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Medicinal Research Reviews
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August 2, 2007
Search for new antagonist ligands for adenosine receptors from QSAR point of view. How close are we?
Maykel Pérez González, Carmen Terán, Marta Teijeira
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2005
A topological function based on spectral moments for predicting affinity toward A3 adenosine receptors
Maykel Pérez González, Carmen Terán, Marta Teijeira
Bioorganic & Medicinal Chemistry
|
March 21, 2007
2D-autocorrelation descriptors for predicting cytotoxicity of naphthoquinone ester derivatives against oral human epidermoid carcinoma
Liane Saíz-Urra, Maykel Pérez González, Marta Teijeira
Bioorganic & Medicinal Chemistry
|
September 12, 2006
QSAR studies about cytotoxicity of benzophenazines with dual inhibition toward both topoisomerases I and II: 3D-MoRSE descriptors and statistical considerations about variable selection
Liane Saíz-Urra, Maykel Pérez González, Marta Teijeira
European Journal of Medicinal Chemistry
|
October 12, 2010
Synthesis and cytostatic activity of purine nucleosides derivatives of allofuranose
Pedro Besada, Tamara Costas, Marta Teijeira, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
Geometry, topology, and atom-weights assembly descriptors to predicting A1 adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
European Journal of Medicinal Chemistry
|
October 29, 2005
Radial distribution function descriptors: an alternative for predicting A2 A adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Bulletin of Mathematical Biology
|
October 25, 2006
QSAR studies using radial distribution function for predicting A1 adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Current Topics in Medicinal Chemistry
|
December 17, 2008
Variable selection methods in QSAR: an overview
Maykel Pérez González, Carmen Terán, Liane Saíz-Urra, et al.
Current Medicinal Chemistry
|
August 22, 2006
Quantitative structure activity relationships as useful tools for the design of new adenosine receptor ligands. 1. Agonist
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 29) with videos related to
Sort By:
Page
of 3
Medicinal Research Reviews
|
August 2, 2007
Search for new antagonist ligands for adenosine receptors from QSAR point of view. How close are we?
Maykel Pérez González, Carmen Terán, Marta Teijeira
Bioorganic & Medicinal Chemistry Letters
|
December 17, 2005
A topological function based on spectral moments for predicting affinity toward A3 adenosine receptors
Maykel Pérez González, Carmen Terán, Marta Teijeira
Bioorganic & Medicinal Chemistry
|
March 21, 2007
2D-autocorrelation descriptors for predicting cytotoxicity of naphthoquinone ester derivatives against oral human epidermoid carcinoma
Liane Saíz-Urra, Maykel Pérez González, Marta Teijeira
Bioorganic & Medicinal Chemistry
|
September 12, 2006
QSAR studies about cytotoxicity of benzophenazines with dual inhibition toward both topoisomerases I and II: 3D-MoRSE descriptors and statistical considerations about variable selection
Liane Saíz-Urra, Maykel Pérez González, Marta Teijeira
European Journal of Medicinal Chemistry
|
October 12, 2010
Synthesis and cytostatic activity of purine nucleosides derivatives of allofuranose
Pedro Besada, Tamara Costas, Marta Teijeira, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
Geometry, topology, and atom-weights assembly descriptors to predicting A1 adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
European Journal of Medicinal Chemistry
|
October 29, 2005
Radial distribution function descriptors: an alternative for predicting A2 A adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Bulletin of Mathematical Biology
|
October 25, 2006
QSAR studies using radial distribution function for predicting A1 adenosine receptors agonists
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Current Topics in Medicinal Chemistry
|
December 17, 2008
Variable selection methods in QSAR: an overview
Maykel Pérez González, Carmen Terán, Liane Saíz-Urra, et al.
Current Medicinal Chemistry
|
August 22, 2006
Quantitative structure activity relationships as useful tools for the design of new adenosine receptor ligands. 1. Agonist
Maykel Pérez González, Carmen Terán, Marta Teijeira, et al.
Page
of 3