science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_20/w
Goto
Sponge
NotDistinct
Permalink
An Entity of Type :
bibo:Issue
, within Data Space :
scienceplus.abes.fr
associated with source
document(s)
Type:
work
Issue
New Facet based on Instances of this Class
Attributs
Valeurs
type
work
Issue
Is Part Of
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38
has manifestation of work
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_20/m/print
http://hub.abes.fr/acs/periodical/jmcmar/1995/volume_38/issue_20/m/web
issue
20
is
Is Part Of
of
Synthesis and Antiviral Activity of 8-Aza Analogs of Chiral [2-(Phosphonomethoxy)propyl]guanines
Pyrazinoic Acid Esters with Broad Spectrum in Vitro Antimycobacterial Activity
Synthesis of Tight Binding Inhibitors and Their Action on the Proprotein-Processing Enzyme Furin
Masthead
A New Paclitaxel Photoaffinity Analog with a 3-(4-Benzoylphenyl)propanoyl Probe for Characterization of Drug-Binding Sites on Tubulin and P-Glycoprotein
Pseudodipeptide Inhibitors of Protein Farnesyltransferase
Synthesis and Evaluation of Certain Thiosangivamycin Analogs as Potential Inhibitors of Cell Proliferation and Human Cytomegalovirus
Development of a Potent Thrombin Receptor Ligand
Design, synthesis, and structure-activity Relationships of a new series of .alpha.-adrenergic agonists: spiro[(1,3-diazacycylpent-1-ent)-5,2'-(1',2',3',4'-tetrahydronaphthalene)]
Novel Deltorphin Heptapeptide Analogs with Potent .delta. Agonist, .delta. Antagonist, or Mixed .mu. Antagonist/.delta. Agonist Properties
Mononucleoside Phosphotriester Derivatives with S-Acyl-2-thioethyl Bioreversible Phosphate-Protecting Groups: Intracellular Delivery of 3'-Azido-2',3'-dideoxythymidine 5'-Monophosphate
Cyclization-Activated Prodrugs: N-(Substituted 2-hydroxyphenyl and 2-hydroxypropyl)carbamates Based on Ring-Opened Derivatives of Active Benzoxazolones and Oxazolidinones as Mutual Prodrugs of Acetaminophen
Ribose-Modified Adenosine Analogs as Potential Partial Agonists for the Adenosine Receptor
Synthesis and Biological Evaluation of N6-Cycloalkyl Derivatives of 1-Deazaadenine Nucleosides: A New Class of Anti-Human Immunodeficiency Virus Agents
New Antihistamines: Substituted Piperazine and Piperidine Derivatives as Novel H1-Antagonists
In Vivo and in Vitro Studies on the Neurotoxic Potential of 6-Hydroxydopamine Analogs
Antiinflammatory 4,5-Diarylpyrroles. 2. Activity as a Function of Cyclooxygenase-2 Inhibition
Resolution and in Vitro and Initial in Vivo Evaluation of Isomers of Iodine-125-Labeled 1-Azabicyclo[2.2.2]oct-3-yl .alpha.-Hydroxy-.alpha.-(1-iodo-1-propen-3-yl)-.alpha.-phenylacetate: A High-Affinity Ligand for the Muscarinic Receptor
Synthesis and Antiproliferative and Antiviral Activity of 2'-Deoxy-2'-fluoroarabinofuranosyl Analogs of the Nucleoside Antibiotics Toyocamycin and Sangivamycin
Synthesis and Antimalarial Activities of Several Fluorinated Artemisinin Derivatives
1-(Fluorobenzyl)-4-amino-1H-1,2,3-triazolo[4,5-c]pyridines: Synthesis and Anticonvulsant Activity
Book Reviews
A Molecular Dynamics Approach to Receptor Mapping: Application to the 5HT3 and .beta.2-Adrenergic Receptors
Peptidyl .alpha.-ketoheterocyclic inhibitors of human neutrophil elastase. 3. In vitro and in vivo potency of a series of peptidyl .alpha.-ketobenzoxazoles
Characterization of Potent and Selective Antagonists at Postsynaptic 5-HT1A Receptors in a Series of N4-Substituted Arylpiperazines
Novel 4'-Substituted and 4',4''-Disubstituted 3.alpha.-(Diphenylmethoxy)tropane Analogs as Potent and Selective Dopamine Uptake Inhibitors
Chiral Dioxolane Inhibitors of Leukotriene Biosynthesis: Structure-Activity Relationships and Syntheses Using Asymmetric Dihydroxylation
Synthesis and Antifungal Activity of New Azole Derivatives Containing an N-Acylmorpholine Ring
Synthesis and Anti-DNA Viral Activities in Vitro of Certain 2,4-Disubstituted- 7-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)pyrrolo[2,3-d]pyrimidine Nucleosides
Probing the Hydrophobic Pocket of the Active Site of Aromatase with 4-Phenoxy-7.alpha.-(phenylthio)-4-androstene-3,17-dione
Synthesis, X-ray Crystallography, and Pharmacokinetics of Novel Azomethine Prodrugs of (R)-.alpha.-Methylhistamine: Highly Potent and Selective Histamine H3 Receptor Agonists
Design, Synthesis, and Antiviral Activity of Certain 2,5,6-Trihalo-1-(.beta.-D-ribofuranosyl)benzimidazoles
Synthesis and Anticonvulsant Activity of Enaminones. 3. Investigations on 4'-, 3'-, and 2'-Substituted and Polysubstituted Anilino Compounds, Sodium Channel Binding Studies, and Toxicity Evaluations1,2
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata