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http://hub.abes.fr/acs/periodical/joceah/1998/volume_63/issue_10/101021jo972051t/authorship/4
http://hub.abes.fr/acs/periodical/joceah/2001/volume_66/issue_16/101021jo010159/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2003/volume_68/issue_22/101021jo035062x/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_12/101021jm8001313/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2006/volume_71/issue_9/101021jo0600095/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_26/101021jm010949b/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2008/volume_73/issue_17/101021jo800769m/authorship/1
http://hub.abes.fr/acs/periodical/bichaw/2002/volume_41/issue_9/101021bi011652i/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_6/101021jm0496741/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_17/101021jm980620z/authorship/1
http://hub.abes.fr/acs/periodical/joceah/2005/volume_70/issue_5/101021jo0481046/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_23/101021jm060945c/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_24/101021jm000980y/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1983/volume_48/issue_24/101021jo00172a014/authorship/4
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Synthesis and PharmacologicalEvaluation of Huprine−TacrineHeterodimers: Subnanomolar DualBinding Site AcetylcholinesteraseInhibitors
3D Structure of Torpedo californica Acetylcholinesterase Complexed with HuprineX at 2.1 Å Resolution: Kinetic and Molecular Dynamic Correlates,
Synthesis of Several Halobisnoradamantane Derivatives and TheirReactivity through the SRN1 Mechanism
New Tacrine−Huperzine A Hybrids (Huprines): Highly Potent Tight-BindingAcetylcholinesterase Inhibitors of Interest for the Treatment of Alzheimer'sDisease
Binding of 13-Amidohuprines to Acetylcholinesterase: Exploring the Ligand-InducedConformational Change of the Gly117-Gly118 Peptide Bond in the Oxyanion Hole
Novel Donepezil-Based Inhibitors of Acetyl- and Butyrylcholinesterase and Acetylcholinesterase-Induced β-Amyloid Aggregation
Synthesis and Absolute Configuration of Novel N,O-Psiconucleosides Using (R)-N-Phenylpantolactam as a Resolution Agent
Synthesis, in Vitro Pharmacology, and Molecular Modeling of Very PotentTacrine−Huperzine A Hybrids as Acetylcholinesterase Inhibitors of PotentialInterest for the Treatment of Alzheimer's Disease
Generation and Reactions of Two NewFunctionalizedTricyclo[3.3.0.03,7]oct-1(5)-ene Derivatives
Synthesis, in Vitro Pharmacology, and Molecular Modeling of syn-Huprines asAcetylcholinesterase Inhibitors
Highly Diastereoselective One-Pot Synthesis ofSpiro{cyclopenta[a]indene-2,2‘-indene}diones from 1-Indanones andAromatic Aldehydes
π−π-Interactions in Pentacyclo-[8.2.1.1.2,51.4,718,11]hexadeca-1,7-diene
Application of empirical potential energy calculations to organic chemistry. Part 19. Conformational preference in 2,4-dimethoxybicyclo[3.3.1]nonan-9-one and related molecules. Analysis of vicinal NMR coupling constants in multiple rotor system by combined molecular mechanics and generalized Karplus equation
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