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Albert A Antolin

Showing results (11-20 of 29) with videos related to

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Cell Chemical Biology|December 19, 2017
Objective, Quantitative, Data-Driven Assessment of Chemical ProbesAlbert A Antolin, Joseph E Tym, Angeliki Komianou, et al.
Journal of Cheminformatics|June 1, 2022
canSAR chemistry registration and standardization pipelineDaniela Dolciami, Eloy Villasclaras-Fernandez, Christos Kannas, et al.
Scientific Reports|February 19, 2020
The kinase polypharmacology landscape of clinical PARP inhibitorsAlbert A Antolin, Malaka Ameratunga, Udai Banerji, et al.
Journal of Molecular Graphics & Modelling|September 24, 2013
Exploring the effect of PARP-1 flexibility in docking studiesAlbert A Antolin, Andrea Carotti, Roberto Nuti, et al.
The Science of the Total Environment|December 16, 2023
Short-term exposure to environmental levels of nicotine and cotinine impairs visual motor response in zebrafish larvae through a similar mode of action: Exploring the potential role of zebrafish α7 nAChRMarina Bellot, Leticia Manen, Eva Prats, et al.
Nucleic Acids Research|December 18, 2015
canSAR: an updated cancer research and drug discovery knowledgebaseJoseph E Tym, Costas Mitsopoulos, Elizabeth A Coker, et al.
European Journal of Medicinal Chemistry|January 6, 2026
Promiscuously bioactive compounds are prevalent in widely used commercial drug repurposing librariesHuabin Hu, James Bowers, Justin Shumate, et al.
Nucleic Acids Research|November 18, 2024
The Chemical Probes Portal - 2024: update on this public resource to support best-practice selection and use of small molecules in biomedical researchDomenico Sanfelice, Albert A Antolin, Alisa Crisp, et al.
Cell Chemical Biology|February 9, 2024
Identification of differential biological activity and synergy between the PARP inhibitor rucaparib and its major metaboliteHuabin Hu, Carme Serra, Wenjie Zhang, et al.
Clinical and Translational Medicine|April 17, 2024
Computational repurposing of oncology drugs through off-target drug binding interactions from pharmacological databasesImogen R Walpole, Farzana Y Zaman, Peinan Zhao, et al.
Pageof 3

Showing results (11-20 of 29) with videos related to

Sort By:
Pageof 3
Cell Chemical Biology|December 19, 2017
Objective, Quantitative, Data-Driven Assessment of Chemical ProbesAlbert A Antolin, Joseph E Tym, Angeliki Komianou, et al.
Journal of Cheminformatics|June 1, 2022
canSAR chemistry registration and standardization pipelineDaniela Dolciami, Eloy Villasclaras-Fernandez, Christos Kannas, et al.
Scientific Reports|February 19, 2020
The kinase polypharmacology landscape of clinical PARP inhibitorsAlbert A Antolin, Malaka Ameratunga, Udai Banerji, et al.
Journal of Molecular Graphics & Modelling|September 24, 2013
Exploring the effect of PARP-1 flexibility in docking studiesAlbert A Antolin, Andrea Carotti, Roberto Nuti, et al.
The Science of the Total Environment|December 16, 2023
Short-term exposure to environmental levels of nicotine and cotinine impairs visual motor response in zebrafish larvae through a similar mode of action: Exploring the potential role of zebrafish α7 nAChRMarina Bellot, Leticia Manen, Eva Prats, et al.
Nucleic Acids Research|December 18, 2015
canSAR: an updated cancer research and drug discovery knowledgebaseJoseph E Tym, Costas Mitsopoulos, Elizabeth A Coker, et al.
European Journal of Medicinal Chemistry|January 6, 2026
Promiscuously bioactive compounds are prevalent in widely used commercial drug repurposing librariesHuabin Hu, James Bowers, Justin Shumate, et al.
Nucleic Acids Research|November 18, 2024
The Chemical Probes Portal - 2024: update on this public resource to support best-practice selection and use of small molecules in biomedical researchDomenico Sanfelice, Albert A Antolin, Alisa Crisp, et al.
Cell Chemical Biology|February 9, 2024
Identification of differential biological activity and synergy between the PARP inhibitor rucaparib and its major metaboliteHuabin Hu, Carme Serra, Wenjie Zhang, et al.
Clinical and Translational Medicine|April 17, 2024
Computational repurposing of oncology drugs through off-target drug binding interactions from pharmacological databasesImogen R Walpole, Farzana Y Zaman, Peinan Zhao, et al.
Pageof 3