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Filip Miljković

Showing results (1-10 of 35) with videos related to

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Molecular Informatics|March 31, 2018
Evaluation of Kinase Inhibitor Selectivity Using Cell-based Profiling DataFilip Miljković, Jürgen Bajorath
ACS Omega|July 20, 2018
Reconciling Selectivity Trends from a Comprehensive Kinase Inhibitor Profiling Campaign with Known Activity DataFilip Miljković, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|December 4, 2019
Data structures for computational compound promiscuity analysis and exemplary applications to inhibitors of the human kinomeFilip Miljković, Jürgen Bajorath
Future Science OA|August 21, 2019
Data structures for compound promiscuity analysis: promiscuity cliffs, pathways and promiscuity hubs formed by inhibitors of the human kinomeFilip Miljković, Jürgen Bajorath
Molecules (Basel, Switzerland)|September 26, 2018
Data-Driven Exploration of Selectivity and Off-Target Activities of Designated Chemical ProbesFilip Miljković, Jürgen Bajorath
ACS Omega|September 18, 2018
Exploring Selectivity of Multikinase Inhibitors across the Human KinomeFilip Miljković, Jürgen Bajorath
Molecular Pharmaceutics|September 6, 2024
Kinase Drug Discovery: Impact of Open Science and Artificial IntelligenceFilip Miljković, Jürgen Bajorath
Journal of Medicinal Chemistry|May 22, 2023
Data-Driven Global Assessment of Protein Kinase Inhibitors with Emphasis on Covalent CompoundsElena Xerxa, Filip Miljković, Jürgen Bajorath
Future Science OA|September 9, 2017
Identifying relationships between unrelated pharmaceutical target proteins on the basis of shared active compoundsFilip Miljković, Ryo Kunimoto, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|March 28, 2019
Systematic computational identification of promiscuity cliff pathways formed by inhibitors of the human kinomeFilip Miljković, Martin Vogt, Jürgen Bajorath
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Molecular Informatics|March 31, 2018
Evaluation of Kinase Inhibitor Selectivity Using Cell-based Profiling DataFilip Miljković, Jürgen Bajorath
ACS Omega|July 20, 2018
Reconciling Selectivity Trends from a Comprehensive Kinase Inhibitor Profiling Campaign with Known Activity DataFilip Miljković, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|December 4, 2019
Data structures for computational compound promiscuity analysis and exemplary applications to inhibitors of the human kinomeFilip Miljković, Jürgen Bajorath
Future Science OA|August 21, 2019
Data structures for compound promiscuity analysis: promiscuity cliffs, pathways and promiscuity hubs formed by inhibitors of the human kinomeFilip Miljković, Jürgen Bajorath
Molecules (Basel, Switzerland)|September 26, 2018
Data-Driven Exploration of Selectivity and Off-Target Activities of Designated Chemical ProbesFilip Miljković, Jürgen Bajorath
ACS Omega|September 18, 2018
Exploring Selectivity of Multikinase Inhibitors across the Human KinomeFilip Miljković, Jürgen Bajorath
Molecular Pharmaceutics|September 6, 2024
Kinase Drug Discovery: Impact of Open Science and Artificial IntelligenceFilip Miljković, Jürgen Bajorath
Journal of Medicinal Chemistry|May 22, 2023
Data-Driven Global Assessment of Protein Kinase Inhibitors with Emphasis on Covalent CompoundsElena Xerxa, Filip Miljković, Jürgen Bajorath
Future Science OA|September 9, 2017
Identifying relationships between unrelated pharmaceutical target proteins on the basis of shared active compoundsFilip Miljković, Ryo Kunimoto, Jürgen Bajorath
Journal of Computer-Aided Molecular Design|March 28, 2019
Systematic computational identification of promiscuity cliff pathways formed by inhibitors of the human kinomeFilip Miljković, Martin Vogt, Jürgen Bajorath
Pageof 4