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Synthesis of Purine Conjugates with Bis-Carboranyl Derivatives of (S)-Lysine or (S)-Glutamic Acid
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Nucleoside–Metallacarborane Conjugates for Base‐Specific Metal Labeling of DNA
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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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Boron Clusters − A New Entity for DNA‐Oligonucleotide Modification
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Multicomponent Synthesis of Purines and Pyrimidines: From the Origin of Life to New Sustainable Approaches for Drug‐Discovery Applications
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Metallacarboranes as Labels for Multipotential Electrochemical Coding of DNA. [3‐Chromium bis(dicarbollide)](‐1)ate and Its Nucleoside Conjugates
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Boron neutron capture therapy (BNCT): a unique role in radiotherapy with a view to entering the accelerator-based BNCT era
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New boron-containing 2′-deoxyadenosines
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New nido-carborane-containing conjugates of purine: synthesis and antiviral activity
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Synthesis of novel biotin-based carborane amides
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Purification of Laboratory Chemicals
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The evolution of nucleoside analogue antivirals: A review for chemists and non-chemists. Part 1: Early structural modifications to the nucleoside scaffold
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A heparin conjugate, LHbisD4, inhibits lymphangiogenesis and attenuates lymph node metastasis by blocking VEGF-C signaling pathway
inferredcites →https://doi.org/10.1016/j.bmc.2005.12.060openalex-extracted
The purines: Potent and versatile small molecule inhibitors and modulators of key biological targets
inferredcites →https://doi.org/10.1016/j.bmc.2008.07.043openalex-extracted
Design and SAR of new substituted purines bearing aryl groups at N9 position as HIV-1 Tat–TAR interaction inhibitors
inferredcites →https://doi.org/10.1016/j.bmc.2012.09.039openalex-extracted
Effect of adenosine modified with a boron cluster pharmacophore on reactive oxygen species production by human neutrophils
inferredcites →https://doi.org/10.1016/j.bmc.2016.08.028openalex-extracted
In vitro antileukemic activity of novel adenosine derivatives bearing boron cluster modification
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Novel lopinavir analogues incorporating heterocyclic replacements of six-member cyclic urea––synthesis and structure–activity relationships
inferredcites →https://doi.org/10.1016/j.bmcl.2014.05.010openalex-extracted
Modulation of human neutrophil activity by adenosine modified with a carborane pharmacophore
inferredcites →https://doi.org/10.1016/j.ccr.2020.213753openalex-extracted
Carborane-containing amino acids and peptides: Synthesis, properties and applications
inferredcites →https://doi.org/10.1016/j.drudis.2017.08.009openalex-extracted
Towards carborane-functionalised structures for the treatment of brain cancer
inferredcites →https://doi.org/10.1016/j.ejmech.2021.113607openalex-extracted
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
inferredcites →https://doi.org/10.1016/j.ejps.2017.09.036openalex-extracted
Insight into lipophilicity of deoxyribonucleoside‑boron cluster conjugates
inferredcites →https://doi.org/10.1016/j.elecom.2006.12.010openalex-extracted
Nucleoside–metallacarborane conjugates for multipotential electrochemical coding of DNA
inferredcites →https://doi.org/10.1016/j.jorganchem.2005.01.043openalex-extracted
Acidic hydrolysis of N-acyl-1-substituted 3-amino-1,2-dicarba-closo-dodecaboranes
inferredcites →https://doi.org/10.1016/j.jorganchem.2005.01.056openalex-extracted
Synthesis of carborane analogues of γ-aminobutanoic acid
inferredcites →https://doi.org/10.1016/j.jorganchem.2008.12.061openalex-extracted
Nucleoside–boron cluster conjugates – Beyond pyrimidine nucleosides and carboranes
inferredcites →https://doi.org/10.1016/j.jorganchem.2011.08.031openalex-extracted
A convenient approach towards boron cluster modifications with adenosine and 2′-deoxyadenosine
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Reactions of closo-dodecaborate amines. Towards novel bis-(closo-dodecaborates) and closo-dodecaborate conjugates with lipids and non-natural nucleosides
inferredcites →https://doi.org/10.1016/j.omto.2022.01.005openalex-extracted
Carboranes as unique pharmacophores in antitumor medicinal chemistry
inferredcites →https://doi.org/10.1016/j.poly.2005.06.046openalex-extracted
Preparative and structural studies on sulfur-linked carborane icosahedra: 2-Phenyl-ortho-carboranyl-sulfur systems (2-Ph-1,2-C2B10H10)2X (X=S, S2 or SO), and ortho-carboran-di-yl systems (1,2-C2B10H10Y)2 (Y=S or SO)
