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Ajit Dhananjay Jagtap

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Journal of Medicinal Chemistry|October 12, 2023
Inhibiting HCMV pUL89-C Endonuclease with Metal-Binding CompoundsAjit Dhananjay Jagtap, Robert J Geraghty, Zhengqiang Wang
Current Medicinal Chemistry|November 30, 2016
Ureas: Applications in Drug DesignAjit Dhananjay Jagtap, Nagendra Bharatrao Kondekar, Amit A Sadani, et al.
Bioorganic Chemistry|January 11, 2020
4-Substituted 2-amino-3,4-dihydroquinazolines with a 3-hairpin turn side chain as novel inhibitors of BACE-1Ajit Dhananjay Jagtap, Nagendra B Kondekar, Pei-Yun Hung, et al.
European Journal of Medicinal Chemistry|July 19, 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 inhibitorHsiao-Chun Wang, Ajit Dhananjay Jagtap, Pei-Teh Chang, et al.
European Journal of Medicinal Chemistry|August 5, 2014
Novel acylureidoindolin-2-one derivatives as dual Aurora B/FLT3 inhibitors for the treatment of acute myeloid leukemiaAjit Dhananjay Jagtap, Pei-Teh Chang, Jia-Rong Liu, et al.
Journal of Medicinal Chemistry|July 18, 2023
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 FibrosisWei-Chieh Yu, Tsung-Yu Yeh, Chih-Hung Ye, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Journal of Medicinal Chemistry|October 12, 2023
Inhibiting HCMV pUL89-C Endonuclease with Metal-Binding CompoundsAjit Dhananjay Jagtap, Robert J Geraghty, Zhengqiang Wang
Current Medicinal Chemistry|November 30, 2016
Ureas: Applications in Drug DesignAjit Dhananjay Jagtap, Nagendra Bharatrao Kondekar, Amit A Sadani, et al.
Bioorganic Chemistry|January 11, 2020
4-Substituted 2-amino-3,4-dihydroquinazolines with a 3-hairpin turn side chain as novel inhibitors of BACE-1Ajit Dhananjay Jagtap, Nagendra B Kondekar, Pei-Yun Hung, et al.
European Journal of Medicinal Chemistry|July 19, 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 inhibitorHsiao-Chun Wang, Ajit Dhananjay Jagtap, Pei-Teh Chang, et al.
European Journal of Medicinal Chemistry|August 5, 2014
Novel acylureidoindolin-2-one derivatives as dual Aurora B/FLT3 inhibitors for the treatment of acute myeloid leukemiaAjit Dhananjay Jagtap, Pei-Teh Chang, Jia-Rong Liu, et al.
Journal of Medicinal Chemistry|July 18, 2023
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 FibrosisWei-Chieh Yu, Tsung-Yu Yeh, Chih-Hung Ye, et al.
Pageof 1