Endosulfine alpha maintains spindle pole integrity by recruiting Aurora A during mitosis von Kim, Seul, Jun, Kyoungho, Kim, Ye-Hyun, Jung, Kwan-Young, Oh, Jeong Su, Kim, Jae-Sung

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γ‐Functionalization of α,β‐Unsaturated Nitriles under Mild Conditions: Versatile Synthesis of 4‐Aryl‐2‐Bromopyridines von Sim, Jaeuk, Viji, Mayavan, Rhee, Jeongtae, Jo, Hyeju, Cho, Suk Joon, Park, Yunjeong, Seo, Seung‐Yong, Jung, Kwan‐Young, Lee, Heesoon, Jung, Jae‐Kyung

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MASTL inhibition promotes mitotic catastrophe through PP2A activation to inhibit cancer growth and radioresistance in breast cancer cells von Yoon, Yi Na, Choe, Min Ho, Jung, Kwan-Young, Hwang, Sang-Gu, Oh, Jeong Su, Kim, Jae-Sung

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Crystal structure of [1,2,4]triazolo[4,3-b]pyridazine derivatives as BRD4 bromodomain inhibitors and structure–activity relationship study von Kim, Jung-Hoon, Pandit, Navin, Yoo, Miyoun, Park, Tae Hyun, Choi, Ji U, Park, Chi Hoon, Jung, Kwan-Young, Lee, Byung Il

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Synthesis and Structure-Activity Relationships of Aristoyagonine Derivatives as Brd4 Bromodomain Inhibitors with X-ray Co-Crystal Research von Yoo, Minjin, Park, Tae Hyun, Yoo, Miyoun, Kim, Yeongrin, Lee, Joo-Youn, Lee, Kyu Myung, Ryu, Seong Eon, Lee, Byung Il, Jung, Kwan-Young, Park, Chi Hoon

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A Novel Way of Preventing Postoperative Pancreatic Fistula by Directly Injecting Profibrogenic Materials into the Pancreatic Parenchyma von Lee, Sang Chul, Hong, Tae Ho, Kim, Ok-Hee, Cho, Suk Joon, Kim, Kee-Hwan, Song, Jin Sook, Hwang, Kyu-Seok, Jung, Jae-Kyung, Hong, Ha-Eun, Seo, Haeyeon, Choi, Ho Joong, Ahn, Joseph, Lee, Tae Yoon, Rim, Eunyoung, Jung, Kwan-Young, Kim, Say-June

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Crystal structures of human NSDHL and development of its novel inhibitor with the potential to suppress EGFR activity von Kim, Dong-Gyun, Cho, Sujin, Lee, Kyu-Yeon, Cheon, Seung-Ho, Yoon, Hye-Jin, Lee, Joo-Youn, Kim, Dongyoon, Shin, Kwang-Soo, Koh, Choong-Hyun, Koo, Ji Sung, Choi, Yuri, Lee, Hyung Ho, Oh, Yu-Kyoung, Jeong, Yoo-Seong, Chung, Suk-Jae, Baek, Moonkyu, Jung, Kwan-Young, Lim, Hyo Jin, Kim, Hyoun Sook, Park, Sung Jean, Lee, Jeong-Yeon, Lee, Sang Jae, Lee, Bong-Jin

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Discovery and Characterization of a Novel MASTL Inhibitor MKI-2 Targeting MASTL-PP2A in Breast Cancer Cells and Oocytes von Kang, Minsung, Kim, Chijung, Leem, Jiyeon, Kim, Ye-hyun, Kwon, Young-ju, Yoon, Yi Na, Chae, Chong Hak, Ahn, Jiyeon, Jung, Kwan-Young, Oh, Jeong Su, Kim, Jae-Sung

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PCW-1001, a Novel Pyrazole Derivative, Exerts Antitumor and Radio-Sensitizing Activities in Breast Cancer von Kang, Minsung, Pandit, Navin, Kim, Ah-Young, Cho, Suk Joon, Kwon, Young-Ju, Ahn, Jiyeon, Lee, Kyu Myung, Wu, Sangwook, Oh, Jeong Su, Jung, Kwan-Young, Kim, Jae-Sung

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MKI-1, a Novel Small-Molecule Inhibitor of MASTL, Exerts Antitumor and Radiosensitizer Activities Through PP2A Activation in Breast Cancer von Kim, Ah-Young, Yoon, Yi Na, Leem, Jiyeon, Lee, Jee-Young, Jung, Kwan-Young, Kang, Minsung, Ahn, Jiyeon, Hwang, Sang-Gu, Oh, Jeong Su, Kim, Jae-Sung

