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Janos Sapi

Showing results (21-30 of 29) with videos related to

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International Journal of Molecular Sciences|July 9, 2022
Inhibition of Recruitment and Activation of Neutrophils by Pyridazinone-Scaffold-Based CompoundsAurélie Moniot, Julien Braux, Renaud Siboni, et al.
Journal of Medicinal Chemistry|January 8, 2016
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic StudiesBenedetta Cornelio, Marie Laronze-Cochard, Mariangela Ceruso, et al.
European Journal of Medicinal Chemistry|May 10, 2019
5-Arylisothiazol-3(2H)-one-1,(1)-(di)oxides: A new class of selective tumor-associated carbonic anhydrases (hCA IX and XII) inhibitorsBenedetta Cornelio, Marie Laronze-Cochard, Raimundo Miambo, et al.
European Journal of Medicinal Chemistry|February 7, 2018
Synthesis and biological evaluation of pyridazinone derivatives as potential anti-inflammatory agentsChantal Barberot, Aurélie Moniot, Ingrid Allart-Simon, et al.
Bioorganic & Medicinal Chemistry|September 11, 2008
Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with improved selectivityGwennaël Ledour, Gautier Moroy, Matthieu Rouffet, et al.
Bioorganic & Medicinal Chemistry|May 22, 2007
Simultaneous presence of unsaturation and long alkyl chain at P'1 of Ilomastat confers selectivity for gelatinase A (MMP-2) over gelatinase B (MMP-9) inhibition as shown by molecular modelling studiesGautier Moroy, Clément Denhez, Haquima El Mourabit, et al.
Cancers|December 10, 2021
Pyridazinone Derivatives Limit Osteosarcoma-Cells Growth In Vitro and In VivoAurélie Moniot, Julien Braux, Camille Bour, et al.
Chembiochem : a European Journal of Chemical Biology|November 19, 2016
Structure-Activity Relationships of Benzenesulfonamide-Based Inhibitors towards Carbonic Anhydrase Isoform SpecificityAvni Bhatt, Brian P Mahon, Vinicius Wilian D Cruzeiro, et al.
Organic & Biomolecular Chemistry|August 25, 2010
Synthesis and biological evaluation of new penta- and heptacyclic indolo- and quinolinocarbazole ring systems obtained via Pd(0) catalysed reductive N-heteroannulationMarie Laronze-Cochard, Fabien Cochard, Etienne Daras, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
International Journal of Molecular Sciences|July 9, 2022
Inhibition of Recruitment and Activation of Neutrophils by Pyridazinone-Scaffold-Based CompoundsAurélie Moniot, Julien Braux, Renaud Siboni, et al.
Journal of Medicinal Chemistry|January 8, 2016
4-Arylbenzenesulfonamides as Human Carbonic Anhydrase Inhibitors (hCAIs): Synthesis by Pd Nanocatalyst-Mediated Suzuki-Miyaura Reaction, Enzyme Inhibition, and X-ray Crystallographic StudiesBenedetta Cornelio, Marie Laronze-Cochard, Mariangela Ceruso, et al.
European Journal of Medicinal Chemistry|May 10, 2019
5-Arylisothiazol-3(2H)-one-1,(1)-(di)oxides: A new class of selective tumor-associated carbonic anhydrases (hCA IX and XII) inhibitorsBenedetta Cornelio, Marie Laronze-Cochard, Raimundo Miambo, et al.
European Journal of Medicinal Chemistry|February 7, 2018
Synthesis and biological evaluation of pyridazinone derivatives as potential anti-inflammatory agentsChantal Barberot, Aurélie Moniot, Ingrid Allart-Simon, et al.
Bioorganic & Medicinal Chemistry|September 11, 2008
Introduction of the 4-(4-bromophenyl)benzenesulfonyl group to hydrazide analogs of Ilomastat leads to potent gelatinase B (MMP-9) inhibitors with improved selectivityGwennaël Ledour, Gautier Moroy, Matthieu Rouffet, et al.
Bioorganic & Medicinal Chemistry|May 22, 2007
Simultaneous presence of unsaturation and long alkyl chain at P'1 of Ilomastat confers selectivity for gelatinase A (MMP-2) over gelatinase B (MMP-9) inhibition as shown by molecular modelling studiesGautier Moroy, Clément Denhez, Haquima El Mourabit, et al.
Cancers|December 10, 2021
Pyridazinone Derivatives Limit Osteosarcoma-Cells Growth In Vitro and In VivoAurélie Moniot, Julien Braux, Camille Bour, et al.
Chembiochem : a European Journal of Chemical Biology|November 19, 2016
Structure-Activity Relationships of Benzenesulfonamide-Based Inhibitors towards Carbonic Anhydrase Isoform SpecificityAvni Bhatt, Brian P Mahon, Vinicius Wilian D Cruzeiro, et al.
Organic & Biomolecular Chemistry|August 25, 2010
Synthesis and biological evaluation of new penta- and heptacyclic indolo- and quinolinocarbazole ring systems obtained via Pd(0) catalysed reductive N-heteroannulationMarie Laronze-Cochard, Fabien Cochard, Etienne Daras, et al.
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