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European Journal of Medicinal Chemistry
|
March 15, 2016
Iminolactones as tools for inversion of the absolute configuration of α-amino acids and as inhibitors of cancer cell proliferation
Christina Mernøe Jensen, Hsiao-Qing Chow, Ming Chen, et al.
The FEBS Journal
|
March 29, 2014
L-Asp is a useful tool in the purification of the ionotropic glutamate receptor A2 ligand-binding domain
Christian Krintel, Karla Frydenvang, Anna Ceravalls de Rabassa, et al.
Molecules (Basel, Switzerland)
|
April 12, 2020
Structure Elucidation of Prenyl- and Geranyl-Substituted Coumarins in <i>Gerbera piloselloides</i> by NMR Spectroscopy, Electronic Circular Dichroism Calculations, and Single Crystal X-ray Crystallography
Tuo Li, Xue Ma, Daniil Fedotov, et al.
FEBS Letters
|
February 18, 2024
The positive allosteric modulator BPAM344 and L-glutamate introduce an active-like structure of the ligand-binding domain of GluK2
Yasmin Bay, Mie Egeberg Jeppesen, Karla Frydenvang, et al.
European Journal of Medicinal Chemistry
|
March 10, 2007
Synthesis and pharmacological evaluation of novel conformationally constrained homologues of glutamic acid
Paola Conti, Antonio Caligiuri, Andrea Pinto, et al.
Chemistry & Biodiversity
|
February 24, 2009
New analogues of epiboxidine incorporating the 4,5-dihydroisoxazole nucleus: synthesis, binding affinity at neuronal nicotinic acetylcholine receptors, and molecular modeling investigations
Clelia Dallanoce, Pietro Magrone, Paola Bazza, et al.
Journal of Medicinal Chemistry
|
December 5, 2008
Novel high-affinity and selective biaromatic 4-substituted gamma-hydroxybutyric acid (GHB) analogues as GHB ligands: design, synthesis, and binding studies
Signe Høg, Petrine Wellendorph, Birgitte Nielsen, et al.
Journal of Medicinal Chemistry
|
September 20, 2011
A new phenylalanine derivative acts as an antagonist at the AMPA receptor GluA2 and introduces partial domain closure: synthesis, resolution, pharmacology, and crystal structure
Ewa Szymańska, Karla Frydenvang, Alberto Contreras-Sanz, et al.
European Journal of Pharmacology
|
August 13, 2004
Carbamoylcholine homologs: synthesis and pharmacology at nicotinic acetylcholine receptors
Anders A Jensen, Ivan Mikkelsen, Bente Frølund, et al.
Biophysical Journal
|
June 9, 2016
Enthalpy-Entropy Compensation in the Binding of Modulators at Ionotropic Glutamate Receptor GluA2
Christian Krintel, Pierre Francotte, Darryl S Pickering, et al.
Page
of 9
Search research articles
Search
Showing results (31-40 of 81) with videos related to
Sort By:
Page
of 9
European Journal of Medicinal Chemistry
|
March 15, 2016
Iminolactones as tools for inversion of the absolute configuration of α-amino acids and as inhibitors of cancer cell proliferation
Christina Mernøe Jensen, Hsiao-Qing Chow, Ming Chen, et al.
The FEBS Journal
|
March 29, 2014
L-Asp is a useful tool in the purification of the ionotropic glutamate receptor A2 ligand-binding domain
Christian Krintel, Karla Frydenvang, Anna Ceravalls de Rabassa, et al.
Molecules (Basel, Switzerland)
|
April 12, 2020
Structure Elucidation of Prenyl- and Geranyl-Substituted Coumarins in <i>Gerbera piloselloides</i> by NMR Spectroscopy, Electronic Circular Dichroism Calculations, and Single Crystal X-ray Crystallography
Tuo Li, Xue Ma, Daniil Fedotov, et al.
FEBS Letters
|
February 18, 2024
The positive allosteric modulator BPAM344 and L-glutamate introduce an active-like structure of the ligand-binding domain of GluK2
Yasmin Bay, Mie Egeberg Jeppesen, Karla Frydenvang, et al.
European Journal of Medicinal Chemistry
|
March 10, 2007
Synthesis and pharmacological evaluation of novel conformationally constrained homologues of glutamic acid
Paola Conti, Antonio Caligiuri, Andrea Pinto, et al.
Chemistry & Biodiversity
|
February 24, 2009
New analogues of epiboxidine incorporating the 4,5-dihydroisoxazole nucleus: synthesis, binding affinity at neuronal nicotinic acetylcholine receptors, and molecular modeling investigations
Clelia Dallanoce, Pietro Magrone, Paola Bazza, et al.
Journal of Medicinal Chemistry
|
December 5, 2008
Novel high-affinity and selective biaromatic 4-substituted gamma-hydroxybutyric acid (GHB) analogues as GHB ligands: design, synthesis, and binding studies
Signe Høg, Petrine Wellendorph, Birgitte Nielsen, et al.
Journal of Medicinal Chemistry
|
September 20, 2011
A new phenylalanine derivative acts as an antagonist at the AMPA receptor GluA2 and introduces partial domain closure: synthesis, resolution, pharmacology, and crystal structure
Ewa Szymańska, Karla Frydenvang, Alberto Contreras-Sanz, et al.
European Journal of Pharmacology
|
August 13, 2004
Carbamoylcholine homologs: synthesis and pharmacology at nicotinic acetylcholine receptors
Anders A Jensen, Ivan Mikkelsen, Bente Frølund, et al.
Biophysical Journal
|
June 9, 2016
Enthalpy-Entropy Compensation in the Binding of Modulators at Ionotropic Glutamate Receptor GluA2
Christian Krintel, Pierre Francotte, Darryl S Pickering, et al.
Page
of 9