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Showing results (21-30 of 34) with videos related to

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Bioorganic & Medicinal Chemistry Letters|May 1, 2001
Structure determination and comparison of BM567, a sulfonylurea, with terbogrel, two compounds with dual action, thromboxane receptor antagonism and thromboxane synthase inhibitionC Michaux, S Rolin, J M Dogné, et al.
Journal of Inorganic Biochemistry|September 22, 2001
Synthesis and structural analysis of the copper(II) complexes of N2-(2-pyridylmethyl)-2-pyridinecarboxamideF Lebon, M Ledecq, M Dieu, et al.
The Journal of Pharmacy and Pharmacology|May 24, 2001
Design, synthesis and biological evaluation of a sulfonylcyanoguanidine as thromboxane A2 receptor antagonist and thromboxane synthase inhibitorJ M Dogné, J Wouters, S Rolin, et al.
Journal of Medicinal Chemistry|April 1, 1991
Synthesis and biochemical evaluation of baclofen analogues locked in the baclofen solid-state conformationA Mann, T Boulanger, B Brandau, et al.
Journal of Medicinal Chemistry|May 29, 1992
Structure and molecular modeling of GABAA receptor antagonistsD Rognan, T Boulanger, R Hoffmann, et al.
Antiviral Research|May 1, 1996
Relationship between structural properties and affinity for herpes simplex virus type 1 thymidine kinase of bromine substituted 5-heteroaromatic 2'-deoxyuridinesI Creuven, C Evrard, A Olivier, et al.
Bioorganic & Medicinal Chemistry|November 1, 1995
Structure-affinity relationships of baclofen and 3-heteroaromatic analoguesB Pirard, P A Carrupt, B Testa, et al.
Journal of Medicinal Chemistry|January 1, 1989
Stereoelectronic study of zetidoline, a dopamine D2 receptor antagonistS Collin, G Evrard, D P Vercauteren, et al.
Journal of Neural Transmission. Supplementum|January 1, 1994
Experimental and theoretical study of reversible monoamine oxidase inhibitors: structural approach of the active site of the enzymeJ Wouters, F Moureau, D P Vercauteren, et al.
Antiviral Research|August 1, 1994
Stereoelectronic properties of five anti-HSV-1 2'-deoxynucleosides analogues with heterocyclic substituents in the 5-position: a comparison with BVDUA Olivier, I Creuven, C Evrard, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

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Pageof 4
Bioorganic & Medicinal Chemistry Letters|May 1, 2001
Structure determination and comparison of BM567, a sulfonylurea, with terbogrel, two compounds with dual action, thromboxane receptor antagonism and thromboxane synthase inhibitionC Michaux, S Rolin, J M Dogné, et al.
Journal of Inorganic Biochemistry|September 22, 2001
Synthesis and structural analysis of the copper(II) complexes of N2-(2-pyridylmethyl)-2-pyridinecarboxamideF Lebon, M Ledecq, M Dieu, et al.
The Journal of Pharmacy and Pharmacology|May 24, 2001
Design, synthesis and biological evaluation of a sulfonylcyanoguanidine as thromboxane A2 receptor antagonist and thromboxane synthase inhibitorJ M Dogné, J Wouters, S Rolin, et al.
Journal of Medicinal Chemistry|April 1, 1991
Synthesis and biochemical evaluation of baclofen analogues locked in the baclofen solid-state conformationA Mann, T Boulanger, B Brandau, et al.
Journal of Medicinal Chemistry|May 29, 1992
Structure and molecular modeling of GABAA receptor antagonistsD Rognan, T Boulanger, R Hoffmann, et al.
Antiviral Research|May 1, 1996
Relationship between structural properties and affinity for herpes simplex virus type 1 thymidine kinase of bromine substituted 5-heteroaromatic 2'-deoxyuridinesI Creuven, C Evrard, A Olivier, et al.
Bioorganic & Medicinal Chemistry|November 1, 1995
Structure-affinity relationships of baclofen and 3-heteroaromatic analoguesB Pirard, P A Carrupt, B Testa, et al.
Journal of Medicinal Chemistry|January 1, 1989
Stereoelectronic study of zetidoline, a dopamine D2 receptor antagonistS Collin, G Evrard, D P Vercauteren, et al.
Journal of Neural Transmission. Supplementum|January 1, 1994
Experimental and theoretical study of reversible monoamine oxidase inhibitors: structural approach of the active site of the enzymeJ Wouters, F Moureau, D P Vercauteren, et al.
Antiviral Research|August 1, 1994
Stereoelectronic properties of five anti-HSV-1 2'-deoxynucleosides analogues with heterocyclic substituents in the 5-position: a comparison with BVDUA Olivier, I Creuven, C Evrard, et al.
Pageof 4