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Efficacy and safety of a novel topical agent for gallstone dissolution: 2-methoxy-6-methylpyridine von Choi, Ho Joong, Cho, Suk Joon, Kim, Ok-Hee, Song, Jin Sook, Hong, Ha-Eun, Lee, Sang Chul, Kim, Kee-Hwan, Lee, Sang Kuon, You, Young Kyoung, Hong, Tae Ho, Kim, Eun Young, Park, Jung Hyun, Na, Gun Hyung, Do You, Dong, Han, Jae Hyun, Park, Jae Woo, Kwak, Bong Jun, Lee, Tae Yun, Ahn, Joseph, Lee, Hwan Hee, Kang, Seung Kyu, Hwang, Kyu-Seok, Jung, Jae-Kyung, Jung, Kwan-Young, Kim, Say-June

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Deacetylation of Unactivated Amide Bonds in Heterocyclic Systems Using t‐BuOK von Yoo, Minjin, Jung, Kwan‐Young

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PCW-A1001, AI-assisted de novo design approach to design a selective inhibitor for FLT-3(D835Y) in acute myeloid leukemia von Jang, Seong Hun, Sivakumar, Dakshinamurthy, Mudedla, Sathish Kumar, Choi, Jaehan, Lee, Sungmin, Jeon, Minjun, Bvs, Suneel Kumar, Hwang, Jinha, Kang, Minsung, Shin, Eun Gyeong, Lee, Kyu Myung, Jung, Kwan-Young, Kim, Jae-Sung, Wu, Sangwook

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Identification of a novel SIRT7 inhibitor as anticancer drug candidate von Kim, Ji-Hye, Kim, Dahee, Cho, Suk Joon, Jung, Kwan-Young, Kim, Jong-Hoon, Lee, Jun Mi, Jung, Hee Jung, Kim, Kwang Rok

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Structure-activity relationships of thiazole and thiadiazole derivatives as potent and selective human adenosine A3 receptor antagonists von JUNG, Kwan-Young, KIM, Soo-Kyung, GAO, Zhan-Guo, GROSS, Ariel S, MELMAN, Neli, JACOBSON, Kenneth A, KIM, Yong-Chul

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Perturbation of the c‑Myc–Max Protein–Protein Interaction via Synthetic α‑Helix Mimetics von Jung, Kwan-Young, Wang, Huabo, Teriete, Peter, Yap, Jeremy L, Chen, Lijia, Lanning, Maryanna E, Hu, Angela, Lambert, Lester J, Holien, Toril, Sundan, Anders, Cosford, Nicholas D. P, Prochownik, Edward V, Fletcher, Steven

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Inhibition of SIRT7 overcomes sorafenib acquired resistance by suppressing ERK1/2 phosphorylation via the DDX3X-mediated NLRP3 inflammasome in hepatocellular carcinoma von Kim, Yuna, Jung, Kwan-Young, Kim, Yun Hak, Xu, Pan, Kang, Baeki E., Jo, Yunju, Pandit, Navin, Kwon, Jeongho, Gariani, Karim, Gariani, Joanna, Lee, Junguee, Verbeek, Jef, Nam, Seungyoon, Bae, Sung-Jin, Ha, Ki-Tae, Yi, Hyon-Seung, Shong, Minho, Kim, Kyun-Hwan, Kim, Doyoun, Jung, Hee Jung, Lee, Chang-Woo, Kim, Kwang Rok, Schoonjans, Kristina, Auwerx, Johan, Ryu, Dongryeol

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Antihelminthic drug niclosamide inhibits CIP2A and reactivates tumor suppressor protein phosphatase 2A in non-small cell lung cancer cells von Kim, Myeong-ok, Choe, Min Ho, Yoon, Yi Na, Ahn, Jiyeon, Yoo, Minjin, Jung, Kwan-Young, An, Sungkwan, Hwang, Sang-Gu, Oh, Jeong Su, Kim, Jae-Sung

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Small-molecule inhibitors of dimeric transcription factors: Antagonism of protein-protein and protein-DNA interactions von Yap, Jeremy L, Chauhan, Jay, Jung, Kwan-Young, Chen, Lijia, Prochownik, Edward V, Fletcher, Steven

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Pharmacophore identification of c-Myc inhibitor 10074-G5 von Yap, Jeremy L., Wang, Huabo, Hu, Angela, Chauhan, Jay, Jung, Kwan-Young, Gharavi, Robert B., Prochownik, Edward V., Fletcher, Steven

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