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http://hub.abes.fr/acs/periodical/jacsat/1986/volume_108/issue_12/101021ja00272a052/authorship/1
http://hub.abes.fr/oup/periodical/proeng/1990/volume_4/issue_1/101093protein411/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_2/101021jm0300072/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_12/101021jm049276y/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_3/101021jm0492958/authorship/18
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_22/101021jm060955d/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_17/101021jm070105d/authorship/19
http://hub.abes.fr/acs/periodical/bichaw/2001/volume_40/issue_31/101021bi010186u/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_7/101021jm061247v/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_21/101021jm060777o/authorship/16
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_19/101021jm050458h/authorship/22
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_5/101021jm701096v/authorship/17
http://hub.abes.fr/acs/periodical/bichaw/2007/volume_46/issue_33/101021bi7008745/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1996/volume_39/issue_2/101021jm9507183/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_13/101021jm701397k/authorship/9
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_8/101021jo0500131/authorship/11
http://hub.abes.fr/acs/periodical/bichaw/2003/volume_42/issue_3/101021bi0205449/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_7/101021jm061280h/authorship/23
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_17/101021jm060818g/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_8/101021jm061436d/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_8/101021jm000468c/authorship/9
http://hub.abes.fr/acs/periodical/bichaw/2006/volume_45/issue_24/101021bi060184f/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_12/101021jm051283e/authorship/8
http://hub.abes.fr/acs/periodical/joceah/1986/volume_51/issue_23/101021jo00373a001/authorship/1
http://hub.abes.fr/acs/periodical/jacsat/1985/volume_107/issue_8/101021ja00294a075/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1987/volume_109/issue_10/101021ja00244a037/authorship/3
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Host-guest complexation. 40. Synthesis and complexation of macrocyclic hosts containing cyclic ureas, anisyls, and steric barriers
Complementary solutes enter nonpolar preorganized cavities in lipophilic noncomplementary media
Design, Synthesis, and Structural Analysis of Influenza NeuraminidaseInhibitors Containing Pyrrolidine Cores
Discovery of ((4R,5S)-5-Amino-4-(2,4,5-trifluorophenyl)cyclohex-1-enyl)-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)methanone(ABT-341), a Highly Potent, Selective, OrallyEfficacious, and Safe Dipeptidyl Peptidase IVInhibitor for the Treatment of Type 2 Diabetes
An Unusual IntramolecularHetero-Diels−Alder Cycloaddition
Design, Synthesis, and Biological Activity of5,10-Dihydro-dibenzo[b,e][1,4]diazepin-11-one-Based Potent and Selective Chk-1 Inhibitors
Species Specificity of Amidine-Based Urokinase Inhibitors
Identification of Novel Binding Interactions in the Development of Potent,Selective 2-Naphthamidine Inhibitors of Urokinase. Synthesis, StructuralAnalysis, and SAR of N-Phenyl Amide 6-Substitution
Novel Transient Receptor Potential Vanilloid 1 Receptor Antagonists for theTreatment of Pain: Structure−Activity Relationships for Ureas with Quinoline,Isoquinoline, Quinazoline, Phthalazine, Quinoxaline, and Cinnoline Moieties
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of(5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IVInhibitors
3-Amino-benzo[d]isoxazoles as Novel Multitargeted Inhibitors of Receptor Tyrosine Kinases
Crystal Structures of DPP-IV (CD26) from Rat Kidney Exhibit FlexibleAccommodation of Peptidase-Selective Inhibitors
New Shapes in HIV protease inhibitors
Pharmacological and Functional Comparison of the Polo-like Kinase Family: Insight into Inhibitor and Substrate Specificity
A Novel, Picomolar Inhibitor of Human Immunodeficiency Virus Type 1Protease
Thienopyrimidine Ureas as Novel and Potent Multitargeted Receptor TyrosineKinase Inhibitors
Discovery of 2-[4-{{2-(2S,5R)-2-Cyano-5-ethynyl-1-pyrrolidinyl]-2-oxoethyl]amino]-4-methyl-1-piperidinyl]-4-pyridinecarboxylic Acid (ABT-279): A Very Potent, Selective,Effective, and Well-Tolerated Inhibitor of Dipeptidyl Peptidase-IV, Useful for the Treatment ofDiabetes
Structure-Based Design, Synthesis, and Biological Evaluation of Potent and SelectiveMacrocyclic Checkpoint Kinase 1 Inhibitors
Influenza Neuraminidase Inhibitors: Structure-Based Design of a Novel InhibitorSeries
Discovery, Structure−Activity Relationship, and Pharmacological Evaluation of (5-Substituted-pyrrolidinyl-2-carbonyl)-2-cyanopyrrolidines as Potent Dipeptidyl Peptidase IV Inhibitors.
Discovery and Structure−Activity Relationships of Piperidinone- and Piperidine-ConstrainedPhenethylamines as Novel, Potent, and Selective Dipeptidyl Peptidase IV Inhibitors
Discovery of N-(4-(3-Amino-1H-indazol-4-yl)phenyl)-N‘-(2-fluoro-5-methylphenyl)urea(ABT-869), a 3-Aminoindazole-Based Orally Active Multitargeted Receptor Tyrosine KinaseInhibitor
7-Aminopyrazolo[1,5-a]pyrimidines as Potent Multitargeted Receptor Tyrosine Kinase Inhibitors
Structure-Based Characterization and Optimization of Novel HydrophobicBinding Interactions in a Series of Pyrrolidine Influenza NeuraminidaseInhibitors
Host-guest complexation. 42. Preorganization strongly enhances the tendancy of hemispherands to form hemispheraplexes
The catalytic oxidation of dithiols by a semisynthetic enzyme
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