inferredcites →https://doi.org/10.1016/j.poly.2012.05.036openalex-extracted
Novel bis[(1,2,3-triazolyl)methyl]carborane derivatives via regiospecific copper-catalyzed 1,3-dipolar cycloaddition
inferredcites →https://doi.org/10.1016/s0020-1693(00)81619-9openalex-extracted
Dichloro(6-aminoethylaminopurine)platinum(II) and its hydroxy analogues: Synthesis and preliminary evaluation
inferredcites →https://doi.org/10.1016/s0022-328x(99)00129-1openalex-extracted
Nucleic acids and nucleosides containing carboranes
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Challenges and Opportunities for the Application of Boron Clusters in Drug Design
inferredcites →https://doi.org/10.1021/acs.joc.2c00151openalex-extracted
N-Aminoacyl-3-amino-nido-carboranes as a Group of Boron-Containing Derivatives of Natural Amino Acids
inferredcites →https://doi.org/10.1021/acs.organomet.9b00228openalex-extracted
Tethered N-Heterocyclic Carbene-Carboranyl Silver Complexes for Cancer Therapy
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Multitargeted Compounds Derived from (2,5-Dioxopyrrolidin-1-yl)(phenyl)-Acetamides as Candidates for Effective Anticonvulsant and Antinociceptive Agents
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Rapid Cage Degradation of 1-Formyl- and 1-Alkyloxycarbonyl-Substituted 1,2-Dicarba-closo-dodecaboranes by Water or Methanol in Polar Organic Solvents
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The preparation and characterization of several meso-tetracarboranylporphyrins
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Efficacy of Base-Modification on Target Binding of Small Molecule DNA Aptamers
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Carborane- or Metallacarborane-Linked Nucleotides for Redox Labeling. Orthogonal Multipotential Coding of all Four DNA Bases for Electrochemical Analysis and Sequencing
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Insights into Soluble Guanylyl Cyclase Activation Derived from Improved Heme-Mimetics
inferredcites →https://doi.org/10.1021/la702852eopenalex-extracted
Aggregation Behavior of Nucleoside−Boron Cluster Conjugates in Aqueous Solutions
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DNA-Dinucleotides Bearing a 3‘,3‘-Cobalt- or 3‘,3‘-Iron-1,2,1‘,2‘-dicarbollide Complex
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Lithiacarboranes and 1,2,4-triazine 4-oxides: S N H reactions and ring transformations
inferredcites →https://doi.org/10.1039/b203730kopenalex-extracted
Synthesis of a porphyrin-labelled carboranyl phosphate diester: a potential new drug for boron neutron capture therapy of cancer
inferredcites →https://doi.org/10.1039/c4nj01096eopenalex-extracted
Nucleoside bearing boron clusters and their phosphoramidites – building blocks for modified oligonucleotide synthesis
inferredcites →https://doi.org/10.1039/d2nj02994dopenalex-extracted
(7,8-Dicarba- nido -undecaboran-7-yl)acetic acid: synthesis of individual enantiomers and the first example of the determination of the absolute configuration of chiral monosubstituted nido -carborane
inferredcites →https://doi.org/10.1070/rcr4772openalex-extracted
Purine derivatives with antituberculosis activity
inferredcites →https://doi.org/10.1080/00397919508011794openalex-extracted
Easy Synthesis of Unnatural Siderophores
inferredcites →https://doi.org/10.1080/15257770701548733openalex-extracted
2′-Deoxyadenosine Bearing Hydrophobic Carborane Pharmacophore
inferredcites →https://doi.org/10.1134/s0012500810090090openalex-extracted
1,3-Dipolar cycloaddition of [(o-carboran-1-yl)methyl]azide to alkynes
inferredcites →https://doi.org/10.1248/cpb.c17-00997openalex-extracted
Syntheses and Biological Evaluation of Novel Hydroxamic Acid Derivatives Containing Purine Moiety as Histone Deacetylase Inhibitors
inferredcites →https://doi.org/10.3390/cancers13153855openalex-extracted
Interaction of Adenosine, Modified Using Carborane Clusters, with Ovarian Cancer Cells: A New Anticancer Approach against Chemoresistance
inferredcites →https://doi.org/10.3390/ijms19113501openalex-extracted
DNA Modified with Boron–Metal Cluster Complexes [M(C2B9H11)2]—Synthesis, Properties, and Applications
inferredcites →https://doi.org/10.3390/ijms232213726openalex-extracted
Carborane-Containing Folic Acid bis-Amides: Synthesis and In Vitro Evaluation of Novel Promising Agents for Boron Delivery to Tumour Cells
inferredcites →https://doi.org/10.3390/molecules23081846openalex-extracted
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
inferredcites →https://doi.org/10.3390/ph15050573openalex-extracted
Substituted Purines as High-Affinity Histamine H3 Receptor Ligands
inferredcites →https://doi.org/10.4155/fmc-2018-0517openalex-extracted
Comparative Study of inorganic, Boron-Rich Cluster and Organic, Phenyl Adenosine Modifications: Synthesis and Properties
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