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            <title>Contribution of Phosphates
and Adenine to the Potency
of Adenophostins at the IP3 Receptor: Synthesis of All
Possible Bisphosphates of Adenophostin A</title>
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            <title>Minimization of Human Relaxin-3
Leading to High-Affinity Analogues with Increased Selectivity for
Relaxin-Family Peptide 3 Receptor (RXFP3) over RXFP1</title>
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            <title>Pyridone Methylsulfone
Hydroxamate LpxC Inhibitors for the Treatment of Serious Gram-Negative
Infections</title>
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            <title>Aberrant Cyclization Affords
a C-6 Modified Cyclic Adenosine 5′-Diphosphoribose Analogue
with Biological Activity in Jurkat T Cells</title>
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            <title>3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: A Novel Template
for the Design of Highly Selective
A2B Adenosine Receptor Antagonists</title>
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            <title>Structure–Activity
Relationship of Novel Menaquinone-4 Analogues: Modification of the
Side Chain Affects their Biological Activities</title>
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            <title>A Tribute to Joseph G.
Cannon, 1926–2011</title>
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            <description>Journal of Medicinal ChemistryDOI: 10.1021/jm300081m (Source: Journal of Medicinal Chemistry)</description>
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            <title>Synthesis and Biological
Activity of 6-Substituted
Pyrrolo[2,3-d]pyrimidine Thienoyl Regioisomers as
Inhibitors of de Novo Purine Biosynthesis with Selectivity for Cellular
Uptake by High Affinity Folate Receptors and the Proton-Coupled Folate
Transporter over the Reduced Folate Carrier</title>
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            <title>5-Imino-1,2,4-Thiadiazoles:
First Small Molecules
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            <title>Homobivalent Ligands of
the Atypical Antipsychotic
Clozapine: Design, Synthesis, and Pharmacological Evaluation</title>
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            <description>Journal of Medicinal ChemistryDOI: 10.1021/jm201420s (Source: Journal of Medicinal Chemistry)</description>
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            <title>Correction to Malaria-Infected
Mice Are Completely Cured by One 6 mg/kg Oral Dose of a New Monomeric
Trioxane Sulfide Combined with Mefloquine</title>
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            <title>1,4-Dioxane, a Suitable
Scaffold for the Development
of Novel M3 Muscarinic Receptor Antagonists</title>
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            <title>3-Fluoro- and 3,3-Difluoro-3,4-dideoxy-KRN7000
Analogues as New Potent Immunostimulator Agents: Total Synthesis and
Biological Evaluation in Human Invariant Natural Killer T Cells and
Mice</title>
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            <description>Journal of Medicinal ChemistryDOI: 10.1021/jm201368m (Source: Journal of Medicinal Chemistry)</description>
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            <title>[1,2,4]Triazol-3-ylsulfanylmethyl)-3-phenyl-[1,2,4]oxadiazoles:
Antagonists of the Wnt Pathway That Inhibit Tankyrases 1 and 2 via
Novel Adenosine Pocket Binding</title>
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            <description>Journal of Medicinal ChemistryDOI: 10.1021/jm2011222 (Source: Journal of Medicinal Chemistry)</description>
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            <title>Trivalent Ultrashort Lipopeptides
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Antifungal Agents</title>
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            <title>Ligand-Based Design of
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            <title>Synthesis and Toxicopharmacological
Evaluation of m-Hydroxymexiletine, the First Metabolite
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More Potent Than the Parent Compound on Voltage-Gated Sodium Channels</title>
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            <title>The 1.8 Å Crystal
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a Mode of Action for T2 Ribonucleases As Antitumorigenic Agents</title>
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            <title>A Synthetic Chalcone as
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            <title>Diverse Heterocyclic Scaffolds
as Allosteric Inhibitors
of AKT</title>
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            <title>Discovery of 1,2,4-Triazine
Derivatives as Adenosine
A2A Antagonists using Structure Based Drug Design</title>
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            <title>Discovery and Structure–Activity
Relationship
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for Huntington’s Disease</title>
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Efflux Implications for Drug Discovery</title>
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Hybrids as Multifunctional Agents for the Treatment of Alzheimer’s
Disease, with Cholinergic, Antioxidant, and β-Amyloid-Reducing
Properties</title>
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            <title>Directed R-Group Combination
Graph: A Methodology
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of Analogues</title>
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