von Park, Chul Min, Kim, So Young, Park, Woo Kyu, Park, No Sang, Seong, Churl Min

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Synthesis and SAR of (piperazin-1-yl-phenyl)-arylsulfonamides: A novel series of atypical antipsychotic agents von Park, Chul Min, Kim, So Young, Park, Woo Kyu, Choi, Jung Hwan, Seong, Churl Min

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Dendritic oligoguanidines as intracellular translocators von Chung, Hyun-Ho, Harms, Guido, Min Seong, Churl, Choi, Byung Hyune, Min, Changhee, Taulane, Joseph P., Goodman, Murray

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Corrigendum to “Individual and common inhibitors of coronavirus and picornavirus main proteases” [FEBS Lett. 583 (2009) 549–555] von Kuo, Chih-Jung, Liu, Hun-Ge, Lo, Yueh-Kuei, Seong, Churl-Min, Lee, Kee-In, Jung, Young-Sik, Liang, Po-Huang

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Atom-transfer addition and annulation reactions of iodomalonates von Curran, Dennis P, Chen, Meng Hsin, Spletzer, Eric, Seong, Churl Min, Chang, Chi Tai

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Atom-transfer addition, annulation, and macrocyclization reactions of iodomalononitriles von Curran, Dennis P, Seong, Churl Min

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1-(Arylsulfonyl)-2,3-dihydro-1H-quinolin-4-one derivatives as 5-HT₆ serotonin receptor ligands von Park, Chul Min, Choi, Jin Il, Choi, Jung Hwan, Kim, So Young, Park, Woo Kyu, Seong, Churl Min

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Peptidomimetic inhibitors of p21ras farnesyltransferase: Hydrophobic functionalization leads to disruption of p21ras membrane association in whole cells von Qian, Yimin, Blaskovich, Michelle A., Seong, Churl-Min, Vogt, Andreas, Hamilton, Andrew D., Sebti, Said M.

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1-(Arylsulfonyl)-2,3-dihydro-1H-quinolin-4-one derivatives as 5-HT sub(6) serotonin receptor ligands von Park, Chul Min, Choi, Jin Il, Choi, Jung Hwan, Kim, So Young, Park, Woo Kyu, Seong, Churl Min

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1-(Arylsulfonyl)-2,3-dihydro-1 H-quinolin-4-one derivatives as 5-HT 6 serotonin receptor ligands von Park, Chul Min, Choi, Jin Il, Choi, Jung Hwan, Kim, So Young, Park, Woo Kyu, Seong, Churl Min

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Synthesis and structure-activity relationship of 1H-indole-3- carboxylic acid pyridine-3-ylamides: A novel series of 5-HT sub(2C) receptor antagonists von Park, Chul Min, Kim, So Young, Park, Woo Kyu, Park, No Sang, Seong, Churl Min

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Discovery of 3-aryl-3-methyl-1H-quinoline-2,4-diones as a new class of selective 5-HT sub(6) receptor antagonists von Seong, Churl Min, Park, Woo Kyu, Park, Chul Min, Kong, Jae Yang, Park, No Sang

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Discovery of 3-aryl-3-methyl-1 H-quinoline-2,4-diones as a new class of selective 5-HT 6 receptor antagonists von Seong, Churl Min, Park, Woo Kyu, Park, Chul Min, Kong, Jae Yang, Park, No Sang

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Synthesis and structure–activity relationship of 1 H-indole-3-carboxylic acid pyridine-3-ylamides: A novel series of 5-HT 2C receptor antagonists von Park, Chul Min, Kim, So Young, Park, Woo Kyu, Park, No Sang, Seong, Churl Min

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Bioisosterism: interchange of 4-OH to 4-NH2 in vanillin or homovanillin ring of capsaicinoids von Cho, S J, Jung, Y S, Seong, C M, Park, W K, Kong, J Y, Park, N S

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Homovanillic amide derivatives as capsaicin analogs and their analgesic activity von Baek, G H, Jung, Y S, Cho, S J, Seong, C M, Park, N S

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