A. Jagtap

Isoindole-1 , 3-dione-based α ,-diketo acid bioisosteres as hepatitis C virus NS 5 B polymerase inhibitors

J. Chern, P. Chang, R. R. Deore, 2014 .

Bioisosteric replacement of an acylureido moiety attached to an indolin-2-one scaffold with a malonamido or a 2/4-pyridinoylamido moiety produces a selectively potent Aurora-B inhibitor.

J. Chern, Hsiang-Wen Tseng, Chih-Peng Liu, 2014, European journal of medicinal chemistry.

Novel acylureidoindolin-2-one derivatives as dual Aurora B/FLT3 inhibitors for the treatment of acute myeloid leukemia.

J. Chern, Li-Jiuan Shen, Hsiang-Wen Tseng, 2014, European journal of medicinal chemistry.

Discovery of HDAC6, HDAC8, and 6/8 Inhibitors and Development of Cell-Based Drug Screening Models for the Treatment of TGF-β-Induced Idiopathic Pulmonary Fibrosis.

J. Chern, Shau-Ping Lin, Shuei-Liong Lin, 2023, Journal of medicinal chemistry.

Ureas: Applications in Drug Design.

J. Chern, A. Jagtap, Amit A. Sadani, 2017, Current medicinal chemistry.

4-Substituted 2-amino-3,4-dihydroquinazolines with a 3-hairpin turn side chain as novel inhibitors of BACE-1.

J. Chern, Chia-Ron Yang, G. Chen, 2019, Bioorganic chemistry.

Inhibiting HCMV pUL89-C Endonuclease with Metal-Binding Compounds.

R. Geraghty, Zhengqiang Wang, A. Jagtap, 2023, Journal of medicinal chemistry.