science
plus
.abes.fr
|
explorer
À propos de :
Melchiorre Carlo
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
foaf:Person
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
Person
New Facet based on Instances of this Class
Attributs
Valeurs
type
Person
name
Melchiorre Carlo
familyName
Melchiorre
Given name
Carlo
is
relates
of
http://hub.abes.fr/acs/periodical/jmcmar/1988/volume_31/issue_9/101021jm00117a030/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1974/volume_17/issue_4/101021jm00250a019/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28/issue_11/101021jm00149a017/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/1988/volume_31/issue_12/101021jm00120a009/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_1/101021jm00121a017/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1994/volume_37/issue_20/101021jm00046a021/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1977/volume_20/issue_3/101021jm00213a016/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_9/101021jm011067f/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_22/101021jm8009684/authorship/12
http://hub.abes.fr/acs/periodical/joceah/1974/volume_39/issue_20/101021jo00934a026/authorship/3
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_20/101021jm070559a/authorship/16
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_7/101021jm800210c/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_15/101021jm020835f/authorship/11
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_23/101021jm0608762/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_1/101021jm000991r/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_26/101021jm0494366/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_26/101021jm701225u/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_8/101021jm011066n/authorship/11
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_24/101021jm0155594/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_15/101021jm800577j/authorship/14
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_23/101021jm030952q/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_1/101021jm049156q/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_1/101021jm049153d/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_3/101021jm000995w/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2003/volume_46/issue_6/101021jm021055/authorship/11
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_17/101021jm800637b/authorship/5
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_2/101021jm049112h/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_24/101021jm049782n/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_3/101021jm7009364/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_23/101021jm00075a032/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1984/volume_27/issue_12/101021jm00378a001/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1987/volume_30/issue_1/101021jm00384a034/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1989/volume_32/issue_1/101021jm00121a011/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1990/volume_33/issue_11/101021jm00173a004/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_11/101021jm00063a002/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/1993/volume_36/issue_6/101021jm00058a005/authorship/7
http://hub.abes.fr/acs/periodical/joceah/1975/volume_40/issue_15/101021jo00903a025/authorship/2
http://hub.abes.fr/acs/periodical/jmcmar/1978/volume_21/issue_11/101021jm00209a007/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1985/volume_28/issue_9/101021jm00147a042/authorship/5
http://hub.abes.fr/springer/periodical/210/1995/volume_352/issue_3/B962FC631366585BE053120B220A4B9B/authorship/4
is
Author
of
Cholinergic compounds. 9. Cyclohexane analogs of deoxamuscarine and derivatives
Differential blockade of muscarinic receptor subtypes by polymethylene tetraamines. Novel class of selective antagonists of cardiac M-2 muscarinic receptors
2-[[[2-(2,6-Dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzoxathian: a new antagonist with high potency and selectivity towards .alpha.1-adrenoreceptors
Structure-activity relationships in 1,4-benzodioxan-related compounds. 4. Effect of aryl and alkyl substituents at position 3 on .alpha.-adrenoreceptor blocking activity
Synthesis and identification by shift reagents of isomeric 2-methyl-2-n-propylcyclopentane-1,3-diols
Structure-activity relationships among methoctramine-related polymethylenetetramines. Chain length and substituent effects on M-2 muscarinic receptor blocking activity
