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Journal of Medicinal Chemistry
|
December 22, 2006
2-substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity
Mathew P Leese, Bertrand Leblond, Andrew Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX
Vincenzo Alterio, Mika Hilvo, Anna Di Fiore, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 10, 2020
Biochemical and structural characterisation of a protozoan beta-carbonic anhydrase from <i>Trichomonas vaginalis</i>
Linda J Urbański, Anna Di Fiore, Latifeh Azizi, et al.
Chemical Communications (Cambridge, England)
|
October 11, 2016
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition
Vincenzo Alterio, Roberta Cadoni, Davide Esposito, et al.
Journal of Medicinal Chemistry
|
April 29, 2017
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides
Elvira Bruno, Maria Rosa Buemi, Anna Di Fiore, et al.
European Journal of Medicinal Chemistry
|
September 7, 2023
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia
Andrea Angeli, Laura Micheli, Rita Turnaturi, et al.
European Journal of Medicinal Chemistry
|
December 12, 2018
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety
Maria Rosa Buemi, Anna Di Fiore, Laura De Luca, et al.
Molecular Cancer Therapeutics
|
August 30, 2008
Anticancer steroid sulfatase inhibitors: synthesis of a potent fluorinated second-generation agent, in vitro and in vivo activities, molecular modeling, and protein crystallography
L W Lawrence Woo, Delphine S Fischer, Christopher M Sharland, et al.
Journal of Medicinal Chemistry
|
February 12, 2008
Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents
Mathew P Leese, Fabrice L Jourdan, Keira Gaukroger, et al.
The Journal of Biological Chemistry
|
August 16, 2008
Biochemical characterization of CA IX, one of the most active carbonic anhydrase isozymes
Mika Hilvo, Lina Baranauskiene, Anna Maria Salzano, et al.
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Search research articles
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Showing results (51-60 of 60) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 60 results.
Journal of Medicinal Chemistry
|
December 22, 2006
2-substituted estradiol bis-sulfamates, multitargeted antitumor agents: synthesis, in vitro SAR, protein crystallography, and in vivo activity
Mathew P Leese, Bertrand Leblond, Andrew Smith, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
October 7, 2009
Crystal structure of the catalytic domain of the tumor-associated human carbonic anhydrase IX
Vincenzo Alterio, Mika Hilvo, Anna Di Fiore, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
June 10, 2020
Biochemical and structural characterisation of a protozoan beta-carbonic anhydrase from <i>Trichomonas vaginalis</i>
Linda J Urbański, Anna Di Fiore, Latifeh Azizi, et al.
Chemical Communications (Cambridge, England)
|
October 11, 2016
Benzoxaborole as a new chemotype for carbonic anhydrase inhibition
Vincenzo Alterio, Roberta Cadoni, Davide Esposito, et al.
Journal of Medicinal Chemistry
|
April 29, 2017
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides
Elvira Bruno, Maria Rosa Buemi, Anna Di Fiore, et al.
European Journal of Medicinal Chemistry
|
September 7, 2023
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia
Andrea Angeli, Laura Micheli, Rita Turnaturi, et al.
European Journal of Medicinal Chemistry
|
December 12, 2018
Exploring structural properties of potent human carbonic anhydrase inhibitors bearing a 4-(cycloalkylamino-1-carbonyl)benzenesulfonamide moiety
Maria Rosa Buemi, Anna Di Fiore, Laura De Luca, et al.
Molecular Cancer Therapeutics
|
August 30, 2008
Anticancer steroid sulfatase inhibitors: synthesis of a potent fluorinated second-generation agent, in vitro and in vivo activities, molecular modeling, and protein crystallography
L W Lawrence Woo, Delphine S Fischer, Christopher M Sharland, et al.
Journal of Medicinal Chemistry
|
February 12, 2008
Structure-activity relationships of C-17 cyano-substituted estratrienes as anticancer agents
Mathew P Leese, Fabrice L Jourdan, Keira Gaukroger, et al.
The Journal of Biological Chemistry
|
August 16, 2008
Biochemical characterization of CA IX, one of the most active carbonic anhydrase isozymes
Mika Hilvo, Lina Baranauskiene, Anna Maria Salzano, et al.
Page
of 6