Amanote Research
Register
Sign In
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
doi 10.1021/acs.jmedchem.5b01998.s004
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
Purine (N)Methanocarba Nucleoside Derivatives Lacking an Exocyclic Amine as Selective A3 Adenosine Receptor Agonists
2-Dialkynyl Derivatives of (N)-Methanocarba Nucleosides: ‘Clickable’ A3 Adenosine Receptor-Selective Agonists
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Direct Comparison of (N)-Methanocarba and Ribose-Containing 2Arylalkynyladenosine Derivatives as A3 Receptor Agonists
Orthogonal Activation of the Reengineered A3 Adenosine Receptor (Neoceptor) Using Tailored Nucleoside Agonists
Tricyclic Imidazoline Derivatives as Potent and Selective Adenosine A1 Receptor Antagonists
Exploring Distal Regions of the A3 Adenosine Receptor Binding Site: Sterically Constrained N6-(2-Phenylethyl)adenosine Derivatives as Potent Ligands
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Purine Excretion by Mouse Peritoneal Macrophages Lacking Adenosine Deaminase Activity.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Radiolabeling and Efficient Synthesis of Tritiated 2-Chloro-N6-(3-Iodobenzyl)adenosine-5′-N-Methyluron-Amide, a Potent, Selective A3 Adenosine Receptor Agonist
Journal of Labelled Compounds and Radiopharmaceuticals
Organic Chemistry
Nuclear Medicine
Radiology
Biochemistry
Analytical Chemistry
Imaging
Spectroscopy
Drug Discovery
Design of an Adenosine Phosphorylase by Active-Site Modification of Murine Purine Nucleoside Phosphorylase
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
