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Journal of Enzyme Inhibition and Medicinal Chemistry
|
August 22, 2006
N-arylsulfonyl-2-vinyltryptamines as new 5-HT6 serotonin receptor ligands
Marion Raoul, Dominique Patigny, Frédréic Fabis, et al.
Biochemical Pharmacology
|
December 15, 2010
Inhibition of human leukocyte elastase, plasmin and matrix metalloproteinases by oleic acid and oleoyl-galardin derivative(s)
Gautier Moroy, Erika Bourguet, Martine Decarme, et al.
European Journal of Medicinal Chemistry
|
May 27, 2009
Synthesis and biological evaluation of novel 4,5-bis(dialkylaminoalkyl)-substituted acridines as potent telomeric G-quadruplex ligands
Marie Laronze-Cochard, Young-Min Kim, Bertrand Brassart, et al.
Chemmedchem
|
November 7, 2012
Cyclopropyl-tryptamine analogues: synthesis and biological evaluation as 5-HT(6) receptor ligands
Claude Szalata, Jan Szymoniak, Frédéric Fabis, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
April 10, 2003
Cytotoxic bis-3,4-dihydro-beta-carbolines and bis-beta-carbolines
Wei-Qun Jiang, Catherine Charlet-Fagnère, Janos Sapi, et al.
Chirality
|
September 5, 2015
Diastereomer Interconversion via Enolization: A Case Study
Andrea Renzetti, Antonello Di Crescenzo, Feilin Nie, et al.
European Journal of Dermatology : EJD
|
September 16, 2010
The NC1 domain of type XIX collagen inhibits melanoma cell migration
Aida Toubal, Laurent Ramont, Christine Terryn, et al.
Journal of Chromatography. A
|
June 30, 2006
Multiple dual-mode centrifugal partition chromatography, a semi-continuous development mode for routine laboratory-scale purifications
Eldra Delannay, Alix Toribio, Leslie Boudesocque, et al.
Bioconjugate Chemistry
|
March 2, 2016
Design, Synthesis, and Use of MMP-2 Inhibitor-Conjugated Quantum Dots in Functional Biochemical Assays
Erika Bourguet, Kristina Brazhnik, Alyona Sukhanova, et al.
RSC Medicinal Chemistry
|
May 28, 2021
Pyridazinone derivatives as potential anti-inflammatory agents: synthesis and biological evaluation as PDE4 inhibitors
Ingrid Allart-Simon, Aurélie Moniot, Nicolo Bisi, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Journal of Enzyme Inhibition and Medicinal Chemistry
|
August 22, 2006
N-arylsulfonyl-2-vinyltryptamines as new 5-HT6 serotonin receptor ligands
Marion Raoul, Dominique Patigny, Frédréic Fabis, et al.
Biochemical Pharmacology
|
December 15, 2010
Inhibition of human leukocyte elastase, plasmin and matrix metalloproteinases by oleic acid and oleoyl-galardin derivative(s)
Gautier Moroy, Erika Bourguet, Martine Decarme, et al.
European Journal of Medicinal Chemistry
|
May 27, 2009
Synthesis and biological evaluation of novel 4,5-bis(dialkylaminoalkyl)-substituted acridines as potent telomeric G-quadruplex ligands
Marie Laronze-Cochard, Young-Min Kim, Bertrand Brassart, et al.
Chemmedchem
|
November 7, 2012
Cyclopropyl-tryptamine analogues: synthesis and biological evaluation as 5-HT(6) receptor ligands
Claude Szalata, Jan Szymoniak, Frédéric Fabis, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry
|
April 10, 2003
Cytotoxic bis-3,4-dihydro-beta-carbolines and bis-beta-carbolines
Wei-Qun Jiang, Catherine Charlet-Fagnère, Janos Sapi, et al.
Chirality
|
September 5, 2015
Diastereomer Interconversion via Enolization: A Case Study
Andrea Renzetti, Antonello Di Crescenzo, Feilin Nie, et al.
European Journal of Dermatology : EJD
|
September 16, 2010
The NC1 domain of type XIX collagen inhibits melanoma cell migration
Aida Toubal, Laurent Ramont, Christine Terryn, et al.
Journal of Chromatography. A
|
June 30, 2006
Multiple dual-mode centrifugal partition chromatography, a semi-continuous development mode for routine laboratory-scale purifications
Eldra Delannay, Alix Toribio, Leslie Boudesocque, et al.
Bioconjugate Chemistry
|
March 2, 2016
Design, Synthesis, and Use of MMP-2 Inhibitor-Conjugated Quantum Dots in Functional Biochemical Assays
Erika Bourguet, Kristina Brazhnik, Alyona Sukhanova, et al.
RSC Medicinal Chemistry
|
May 28, 2021
Pyridazinone derivatives as potential anti-inflammatory agents: synthesis and biological evaluation as PDE4 inhibitors
Ingrid Allart-Simon, Aurélie Moniot, Nicolo Bisi, et al.
Page
of 3