science
plus
.abes.fr
|
explorer
À propos de :
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/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/2002/volume_45
has manifestation of work
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/m/print
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_25/m/web
Date Copyrighted
2002
Rights
Copyright © 2002 American Chemical Society
issue
25
Rights Holder
American Chemical Society
is
Is Part Of
of
A New Series of Estrogen Receptor Modulators That Display Selectivity forEstrogen Receptor β
Structural Studies on Hgr3 Orphan Receptor Ligand Prolactin-ReleasingPeptide
Relationships between Structure and Interaction Kinetics for HIV-1 ProteaseInhibitors
Syntheses and Structure−Activity Relationships of Nonnatural β-C-Nucleoside5‘-Triphosphates Bearing an Aromatic Nucleobase with Phenolic HydroxyGroups: Inhibitory Activities against DNA Polymerases
A Thymidine Phosphorylase-StableAnalogue of BVDU with SignificantAntiviral Activity
Crystal Structures of Dipeptides Containing the Dmt-Tic Pharmacophore
Antitumor Imidazotetrazines. 41. Conjugation of the Antitumor AgentsMitozolomide and Temozolomide to Peptides and Lexitropsins Bearing DNAMajor and Minor Groove-Binding Structural Motifs
Synthesis and Structure−Activity Relationships of Novel 7-Substituted1,4-Dihydro-4-oxo-1-(2-thiazolyl)-1,8-naphthyridine-3-carboxylic Acids asAntitumor Agents. Part 1
Synthesis and Antimycobacterial Activity of Pyrazine and QuinoxalineDerivatives
Discovery of 8-Hydroxyadenines as aNovel Type of Interferon Inducer
Potent δ-Opioid Receptor Agonists Containing the Dmt−Tic Pharmacophore
Enzymes. A Practical Introduction to Structure,Mechanism, and Data Analysis. Second Edition By Robert A. Copeland. Wiley-VCH, New York. 2000.xvi + 397 pp. 16 × 24.5 cm. ISBN 0-471-35929-7. $99.95.
QSAR Evaluation of the Ch'an Su and Related Bufadienolides against theColchicine-Resistant Primary Liver Carcinoma Cell Line PLC/PRF/5
Design and Synthesis of Dipeptide Nitriles as Reversible and Potent CathepsinS Inhibitors
Probing the Cysteine-34 Position of Endogenous Serum Albumin withThiol-Binding Doxorubicin Derivatives. Improved Efficacy of an Acid-SensitiveDoxorubicin Derivative with Specific Albumin-Binding Properties Compared toThat of the Parent Compound
Comparative Molecular Field Analysis of Substrates for an ArylSulfotransferase Based on Catalytic Mechanism and Protein HomologyModeling
Structural Basis for Understanding Structure−Activity Relationships for the Glutamate BindingSite of the NMDA Receptor.
Telomerase Inhibition, TelomereShortening, and Decreased CellProliferation by Cell Permeable2‘-O-Methoxyethyl Oligonucleotides
Pyrimidoquinazoline-Based Antitumor Agents. Design of Topoisomerase II toDNA Cross-linkers with Activity against Protein Kinases
Antitumor Imidazotetrazines. 40. Radiosyntheses of [4-11C-Carbonyl]- and[3-N-11C-Methyl]-8-carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one(Temozolomide) for Positron Emission Tomography (PET) Studies
Improving the Oral Efficacy of CNS DrugCandidates: Discovery of Highly OrallyEfficacious Piperidinyl Piperidine M2Muscarinic Receptor Antagonists
Use of ab Initio Calculations To Predict the Biological Potency ofCarboxylesterase Inhibitors
Perfluorooctyl Bromide Has Limited Membrane Solubility and Is Located at theBilayer Center. Locating Small Molecules in Lipid Bilayers throughParamagnetic Enhancements of NMR Relaxation
Alternative Linked Data Documents:
ODE
Content Formats:
RDF
ODATA
Microdata