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Adenosine and 2′‐Deoxyadenosine Modified with Boron Cluster Pharmacophores as New Classes of Human Blood Platelet Function Modulators
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0471142700.nc0437s38openalex-snapshot
Nucleoside Modification with Boron Clusters and Their Metal Complexes
inferredcites →https://doi.org/10.1002/chem.200600740openalex-snapshot
Nucleoside–Metallacarborane Conjugates for Base‐Specific Metal Labeling of DNA
inferredcites →https://doi.org/10.1016/0049-3848(87)90172-1openalex-snapshot
Evidence for an anti-aggregatory effect of adenosine at physiological concentrations and for its role in the action of dipyridamole
inferredcites →https://doi.org/10.1016/0049-3848(89)90294-6openalex-snapshot
Rapid photometric method for estimation of platelet count in blood plasma or platelet suspension
inferredcites →https://doi.org/10.1016/0049-3848(95)93881-yopenalex-snapshot
Platelet aggregation monitored in a 96 well microplate reader is useful for evaluation of platelet agonists and antagonists
inferredcites →https://doi.org/10.1016/0076-6879(89)69045-3openalex-snapshot
[1] Isolation of human platelets from plasma by centrifugation and washing
inferredcites →https://doi.org/10.1016/j.bcp.2004.06.011openalex-snapshot
2-Substituted adenosine derivatives: affinity and efficacy at four subtypes of human adenosine receptors
inferredcites →https://doi.org/10.1016/j.bmc.2003.12.041openalex-snapshot
Synthesis and biological activity of 2-alkylated deoxyadenosine bisphosphate derivatives as P2Y1 receptor antagonists
inferredcites →https://doi.org/10.1016/j.cardiores.2004.11.008openalex-snapshot
Adenosine-mediated cardioprotection in the aging myocardium
inferredcites →https://doi.org/10.1016/j.it.2003.11.003openalex-snapshot
Adenosine: an endogenous regulator of innate immunity
inferredcites →https://doi.org/10.1016/j.pharmthera.2005.04.013openalex-snapshot
Adenosine 5′-triphosphate and adenosine as endogenous signaling molecules in immunity and inflammation
inferredcites →https://doi.org/10.1016/j.tetlet.2005.04.046openalex-snapshot
General method for the synthesis of 2′-O-carboranyl-nucleosides
inferredcites →https://doi.org/10.1016/s0010-8545(00)00262-9openalex-snapshot
Metallacarboranes in the new millennium
inferredcites →https://doi.org/10.1016/s0010-8545(02)00087-5openalex-snapshot
The medicinal chemistry of carboranes
inferredcites →https://doi.org/10.1016/s0014-2999(98)00461-0openalex-snapshot
Modulation of the chemotactic peptide- and immunoglobulin G-triggered respiratory burst in human neutrophils by exogenous and endogenous adenosine
inferredcites →https://doi.org/10.1016/s0049-3848(01)00412-1openalex-snapshot
Adenosine increases human platelet levels of 3′,5′-cGMP through nitric oxide
inferredcites →https://doi.org/10.1016/s0960-894x(01)00438-3openalex-snapshot
Utility of boron clusters for drug design. Hansch–fujita hydrophobic parameters π of dicarba-closo-dodecaboranyl groups
inferredcites →https://doi.org/10.1016/s0968-0896(98)00038-8openalex-snapshot
Adenosine receptors: new opportunities for future drugs
inferredcites →https://doi.org/10.1021/ic00117a018openalex-snapshot
Iodination Reactions of Icosahedral para-Carborane and the Synthesis of Carborane Derivatives with Boron-Carbon Bonds
inferredcites →https://doi.org/10.1021/jm049029uopenalex-snapshot
Design, Synthesis, and Antiviral Activity of Adenosine 5‘-Phosphonate Analogues as Chain Terminators against Hepatitis C Virus
inferredcites →https://doi.org/10.1021/jm9707737openalex-snapshot
2‘-C-Methyl Analogues of Selective Adenosine Receptor Agonists: Synthesis and Binding Studies
inferredcites →https://doi.org/10.1023/a:1005756929011openalex-snapshot
Chemistry and biology of some low molecular weight boron compounds for Boron Neutron Capture Therapy
inferredcites →https://doi.org/10.1038/nrd1983openalex-snapshot
Adenosine receptors as therapeutic targets
inferredcites →https://doi.org/10.1038/sj.bjp.0703045openalex-snapshot
A2A adenosine receptors in human peripheral blood cells
inferredcites →https://doi.org/10.1053/euhj.2000.2515openalex-snapshot
Platelet activation: assessment and quantification
inferredcites →https://doi.org/10.1080/15257770701548733openalex-snapshot
2′-Deoxyadenosine Bearing Hydrophobic Carborane Pharmacophore
inferredcites →https://doi.org/10.1093/cvr/27.1.18openalex-snapshot
Role of adenosine and its interaction with adrenoceptor activity in ischaemic and reperfusion injury of the myocardium
inferredcites →https://doi.org/10.1093/jac/dkg405openalex-snapshot
Ribavirin, viramidine and adenosine-deaminase-catalysed drug activation: implication for nucleoside prodrug design
