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Journal of Chemical Information and Modeling
|
October 24, 2008
Targets looking for drugs: a multistep computational protocol for the development of structure-based pharmacophores and their applications for hit discovery
Cristina Tintori, Valentina Corradi, Matteo Magnani, et al.
The FEBS Journal
|
May 23, 2009
Possible binding site for paclitaxel at microtubule pores
Matteo Magnani, Giorgio Maccari, José M Andreu, et al.
The FEBS Journal
|
June 29, 2006
The betaI/betaIII-tubulin isoforms and their complexes with antimitotic agents. Docking and molecular dynamics studies
Matteo Magnani, Francesco Ortuso, Simonetta Soro, et al.
Journal of Chemical Information and Modeling
|
May 23, 2006
A genetic-function-approximation-based QSAR model for the affinity of arylpiperazines toward alpha1 adrenoceptors
Laura Maccari, Matteo Magnani, Giovannella Strappaghetti, et al.
Scientific Reports
|
August 19, 2025
Anatomy of a Swedish population-scale network
Georgios Panayiotou, Inga K Wohlert, Miia Bask, et al.
Journal of Chemical Information and Modeling
|
August 24, 2010
Molecular interaction fields and 3D-QSAR studies of p53-MDM2 inhibitors suggest additional features of ligand-target interaction
Cristina Dezi, Andrea Carotti, Matteo Magnani, et al.
Chemmedchem
|
August 8, 2006
Ligand-based virtual screening, parallel solution-phase and microwave-assisted synthesis as tools to identify and synthesize new inhibitors of mycobacterium tuberculosis
Fabrizio Manetti, Matteo Magnani, Daniele Castagnolo, et al.
Chemmedchem
|
February 14, 2007
Inhibition of Bcr-Abl phosphorylation and induction of apoptosis by pyrazolo[3,4-d]pyrimidines in human leukemia cells
Fabrizio Manetti, Annalisa Pucci, Matteo Magnani, et al.
Bioorganic & Medicinal Chemistry
|
August 30, 2008
Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis
Daniele Castagnolo, Alessandro De Logu, Marco Radi, et al.
Journal of Medicinal Chemistry
|
February 9, 2008
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines
Fabrizio Manetti, Chiara Brullo, Matteo Magnani, et al.
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of 3
Search research articles
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Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
Journal of Chemical Information and Modeling
|
October 24, 2008
Targets looking for drugs: a multistep computational protocol for the development of structure-based pharmacophores and their applications for hit discovery
Cristina Tintori, Valentina Corradi, Matteo Magnani, et al.
The FEBS Journal
|
May 23, 2009
Possible binding site for paclitaxel at microtubule pores
Matteo Magnani, Giorgio Maccari, José M Andreu, et al.
The FEBS Journal
|
June 29, 2006
The betaI/betaIII-tubulin isoforms and their complexes with antimitotic agents. Docking and molecular dynamics studies
Matteo Magnani, Francesco Ortuso, Simonetta Soro, et al.
Journal of Chemical Information and Modeling
|
May 23, 2006
A genetic-function-approximation-based QSAR model for the affinity of arylpiperazines toward alpha1 adrenoceptors
Laura Maccari, Matteo Magnani, Giovannella Strappaghetti, et al.
Scientific Reports
|
August 19, 2025
Anatomy of a Swedish population-scale network
Georgios Panayiotou, Inga K Wohlert, Miia Bask, et al.
Journal of Chemical Information and Modeling
|
August 24, 2010
Molecular interaction fields and 3D-QSAR studies of p53-MDM2 inhibitors suggest additional features of ligand-target interaction
Cristina Dezi, Andrea Carotti, Matteo Magnani, et al.
Chemmedchem
|
August 8, 2006
Ligand-based virtual screening, parallel solution-phase and microwave-assisted synthesis as tools to identify and synthesize new inhibitors of mycobacterium tuberculosis
Fabrizio Manetti, Matteo Magnani, Daniele Castagnolo, et al.
Chemmedchem
|
February 14, 2007
Inhibition of Bcr-Abl phosphorylation and induction of apoptosis by pyrazolo[3,4-d]pyrimidines in human leukemia cells
Fabrizio Manetti, Annalisa Pucci, Matteo Magnani, et al.
Bioorganic & Medicinal Chemistry
|
August 30, 2008
Synthesis, biological evaluation and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis
Daniele Castagnolo, Alessandro De Logu, Marco Radi, et al.
Journal of Medicinal Chemistry
|
February 9, 2008
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines
Fabrizio Manetti, Chiara Brullo, Matteo Magnani, et al.
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of 3