1,4-Dihydropyrazolo[4,3-d]imidazole phenyl derivatives : A Novel Type Ⅱ Raf kinase inhibitors
Hana Yu, Yunkyung Jung, Hwan Kim, Junghun Lee, Chang-Hyun Oh, Kyung Ho Yoo, Taebo Sim and Jung-Mi Hah
Bioorg. Med. Chem. Lett., 2010
42
QM/MM based 3D QSAR models for potent B Raf inhibitors
Jae Yoon Chung, Hwan Won Chung, Seung Joo Cho, Art E. Cho, Jung-Mi Hah
J. Computer-Aided Molecular Design, 2010
43
Discovery and Initial SAR of Pyrimidin-4-yl-1H-imidazole derivatives with Antiproliferative activity against Melanoma cell lines
Junghun Lee, Hwan Kim, Hana Yu, Jae Yoon Chung, Chang-Hyun Oh, Kyung Ho Yoo, Taebo Sim, and Jung-Mi Hah
Bioorg. Med. Chem. Lett., 2010
44
Synthesis and antiproliferative activity of pyrrolo[3,2-b]pyridine derivatives against melanoma
Hee-Jin Kim, Myung-Ho Jung, Hwan Kim, Mohammed I, El-Gamal, So Ha Lee, Kyung Ho Yoo, Tae Bo Sim, Jung-Mi Hah, Jung-Hyuck Cho, Jung Hoon Choi, Chang-Hyun Oh
Bioorg. Med. Chem. Lett., 2009
45
Correlation between Performance of QM/MM Docking and Simple Classification of Binding Sites
Jae Yoon Chung, Art E Cho, Jung-Mi Hah
J. Chem. Inf. Model., 2009
46
Hologram and Receptor-Guided 3D QSAR Analysis of Anilinopyridine JNK3 Inhibitors
Jae Yoon Chung, Art E Cho, Jung-Mi Hah
Bull. Kor. Chem. Soc., 2009
47
Synthesis of pyrrolo[2,3-d]pyrimidine derivatives and their antiproliferative activity against melanoma cell line
Myung-Ho Jung, Hwan Kim, Won-Kyung Choi, Mohammed I. El-Gamal, Jin-Hun Park, , So Ha Lee, Kyung Ho Yoo, Tae Bo Sim, Jung-mi Hah, Jung-Hyuck cho, Jung Hoon Choi, Chang-Hyun Oh
Bioorg. Med. Chem. Lett., 2009
48
Aminoquinoline Derivatives with Antiproliferative Activity Against Melanoma Cell Line
Bong Soo Nam, Hwan Kim, Chang-Hyun Oh, So Ha Lee, Seung Joo Cho, Tae Bo Sim, Jung-Mi Hah, Dong Jin Kim, Jung Hoon choi, Kyung Ho Yoo
Bioorg. Med. Chem. Lett., 2009
49
Pharmacophore based 3D-QSAR study of VEGFR-2 inhibitors
M. M. Neaz, F. A. Pasha, M. Muddassar, So Ha Lee, Taebo Sim, Jung-Mi Hah, Seung Joo Cho
Med. Chem. Res., 2009
50
Light-Mediated Liberation of Enzymatic Activity: “Small Molecule” Caged Protein Equivalents