science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_9/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/1999/volume_42
has manifestation of work
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_9/m/print
http://hub.abes.fr/acs/periodical/jmcmar/1999/volume_42/issue_9/m/web
Date Copyrighted
1999
Rights
Copyright © 1999 American Chemical Society
issue
9
Rights Holder
American Chemical Society
is
Is Part Of
of
Synthesis of a Series of Stromelysin-Selective Thiadiazole Urea MatrixMetalloproteinase Inhibitors
Emerging Molecular Approaches to Pain Therapy
Design and Synthesis of Imidazoline Derivatives Active on Glucose Homeostasisin a Rat Model of Type II Diabetes. 2. Syntheses and Biological Activities of1,4-Dialkyl-, 1,4-Dibenzyl, and 1-Benzyl-4-alkyl-2-(4‘,5‘-dihydro-1‘H-imidazol-2‘-yl)piperazines and Isosteric Analogues of Imidazoline
Comparative Molecular Field Analysis of Hydantoin Binding to the NeuronalVoltage-Dependent Sodium Channel
Novel Potent and Selective Central 5-HT3 Receptor Ligands Provided withDifferent Intrinsic Efficacy. 2. Molecular Basis of the Intrinsic Efficacy ofArylpiperazine Derivatives at the Central 5-HT3 Receptors
Potent 1,3-Disubstituted-9H-pyrido[3,4-b]indoles as New Lead Compounds inAntifilarial Chemotherapy,
Substrate Specificity and Stereoselectivity of Rat BrainMicrosomal Anandamide Amidohydrolase
δ Opioid Affinity and Selectivity of 4-Hydroxy-3-methoxyindolomorphinanAnalogues Related to Naltrindole
Synthesis of 2,8-Disubstituted Imidazo[1,5-a]pyrimidines with Potent AntitumorActivity
Phytomedicines of Europe. Chemistry and Biological Activity. ACS Symposium Series 691 Edited by Larry D. Lawson and Rudolf Bauer. AmericanChemical Society, Washington, DC. 1998. x + 324 pp.15.5 × 23.5 cm. ISBN 0-8412-3559-7. $115.00.
Structure−Activity Relationships of Bisphosphate Nucleotide Derivatives asP2Y1 Receptor Antagonists and Partial Agonists
Medicinal Chemistry: Today and Tomorrow Edited by Mikio Yamazaki. International Union of Pureand Applied Chemistry, Blackwell Science Ltd., Oxford.1997. x + 278 pp. 19.5 × 23 cm. ISBN 0-632-04272-9.£55.00.
Designer Drugs Directory By Karel Valter andPhilippe Arrizabalaga. Edited by Jean-Claude Landry.Elsevier Science, Lausanne, Switzerland. 1998. 212 pp.17 x 25 cm. ISBN 0-444-20525-X. $154.00.
SQ: A Program for Rapidly Producing Pharmacophorically Relevent MolecularSuperpositions
Novel Approach To Predicting P450-Mediated Drug Metabolism: Developmentof a Combined Protein and Pharmacophore Model for CYP2D6
Potent Estrogenic Agonists BearingDicarba-closo-dodecaborane as aHydrophobic Pharmacophore
cycloSal-Pronucleotides of 2‘-Fluoro-ara- and 2‘-Fluoro-ribo-2‘,3‘-dideoxyadenosine as a Strategy to Bypass a Metabolic Blockade
Development of Fluorine-18-Labeled 5-HT1A Antagonists
Novel Derivatives of 2-Pyridinemethylamine as Selective, Potent, and OrallyActive Agonists at 5-HT1A Receptors
Cyclobutane Quisqualic Acid Analogues as Selective mGluR5a MetabotropicGlutamic Acid Receptor Ligands
Novel CDC25A Phosphatase Inhibitors from Pyrolysis of 3-α-Azido-B-homo-6-oxa-4-cholesten-7-one on Silica Gel
Agonist Selectivity of mGluR1 and mGluR2 Metabotropic Receptors: A DifferentEnvironment but Similar Recognition of an Extended Glutamate Conformation
cycloSal-Pronucleotides of 2‘,3‘-Dideoxyadenosine and2‘,3‘-Dideoxy-2‘,3‘-didehydroadenosine: Synthesis and Antiviral Evaluation of aHighly Efficient Nucleotide Delivery System
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata