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http://hub.abes.fr/acs/periodical/cmatex/2008/volume_20/issue_19/101021cm801335j/authorship/3
http://hub.abes.fr/acs/periodical/ancham/2005/volume_77/issue_2/101021ac048485n/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_26/101021jm058261c/authorship/6
http://hub.abes.fr/acs/periodical/jnprdf/2006/volume_69/issue_6/101021np060094b/authorship/9
http://hub.abes.fr/acs/periodical/joceah/2004/volume_69/issue_16/101021jo040159k/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_15/101021jm070393d/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_9/101021jm049031l/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_11/101021jm060122n/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_15/101021jm060287w/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/101021jm020330p/authorship/4
http://hub.abes.fr/acs/periodical/orgnd7/2007/volume_26/issue_9/101021om060898m/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_2/101021jm0608614/authorship/7
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_5/101021jo020704m/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_28/101021ja052604e/authorship/8
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_15/101021ja077620l/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_12/101021jm034249d/authorship/4
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http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_20/101021jm050135l/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_14/101021jm058175c/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_3/101021jm050700k/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_13/101021jm8000482/authorship/8
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http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_19/101021jm800532x/authorship/4
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http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_15/101021ja042258l/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/2005/volume_127/issue_29/101021ja051147z/authorship/12
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http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_14/101021jm0601699/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_16/101021jm061325e/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_24/101021jm800913d/authorship/8
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http://hub.abes.fr/acs/periodical/jacsat/1996/volume_118/issue_5/101021ja952964/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_19/101021ja0688732/authorship/8
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Further Structural Exploration of Trisubstituted Asymmetric Pyran Derivatives(2S,4R,5R)-2-Benzhydryl-5-benzylamino-tetrahydropyran-4-ol and Their CorrespondingDisubstituted (3S,6S) Pyran Derivatives: A Proposed Pharmacophore Model for High-AffinityInteraction with the Dopamine, Serotonin, and Norepinephrine Transporters
Probes for Narcotic Receptor Mediated Phenomena. 37. Synthesis and Opioid Binding Affinity of the Final Pair of Oxide-Bridged Phenylmorphans, the Ortho- and Para-b-Isomers and Their N-Phenethyl Analogues, and the Synthesis of the N-Phenethyl Analogues of the Ortho- and Para-d-Isomers
General Approach for the Synthesis of Sarpagine Indole Alkaloids.Enantiospecific Total Synthesis of (+)-Vellosimine,(+)-Normacusine B, (−)-Alkaloid Q3, (−)-Panarine,(+)-Na-Methylvellosimine, and (+)-Na-Methyl-16-epipericyclivine
Enantiospecific Synthesis of (+)-Alstonisine via a Stereospecific Osmylation Process
Structure-Based Design of Potent Non-Peptide MDM2 Inhibitors
Adamantyl Cannabinoids: A Novel Class of Cannabinergic Ligands
N-Substituted cis-4a-(3-Hydroxyphenyl)-8a-methyloctahydroisoquinolines AreOpioid Receptor Pure Antagonists
Chemistry of the Diazeniumdiolates. O- versus N-Alkylation ofthe RNH[N(O)NO]- Ion
Crystal Structures of Dipeptides Containing the Dmt-Tic Pharmacophore
Synthetic Studies of Neoclerodane Diterpenes from Salvia divinorum: Preparation andOpioid Receptor Activity of Salvinicin Analogues
Design and Comprehensive Conformational Studies ofTyr1-cyclo(d-Pen2-Gly3-Phe4-l-3-Mpt5) andTyr1-cyclo(d-Pen2-Gly3-Phe4-d-3-Mpt5): NovelConformationally Constrained Opioid Peptides
Sculpting the Bicyclo[3.1.0]hexane Template of CarbocyclicNucleosides to Improve Recognition by Herpes ThymidineKinase
Conformational Analysis of the cis- and trans-Adducts of the Pictet−Spengler Reaction.Evidence for the Structural Basis for the C(1)−N(2) Scission Process in the cis- totrans-Isomerization
A Hybrid Quantum Dot−Antibody Fragment FluorescenceResonance Energy Transfer-Based TNT Sensor
Functionalization of the 6,14-Bridge of theOrvinols. 2.1 Preparation of 18- and19-Hydroxyl-Substituted Thevinols andTheir Treatment with Benzyl Bromide
A Virtual Screen for Diverse Ligands: Discovery of Selective G Protein-Coupled Receptor Antagonists
Synthesis, in Vitro Affinity, and Efficacyof a Bis 8-Ethynyl-4H-imidazo[1,5a]-[1,4]benzodiazepine Analogue, the FirstBivalent α5 Subtype Selective BzR/GABAA Antagonist
Chemistry of the Diazeniumdiolates: Z ⇌ E Isomerism
Ru2(ap)4(σ-oligo(phenyleneethynyl)) Molecular Wires: Synthesis andElectronic Characterization
Potent Cannabinergic Indole Analogues as Radioiodinatable Brain ImagingAgents for the CB1 Cannabinoid Receptor
Enantiomerically Pure Hexahydropyrazinoquinolines as Potent and SelectiveDopamine 3 Subtype Receptor Ligands
Synthesis and Pharmacological Characterization of Nicotinic Acetylcholine Receptor Propertiesof (+)- and (−)-Pyrido-[3,4-b]homotropanes
Synthesis and Monoamine Transporter Binding Properties of 2,3-Cyclo Analogues of3β-(4‘-Aminophenyl)-2β-tropanemethanol
1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) Analogues: A PromisingClass of Monoamine Uptake Inhibitors
Probes for Narcotic Receptor Mediated Phenomena. 34. Synthesis and Structure−ActivityRelationships of a Potent μ-Agonist δ-Antagonist and an Exceedingly Potent Antinociceptive inthe Enantiomeric C9-Substituted 5-(3-Hydroxyphenyl)-N-phenylethylmorphan Series
Organometallic Supramolecular Mixed-Valence Cobalt(I)/Cobalt(II)Aquo Complexes Stabilized with the Water-Soluble PhosphineLigand p-TPPTP (p-triphenylphosphine triphosphonic acid)
Molecular Packing in Electroclinic Liquid Crystal Elastomer Films
Slow-Onset, Long-Duration, Alkyl Analogues of Methylphenidate with Enhanced Selectivity forthe Dopamine Transporter
Hydrolytic Reactivity Trends among Potential Prodrugs of the O2-Glycosylated Diazeniumdiolate Family. Targeting Nitric Oxide to Macrophages for Antileishmanial Activity
Synthesis of Salvinorin A Analogues as Opioid Receptor Probes
Novel Anticholinesterases Based on the Molecular Skeletons of Furobenzofuranand Methanobenzodioxepine
PABA/NO as an Anticancer Lead: Analogue Synthesis, Structure Revision, Solution Chemistry,Reactivity toward Glutathione, and in Vitro Activity
A Novel Series ofPiperidin-4-yl-1,3-Dihydroindol-2-ones asAgonist and Antagonist Ligands at theNociceptin Receptor
Probes for Narcotic Receptor-Mediated Phenomena. 33.1Construction of a Strained trans-5,6-Ring System by Displacementof a Nitro-Activated Aromatic Fluorine. Synthesis of thePenultimate Oxide-Bridged Phenylmorphans
Conformationally Constrained Analogues of Diacylglycerol. 29. Cells Sort Diacylglycerol-Lactone Chemical Zip Codes to Produce Diverse and Selective Biological Activities
Structure−Activity Relationships for a Novel Series of Dopamine D2-like Receptor Ligands Based on N-Substituted 3-Aryl-8-azabicyclo[3.2.1]octan-3-ol
Self-Assembled TNT Biosensor Based on ModularMultifunctional Surface-Tethered Components
Further Structurally Constrained Analogues ofcis-(6-Benzhydrylpiperidin-3-yl)benzylamine with Elucidation of BioactiveConformation: Discovery of 1,4-Diazabicyclo[3.3.1]nonane Derivatives andEvaluation of Their Biological Properties for the Monoamine Transporters
Rearrangement of 5-Trimethylsilylthebaine on Treatment withL-Selectride: An Efficient Synthesis of (+)-Bractazonine
X-ray structures of the δ opioid antagonist TIPP and a protected derivative of the δ opioid antagonist ICI 174,864
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