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Biochimica Et Biophysica Acta
|
February 8, 1997
Probing the substrate specificity for lipases. II. Kinetic and modeling studies on the molecular recognition of 2-arylpropionic esters by Candida rugosa and Rhizomucor miehei lipases
M Botta, E Cernia, F Corelli, et al.
Journal of Computer-Aided Molecular Design
|
May 18, 2000
Research on anti-HIV-1 agents. Investigation on the CD4-Suradista binding mode through docking experiments
F Manetti, F Corelli, N Mongelli, et al.
Journal of Medicinal Chemistry
|
January 3, 1997
Diltiazem-like calcium entry blockers: a hypothesis of the receptor-binding site based on a comparative molecular field analysis model
F Corelli, F Manetti, A Tafi, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
February 24, 2001
Building a pharmacophore model for a novel class of antitubercular compounds
F Manetti, F Corelli, M Biava, et al.
La Radiologia Medica
|
February 11, 1999
[Automated procedures for radiation protection and quality controls in conventional diagnostic radiology]
A Tofani, M Bechini, A Del Corona, et al.
Bioorganic & Medicinal Chemistry
|
September 8, 1998
Synthesis and binding mode of heterocyclic analogues of suramin inhibiting the human basic fibroblast growth factor
F Manetti, V Cappello, M Botta, et al.
Current Medicinal Chemistry
|
June 10, 2011
Targeting the human DEAD-box polypeptide 3 (DDX3) RNA helicase as a novel strategy to inhibit viral replication
A Garbelli, M Radi, F Falchi, et al.
Journal of Medicinal Chemistry
|
June 19, 2001
Synthesis, biological evaluation, and pharmacophore generation of new pyridazinone derivatives with affinity toward alpha(1)- and alpha(2)-adrenoceptors
R Barbaro, L Betti, M Botta, et al.
Journal of Medicinal Chemistry
|
December 14, 2001
Synthesis, biological evaluation, and pharmacophore generation of uracil, 4(3H)-pyrimidinone, and uridine derivatives as potent and selective inhibitors of parainfluenza 1 (Sendai) virus
R Saladino, C Crestini, A T Palamara, et al.
Biochimica Et Biophysica Acta
|
November 23, 2000
Design and realization of a tailor-made enzyme to modify the molecular recognition of 2-arylpropionic esters by Candida rugosa lipase
F Manetti, D Mileto, F Corelli, 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
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Biochimica Et Biophysica Acta
|
February 8, 1997
Probing the substrate specificity for lipases. II. Kinetic and modeling studies on the molecular recognition of 2-arylpropionic esters by Candida rugosa and Rhizomucor miehei lipases
M Botta, E Cernia, F Corelli, et al.
Journal of Computer-Aided Molecular Design
|
May 18, 2000
Research on anti-HIV-1 agents. Investigation on the CD4-Suradista binding mode through docking experiments
F Manetti, F Corelli, N Mongelli, et al.
Journal of Medicinal Chemistry
|
January 3, 1997
Diltiazem-like calcium entry blockers: a hypothesis of the receptor-binding site based on a comparative molecular field analysis model
F Corelli, F Manetti, A Tafi, et al.
Farmaco (Societa Chimica Italiana : 1989)
|
February 24, 2001
Building a pharmacophore model for a novel class of antitubercular compounds
F Manetti, F Corelli, M Biava, et al.
La Radiologia Medica
|
February 11, 1999
[Automated procedures for radiation protection and quality controls in conventional diagnostic radiology]
A Tofani, M Bechini, A Del Corona, et al.
Bioorganic & Medicinal Chemistry
|
September 8, 1998
Synthesis and binding mode of heterocyclic analogues of suramin inhibiting the human basic fibroblast growth factor
F Manetti, V Cappello, M Botta, et al.
Current Medicinal Chemistry
|
June 10, 2011
Targeting the human DEAD-box polypeptide 3 (DDX3) RNA helicase as a novel strategy to inhibit viral replication
A Garbelli, M Radi, F Falchi, et al.
Journal of Medicinal Chemistry
|
June 19, 2001
Synthesis, biological evaluation, and pharmacophore generation of new pyridazinone derivatives with affinity toward alpha(1)- and alpha(2)-adrenoceptors
R Barbaro, L Betti, M Botta, et al.
Journal of Medicinal Chemistry
|
December 14, 2001
Synthesis, biological evaluation, and pharmacophore generation of uracil, 4(3H)-pyrimidinone, and uridine derivatives as potent and selective inhibitors of parainfluenza 1 (Sendai) virus
R Saladino, C Crestini, A T Palamara, et al.
Biochimica Et Biophysica Acta
|
November 23, 2000
Design and realization of a tailor-made enzyme to modify the molecular recognition of 2-arylpropionic esters by Candida rugosa lipase
F Manetti, D Mileto, F Corelli, et al.
Page
of 3