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Beining Chen

Showing results (31-40 of 52) with videos related to

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The Review of Scientific Instruments|July 8, 2025
Development and application of an ion sensitive probe for helicon plasma diagnosticsGeyi Chen, Ruixin Yuan, Zuyu Zhang, et al.
Journal of Chemical Information and Modeling|March 28, 2006
Virtual screening using binary kernel discrimination: effect of noisy training data and the optimization of performanceBeining Chen, Robert F Harrison, Kitsuchart Pasupa, et al.
Analytical Chemistry|April 2, 2002
Rational design of a polymer specific for microcystin-LR using a computational approachIva Chianella, Manuela Lotierzo, Sergey A Piletsky, et al.
Journal of Chemical Information and Modeling|September 19, 2019
Development and Application of a Data-Driven Reaction Classification Model: Comparison of an Electronic Lab Notebook and Medicinal Chemistry LiteratureGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
Journal of Computer-Aided Molecular Design|January 6, 2007
Evaluation of machine-learning methods for ligand-based virtual screeningBeining Chen, Robert F Harrison, George Papadatos, et al.
Journal of Computer-Aided Molecular Design|March 1, 2020
Enhancing reaction-based de novo design using a multi-label reaction class recommenderGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
European Journal of Medicinal Chemistry|May 4, 2007
Synthesis and evaluation of a focused library of pyridine dicarbonitriles against prion diseaseKai Guo, Roger Mutter, William Heal, et al.
Molecular Informatics|November 9, 2021
RENATE: A Pseudo-retrosynthetic Tool for Synthetically Accessible de novo DesignGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
The Journal of Organic Chemistry|October 14, 2014
Regioselective synthesis of 3-aminoimidazo[1,2-a]-pyrimidines under continuous flow conditionsAshlie J E Butler, Mark J Thompson, Patrick J Maydom, et al.
Chemmedchem|July 17, 2010
Improved 2,4-diarylthiazole-based antiprion agents: switching the sense of the amide group at C5 leads to an increase in potencyMark J Thompson, Jennifer C Louth, Gemma K Greenwood, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
The Review of Scientific Instruments|July 8, 2025
Development and application of an ion sensitive probe for helicon plasma diagnosticsGeyi Chen, Ruixin Yuan, Zuyu Zhang, et al.
Journal of Chemical Information and Modeling|March 28, 2006
Virtual screening using binary kernel discrimination: effect of noisy training data and the optimization of performanceBeining Chen, Robert F Harrison, Kitsuchart Pasupa, et al.
Analytical Chemistry|April 2, 2002
Rational design of a polymer specific for microcystin-LR using a computational approachIva Chianella, Manuela Lotierzo, Sergey A Piletsky, et al.
Journal of Chemical Information and Modeling|September 19, 2019
Development and Application of a Data-Driven Reaction Classification Model: Comparison of an Electronic Lab Notebook and Medicinal Chemistry LiteratureGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
Journal of Computer-Aided Molecular Design|January 6, 2007
Evaluation of machine-learning methods for ligand-based virtual screeningBeining Chen, Robert F Harrison, George Papadatos, et al.
Journal of Computer-Aided Molecular Design|March 1, 2020
Enhancing reaction-based de novo design using a multi-label reaction class recommenderGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
European Journal of Medicinal Chemistry|May 4, 2007
Synthesis and evaluation of a focused library of pyridine dicarbonitriles against prion diseaseKai Guo, Roger Mutter, William Heal, et al.
Molecular Informatics|November 9, 2021
RENATE: A Pseudo-retrosynthetic Tool for Synthetically Accessible de novo DesignGian Marco Ghiandoni, Michael J Bodkin, Beining Chen, et al.
The Journal of Organic Chemistry|October 14, 2014
Regioselective synthesis of 3-aminoimidazo[1,2-a]-pyrimidines under continuous flow conditionsAshlie J E Butler, Mark J Thompson, Patrick J Maydom, et al.
Chemmedchem|July 17, 2010
Improved 2,4-diarylthiazole-based antiprion agents: switching the sense of the amide group at C5 leads to an increase in potencyMark J Thompson, Jennifer C Louth, Gemma K Greenwood, et al.
Pageof 6