inferredcites →https://doi.org/10.1097/00001813-200206000-00001openalex-snapshot
A3 adenosine receptor as a target for cancer therapy
inferredcites →https://doi.org/10.1111/j.1474-8673.1996.tb00051.xopenalex-snapshot
Purinoceptors and platelet aggregation
inferredcites →https://doi.org/10.1135/cccc20071646openalex-snapshot
Boron Units as Pharmacophores - New Applications and Opportunities of Boron Cluster Chemistry
inferredcites →https://doi.org/10.1139/v73-569openalex-snapshot
The tert-Butyldimethylsilyl Group as a Protecting Group in Deoxynucleosides
inferredcites →https://doi.org/10.1152/jappl.1994.76.1.5openalex-snapshot
Adenosine, an endogenous anti-inflammatory agent
inferredcites →https://doi.org/10.1161/01.cir.85.3.893openalex-snapshot
Protective effects of adenosine in myocardial ischemia.
inferredcites →https://doi.org/10.1248/cpb.18.2441openalex-snapshot
Studies of Nucleosides and Nucleotides. XLIV. Purine Cyclonucleosides. (2). Synthesis of Cyclonucleosides having 8, 3'-O- and -S-Anhydro Linkage derived from 2'-Deoxyadenosine
inferredcites →https://doi.org/10.2174/1568026033392200openalex-snapshot
Pharmacology of Adenosine A2A Receptors and Therapeutic Applications
inferredcites →https://doi.org/10.2174/1568026033392282openalex-snapshot
Medicinal Chemistry of Adenosine A2A Receptor Agonists
inferredcites →https://doi.org/10.3109/10428190009053539openalex-snapshot
Vidarabine and 2-Deoxycoformycin as Antileukemic Agents Against Monocytic Leukemia
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4489243openalex-extracted
Synthesis of Purine Conjugates with Bis-Carboranyl Derivatives of (S)-Lysine or (S)-Glutamic Acid
inferred← citeshttps://doi.org/10.2139/ssrn.4496950openalex-extracted
Synthesis of Purine Conjugates with Bis-Carboranyl Derivatives of (S)-Lysine or (S)-Glutamic Acid
inferred← citeshttps://doi.org/10.1002/9781119275602.ch1.2openalex-snapshot
Boron Cluster Modifications with Antiviral, Anticancer, and Modulation of Purinergic Receptors’ Activities Based on Nucleoside Structures
inferred← citeshttps://doi.org/10.1002/9781119275602.ch3.1openalex-snapshot
Twenty Years of Research on 3‐Carboranyl Thymidine Analogs (3CTAs)
inferred← citeshttps://doi.org/10.1002/cmdc.201200502openalex-snapshot
Synthesis and Biological Evaluation of Diaryl‐Substituted Carboranes as Inhibitors of Hypoxia Inducible Factor (HIF)‐1 Transcriptional Activity
inferred← citeshttps://doi.org/10.1002/ejoc.201201412openalex-snapshot
Efficient Synthesis of Thiolactoside Glycoclusters by Ruthenium‐Catalyzed Cycloaddition Reaction of Disubstituted Alkynes on Carbohydrate Scaffolds
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Synthesis of novel carborane-containing terminal alkynes
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Carboranes in medicine
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Carboranes in Medicine
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Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors
inferred← citeshttps://doi.org/10.1016/j.bmc.2012.09.039openalex-snapshot
Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils
inferred← citeshttps://doi.org/10.1016/j.bmc.2016.08.028openalex-snapshot
In vitro antileukemic activity of novel adenosine derivatives bearing boron cluster modification
inferred← citeshttps://doi.org/10.1016/j.bmcl.2014.05.010openalex-snapshot
Modulation of human neutrophil activity by adenosine modified with a carborane pharmacophore
inferred← citeshttps://doi.org/10.1016/j.ccr.2026.218206openalex-snapshot
Host–guest supramolecular chemistry of carboranes: structural features and emerging applications in nanotechnology and nanomedicine
inferred← citeshttps://doi.org/10.1016/j.ejmech.2021.113607openalex-snapshot
Synthesis and evaluation of adenosine derivatives as A1, A2A, A2B and A3 adenosine receptor ligands containing boron clusters as phenyl isosteres and selective A3 agonists
inferred← citeshttps://doi.org/10.1016/j.ejps.2017.09.036openalex-snapshot
Insight into lipophilicity of deoxyribonucleoside‑boron cluster conjugates
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2011.08.031openalex-snapshot
A convenient approach towards boron cluster modifications with adenosine and 2′-deoxyadenosine
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2015.06.027openalex-snapshot
Glycoconjugates of polyhedral boron clusters
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.02.009openalex-snapshot
Reactions of closo-dodecaborate amines. Towards novel bis-(closo-dodecaborates) and closo-dodecaborate conjugates with lipids and non-natural nucleosides