Structure-activity relationships in 1,4-benzodioxan related compounds. 3. 3-Phenyl analogs of 2-[[[2-(2,6-dimethoxyphenoxy)ethyl]amino]methyl]-1,4-benzodioxan (WB 4101) as highly selective .alpha.1-adrenoreceptor antagonists
Cyclopentane analog of muscarone
Structure-activity relationships among benextramine-related tetraamine disulfides at peripheral .alpha.-adrenoreceptors
Synthesis and biological activity of some methoctramine-related tetraamines bearing an 11-acetyl-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one moiety as antimuscarinics: a second generation of highly selective M2 muscarinic receptor antagonists
Structure-activity relationships among benextramine-related tetraamine disulfides. Chain length effect on .alpha.-adrenoreceptor blocking activity
Design, Synthesis, and BiologicalEvaluation of Prazosin-RelatedDerivatives as Multipotent Compounds
Structure−Activity Relationships of Acetylcholinesterase NoncovalentInhibitors Based on a Polyamine Backbone. 3. Effect of Replacing the InnerPolymethylene Chain with Cyclic Moieties
Structure−Activity Relationships of Methoctramine-Related Polyamines asMuscular Nicotinic Receptor Noncompetitive Antagonists. 3. Effect of Insertingthe Tetraamine Backbone into a Macrocyclic Structure
Novel Class of Quinone-Bearing Polyamines as Multi-Target-Directed Ligands To CombatAlzheimer's Disease
Multi-Target-Directed Ligands To Combat Neurodegenerative Diseases
Design, Synthesis, and Biological Activityof Methoctramine-Related Polyamines asPutative Gi Protein Activators
Prazosin-Related Compounds. Effect of Transforming thePiperazinylquinazoline Moiety into an Aminomethyltetrahydroacridine Systemon the Affinity for α1-Adrenoreceptors
Design, Synthesis, and Biological Evaluation of Conformationally RestrictedRivastigmine Analogues
Structure−Activity Relationships in 1,4-Benzodioxan-Related Compounds. 7.Selectivity of 4-Phenylchroman Analogues for α1−Adrenoreceptor Subtypes
Structure−Activity Relationships of Acetylcholinesterase NoncovalentInhibitors Based on a Polyamine Backbone. 2. Role of the Substituents on thePhenyl Ring and Nitrogen Atoms of Caproctamine
Rational Approach To DiscoverMultipotent Anti-Alzheimer Drugs
Multitarget-Directed Drug Design Strategy: A Novel Molecule Designed To Block EpidermalGrowth Factor Receptor (EGFR) andTo Exert Proapoptotic Effects
Multi-Target-Directed Drug Design Strategy: From a Dual Binding Site Acetylcholinesterase Inhibitor to a Trifunctional Compound against Alzheimer’s Disease
Inhibition of Acetylcholinesterase, β-Amyloid Aggregation, and NMDA Receptors in Alzheimer’s Disease: A Promising Direction for the Multi-target-Directed Ligands Gold Rush
Multi-target-Directed Ligands To Combat Neurodegenerative Diseases
Hexahydrochromeno[4,3-b]pyrrole Derivatives as AcetylcholinesteraseInhibitors
Analogues of Prazosin That Bear a Benextramine-Related Polyamine BackboneExhibit Different Antagonism toward α1-Adrenoreceptor Subtypes
Structure−Activity Relationships of Acetylcholinesterase Noncovalent Inhibitors Based on a Polyamine Backbone. 4. Further Investigation on the Inner Spacer
Propidium-Based Polyamine Ligands asPotent Inhibitors of Acetylcholinesteraseand Acetylcholinesterase-InducedAmyloid-β Aggregation
Parallel Synthesis and Cytotoxicity Evaluation of a Polyamine−Quinone Conjugates Library
Structure−Activity Relationships of Methoctramine-Related Polyamines asMuscular Nicotinic Receptor Noncompetitive Antagonists. 2. Role ofPolymethylene Chain Lengths Separating Amine Functions and of Substituentson the Terminal Nitrogen Atoms
Molecular properties of the adrenergic .alpha. receptor. 2. Optimum covalent inhibition by two different prototypes of polyamine disulfides
Structure-activity relationships for prazosin and WB 4101 analogs as .alpha.1-adrenoreceptor antagonists
Structure-activity relationships in 1,4-benzodioxan-related compounds. Investigation on the role of the dehydrodioxane ring on .alpha.1-adrenoreceptor blocking activity
Structure-activity relationships in prazosin-related compounds. Effect of replacing a piperazine ring with an alkanediamine moiety on .alpha.1-adrenoreceptor blocking activity
Design, Synthesis, and Biological Activity of Methoctramine-Related Tetraamines Bearing a 11-Acetyl-5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one Moiety: Structural Requirements for Optimum Occupancy of Muscarinic Receptor Subtypes As Revealed by Symmetrical and Unsymmetrical Polyamines
Selective blockade of muscarinic M2 receptors in vivo by the new antagonist tripitramine
Structure-activity relationships in prazosin-related compounds. 2. Role of the piperazine ring on .alpha.-blocking activity
Synthesis of methyloxocyclopentaneacetic acids
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata