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2016.11.032openalex-snapshot
Direct C C coupling of phthalazine-N-oxide with the carboranyl anion – An original approach to C-modification of carboranes
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Insights into molecular structure of adenosine-boron cluster conjugates and theirs phenyl isosters as adenosine receptor ligands: Nuclear magnetic resonance, crystallographic and computational studies
inferred← citeshttps://doi.org/10.1016/j.tetlet.2023.154686openalex-snapshot
Synthesis of purine conjugates with bis-carboranyl derivatives of (S)-lysine or (S)-glutamic acid
inferred← citeshttps://doi.org/10.1016/j.vph.2018.11.005openalex-snapshot
Adenosine receptor agonists deepen the inhibition of platelet aggregation by P2Y12 antagonists
inferred← citeshttps://doi.org/10.1021/acs.jmedchem.5b01932openalex-snapshot
Challenges and Opportunities for the Application of Boron Clusters in Drug Design
inferred← citeshttps://doi.org/10.1021/ci200216zopenalex-snapshot
In Silico Carborane Docking to Proteins and Potential Drug Targets
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Carbaboranes as Pharmacophores: Properties, Synthesis, and Application Strategies
inferred← citeshttps://doi.org/10.1021/cr2000866openalex-snapshot
Boron in Drug Discovery: Carboranes as Unique Pharmacophores in Biologically Active Compounds
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Thiazolylaminomannosides As Potent Antiadhesives of Type 1 Piliated Escherichia coli Isolated from Crohn’s Disease Patients
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QM/MM Calculations Reveal the Different Nature of the Interaction of Two Carborane-Based Sulfamide Inhibitors of Human Carbonic Anhydrase II
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Carboranes in drug discovery, chemical biology and molecular imaging
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Interactions of Boron Clusters and their Derivatives with Serum Albumin
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“Carboranyl-cysteine”—Synthesis, Structure and Self-Assembly Behavior of a Novel α-Amino Acid
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Insights in the rational design of synthetic multivalent glycoconjugates as lectin ligands
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Boron and nucleic acid chemistries: merging the best of both worlds
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Nucleophilic addition reactions to the ethylnitrilium derivative of nido -carborane 10-EtCN-7,8-C 2 B 9 H 11
inferred← citeshttps://doi.org/10.1080/15257770.2013.838259openalex-snapshot
Phosphorylation of Nucleoside-Metallacarborane and Carborane Conjugates by Nucleoside Kinases
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Recent developments with boron as a platform for novel drug design
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Effects of Dual Purinoceptor-dependent Approach on Release of Vascular Endothelial Growth Factor From Human Microvascular Endothelial Cell (HMEC-1) and Endothelial Cell Condition
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Potential for modulation of platelet function via adenosine receptors during inflammation
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Physiologically Active Compounds Based on Membranotropic Cage Carriers–Derivatives of Adamantane and Polyhedral Boron Clusters (Review)
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New Opportunities in Boron Chemistry for Medical Applications
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The Use of Carboranes in Cancer Drug Development
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Molecular Modeling in Drug Design
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Interaction of Adenosine, Modified Using Carborane Clusters, with Ovarian Cancer Cells: A New Anticancer Approach against Chemoresistance
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Dimethyloxonium and Methoxy Derivatives of nido-Carborane and Metal Complexes Thereof
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Comparative Study of Carborane- and Phenyl-Modified Adenosine Derivatives as Ligands for the A2A and A3 Adenosine Receptors Based on a Rigid in Silico Docking and Radioligand Replacement Assay
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The Boron Advantage: The Evolution and Diversification of Boron’s Applications in Medicinal Chemistry
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Comparative Study of inorganic, Boron-Rich Cluster and Organic, Phenyl Adenosine Modifications: Synthesis and Properties
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